Bringing Extinct Species Back to Life | Dr. Beth Shapiro

Dr. Beth Shapiro, PhD, is an evolutionary biologist and Chief Science Officer at Colossal Biosciences. Her work focuses on de-extinction and wildlife conservation efforts. We discuss genetic differences among humans, and how ancient DNA and modern embryology are being used to de-extinct and protect woolly mammoths, dodo birds, and dire wolves, as well as to help conserve endangered species. We also explore the ethical implications of de-extinction and how synthetic biology can help build a more bio diverse and resilient world. Read the full episode show notes at hubermanlab.com. Thank you to our sponsors AG1: https://drinkag1.com/huberman Joovv: https://joovv.com/huberman Eight Sleep: https://eightsleep.com/huberman Function: https://functionhealth.com/huberman Timestamps (00:00:00) Beth Shapiro (00:02:35) What is a Species?, Taxonomy, Bison (00:09:13) Neanderthals, Denisovans, Homo Sapiens (00:12:38) Sponsors: Joovv & Eight Sleep (00:15:27) Hybrid Ancestry, “Grolar” Bears (00:20:30) Homo Sapiens & Neanderthal Interbreeding, Genes; Denisovans (00:25:53) Neanderthal Genes, Immunity, Red Hair; Eye Color (00:30:17) De-Extinction, Species Selection, Woolly Mammoths (00:38:08) Sponsor: AG1 (00:39:21) Bird De-Extinction, Dodo; Reproduction & Genes (00:47:40) Development Biology, Woolly Mammoth, Elephants (00:54:49) Dire Wolf, Synthetic Biology, Ethics (01:03:26) De-Extinction, Ecology, Conservation, Ethics (01:09:22) Ecosystem Resilience, Thylacine; Preventing Extinction, Quolls (01:15:45) Sponsor: Function (01:17:23) Modeling Ecological Impact, Mosquitoes, Gene Drives; Panthers (01:25:50) Advisory Panels, Synthetic Biology Education (01:29:13) Genetic Selection in Humans, Human-Shaped World (01:38:25) Black-Footed Ferrets, Genetic Rescue (01:47:05) Dire Wolf; Ecological Modeling, New Technology & Public Fear (01:55:09) Artificial Wombs; Current Issues, Conservation & Red Wolf (02:01:26) Science Pioneers; Colossal Public Education (02:04:31) Beth’s Science Origin Story; Dinosaurs (02:13:42) Zero-Cost Support, YouTube, Spotify & Apple Follow, Reviews & Feedback, Sponsors, Social Media, Neural Network Newsletter Disclaimer & Disclosures Learn more about your ad choices. Visit megaphone.fm/adchoices

Speaker names marked ? are inferred from speaking time and the show’s known hosts — they are not voice-verified.

• 0:00Speaker 00

  So our dire wolves, they have 20 edits that we picked and we sequenced genomes from fossil dire wolves. We learned from those genomes what genetic changes made those animals bigger, more robust, light colored in coat. And then we engineered those changes into a gray wolf genome to recreate the dire wolf. You know, I often get the question of, why are you thinking about bringing extinct species back to life? Why aren't you thinking about helping living species not become extinct? And the answer is, we are doing both. It is the same tools. It's the same technology. It's the same needs. And when we excite people

• 0:40Speaker 00

  with the idea of mammoths and dodos and thylacines, we get more engagement and enthusiasm and investment in developing the technology that we can use to stop living species from becoming extinct.

• 0:52Andrew D. Huberman?

  Welcome to the Huberman Lab Podcast, where we discuss science and science-based tools for everyday life.

• 1:01Andrew D. Huberman?

  I'm Andrew Huberman, and I'm a professor of neurobiology and ophthalmology at Stanford School of Medicine. My guest today is Dr. Beth Shapiro. Dr. Beth Shapiro is an evolutionary biologist. She was a professor at UC Santa Cruz and an investigator with the Howard Hughes Medical Institute before leaving to become Chief Scientific Officer at Colossal Biosciences. Her work at Colossal is focused on what is called de-extincting species, such as the woolly mammoth, the dodo bird, and the dire wolf, meaning bringing them back to life. But that entire initiative is also about species preservation more broadly and how genomics can be used to improve the global ecosystem. In this episode, we discuss what it means to use ancient DNA to bring back extinct species, which then led us to a broader

• 1:46Andrew D. Huberman?

  discussion about genetic engineering in human health, both of which, by the way, are happening right now. So this is not just a projection into what's coming in the future. As you'll see, Dr. Beth Shapiro is truly a one-of-a-kind thinker. And today, you'll learn the science, the ethical implications, and the positive potential of using genetics to de-extinct species and using genetic selection and genetic tools to change humans. And no, Dr. Beth Shapiro is not planning to bring back dinosaurs, and today, you'll learn why. Before we begin, I'd like to emphasize that this podcast is separate from my teaching and research roles at Stanford. It is, however, part of my desire and effort to bring zero cost to consumer information about science and science-related tools to the general public. In keeping with

• 2:29Andrew D. Huberman?

  that theme, today's episode does include sponsors. And now for my discussion with Dr. Beth Shapiro. Dr. Beth Shapiro, welcome.

• 2:37Speaker 00

  Thank you.

• 2:38Andrew D. Huberman?

  Longtime fan of your work.

• 2:39Speaker 00

  Same.

• 2:40Andrew D. Huberman?

  Love animals, love stories about animals that aren't around anymore. Heard that you're going to bring back the woolly mammoths, the dodo bird, and that you might have already done something to contribute to the proliferation of the black-footed ferret. I'm a big fan of mustelids, of which ferrets are. We're going to talk about all of that today, including the ethical implications and so on. But I have a very basic question, which is, how do you decide what a species is? Because you have a degree in zoology. I always wanted to get a degree in zoology. But a few years ago, we got this thing called DNA sequencing. We can look at ancient DNA, can look at skeletons. People have done that for a long time. And my understanding is that it's completely revised, the understanding of

• 3:24Andrew D. Huberman?

  the relationship between different animals and the number of branches in these phylogenetic trees. So what have we learned that I think people might appreciate understanding about taxonomy? And like, is my dog as a bulldog mutt really the same as a chihuahua? Are they really the same species?

• 3:41Speaker 00

  Right. That's a really fascinating way to put it. And I think the most important thing that most people probably don't think about is that biology doesn't care what species you are. Species is a human concept. We have this incredible proclivity to want to put things into boxes so that we can talk about them, so that we can have conversations or share stories or share memories. In order to share something, we have to know what to call it. That's one of the reasons language has been so fundamental to the evolution of our species and our social structures. So what is a species? Probably when you learned about species in biology class when you were in middle school, you learned about Ernst

• 4:25Speaker 00

  Mayer's biological species concept.

• 4:27Andrew D. Huberman?

  Kingdom phylum, order, genus, species, like this kind of thing, clade, you know?

• 4:31Speaker 00

  No, that's the taxonomy, right? So we have Linnaeus came up with this idea of doing taxonomy, right? So here's an interesting taxonomy story. I've spent a lot of my career working on bison, for unfortunate reasons, probably, or fun reasons or whatever, but a lot of time working on bison. And bison were called buffalo, buffalo, right? We think of American bison as buffalo. It's the same thing, the same thing. But bison is the taxonomic name that was given to American buffalo by Carl Linnaeus, because when Europeans were going around the world and finding for the first time, Europeans had seen all these different animals, if they saw a big animal that looked like it would make a good coat,

• 5:11Speaker 00

  that was called a buff coat, they called it a buffalo or a buffalo, right? So we have African buffalo and Asian buffalo and American buffalo, and they are not related to each other at all, if you look at their DNA. But they all have the same name because they all made a good coat at some point, or at least there was the idea that they would. But taxonomists found this to be very disturbing. We want to know what animal we're talking about when we say the buffalo. And so this is why Carl Linnaeus comes up with this scheme, the American bison, the American buffalo is called bison, bison. In fact, the plains bison is called bison, bison, bison. That's a genus and a species and a subspecies that are all the same thing.

• 5:53Andrew D. Huberman?

  That's the Latin name, bison, bison, bison?

• 5:55Speaker 00

  Bison, bison, bison.

• 5:56Andrew D. Huberman?

  It's almost as humorous as, I think it's gorilla, gorilla?

• 5:59Speaker 00

  Yes.

• 6:00Andrew D. Huberman?

  Or the gorilla?

• 6:00Speaker 00

  Gorilla, gorilla. And llama, llama. That's one of my favorites, too.

• 6:02Andrew D. Huberman?

  Love it.

• 6:03Speaker 00

  Anyway, taxonomy. So we have these taxonomic ways of thinking about things, and that sorts everything into your deep evolutionary history. But species concepts are what people use to try to say, okay, I have this animal. Is it in the same species as this other animal or a different species from this animal? And the species concept that you probably learned, Ernst Mayer's, is the biological species concept, which says, if they can breed and their offspring are fertile, then they're the same species.

• 6:30Andrew D. Huberman?

  Which seems like a good place to start.

• 6:33Speaker 00

  It's a good place to start.

• 6:34Andrew D. Huberman?

  Because even in my understanding from my fly biologist friends, is that you can't mate drosophila with another species of fly and get a fertile offspring. So even among flies, there's some restriction. And what's wild is that flies and mammals of all sorts seem to know. Like, they actually don't try to mate, in most cases. They don't try to mate with other species, which is fascinating in its own right.

• 6:58Speaker 00

  We might beg to disagree there. I mean, if you've seen your dog tries, your dog probably tries to mate anything it comes across.

• 7:04Andrew D. Huberman?

  He just hit seven months. I've not seen him hump a single time. He's still intact. This time, I'm keeping my dog intact. We can talk about the reasons for that. It's health reasons. I might get him a vasectomy. People, we never talk about this, right? You can keep your dog intact and just give him a vasectomy if you don't want him to breed. Right? Yeah. Right? A guest on this podcast said that, an animal expert from the Carolins.

• 7:22Speaker 00

  That makes so much sense.

• 7:23Andrew D. Huberman?

  She said, you know, in Scandinavia, it's actually, she claims, and I believe her, that it's illegal to neuter a male dog unless there's a health reason. In Scandinavia and Australia, the inverse is true. Of course, they're upside down, but we'll forgive them for that. But yeah, they need their hormones for proper brain development.

• 7:40Speaker 00

  Right.

• 7:40Andrew D. Huberman?

  And we worry about them running around and breeding. There is this thing called the vasectomy, which is actually less invasive a procedure than the full neuter. Anyway, we don't want to digress too much. Like, my dog doesn't try and mate. I didn't see my previous dog try and mate with cats or with, or even chihuahuas, you know?

• 7:57Speaker 00

  Do you think Neanderthals and humans are different species?

• 8:00Andrew D. Huberman?

  I don't know, but I want to know if we are all the same species. This is an edgy topic, right? But if humans, I mean, if it's somewhat based on nomenclature, and if there's enough genetic variation out there, is it the case that people that we call people are actually divergent enough in terms of their DNA, that two people are not necessarily both homo sapiens, that there's some homo sapiens with an asterisk? I'm not trying to cast any hierarchy. They can just be different.

• 8:30Speaker 00

  So you're referring to a different species concept, which is the genetic species concept, where an organism is classified based on some threshold of sequence similarity. And that is a species concept that is as valid and valuable a species concept as the biological species concept, which says you can't interbreed. If you're interested in conserving species, you might use a geographic species concept that says, if you live here, you're a Florida panther, but if you live in Texas, you're a Texas panther. We're going to call you different species. Biology doesn't care about your species concept. Your species concept is something that you have adopted to have a conversation with another person about a particular topic.

• 9:12Andrew D. Huberman?

  Educate us on this Neanderthal piece. I know this is a topic very close to home, given that your husband works on these issues, and we can, maybe we'll get him on here separately. But feel free to steal his thunder in any way that you feel.

• 9:25Speaker 00

  My husband, Ed Green, was part of Svanti Pava's group when they were assembling the Neanderthal genome. And so he spent a lot of time thinking about Neanderthal. I think what's interesting from a species concept Well, if we start there with what's going on with Neanderthals is we now know, based on studying DNA, both from Neanderthals that used to be alive and a different lineage of human called Denisovan, we call it this, that was first isolated again by Santi Pabu's research group from a tiny little finger bone that they found in a cave, Denisova Cave in Russia, that's why they're called Denisovans. We know that there were multiple different species or lineages, or whatever you want to call them, of human-like people that were

• 10:06Speaker 00

  alive at the same time. And we know that after people moved out of Africa to colonize Europe, they met our ancestors, Homo sapiens, anatomically modern humans, everything you want to call them, they met groups of Neanderthals and they bred with them. So if they were a different species, they were violating the biological species concept at this point. So again, species concepts are just what we make of them. And today, most people have somewhere between 2% and 5% of their DNA that is from this admixture event, this hybridization event between anatomically modern humans dispersing out of Africa and the Neanderthals that were already in Europe.

• 10:48Andrew D. Huberman?

  Many questions about this. First of all, and try not to laugh, the silhouette diagram that we've seen of apes gradually in sort of time sequence, working their way to bipedal and upright. When we see that diagram, is that substantiated by the fossil record?

• 11:04Speaker 00

  It is, yes. We know that the lineage that eventually became us evolved in Africa. We can trace ancestry back to apes and then to primates, or primates and then to apes, and then eventually to us. The fossil record in Africa is very fragmentary. One thing that's really been really fun about working in ancient DNA is the field of paleoanthropology is pretty contentious because there are so few bones that are out there that if someone finds a bone and it's a partial fragment of a jaw with a piece of a tooth in it, they can use that bone to completely revise what we think has happened in human evolutionary history. And maybe they're right and maybe they're not, and they're smart and they've been thinking about these things and they compare it to all the other bones. So there's

• 11:45Speaker 00

  a lot there. What's brilliant about ancient DNA is that if I can find a little pinky bone in a cave in Denisova, right, and I can get DNA from that, I know that my bone has ancestors, right? If I have a bone that might be somewhere on that lineage to human evolution, I don't know that that bone has descendants. I don't know that that bone is part of our actual family tree, or if it's another one of the dead ends that went in a different direction and eventually became extinct. But that is one of the coolest things about being able to sequence one of these bones, because now you know what it is. And now you can line it up against all the DNA from all of the people that are alive

• 12:26Speaker 00

  today and discover things like, we all have ancestry because there was breeding between these lineages because they could, and because I think that if they can, they do.

• 12:38Andrew D. Huberman?

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• 14:03Andrew D. Huberman?

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• 14:44Andrew D. Huberman?

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• 15:27Andrew D. Huberman?

  It's interesting, right? Because if you took the far ends of the spectrum of the, you know, the old world primate, you know, apes, and then the upright human walking, my assumption is that, let's just say you used artificial insemination, that you wouldn't actually get viable, reproductively competent offspring from those. But at some point, you know, two different species, again, it's a nomenclature or two, some point, but two non-genetically similar, I don't want to say identical, because they're not twins, right? So I don't have a language here, forgive me. But you can get breeding across species and get reproductively viable offspring. That has to be the way this happened, right? It couldn't have just been through spontaneous mutations that suddenly took animals from quadrupeds to bipeds.

• 16:11Speaker 00

  No, this is a very long and slow evolutionary process. It's actually a really good question, and I think it's an open question in evolutionary biology. And it's probably different. Evolution does happen because of random mutations that accumulate in a genome. And if you think about what might happen if two lineages are isolated from each other for a really long time, and in different habitats, say, this lineage is adapting to the habitat that's it's in. Maybe it's, you know, very rainy, and there's a lot of water, and there's a lot of floral plants. And over here, it's drier and there's really scrubby plants. There's different selective environments. And as mutations arise in that genome, different ones will go to fixation. The size of the population also matters. If a population

• 16:55Speaker 00

  is really small, even mutations that arise that are bad can become fixed in that population just because the population is small and it just happens by chance. And so over time, these two will become more and more different from each other. So what happens when they come back in contact with each other? I think it will really depend on what those mutations that arose over that time was. It could be that there's a very short evolutionary time, but a mutation has arisen that means the sperm can't fertilize the egg, or the egg can't subdivide properly if you have a hybrid ancestry. Or it could be that nothing really has happened over a really long evolutionary time, and admixture can happen. Humans and

• 17:38Speaker 00

  Neanderthals diverged somewhere 300,000 to 500,000 years ago. That's not very long ago in evolutionary time. Brown bears and polar bears diverged about half a million years ago, and we know that they can readily interbreed and do whenever they overlap in habitat. Yeah, they're called growler bears or pizly bears, depending on which direction. I know, they're terrible names, right? You want a different name for this really queen.

• 18:03Andrew D. Huberman?

  Especially if you're a bear.

• 18:04Speaker 00

  Yeah. But that's been happening throughout their evolutionary history. We can see this because using ancient DNA, we were able to go back, we found a polar bear off the coast of Alaska that probably lived more than 100,000 years ago. And it had ancestry that we see in brown bears everywhere in the world, suggesting that that bear's ancestors at some point, or that bear's descendants had hybridized with brown bears, and that DNA got passed around. We know that during the last ice age, there were polar bears that got trapped on the ABC Islands in southeast Alaska. And when brown bears expanded from the mainland, they interbred with those polar bears. And brown bears, all alive in North America today, have polar bear ancestry that is because of that interbreeding 20,000 years ago or so.

• 18:49Andrew D. Huberman?

  Wow.

• 18:49Speaker 00

  Yeah. So in that case, a half a million years had gone by, they're really adapted to different habitats, and yet they can interbreed. But what's most interesting, and I think is relevant to your question, is that those hybrid bears only ever live and survive as brown bears. We see no evidence of brown bear DNA getting into polar bears. And that is, again, because of how evolution has worked. And especially interesting because it only really happens in the direction where the mom is a polar bear and the dad is a brown bear. Polar bears are induced ovulators, so the presence of a male will call them to ovulate, cause them to ovulate. So you can imagine a situation where a brown bear wakes

• 19:31Speaker 00

  up from hibernation, goes on to polar bear habitat to scavenge for food, comes across a polar bear female, induces ovulation, and they mate. The other way around, where a polar bear male finds a seasonally ovulating brown bear female, probably wouldn't happen because the timing of overlap wouldn't be right. And also, he would probably kill her rather than mate her because of the size difference and difference in what they're doing. So why is it then that since bears live with their moms, all the brown bears that we see that have polar bear ancestry are brown bears, not polar bears? We were working with some polar bear biologists, we were doing this analysis many years ago. And their hypothesis was simply that if you have brown bear ancestry, you don't have perfectly white fur, and you cannot successfully hunt seals. So it is just adaptation that

• 20:16Speaker 00

  means that that admixture doesn't work, right? So even though there's no problem with sperm and egg mixing, and the animal is born, they cannot survive as polar bears. And so polar bear stays separate from brown bear in that way.

• 20:30Andrew D. Huberman?

  I'm going to bring up dogs again, but in the back of my mind is a conversation about humans and this question about different species of, prior to Homo sapiens, or Homo sapiens and nearby species having reproductively competent offspring. So in the dog world, it's well known that the English Bulldog, which has a big head, small hips, is the byproduct of many crossings, but it's basically the bull mastiff and the pug. And this was an attempt to generate an animal with a short snout so it could clamp down for bull baiting, which fortunately is an illegal sport now, to clamp down and not get shaken off by the bull very easily. The floppy face is associated with a lack of pain receptors. So a bunch of things in the bull mastiff lineage that they want,

• 21:13Andrew D. Huberman?

  but they wanted a low center of gravity, so they took the pug. But when you cross them, of course, the females can't give birth because the birth canal just doesn't allow for it.

• 21:21Speaker 00

  Right.

• 21:22Andrew D. Huberman?

  Humans realize this pretty quickly and they learn cesarean section. So I could imagine a situation, although I don't tend to think like this. Today, I'm imagining a situation where Homo sapiens and some other non-Homo sapien human-ish species were having sex, sometimes getting pregnant, but the babies would always die because the birth canal and the structure of the pelvis wasn't quite right to allow the head size through, which, you know, there are a lot of, I hear a lot of arguments that, you know, humans sort of optimized for just enough space so that the large-brained humans, you know, we love to talk about how big our brains are, right, could pass through, but no larger and not much smaller in most cases.

• 22:01Speaker 00

  One of the reasons that giving birth is one of the ways that women have died in our evolutionary history.

• 22:05Andrew D. Huberman?

  Right. And cesarean sections, I probably have changed human evolution in that sense, as has aseptic, you know, conditions and things like that.

• 22:13Speaker 00

  Absolutely. For me, my child was cesarean birth, so.

• 22:16Andrew D. Huberman?

  Right. So I like to think you would have survived anyway. But the, but I could imagine a mutation that was an adaptive mutation where suddenly this other species, which maybe had a smaller pelvis, a female could deliver this child live, the mother survived as well. And then that DNA, you know, propagates so that there are now humans, maybe it's been bred out, but that there are or were humans walking around who are not completely Homo sapien. Or is it not, not possible?

• 22:45Speaker 00

  I don't know about what's known about hip size or anything like this, but, but it is true that humans and our archaic cousins Neanderthals interbred and that people walking around today have Neanderthal DNA.

• 22:57Andrew D. Huberman?

  Two to 5%, you said?

• 22:58Speaker 00

  Two to 5%. What's interesting about that, and it touches a little bit on the adaptation component that you, you raised, is that I think most people, or a lot of people have heard this number, we have 2 to 5% Neanderthal DNA. Less well-understood is that it's a different 2 to 5%. Like, the 2% Neanderthal that is in my genome is different from the 2% or maybe 5% Neanderthal that's in your genome is different than the next person.

• 23:25Andrew D. Huberman?

  So it could be heart, liver, skeleton, and spleen for me, and it could be some other constellation for you.

• 23:30Speaker 00

  Could be anything. And if we were to go around the world today and pick out all of the pieces of Neanderthal DNA that exist in humans today, we would put together more than 90%, possibly more than 95% of the Neanderthal genome, just from people who are alive today. And that tells us that most of the Neanderthal genome was not maladaptive for people, that pretty much all of it could get passed on and live in healthy humans today.

• 24:01Andrew D. Huberman?

  Interesting.

• 24:01Speaker 00

  We don't know what happened in the other direction, right? We, we see Neanderthal bones and there hasn't really been any evidence of humans admiring with Neanderthals. There has been evidence of hybrids between Neanderthals and Denisovans. This is really one of the most exciting things that ancient DNA has been able to contribute, I think, to understanding human disease and human medicine and what it means to be human. Because before we had the Neanderthal genome, if we wanted to know what in our DNA makes us human, we would have to compare all the humans that are alive today with our closest living relative, just a chimpanzee or a bonobo. So there's 3 to 5 million years of time between when we shared a common ancestor and a lot of change happens in 3 to 5 million years in

• 24:45Speaker 00

  your DNA. And some of it is useful, some of it is what makes us human, and most of it is just not. It's just changed because copying errors during copying cells and that's what happens. That's how we're different. Every child that's born has about 100 differences compared to their parents because of copying error in the process of making the sperm and making the eggs that made that kid. So when we got the Neanderthal genome, that 3 million to 5 million year long branch leading to us was shortened to 300,000 to 500,000 years by an order of magnitude. So now, if we want to know what it is that makes us human, we have a much smaller list of mutations or variants that we can look

• 25:26Speaker 00

  at. And because we now know that 95% say of the Neanderthal genome exists in people today, we've narrowed that list down even further to that other 5%. What's going on in that 5% of the genome where no living person has Neanderthal DNA? That is where the stuff that the baby had to have the human version in order for that baby to survive. And that's where we look to see what it is that made us human.

• 25:53Andrew D. Huberman?

  A few years back, when 23andMe and these other companies started making genomics in humans easier and more affordable, a lot of guys boast about Neanderthal DNA being vigor genes, whereas women try and downplay the amount of Neanderthal DNA that they have when they get their results. I found that interesting. Is there any evidence that the Neanderthal genes are quote unquote vigor genes, that they allow for more durability of human, male or female?

• 26:21Speaker 00

  It's an interesting question. If you just look at that 2 to 5% of Neanderthal DNA that we all have, most of it is not anything that is under selection. So you see it at about 3% frequency or so in different populations. What is interesting is when a piece of Neanderthal DNA is suddenly much more common in a population of humans, because that would suggest, I got some DNA from my Neanderthal ancestry and that bit of DNA suddenly made me more fit. Because I had that bit of Neanderthal DNA, I was able to survive and have more kids than everybody else. And so it increases in frequency compared to average. And this has been a really interesting thing to learn when you think about Neanderthal DNA. There are a couple of things that have come out. There are genes that are common in Latin

• 27:03Speaker 00

  American populations that come from Neanderthals that predispose to type 2 diabetes. There is another gene that I think was, again, in a Latin American population that makes people feel, I can't remember if it was more pain or less pain, but it did have to do with pain sensation. And I remember there was a trial of people in Colombia where they got to feel pain in some way. And there's a Neanderthal gene associated with this. But most of the really interesting ones have been at, in immune-related genes. During the pandemic, one of the first alleles that was discovered to be associated with negative risk or bad outcomes of COVID was a gene that came from Neanderthals. So it's a Neanderthal-derived

• 27:43Speaker 00

  gene that was at something like 50% frequency, so way above the 3% average frequency in Asian populations. And it, it made people more susceptible to the virus entering your lungs. And presumably, it only became that high frequency because it was protective against some other disease that was circulating in the past. But the trade-off of that is that it, of course, you know, made them more susceptible to COVID. There was another Neanderthal-associated allele that was actually protective against COVID. So I think our ancestors have been subjected to different diseases and pandemics and things that have happened throughout life. And we see the traces of that in, in ancient DNA. We can

• 28:24Speaker 00

  now go into graveyards in Europe and, and actually isolate plague from dirt and from bones from people who died of plague and look and see how their immune systems and genes have responded to exposure to, to things like this. It's really fascinating.

• 28:39Andrew D. Huberman?

  Wow. My redhead friends like to claim that they have more Neanderthal and therefore more vigor and pain resistance. So I'm guessing the study probably said more pain resistance.

• 28:50Speaker 00

  Probably.

• 28:50Andrew D. Huberman?

  We have pain experts on here that verify that indeed, on average, that redheads tend to require more anesthesia, on average. So that tracks. But were Neanderthals, were a lot of them gingers?

• 29:03Speaker 00

  Yes. This comes from studying at MC1R, a gene associated with the red melanin. Mammoths as well, they had, I mean, you can see mammoth, you can see mammoth mummies with the actual hair and you can see that they're kind of, I don't know if it's because they all bleached to red, but there definitely is a, some evidence from their genome that they had reddish colored hair. Yes.

• 29:21Andrew D. Huberman?

  Interesting. But maybe we could just briefly talk about eye color. Is it true that all blue-eyed people descended from a single blue-eyed human at one point? This almost sounds like some eugenics thing, but that's not why I'm asking. You also see a lot about how true green-eyed people are quite rare. Was there a time when the population of humans on earth had a lot more green-eyed people?

• 29:41Speaker 00

  I think all of the colors, if you, if you look at African populations, mostly, it's like me, dark, dark eyes. I think that's probably the ancestral state. But there are lots of different eye colors that have evolved. And I think they're selected for. I mean, people like things that are different and unique. And so people want to mate that has blue eyes and.

• 29:58Andrew D. Huberman?

  You really think that it was selected for?

• 30:00Speaker 00

  I think probably eye color was, was sexual selection. I, I don't know what other benefits blue eyes could have other than looking very, you know, stoic and cool as you're like trying to hunt down something on the.

• 30:14Andrew D. Huberman?

  Oh, genocides are so much fun because they're, they're willing to just go there. I was gonna ask you this question later, but I'll ask now because it relates to what we're on to now. You know, we tend to think of our lives in, in the time bin of our lives, you know, roughly 100 years if we're lucky, right? You know, at this stage of human evolution, for about 100 years, maybe 80, maybe, you know, if we're fortunate, 90, 100. But as somebody who studies long periods of time and what's happened to our species and other species across long periods of time, I'm always curious about this. I know you have to make your coffee in the morning and do everything, and, you know, manage your life like anybody else in, in the today and in the week and in the month and in the year. But do you, do you sit back and think of all the different tens and hundreds and thousands

• 30:56Andrew D. Huberman?

  and millions of years that you could focus on, I'm going to focus at this time bin, right? It's, it's an interesting way to live. Now, I'm just curious how you pick the problems that you choose to work on, because we'll talk about de-extinction. But, you know, why the woolly mammoth? Why not, like, get the Florida Panthers rebooted completely?

• 31:17Speaker 00

  Why not both?

• 31:18Andrew D. Huberman?

  Why not both? Right. But in terms of just, you know, where to focus, like, why bring back things from way back when as opposed to, you know, maybe we could name a few species that disappeared in the last 200 years, guessing there are quite a few.

• 31:32Speaker 00

  Yeah.

• 31:33Andrew D. Huberman?

  You know, how do you pick? And when you're making that decision, what's guiding it at the ethical level? What's guiding it at the practical level? Like, what, what really are you trying to accomplish? Because the stuff about humans is fun place to play and put in the backdrop, we'll return to it. But your work's really focused on the extinction. And like dinosaurs are one option, woolly mammoths are another. And, you know, just making sure that we don't lose any species that we've got right now also seems like a very, very important, indeed noble pursuit.

• 32:04Speaker 00

  Yes. There's, that's a very complicated set of questions there. I think I'll start with.

• 32:11Speaker 00

  What is motivating? And I think what's motivating is what drives the selection of the species. In fact, it's funny, I wrote a book a long time ago now called How to Clone a Mammoth. And the first chapter was how to pick a species. What are you going to do? How are you going to choose a species to bring back? And there are technical, ethical, ecological, and social reasons to pick any of the species that you can. Technical, these are the easiest, right? We can't bring a dinosaur back to life because we don't have dinosaur DNA. The oldest DNA that we have ever recovered from a bone is from a mammoth bone. A mammoth's bone probably dates to around one to two million years ago. It's hard to know how old it is in that time range because there's not a really clean

• 32:55Speaker 00

  way of dating something within that time range. But it's old. Dinosaurs went extinct more than 66 million years ago. So that's far outside of where we're going to get recoverable DNA.

• 33:05Andrew D. Huberman?

  And that's because the skeletons just don't.

• 33:07Speaker 00

  They're fossilized. They've turned into rock, right?

• 33:10Andrew D. Huberman?

  There's no shred of DNA left.

• 33:12Speaker 00

  Yeah, as soon as an organism dies, the DNA in its cells starts getting chopped up into smaller and smaller and smaller fragments until eventually there's nothing left. This is really by three processes. UV light, we know about this. It's why we wear sunscreen when we go outside. But the UV light hits your DNA and it actually breaks it. And when we're alive, we have proofreading enzymes that will come and fix your DNA. So you don't get cancer every time you go outside. But that is an energy requiring process. And after you die, there's no more energy. So the breaks from UV accumulate. Freezing and thawing is water molecules expand and will physically break the DNA fragment. So that's bad for DNA preservation.

• 33:53Speaker 00

  And most importantly, just microbial decay, the fungi, the bacteria that get into an organism when it's decaying and chew it up to transform that carbon and nitrogen into the next generation of organisms, right? And so that process is slower in some environments than others. Exactly in the same way that your sandwich will rot faster if you leave it in the sun versus in the shelf versus in the fridge versus in the freezer. DNA will preserve for longer in the cold Arctic where things are rapidly buried in frozen dirt and they stay that way for a million years, like this mammoth bone that we were able to recover DNA from. But if you die in a very hot, wet, swampy place like Mauritius, where the dodo lived,

• 34:37Speaker 00

  it's another one of the species that we're working on at Colossal, very little chance you're going to be able to recover DNA from any of the fragments that are on Mauritius Island. And I have tried like hundreds of bones from Mauritius. We have a great dodo genome, but it's from a bird that went to Europe alive on a ship and is part of the collection at the Danish Museum of Natural History. So you have to have a well-preserved sample that you can get DNA from. Ideally, many of them because you want to know what are the DNA changes that made a mammoth a mammoth instead of another type of elephant, right? So many of them will help you to do that. But one is good enough to get some sort of template for what you're going to do. You probably should know what caused that species to go extinct in the first place

• 35:20Speaker 00

  so that you don't bring something back that becomes the first species to be de-extinct and then the first species to be re-extinct.

• 35:29Andrew D. Huberman?

  Or bring back something really nasty that knocks out a bunch of other species.

• 35:33Speaker 00

  Yeah, you have to understand the role that that animal played in the ecosystem and whether that niche is still available. I mean, ecosystems don't live in a vacuum just waiting for something to come back. And in some cases, there's a real ecological driver for the species that we're focusing on. We feel like there is a real ecological role for these species to play, that these ecosystems are destabilized because of extinction. And by bringing back these key ecological interactions, we can make those ecosystems more robust and more resilient in the face of all the crap that people are always throwing at our natural ecosystems.

• 36:10Andrew D. Huberman?

  Could you give me an example of that? So if you were to bring back woolly mammoths, I'm guessing that's not going to save the Amazon forest, but what probably is going to do something useful based on what you just said?

• 36:21Speaker 00

  Yeah, so if you think about what large animals, large herbivores do in their ecosystem, they churn the soil by walking around. They knock down things. Elephants knocked down trees. Mammoths probably lived places above trees, so that wasn't what they were doing. But they were distributing seeds and nutrients. Have you heard of Pleistocene Park? This is up in northeastern Siberia. There are these two scientists, it's actually Sergey Zimov, who's a Russian Academy scientist, and his son Nikita, they've been running this park up in northeastern Siberia for a long time. And they have been really interested in understanding what happens when you restore all of the species that used to live on the tundra to the tundra ecosystem.

• 37:02Speaker 00

  And they have bison that they've brought in from Canada and wild horses and several species of deer and musk ox. And they've seen that having the animals on the landscape that they've fenced off actually causes the plants to come back with more ferocity. So these animals, they have to eat during the winter. So in order to find food, they scrape the snow off of the surface of the dirt. In the absence of these animals, the snow stays on the surface and snow is a very efficient insulator. So it traps the summer heat in that frozen sediment, causes the sediment to melt faster. And when the plants come back, it's a particular type of plant that can live in that moist sediment.

• 37:48Speaker 00

  With the animals, you get a mosaic landscape where there's some parts that are moist and wet. There are other parts that have been exposed and they're dry and colder. And you get broader diversity of plants that are coming back where these animals are. So they are essentially recreating their ecosystem just by being there.

• 38:08Andrew D. Huberman?

  I'd like to take a quick break and acknowledge our sponsor, AG1. I'm excited to share that AG1 has just launched their newest formulation, AG1 Pro. AG1 Pro takes the clinically backed AG1 formula, which is a blend of vitamins, minerals, probiotics, and adaptogens, and adds three important new ingredients, creatine monohydrate, calcium HMB, and zinc carnecine. Each serving has five grams of creatine monohydrate to support muscle strength and performance as well as brain health, calcium HMB to support muscle recovery and reduce muscle breakdown, and zinc carnecine to support and improve the lining of your gut. All three of these ingredients have compelling science to support them, and therefore I love seeing them added to the existing AG1 formula.

• 38:49Andrew D. Huberman?

  As most of you know, I've been taking AG1 every day for nearly 14 years now. I started taking it long before I even knew what a podcast was. It's a great product and it's now made even better with the new AG1 Pro formula. If you would like to try AG1 Pro, you can go to drinkag1.com/huberman to get a special offer. AG1 is giving away a free bottle of omega-3 coenzyme Q10 with your first subscription. Again, go to drinkag1.com/huberman to get a free bottle of omega-3 coenzyme Q10 with your first AG1 subscription. Okay, so you're picking, look, you don't have to pick a species, but you got to pick something of, you know, two or three.

• 39:28Speaker 00

  Right.

• 39:28Andrew D. Huberman?

  I can't say like, we're going to bring back everything from a given era. So.

• 39:33Speaker 00

  So we did technical, ethical, ecological. I think that another answer is what is going to make an impact, right? When I joined Colossal, we didn't have a bird program. But I really wanted there to be a bird de-extinction program because all of the tools that we are developing for de-extinction are the same tools that we can use to use synthetic biology to modify the genomes of living species and help them avoid becoming extinct. And so the kit that we're building from multiplex genome engineering to cellular rejuvenation to IPS cell technologies for wild animals, to even learning the link between particular

• 40:15Speaker 00

  letters of the DNA sequence and what those letters actually do to cause an animal to look the way that it does, right? All of that is applicable across the board. So the stack that we're building for de-extinction, for synthetic biology stack applies to synthetic biology for conservation. So when I joined Colossal and there wasn't a bird program, they had launched the mammoth program, which is a placental mammal, and the thylacine program or Tasmanian tiger, that's a marsupial mammal. But birds are among the most endangered species on the planet and it is not possible to clone birds using somatic cell nuclear transfer, the process that most famously brought us Dolly the sheep, because we don't have access to the egg cells at the right stage.

• 40:57Speaker 00

  So while that process is really pivotal and integral to our mammoth and thylacine and the other mammalian project, it's just not possible to use it for birds. And so I wanted a program that was going to help us develop technologies for birds. So why did we pick the dodo compared to any other bird for the first one?

• 41:17Andrew D. Huberman?

  Cool beak.

• 41:18Speaker 00

  It comes down to that, which I also think is a really important part of talking about this project. And it's the idea of awe. Of being excited about something. We get kids drawing animals that are drawing mammoths and violins and dodos and sending them to us all the time. Ben has put them in frames up around. Some of them are good.

• 41:40Andrew D. Huberman?

  The dodo with its sort of rounded top beak also, and the way the eyes are typically drawn, it also has a kind of cartoonish friendly Toucan Sam type of look.

• 41:51Speaker 00

  It was in Alice in Wonderland. Most of what we know about the dodo is from cartoonish drawings of this animal. There are some, and of course there are skeletons, that we can piece together using the many, many bones in Mauritius that do not have any DNA in them, based on my very best tries.

• 42:05Andrew D. Huberman?

  You didn't choose to bring back like a 75 foot long python, thank goodness. But there may be virtue in doing that.

• 42:11Speaker 00

  There might be, although I think there are plenty of pythons in Florida Everglades right now.

• 42:15Andrew D. Huberman?

  I'm not a snake fan. No disrespect to the snake lovers. But talk about bird developmental genetics for a second, not to scare anyone away, but hang in there. A few years ago, I saw something that two female condors can reproduce.

• 42:29Speaker 00

  Crazy.

• 42:31Andrew D. Huberman?

  Right? And this, of course, for

• 42:32Speaker 00

  It actually wasn't two female condors reproducing. It was one female condor.

• 42:36Andrew D. Huberman?

  One female condor.

• 42:37Speaker 00

  Just having an egg all on her own.

• 42:39Andrew D. Huberman?

  Yeah. And because of the socio-political implications, it's got people in what we're on from Northern California pretty excited. They were like, okay, we don't need men after all, right? That was the, that's always, that was the, you know.

• 42:50Speaker 00

  That's funny, because what I heard was, life finds a way.

• 42:53Andrew D. Huberman?

  So how did one female condor, who we trust her when she says that she never mated with a male condor, or a female condor, we believe her, was able to reproduce?

• 43:05Speaker 00

  My scientific explanation is that meiosis didn't fully separate, and she ended up having a fertilized egg or

• 43:12Andrew D. Huberman?

  We should explain meiosis. So the separating of the, of the

• 43:15Speaker 00

  Of the cells during the very early phase when you're making eggs or making sperm. You're trying to duplicate your cell, but instead of that, you make two versions of the cell that only have one copy each of your chromosomes. So when normally, in normal reproduction, an egg that has one copy of the set of chromosomes and a sperm that has one copy of the set of chromosomes come together, they're fertilized. The resulting eventually embryo has two copies, one from mom and one from dad. In this case, there was no sperm. There was an egg that had both copies, probably because of a mistake during meiosis. Like they didn't separate out properly, and that was able to develop full term.

• 43:52Andrew D. Huberman?

  Was the offspring viable?

• 43:54Speaker 00

  Yes.

• 43:55Andrew D. Huberman?

  What's weird about that, yes. I mean, it's very, very cool and very clear, the way you described it, how that could happen, because you need the two sets of chromosomes. So both sets came from mom, in this case, and only mom. But in humans where that happens, and it does happen on certain chromosomes, these homozygosity effects, they happen under certain conditions, like there are these paternal or maternal imprinted conditions like Prater-Willi syndrome, where paternal DNA gets kicked off and you have two copies from mom, which doesn't sound like a bad thing unless there are things on the paternal chromosome that are required for development.

• 44:30Speaker 00

  Right.

• 44:30Andrew D. Huberman?

  And the reverse also happens, like in Angelman syndrome, I think it is, that all the genes, that everyone healthy walking around out there, you and me, and have genes that only came from our mom and only from dad. And so if you get two copies from mom of a chromosome, or two copies from dad, you end up with like pretty severe deficits in brain development and other things.

• 44:52Speaker 00

  And some things. And you also could never be a boy, because the one gene that turns on that cascade of male development is called SRY. It's on the Y chromosome. So without that gene, you would never be a boy. You would always be a girl. Trisomies, where you get two copies from mom and one copy from dad, those can also be bad because of different levels of gene expression.

• 45:11Andrew D. Huberman?

  Down syndrome.

• 45:12Speaker 00

  Down syndrome is trisomy 21. And there are a few other trisomies that are compatible with life. Trisomy 21 is the most common one, because those people can live, obviously, with some challenges, additional challenges because the additional chromosome, but they can live full lives till relatively middle age.

• 45:30Andrew D. Huberman?

  Is there a way of looking back at the ancient DNA of different species and knowing if they reproduce the way we imagine they reproduce? I'm not talking about the actual verb sex. I'm talking about the, like, somehow sperm and egg met, but, or there was something more like the condor. You were just describing where the females were able to reproduce through these kind of unusual myotic events.

• 45:51Speaker 00

  I think because, well, obviously, sex has evolved a bunch of different times on the, on the animal or the tree of life, right? And so different ways of doing sex have evolved. So we have this XY process where the males are what we call the heterogamous sex. So the males have an X and a Y, and the females have two Xs and they don't have a Y. But birds do it differently. They have the WZ, and it's the females that have the two different chromosomes, the males that don't. And then there are, you know, alligators and crocodiles, and they do sex determination based on the temperature at which the egg is sitting during a very critical period during development.

• 46:29Andrew D. Huberman?

  Oh, yeah. Yeah, there's, there are communities online. I've learned that actually believe this kind of stuff for humans. There are all these theories about how to get a male or a female offspring based on position of intercourse, temperature, location, food. None of it beats chance.

• 46:44Speaker 00

  Right. Or if you really want ICSI, right, which is the process by which you take an egg and you take a particular sperm that you know whether it's carrying the Y chromosome or not, and use that to fertilize the egg.

• 46:55Andrew D. Huberman?

  Can you actually determine the XX or XY of the sperm? They can do that now?

• 47:00Speaker 00

  You can do it.

• 47:01Andrew D. Huberman?

  You can select, so you can do true sexual selection?

• 47:04Speaker 00

  You can. And it's because the Y chromosome is teeny, teeny tiny compared to the X, and so you can centrifuge them. And because they're smaller, they sort out.

• 47:13Andrew D. Huberman?

  Got it. So you can spin sperm around. Don't do this at home. And then based on how the different, things of different weights basically spin out to different depths. And so you can bias the likelihood that you'll get a XY carrying sperm or an XX carrying sperm.

• 47:27Speaker 00

  Or you can use cloning, like we are at Colossal, and like we're thinking about in synthetic biology, where you actually know the sex because you're starting with an actual somatic cell, a tissue cell of that animal, instead of using a sperm and an egg.

• 47:39Andrew D. Huberman?

  So let's talk about that. And before we do that, we should probably do a brief developmental neurobiology lesson. You beautifully told us what meiosis is. You know, sperm or egg, you have 20, well, in humans, it's 23 chromosomes, though you only have half so that they can meet in conception and then start to divide and create more cells that become the embryo, right? And so in these other species, I guess you know how many chromosomes there are, and I must use the woolly mammoth, because it's a fun one. And birds are complicated. As a developmental neurobiologist in my past, the bird stuff gets tricky, reptile stuff.

• 48:12Speaker 00

  Birds are tricky.

• 48:13Andrew D. Huberman?

  They're really tricky.

• 48:14Speaker 00

  Some birds are trickier than others. I did not know until I joined Colossal that there are some birds that have a, what's called a germline restricted chromosome, which doesn't exist in any of their cells except for the germline.

• 48:25Andrew D. Huberman?

  Germline or the sperm and eggs.

• 48:27Speaker 00

  Sperm and eggs. And it comes into being, this chromosome, just in the germline, and then it disappears.

• 48:33Andrew D. Huberman?

  Wow.

• 48:33Speaker 00

  I know. Biology is amazing. But birds have these like mini microchromosomes that are a pain to assemble. And if you're sequencing DNA from an extinct species where the DNA fragments are really short, and you have to do it by taking each one of those really short fragments and trying to figure out where on a whole genome it goes best on a computer. We don't actually do it with our, with like tweezers or anything like that.

• 48:54Andrew D. Huberman?

  But Yeah, the, birds are really cool animals, but they, from reproductive biology standpoint, it's tricky. So with, the woolly mammoth was a mammal?

• 49:03Speaker 00

  Yes.

• 49:04Andrew D. Huberman?

  Okay. And you know that because, I mean, people can say, well, duh, because people normally think, oh, it has fur, it must be a mammal. But that is not necessarily true, right? You have monotremes and all this other stuff. So you know it's a mammal because there's evidence of lactation? How are you deeming it a mammal?

• 49:19Speaker 00

  Using its genome. So we've been able to sequence whole genome sequences, high quality whole genome sequence, with sequences from multiple mammoths that date to the last million and a half years. And we can assemble those genome sequences using a computer. And then we compare them to other animals that are alive today. And we know that the closest living relative of a mammoth is an Asian elephant. And in fact, mammoths and Asian elephants are more closely related to each other than Asian elephants are to African elephants. So mammoths are nested within the elephant family, most closely related to Asian elephants.

• 49:55Andrew D. Huberman?

  Okay. So if you get the, the sequence of DNA from a mammoth, so you know, okay, this is the complete genome. And I think a lot of people probably don't realize that your complete genome is represented in most all of your cells. There are rare exceptions. It's just that not all those genes are expressed, which is why you get a hair cell versus skin cell versus heart cell and so on.

• 50:11Speaker 00

  That's the epigenome.

• 50:12Andrew D. Huberman?

  Right. But the menu is there.

• 50:14Speaker 00

  The menu is there.

• 50:15Andrew D. Huberman?

  Are you growing up DNA in a laboratory?

• 50:17Speaker 00

  No.

• 50:18Andrew D. Huberman?

  That is the mammoth sequence?

• 50:19Speaker 00

  So this is what comes, I think, from Jurassic Park. And this is why I love talking about Jurassic Park, because I think everybody has an idea of how we're doing this because they saw Jurassic Park, or they've thought about this movie. And what happened in Jurassic Park? And I should just say, it was not a documentary. So let's not get carried away here. Okay. What happened in Jurassic Park was scientists found mosquitoes preserved in amber. They stuck a needle into those mosquitoes preserved in animal. They sucked out a bit of stuff that happened to be blood and it had dinosaur DNA. And then they had the little dancing DNA thing tells you about how they piece it together. And you can see the little pieces of dinosaur DNA lining up next to each other.

• 51:04Speaker 00

  And then there's holes and they fill in those holes with frog DNA, which was a weird choice, even at the time, because we already knew that birds are dinosaurs. Right? So why they picked frogs? I don't know. But anyway, they filled in.

• 51:15Andrew D. Huberman?

  Maybe they talked to Richard Harland at Berkeley or something. That's another biology joke. Look it up.

• 51:19Speaker 00

  But that's not actually how we're doing this. What we're doing is somehow easier than that because we know that Asian elephants are the closest living relative of mammoths. We also can, by sequencing a bunch of Asian elephant DNA and sequencing a bunch of mammoth DNA, we can see that they already have almost exactly the same genome sequence.

• 51:41Andrew D. Huberman?

  How similar?

• 51:42Speaker 00

  They're about 99% similar. It depends on how you calculate the percentage and things like that.

• 51:46Andrew D. Huberman?

  As a point of reference, how similar are we to the chimpanzees in terms of percentage similarity of DNA?

• 51:53Speaker 00

  In that counting, it's about the same.

• 51:55Andrew D. Huberman?

  But some people might say, we don't look anything like chimpanzees.

• 51:59Speaker 00

  Well.

• 51:59Andrew D. Huberman?

  99 just sounds like so similar, like you're going to get the same thing.

• 52:02Speaker 00

  Yeah, well, there, I mean, people calculate this in lots of different ways. There's some statistic online that we're 85% the same as a banana or something like that, like a lot of our DNA is. I don't know if that's true, right?

• 52:12Andrew D. Huberman?

  Is the goal to recreate the ancient mammoth? Or is it to create a pseudo hybrid of the ancient mammoth?

• 52:19Speaker 00

  The goal is to think about a mammoth in terms of what it does and what it looks like. And this gets back to this idea that you brought up in the beginning about a species concept. This is one of the most common things that we hear. If you are going by a strictly genetic species concept, where you're saying that a species, an organism is classified just by some threshold of similarity, sequence similarity to something else, that's the only way you can call it that thing. That isn't what we're doing in de-extinction. That's not what anyone doing synthetic biology is thinking about when they're designing or engineering things to solve problems, engineering animals or engineering plants to solve problems that we have in the future.

• 52:57Speaker 00

  The genetic species concept is an idea that was proposed to classify organisms that evolve over a very long evolutionary bifurcating phylogenetic tree process, where accumulation of changes is over many generations over a long time. Our mammoths, our dire wolves are not created by that process. And so that concept really doesn't apply. I think that's where a lot of the disinformation comes. I'm going to just push back a little bit on this because what I don't want is for this sort of definitional gatekeeping to really take over and become the whole story. It's important. It's a question, but it's a narrow one. And I think it crowds out the real discussion about what it is that we're doing, how the

• 53:42Speaker 00

  technologies that we're developing can be applied to ecosystem health, to help stop species from becoming extinct, even as synthetic biology for, for human medicine. So we're not trying to make something that is identical to a particular individual that used to be alive. Our mammoths are millions of letters of DNA code different from each other. So even which one to use would be an open question. Instead, what we're doing is focusing on where all of those mammoths are the same as each other, but different from elephants. And thinking that those places, like we were talking about with humans, those are the places that are important to make a mammoth, a mammoth. And that is where I'm going to focus my energy in bringing back a mammoth, which will be

• 54:27Speaker 00

  an elephant that is capable of living in the habitats that a mammoth lived in. Mammoths will have to live in habitats that exist today and tomorrow. So the mammoths will have to be genetically capable of living with the pathogens and the microbes and the food sources and the microbiome that the elephants that will birth them can survive in today.

• 54:49Andrew D. Huberman?

  When you mentioned species nomenclature gatekeeping, I have a feeling this is based on the publicity around the dire wolf.

• 54:57Speaker 00

  Yes.

• 54:57Andrew D. Huberman?

  Okay. I just, I like to just address things very directly. I want to be very clear. I'm not arguing for species gatekeeping here. That's not what I do. I own a mutt after all.

• 55:07Speaker 00

  It's not even that. It's, it's that somehow this idea of what we should call it, based on this very specific definition of you can only call it this if it's some threshold genetic similarity, is noise. It's not an important part of the conversation. I mean, it's a part of the conversation and it's one that we can have. But if people don't want to call it a dire wolf, just don't, right? It's like.

• 55:28Andrew D. Huberman?

  Well, I think like, like all things media and Hollywood, you know, I think Jurassic Park did an amazing service to science and the excitement around these concepts, but probably did a disservice as well by embedding in people's minds that the idea is to bring back the, the exact same animal.

• 55:44Speaker 00

  But didn't we just say that these dinosaurs were some dinosaur DNA and a whole bunch of frog DNA? Nobody looks at them and goes, no, they're not a dinosaur.

• 55:53Andrew D. Huberman?

  Well, you're a scientist and I am too. Actually, it's funny that you, you mentioned this because my dad's a theoretical physicist. He was involved in chaos theory. He's been a guest on the podcast. I remember when Jurassic Park came out, he didn't dislike it, but the part where he kind of rolled his eyes was there's a description of chaos theory in there and what it means. And in Hollywood, they love to use the example of like a butterfly flaps its wings in Patagonia. And then this thing happens in the, to the barista in, in Brooklyn, you know? And people like to bridge those concepts and they, oh, that's so cool. Like, so it's, it's sticky, as we say, but that's, but he, he was rolling his eyes. He's like, okay, that's not how these things work. And so for people that are experts in the area, it can be a little bit grating at times. But the public, I think, is open, right?

• 56:36Andrew D. Huberman?

  And my experience in doing what I do is that the public, if they just have the knowledge in hand and the way you described it, great. So.

• 56:42Speaker 00

  So our dire wolves, they have 20 edits that we picked. And we, we sequenced genomes from fossil dire wolves. We learned from those genomes, what genetic changes made those animals bigger, more robust, light colored in coat. And then we engineered those changes into a gray wolf genome to recreate the dire wolf. If it looks like a dire wolf and it's able to fill the niche of a dire wolf, I'm happy to call it a dire wolf.

• 57:08Andrew D. Huberman?

  So the dire wolf was a very interesting choice. Clearly you were successful in creating this animal. Sounds like you were very intentional in picking which genes. It wasn't like, oh, we're going to take a couple of genes from the dire wolf and throw them into this, this other wolf and create what we call is the dire wolf. If I were to look at the dire wolf and you said a gray wolf?

• 57:29Speaker 00

  Yes.

• 57:30Andrew D. Huberman?

  Side by side, is the dire wolf larger?

• 57:32Speaker 00

  They are.

• 57:33Andrew D. Huberman?

  On average at the same age? Are there any other features that are visibly different or the other features are more adaptive in terms of gut and ability to live in certain environments and this kind of thing?

• 57:42Speaker 00

  They're muscular. The fur is longer and more full and it's also light colored. I think it's an important thing to understand about how we're selecting these because we are very deliberate about what we're doing. And it's both because we want to, with some fidelity, bring back these extinct traits so that the animals can eventually be released. Now, we're not planning on rewilding dire wolves and we will study the animals and learn about the effect of their genes on their lifespan.

• 58:11Speaker 00

  But the other, other animals, the ultimate goal is to, to eventually have populations of free living animals that the local people are stewarding as, as they like to. And so we, we want to understand how healthy they are, how they're going to interact with the habitat that's there. And we want to make sure that because we with synthetic biology have the power to engineer them in a very deliberate way, that we can do that in a way that's safe. So the hair color is a really interesting example of this and the strategy that we use. So when we sequenced the genomes of the fossil dire wolves, we found that they both had variants, the same variants in two genes that would have made them have light colored coats. But in living gray wolves and dogs, variants in those genes, not the same ones that we

• 58:56Speaker 00

  saw in dire wolves, but close enough to where we would need to do the edits that you have some concern that you would have bystander edits that might cause a problem, can lead to oculocutaneous albinism. So blindness or deafness in these dogs. And we decided that because we're not changing the whole genome, they have to be safe on a gray wolf genetic background, we wouldn't make the trait that way. It just wasn't passing the bar of animal welfare, safety. And so instead we brought back the dire wolf light colored coat using different edits that we know are safe in a gray wolf background because there are light colored domestic dogs and gray wolves. So we used the edits that we know are safe because they exist in living dogs.

• 59:38Andrew D. Huberman?

  Oh, that's cool.

• 59:39Speaker 00

  So we were able to engineer, using all the tools of synthetic biology, this light colored coat that is the dire wolf light colored coat, but using a path that we know is safe. And this is the way that we think about all of our projects. We have to take an Asian elephant and turn it into a woolly animal. That trait requires changing not just the structure of the hair, but of the skin itself. We have to make room for more follicles, sebaceous glands, different approaches to be able to support that woolly coat, right? And we need to be able to do that in a way that results in a healthy animal because these are very long-lived animals, takes 22 months for gestation. They reach sexual maturity at 14 and it's a lot of work.

• 1:00:19Andrew D. Huberman?

  So how many dire wolf wolves are walking around right now in some location?

• 1:00:25Speaker 00

  Right now there is Romulus and Remus and they're almost two years old.

• 1:00:30Andrew D. Huberman?

  Male and female or male?

• 1:00:31Speaker 00

  Romulus, Remus are boys and Kalizi is a girl. She is about 18 months old or so.

• 1:00:36Andrew D. Huberman?

  Is the intention to mate them?

• 1:00:38Speaker 00

  No, they're too closely related. We're stopping them using hormones. So rather than.

• 1:00:43Andrew D. Huberman?

  But they live together.

• 1:00:44Speaker 00

  They live together. She was reared by herself. The boys had each other and she had just her. So she's a little bit on the like. I mean, you would never look at these animals and say, this is the way a wild wolf behaved. They were hand reared, right? But she's a little bit on the specially goofy side, but she's, she's the best. She's adorable.

• 1:01:01Andrew D. Huberman?

  Do you feel safe interacting with them?

• 1:01:02Speaker 00

  Oh, no. We have interacted with them, but the people who work with them a lot that they know feel safe interacting with them. But as they got older, it was very clear that they're wild animals. These are not domestic dogs. Remus is a little bit less skittish than Romulus. He will eventually, if you sit in the middle of where they are, he will eventually kind of sniff around and, and maybe come near you. Romulus wants nothing to do with you, which is funny because they're, they're identical twins, but they're slightly different interacting with people. But it's very clear that they, these are wild, they're so huge, right?

• 1:01:31Andrew D. Huberman?

  Yeah. How big are they?

• 1:01:32Speaker 00

  I don't have the latest measurements on how big they are. And of course it's seasonal for all these different things, but I know that they were, at some point they were at least like 120 pounds, which is big for a gray wolf.

• 1:01:41Andrew D. Huberman?

  That's a big animal. So everything you just said about these dire wolves, would you also say about gray wolves, like you wouldn't want to be alone with one? Some can be skittish, some can be calm, like you.

• 1:01:51Speaker 00

  You know, I have good friends who are somebody you should think about having on, actually, that if you're interested in dog behavior and what we've learned about domestic dogs, I know you have a dog and it's very exciting. Eleanor Carlson is at the Broad Institute and at UMass, and she's done a lot of work with wolf dog hybrids and then also with domestic dogs and trying to map genes to behavior and all these things. And basically showed that breed stereotypes are just not real, that you really can't map genes to behavior, except for Chihuahuas, they're just terrible. I'm just kidding.

• 1:02:20Andrew D. Huberman?

  No, it's okay. We had Caesar Milan on the podcast. He'll be the first to say that in, in almost every decade in the United States, there was the demonized dog breed. It was actually German Shepherds post-World War II. Then it was Dobermans, same reason. Then it was the Bulldog, the English Bulldog, which having had English Bulldog is hilarious to me.

• 1:02:38Speaker 00

  I went to Georgia, so that's never going to be my least favorite dog.

• 1:02:41Andrew D. Huberman?

  Right, exactly. And then now it's pit bulls, right? And statistically, actually, I think most bites come from Chow. At least my uncle, who's a vet, tells me that. But Chow owners, I met some nice Chow's. The blue tongue is pretty cool.

• 1:02:52Speaker 00

  And that's a particular variant. You can imagine, yeah, there's a, there's, color is one of the things that's best understood, I think, especially in domestic dogs, because so many genomes and all these things have been mapped. And that's part of what we have to do in all of these cases is, is how do we figure out what it is that causes the thylacine to have the stripes that it has, or causes the particular types of hair development that happen on a woolly mammoth? These are all huge, open problems in, in evolutionary biology that I get to work on every day in my job.

• 1:03:22Andrew D. Huberman?

  Yeah, clearly you have, clearly you have the, the right job. So you have these three dire wolves. They're not mating. Is the plan to make more of them, to mate them? What's, what's the ultimate goal and intermediate goal?

• 1:03:36Speaker 00

  We will have another pack so that hopefully they will all be born more of them at the same time. So that's, and that's the plan eventually. It's not our priority right now. We're working on other species, but what we'd like to do is have another pack in the space where we are so we can really better understand the impact of the animals on ecosystem. This is really the next rational, logical step in any de-extinction project. I often hear rumors and what are you doing? You're just going to take, get an elephant and make a mammoth and just release it into Alaska? And you're like, no. First of all, no, because it's going to be so hard to make that first mammoth that I'm going to want to make sure that it is safe and cared for and has access to all of everything that it needs.

• 1:04:16Andrew D. Huberman?

  Well, this is the Jurassic Park thing again. It's that they break out, right?

• 1:04:19Speaker 00

  But also, you know, you can't do that. We exist in the regulatory environment of anywhere that these animals are. It's, it's not that we're some crazy scientists on an island like in Jurassic Park. We, we work here. We have IACUC protocols. And if you're doing anything that is releasing animal outside, you're under the regulatory purview of a whole bunch of different agencies. I don't know if you saw, but the very first gene edited organism created specifically for the purposes of conservation, ecosystem restoration, was deregulated by the USDA this week. It's the American chestnut tree. And the challenge with any of these genetically modified organisms that we have, which we're creating, synthetic biology uses a tool to make these things better.

• 1:05:03Speaker 00

  The chestnut tree is one of these stories, like the passenger pigeon, where the American chestnut was the most prolific tree across the eastern forests of North America, all the way through North America, until the early part of the 20th century, when a disease was introduced, believed to be on an import of a Chinese chestnut tree, that caused a fungus to get into these trees and they all died. But it took a decade and a billion trees died.

• 1:05:33Andrew D. Huberman?

  This scares me for a variety of reasons. A few years ago, this would be 2016, 17, I got this strange envelope in the mail to my residence. Do you know about this?

• 1:05:43Speaker 00

  No, but I'm scared.

• 1:05:44Andrew D. Huberman?

  So I was living in the East Bay, California, and I get this envelope and it contains a little kind of like, looks like a small quarter size, plastic like container, just thin, an envelope. And I had a little note and it said, free seeds for gardening.

• 1:05:59Speaker 00

  Oh.

• 1:05:59Andrew D. Huberman?

  And I was like, this is really odd. And I started, you know, fishing around on the internet. Turns out the idea was that massive amounts of seeds were being shipped from China and sent here. Now, this isn't a conspiracy, right? Like if you look at this, there are these, this is sort of attempt to just kind of like put new populations of plants and maybe it was all benevolent. And my friends, actually, one of whom is down at Santa Cruz, I know some plant biologists, they were like, whatever you do, do not put that into the ground outside because these things travel, birds eat them, birds poop, and then stuff gets, grows. And this is how you can decimate important populations of trees and plants. It was the first time I really thought about vegetation on vegetation warfare. Is that what is actually what was happening? Is it, was it the Chinese trying to do this? We don't know.

• 1:06:44Andrew D. Huberman?

  But what is very important is that anytime you plant something, you actually want to talk to the people who understand how different ecosystems of plants coexist, in the same way that you wouldn't put your wolves out into the, you know, into the dog park.

• 1:06:56Speaker 00

  I wouldn't put the wolves out because if, if we released dire wolves, they would compete with gray wolves. And gray wolves are already having enough trouble trying to find a way to survive. And so there's no need, there's no ecological need to release gray wolves into the habitat and so we can use them to study these. But if you think about what you just said, right? I, I think people, we as a lineage, have been messing with the evolution and of the stuff around us.

• 1:07:22Andrew D. Huberman?

  Oh, definitely.

• 1:07:23Speaker 00

  As long as we've existed, right? Initially, just by driving things extinct, not deliberately, right? Like just like, maybe this wasn't a deliberate attempt to have some plants that would outcompete other things.

• 1:07:33Andrew D. Huberman?

  Particular flowers, yeah.

• 1:07:34Speaker 00

  But we did. And we changed ecosystems by going into them and, and getting rid of all the largest animals that were there because we were hunting them. I'm thinking about, you know, our ancestors in, you know, 50,000 years ago in Australia, 30,000 years ago in Asia. And then we domesticated things and, and now we, we conserve things. And when people think about conservation, a lot of people have this idea that it's this beautiful thing where you're just leaving everything alone. But that's not what we're doing. We are deciding how many of them get to live, what they get to eat. We vaccinate them, we protect them from predators. We, I'm not saying that is bad, but I think it's naive to say that it's not us determining what the future of these animals are. And we've also been moving stuff around forever.

• 1:08:17Speaker 00

  Like we have English birds all over the place here and in New Zealand that were brought by people because they liked them, right? They liked them where they were. And I think it's a mistake to imagine that the only good ecosystem is the one that you know right now, because you're, you're claiming a particular slice of history as the thing that is better than everything else. And I think it's more important to think in terms of robustness. And you said, well, go back to the beginning, you, you said something about how when we have multiple things happening, multiple species in, in an ecosystem that are all doing different things, you end up with more biodiversity and richer environments. When there's an overlap in ecologicalness, there's some redundancy there.

• 1:09:01Speaker 00

  And that redundancy is really good for that ecosystem because it means that bad stuff can happen and it can weather that bad stuff. So maybe we shouldn't always think in terms of bringing in something new is bad.

• 1:09:14Andrew D. Huberman?

  I should have planted the seeds. No, I'm totally on board what you're saying when I.

• 1:09:18Speaker 00

  I don't mean to plant the seeds.

• 1:09:19Andrew D. Huberman?

  No, no, no, I'm totally, totally on board with what you're saying. It touches on an important theme that we've certainly never discussed on this podcast, which is very relevant to today's discussion and that people should think about, which is, you know, who gets to decide? It's interesting because there's both a kind of like massive ego inserted into the notion that like, we know best about everything, including the other, all the other species of plants and animals. That's obviously not true, but also that we don't have anything to contribute in terms of our own evolution. That is, I mean, look here, you're a human being bringing back species of past. And some people might think scary, other people might think fantastic. I think why it's hard for people to wrap their head around these things and they default

• 1:10:01Andrew D. Huberman?

  to thinking about, oh, it was better in the past, is because A, most people never experienced that. They have no concept. I think there's a great book that I had to read years ago called The Good Old Days, They Were Terrible. But we hear the good old days and you hear about all like the dysentery, the lack of antibiotics, like, but we tend to look back and say, oh, that was, it must've been so nice back then, everything bucolic and beautiful. You forget all the, the dark side of that. But the other one is that we don't have a window into the future.

• 1:10:26Speaker 00

  Right.

• 1:10:27Andrew D. Huberman?

  And so, you know, I went to school in Santa Barbara and one of the first things you learn there is that there are all these species of fox that are out on the, the Anacapa Island and, and Santa Rosa Island and all these islands that, that the Schumacher brought out there on boats. But no one says they don't belong there. They just say there's this incredible biodiversity out there, which is why it's protected, why we don't have, you know, a lot of tourists walking around out there. We want to protect that. But humans brought those out. But the fact that it was Native Americans and it was, and it was some time ago, leads to our perception like it was good, right? And so the idea that we would remove them, no, we need to protect them. And that makes total sense to me, but it's a default psychology that I think is driving a lot of the quote unquote ethical conversations around this. Because we don't have a window into the future. So let's say these dire wolves, you make more of them.

• 1:11:11Andrew D. Huberman?

  I can get totally on board the idea that then they're wildlands that they are roaming, that, that they're serving other populations of animals and plants. There's new interactions that are, that are benevolent interactions, that are pro-evolution as opposed to devolution. I think the challenge for people is we don't know what that looks like. And it feels like there, there are too many variables to understand. So I'm just wondering how you wrap your head around that when you're talking to people about what you do and, and when you're thinking about what you do.

• 1:11:41Speaker 00

  I'm thinking in terms of helping ecosystems to become more resilient. We know, for example, because of what happened in Yellowstone, the impact that restoring the top predator of an ecosystem that had been removed can have. The gray wolves that were reintroduced into Yellowstone, the population of animals that they ate had become too large and they had eaten away at all of the shrubbery. And so putting the gray wolves back in Yellowstone cascaded all the way down that ecosystem ladder to changing the way the rivers were flowing because the plants were growing back now along the edges of the rivers. The thylacine, which is the Tasmanian tiger, this is the second species that Colossal declared as one of our de-extinction targets.

• 1:12:26Speaker 00

  The thylacine was the top predator in Tasmania. And Tasmania today has problems because that top predator is missing. Have you heard about or seen the awful pictures of the Tasmanian devil facial tumor disease?

• 1:12:41Andrew D. Huberman?

  Yeah, this came up on a few podcasts ago because we had Jared Rutter, who's another Hughes biologist, where some mitochondria, we're talking about, they're no transmissible cancers, but these Tasmanian devils have wound-induced cancer-like problems. So they fight, they scratch each other up, they get cancers, and that population is suffering as a consequence.

• 1:13:02Speaker 00

  And they're so closely related to each other that they can pass them between each other.

• 1:13:07Andrew D. Huberman?

  Oh, so it's the genetic similarity that allows that to happen?

• 1:13:10Speaker 00

  The point is that I, yes, this is terrible, but if we had had the top predators, those sick individuals would have been weeded out of that population and we might not have this problem. So you can see restoring that ecosystem. And also, I'll get back to, you know, I often get the question of, why are you thinking about bringing extinct species back to life? Why aren't you thinking about helping living species not become extinct? And the answer is, we are doing both. It is the same tools, it's the same technology, it's the same needs. And when we excite people with the idea of mammoths and dodos and thylacines, we get more engagement and enthusiasm and investment

• 1:13:54Speaker 00

  in developing the technology that we can use to stop living species from becoming extinct. There's a really great story. Our Colossal Australia partners have been working on a project to try to stop the northern quoll from becoming extinct. Have you ever heard of this guy?

• 1:14:08Andrew D. Huberman?

  I'm familiar with the quoll, most people won't.

• 1:14:10Speaker 00

  It's Q U O L L, so it's a little guy, they're adorable little-

• 1:14:13Andrew D. Huberman?

  They're super cute.

• 1:14:14Speaker 00

  Carnivorous marsupials.

• 1:14:16Andrew D. Huberman?

  Yep.

• 1:14:16Speaker 00

  And they eat amphibians. And in Australia, there is an introduced amphibian called a cane toad that is toxic. It's toxic to dogs, when dogs eat them, they die. It's toxic to everything. When a quoll eats a cane toad, it dies. And that's terrible. And there is a very strong chance in the next few decades that northern quoll is going to become extinct. However, there is a synthetic biology solution to this and it's one that has actually already been made, right? There are mammals that eat toxic toads that live on the other side of the planet, even that eat cane toads, right? And they have a single letter change that changes one amino acid in one gene

• 1:14:59Speaker 00

  that allows them to eat that toxic cane toad and not die. Our Australia, Colossal Australia partners have made those changes in a quoll. And when you measure in a dish the ability of that toxin to break down the cane toad, that single letter change to that quoll's genome could allow that quoll not only to avoid becoming extinct, but to eat cane toads, which currently nothing really can in Australia. So now we can see the real benefit of this massive comparative biology framework. I know which gene it is that I need to change, the stack that allows us to develop the tools to be able to make that change, just that change, and then show that that's the only change that's there. You've made what you wanted to do. And then put that in a living animal can stop a species from becoming extinct.

• 1:15:45Andrew D. Huberman?

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• 1:16:30Andrew D. Huberman?

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• 1:17:12Andrew D. Huberman?

  To learn more, visit functionhealth.com/huberman and use the code HUBERMAN for a $50 credit towards your membership. Again, that's functionhealth.com/huberman. As someone who does a lot of public science, health, education, interaction, there are a couple of things that get the public really worried and that they need reassurance on. Honestly, I think it dates back to the pandemic. There's a lot of distrust about scientists. There is this belief that some scientists are only concerned with themselves. It's an important myth, in my opinion, to dispel the idea that most scientists are not what I believe them to be, which is they're trying very hard to get answers right, to do good for the world, including other species.

• 1:17:54Andrew D. Huberman?

  And they're not so careerist that they're willing to overlook that, independent of the IRB boards and the thing, the constraints that force them to do that. But that is the era we're living in, right? So I think that some people think more now in terms of, you know, scientists are like doing stuff because they can. This has parallel conversations about AI, where people are thinking like, hey, like, have we really thought this one through? And people are scared. But I totally agree with what you're saying. And I want to talk about two species to try and highlight this and how it can be done right. Because I think it's clear that you're trying to do this right, which means for the best possible outcomes for humans and other species. And the first are mosquitoes. And the second are humans. Most people don't care about mosquitoes.

• 1:18:39Andrew D. Huberman?

  But some years ago, I started paying attention to mosquitoes because your very own Howard Hughes director now, I think Leslie Bossall, works on the olfactory system of mosquitoes and other insects. And turns out bugs find mates and find things to suck blood from, et cetera, by odors, and pheromones, but odors. And so there was this idea, oh, mosquitoes have malaria. This wasn't Leslie's idea, but it was like, mosquitoes have malaria, let's just get rid of all the mosquitoes.

• 1:19:08Speaker 00

  Right.

• 1:19:08Andrew D. Huberman?

  And the biologists were like, no, you can't do that because then the birds are going to suffer because they eat the mosquitoes, and on, and on, and on. And this stuff can really domino. It sounds like a great idea, it's a terrible idea. Or let's just make mosquitoes that can't reproduce. That's a great way to do it, right? Or let's just do N half of them, right? There were these ideas just kind of thrown out there that with genetics, you can do that. You just release a few of these little suckers into the wild and there is the potential that they mate and proliferate and just enough to eradicate a population or half a population. It's harder to do than that. So people didn't know this was like being explored, but smart people put the brakes on it. So let's talk about mosquitoes. They clearly carry pathogens that harm people, but they're also important for ecosystems,

• 1:19:53Andrew D. Huberman?

  vitally important for certain ecosystems. So how do you think about plucking out a node in an ecosystem, like a species, or introducing a species back into an ecosystem and thinking about the ramifications? It's hard to model behavior in one species, let alone interactions between species. How do you wrap your head around that? With the, maybe the mosquito would be, I hope, a simple example of this.

• 1:20:17Speaker 00

  Mosquitoes are a hard one. And I think that they do cause a lot of death and disease, but not all mosquitoes. So the, you know, only certain species of mosquitoes carry malaria and dengue and other diseases that are known to affect people. And also, those mosquitoes have much higher population density because of the way that people have built our towns than they would have had in natural ecosystems. So for something like a mosquito that is extremely overpopulated and carrying a devastating disease, I would think that there actually is reason to think that it is safe in an ecosystem to at least bring that population back down to a size that it would have been in a natural ecosystem. And a lot of problem with mosquitoes is because people leave

• 1:21:02Speaker 00

  just tubs of water or water that isn't circulating out and they lay a billion eggs and then you have many more mosquitoes. It's not true in the Arctic. In the Arctic, there's a bazillion mosquitoes and no people, and it's really miserable. But I've spent a lot of time in my life.

• 1:21:13Andrew D. Huberman?

  Yeah, I heard you describing that elsewhere, and it sounds horrible. So I do not like mosquitoes. I don't like mosquito bites. And I get it, like, at first blush, I'm like, get rid of all the mosquitoes. But it's a lot more complicated than that.

• 1:21:24Speaker 00

  Maybe engineer mosquitoes that they can't carry the disease, rather than engineer the mosquitoes to be dead. I mean, there are ways that I think we can use synthetic biology and gene drives is the thing you were getting at, where you release something that is created by synthetic drive into the wild, and then it passes on to the next generation. I actually think that gene drives are an incredibly powerful way that we have at our fingertips, where with the appropriate safety measures and care in place, we should think about how we might deploy these tools. You can make a gene drive so it only lasts for a fixed number of generations. And also, because they tend not to make things reproduce, there is incredibly strong natural selection against them. Anything that breaks a gene drive and lets something reproduce is going to be favored in a population, right? So gene

• 1:22:09Speaker 00

  drives are going to be difficult to get to persist, and there are many switches that we could build into them to make them last for a short period of time. But there are some species that have taken over. You talk about your plants that you got. In this part of the world, there's cheat grass everywhere, and it's highly flammable, and it grows alongside the rose, and it's Mediterranean in origin. And the only way we are ever going to get the cheat grass down enough to be able to let the native California grasses come back is if we get rid of the cheat grasses for a few generations.

• 1:22:40Andrew D. Huberman?

  Do you think this is one of the reasons there's so many fires?

• 1:22:43Speaker 00

  They're very flammable, and they also don't have very deep roots. So in California, it's very dry, right? California native grasses have much deeper roots, and so they stay green longer. So they're sequestering carbon, and they're not as flammable for longer into the season. These shallow-rooted Mediterranean grasses dry out super quickly. So as soon as it's fire season, like it is now, they're ready to go, right? And it's not just here. It's all across the western part of North America. And this is a problem. And it's a problem because it causes huge amounts of damage to forest ecosystems, huge amounts of property damage when fires take off and they're out competing these grasses. This is a situation where I would say, let's think about how we might safely deploy something like a gene drive that can remove something, or at least tamp something down enough to

• 1:23:26Speaker 00

  allow that ecosystem to become, again, once again, more robust and resilient. As far as, you know, what do we think about adding things back into an ecosystem? This is one of the reasons that every de-extinction project, or every species translocation project, is staged and thoughtful. When people moved Texas Panthers into Florida in the mid 1990s to try to stop Florida Panthers from becoming extinct, they had developed crooked tails and cowlicks and cryptorchidism. Their testicles didn't descend, and they were going to become extinct. This was an inbreeding depression. There were only a few individuals, so they only bred with individuals they were related to. There was no choice. You bring in the

• 1:24:08Speaker 00

  Texas Panthers, and the Panthers recovered. All of these diseases disappeared for a short period. Now they're inbreeding again, because the population is cut off from Texas, and so they'll have to keep doing it. We have to be the stewards of these ecosystems that we're creating. But that's in our power. We can do a ton of analyses about potential risks and rewards of what might happen when we modify an ecosystem. And we do it all the time, sometimes to good ends and sometimes to bad ends. What we can't do, and I think this is sometimes where the conversation gets lost, is if you look around, we see

• 1:24:49Speaker 00

  habitats around the planet that are suffering because of changes that people have made. Within those habitats, there are species that are teetering at the edge of extinction. And the only strategy that they have to survive is natural selection, evolution and natural selection. The rate of change of these ecosystems is too fast for that to work. If we say, these technologies that we have, whether it's translocations, or assisted reproduction, or genetic modification and synthetic biology and de-extinction, if we say that those technologies are too risky, we are accepting the outcome of doing nothing,

• 1:25:33Speaker 00

  which is also a decision. And I think that's where, a lot of times, the conversation gets lost. Doing nothing is not not deciding. Doing nothing is saying, we accept the fact that we are going to have a future that is less biodiverse than the present.

• 1:25:50Andrew D. Huberman?

  It's amazing how people are perfectly happy to allow the negative default outcome to emerge, even though it's the consequence of humans. But they are wary of humans intervening to a potentially better outcome. I think it gets back to this issue of trust in scientists. And it also raises the question of who decides? I'm very opinionated about this when it comes to public health policy. I think what the pandemic taught us, regardless of where people sat on vaccines and lockdowns, if nothing else, it taught us something absolutely essential, which is you can't have one person be the spokesperson.

• 1:26:25Speaker 00

  Right.

• 1:26:25Andrew D. Huberman?

  People need to hear from a group, including the dissenters in that group, and why they arrived at a particular decision.

• 1:26:33Speaker 00

  I should be clear. For all of the species that we're working on, we have advisory panels that are built from local people. We have the Tasmanian Advisory Panel that has politicians and people who grow forests to log them, and people who work with the animals, and people who are scientists and conservation biologists. And we have regular meetings with all of our different advisory groups to talk about what the future might look like, well before we have a phyllosine to be able to to release anywhere. Our MOA project is led by the Naitahu Research Center in South Island of New Zealand. And these Maori people are the people who will be the long-term stewards of the MOA. And the decision about how many to make, which MOA to make, where to release them, how to release them,

• 1:27:16Andrew D. Huberman?

  Right.

• 1:27:16Speaker 00

  It's their decision, in consultation with other people who will be impacted by this. And I think that's really important. The other thing that I think we do well is this, right? I mean, I am not a scientist hiding up in an ivory tower somewhere. I'm here, talking to you, and talking to as many people as I can, to tell people all about what we even get yelled at for this. Why is colossal always talking about what colossal's doing? Well, would you rather we not tell you? I mean,

• 1:27:43Andrew D. Huberman?

  I think the education piece is the critical piece. I think it's great that

• 1:27:46Speaker 00

  But it's also hard.

• 1:27:47Andrew D. Huberman?

  colossal is doing this.

• 1:27:47Speaker 00

  I mean, it is true. I think we are all desperate for, when the dire wolf story broke, and there was a small subset of scientists who were just yelling at me that I wasn't allowed to call the dire wolf. And there are a bunch of people who were like, wow, I can't believe you learned from a bone and actually used the tools of synthetic biology to engineer extinct traits into a living animal, and now you have living dire wolves, right? And there were people who were scared of it, and people who loved it. And there were a bunch of people who said the word extinction and synthetic biology for the very first time in their lives. And I got emails from my colleagues at universities who said, the undergraduates were coming into their ecology classes and their sociology

• 1:28:29Speaker 00

  classes, their anthropology classes. Some of them were mad, and some of them were excited, but they were talking about it. And they were talking about it as if they had some agency in the world that they were inheriting. And we hear that from middle schoolers and high schoolers. And I think that is really something tremendous about what we're doing. People need to feel excited and positive, and they need to feel awe. And when I saw the dire wolves for the first time, that's what I felt, is genuine awe, right? And there's something about that that just makes the world a better place. It makes people happier and healthier. And I love that I get to talk about it and do this hard science, like really hard science, with a bunch of smart people every day.

• 1:29:13Andrew D. Huberman?

  As long as we're wading into deep water here, let's talk about the really deep water, which is humans.

• 1:29:18Speaker 00

  Okay.

• 1:29:19Andrew D. Huberman?

  So, we have this thing called IVF, where people can make embryos and select what are deemed, at this point, healthy versus unhealthy. So people are doing genetic selection in humans through technology, right? People don't really stop too often and think, oh, yeah, you know, how is that disrupting the human ecosystem in any different number of ways? But a few years back, there was a guy in China, actually, who had been a postdoc at Stanford, who decided to use gene editing to modify the genome of some babies, disrupted the HIV receptor. And there are two stories about this. I don't know which one is true. One story is that they did it for benevolent reasons, to prevent these babies from getting

• 1:30:02Andrew D. Huberman?

  HIV from either an infected parent, or to just protect them against HIV.

• 1:30:06Speaker 00

  The father was HIV positive.

• 1:30:08Andrew D. Huberman?

  The other story that was running in parallel was that there was, that this modification might have some impact on hippocampal or other brain circuit function that might make them hyperintelligent in one dimension. So this was kind of more of a, like a eugenics experiment. That was the idea. And it was very interesting how this emerged. Not in the general public, like, that was interesting in its own right. But there was this short moment of about a week, where it wasn't clear if this guy was going to win a Nobel Prize and be celebrated, or was going to be put in prison.

• 1:30:39Speaker 00

  Yeah, I remember this. It was Antonio Regolado broke the story about a week before the big CRISPR conference.

• 1:30:44Andrew D. Huberman?

  There were these emails that suddenly came out. And it was very clear, like, people were kind of tap dancing around this guy, like, what's going to happen to him? Do I want to be associated with this and glean some of the benefit? Or is he going to be demonized? In which case, I want nothing to do with this guy. He's like, he's blacklisted. It turns out it was the latter, right? And the Chinese government said, yeah, we're going to shut down his lab. He's going to be punished.

• 1:31:07Andrew D. Huberman?

  I don't know what's happening, if he's running experiments, or if he's in prison, or what's happening. But this was so interesting, right? Because since then, there's been no fewer than four major companies launched for deep sequencing of embryos, both from IVF, but also non IVF babies. And I have people coming up to me, saying, hey, guess what? We just got to screen these embryos, and we were told which of them is going to have the highest IQ, and which of them is going to be tallest, and which of them is going to be this, and which one and that. And so, some of these companies are geared towards ruling out disease.

• 1:31:42Speaker 00

  Right.

• 1:31:43Andrew D. Huberman?

  Others are geared towards trying to optimize for best possible outcome.

• 1:31:48Speaker 00

  Right.

• 1:31:48Andrew D. Huberman?

  Now, this gets people riled up, because it's very expensive at this point, so that has other implications.

• 1:31:53Speaker 00

  Right.

• 1:31:54Andrew D. Huberman?

  And it's easy to say, oh, well, that's like eugenics. But when people select who, assuming they do it voluntarily, who to have children with, they're selecting on the basis of a number of features. Some physical, some emotional, some resource-related, some cognitive, you know? And so, there's a lot of this happening, happens in the animal kingdom.

• 1:32:16Speaker 00

  Yeah.

• 1:32:16Andrew D. Huberman?

  And in humans, it's happening now at the level of genetic sequencing. And I think we're headed for big discussions about ethics, about changing, quote-unquote, "ecosystems."

• 1:32:27Speaker 00

  Right.

• 1:32:27Andrew D. Huberman?

  Through genetic selection of humans. It's started, it's happening.

• 1:32:30Speaker 00

  There's a really fascinating story that comes partly out of ancient human DNA literature, and speaks directly to this. This idea that, I think we feel uncomfortable with things, we feel comfortable with new technologies initially, because there's kind of this reptile brain thing going on, where first, we have to decide if we're scared of it, before we can decide if we're curious of something, right? So there's initial pushback there. But we are doing, as you say, genetic selection on humans by choosing our mates. And it makes us uncomfortable even to think about that. But here is a relatively benign example to show that that's true. And it has to do with human height, right?

• 1:33:12Speaker 00

  So, we know, unlike IQ, which is very difficult to pin down which bits of your genome mean IQ, and IQ as measured by what, and what are you at, and it's different in different cultures, and so that's hard. But height is relatively easy, and we know that it's heritable. So we know that there's bits in your DNA that can mean that you're tall or short. I'm five feet tall, so I didn't get any of the tall genes, right? I'm little. But, we know now, by looking at the ancient human DNA, that in Europe, at least, where there's a lot of very tall people in Northern Europe, right? The Dutch are extremely tall.

• 1:33:43Andrew D. Huberman?

  They're very tall.

• 1:33:44Speaker 00

  I remember going to the Netherlands, and imagining that I was going to be speciating there, where I would be walking in between people, as they were above me, you know? Like, driving a tiny car, with a lot of big trucks on the highways, and anyway, that's kind of what I feel like when I walk around the Netherlands.

• 1:33:56Andrew D. Huberman?

  The Dutch are very tall, very kind, but very tall.

• 1:33:58Speaker 00

  Very tall. But we know that a lot of these genes were first introduced into Europe with the Step people, at about 4,700 years ago, at the Yamnaya. And that, originally, they were migrating. And for a long time, we thought that people were just getting taller because of environment. They were learning more about health, they're learning more about what they should eat. And yes, there is some true to that. But height in Northern Europe has kind of plateaued now, and people have reached what seems to be the tallest you can be with this set of genes that exist in people today. But it is there, it's in Northern Europe, it's not in other parts of the world, right? And so, there is human genetic selection for a trait that we can visibly see, that makes people look different from each other. That isn't because somebody's picking an embryo and a sperm in a dish.

• 1:34:43Speaker 00

  So, we would be naive to imagine that it doesn't happen, that it hasn't happened throughout our evolutionary history, or that we can control it. But I think what offends us about it, this innate reptilian brain part of us, is that while we don't care that a chihuahua and a boxer, we pick, we engineer to have different traits, because they have different roles in the society, because we have created the roles for them in society, we created them, they were once gray wolves. We like to think of people as not having niches to fill, as having some freedom of choice, to be able to pick what they want to do and what they want to be. And this idea that one generation might do something to take that away from the next

• 1:35:28Speaker 00

  generation, just sits really uncomfortably with us.

• 1:35:32Andrew D. Huberman?

  It's wonderful that you're doing public education on these things, because I think people really need to understand that there are well-meaning scientists, who are not just trying to figure out, you know, what would happen if. And I think that it's clear that there are going to be more things like this, right? And so, we have to navigate forward with that. Similar to AI, it's not going anywhere, just like smartphones aren't going anywhere. And the question is, what is the best use of this, the safest uses? And where can it evolve our thinking in our lives in really unforeseen ways, unforeseen positive ways?

• 1:36:03Speaker 00

  We're really only just beginning to see this. I mean, you know, the story of baby KJ, the first child who was cured of a genetic disease using the tools of synthetic biology. This was a child that was born with a urea cycle deficiency, his blood was building up in ammonia. And because people, scientists, had done a ton of research on this particular condition, and really understood a lot of what was happening, they were able to identify the cause of this genetic disease. And then it was a collaboration between academic, industry, NIH, the Children's Hospital Philadelphia, where he was born, all this huge collaboration came together, took six months, designed a base editor, CRISPR base editor, to target his particular cells,

• 1:36:48Speaker 00

  come up with a delivery mechanism to get it into his liver, do all of the testing that you need to do to make sure that it's safe, and then give him a CRISPR medicine, a bespoke CRISPR medicine, as a six-month-old kid, three times, and he is cured of this disease, and will live a normal life.

• 1:37:04Andrew D. Huberman?

  Amazing. And no one accuses those doctors of playing God. Right? That's what's so funny, I mean, here, I guess we're sort of exploring in the background, like, what establishes the line?

• 1:37:15Speaker 00

  But why not? How is that not playing God in the same way that anything is playing God? I think we play God every day, and, you know, in Judaism, there's actually the idea that you're supposed to take care of the natural world out there, so you're actually playing human, in this case, instead of playing God, when you're using the tools available to you to actually make the world and the people around you better and healthier. When we took a gray wolf, and decided we were going to let its puppies live in our campsite as hunter-gatherers 30,000 years ago, we were making a decision that impacted another species. As we took teacinte and turned it into corn, every decision that we make about which populations of species to protect, and which not to protect, to decide to allow coals to have this genetic

• 1:37:58Speaker 00

  modification, so they can survive in the habitat that we changed by introducing cane toads, these are all decisions we make, that fall into that category of exerting human influence on the world. But the world today is a human world, and the species that live today, and thrive today, are those that have figured out how best to do that, in the niches that we have created for it. And we need to just deal with that, get better at it, use the tools at our disposal.

• 1:38:24Andrew D. Huberman?

  Can I ask you about ferrets?

• 1:38:26Speaker 00

  You can.

• 1:38:27Andrew D. Huberman?

  And I also want to talk about stuff that lives underwater. That ecosystem has all sorts of issues that it needs to deal with. Humans probably have to intervene really quick, or we're going to be in trouble. So, ferrets, they're not rats, they're carnivores, great binocular vision, great hunters, but a few years back, the black-footed ferrets were almost extinct. My understanding, this might be wrong, was that it was that the prairie dog population got out of control, when the numbers of black-footed ferrets were diminished. And as a consequence, the grasslands were being eaten up like crazy, and that had all sorts of downstream, negative consequences. So it was important to reestablish the black-footed ferrets, not just because they're cute. And my understanding is that it was one ferret, Scarface, who sired like 300 litters, or

• 1:39:12Andrew D. Huberman?

  more, and they were able to resuscitate, or at least partially resuscitate, the population. So I'm curious, which elements of that recollection are false, and also, whether or not there's any concern about diversity, given that it was one male siring all these litters, and so you get a bunch of kits, and they're mating. But mating of close relatives is bad for genomes, for reasons that sort of emerged earlier, is you get homozygosity, you get genes that are too similar.

• 1:39:40Speaker 00

  Right.

• 1:39:41Andrew D. Huberman?

  And then if you have, most people are dominant alleles, you know, where you only need one copy, okay, that's a separate matter, but when normally, many mutations, you need two copies, recessive alleles, but if you get genes that are very similar, between brother and sister, you're likely to have two recessive alleles, and you get bad mutations, and you can get deformities, and sterilities, and a low IQ. It's a very interesting thing, that throughout all species, inbreeding is bad.

• 1:40:07Speaker 00

  To a point. The island foxes, the Channel Island foxes that you talked about, this is a really fascinating example of a population that was so small for such a long time, and lived in a pretty steady environment, with no creditors, that they went through that bottleneck, where all of those bad mutations were expressed, and purged from the population. And they have almost identical genomes, they have almost no genetic diversity, and they are perfectly healthy.

• 1:40:33Andrew D. Huberman?

  Wow, okay.

• 1:40:34Speaker 00

  I don't know if something happened to that habitat, if they wouldn't be able to survive, because there's no diversity of, you know, if a disease came in, they would all be susceptible, rather than some versus not.

• 1:40:44Andrew D. Huberman?

  And that's a very protected region, I know that, because my college girlfriend was an environmental studies major, and they used to go out there, and it's very protective, you can't just like, take a boat and like, stomp around the, those islands.

• 1:40:55Speaker 00

  But it's fascinating.

• 1:40:56Andrew D. Huberman?

  It is fascinating, it is fascinating. But in general, my understanding is that breeding with close relatives.

• 1:41:01Speaker 00

  Close relatives is bad.

• 1:41:02Andrew D. Huberman?

  Really bad, certainly for humans, which is why in Iceland and Scandinavia, there's these incredible genetic records, dating back to when there were fewer foreign opportunities to mate with foreigners, right?

• 1:41:13Speaker 00

  Yes.

• 1:41:13Andrew D. Huberman?

  We were going to be blunt about it. So, what's the deal with these black-footed ferrets? Because it's an example of this, a dynamic tension between trying to reestablish a population, and wanting enough genetic diversity.

• 1:41:25Speaker 00

  Yeah, and it's also a great example of how we can use multiple tools that we have for genetic rescue simultaneously, to help a species. I should say, the Black-footed Ferret Project is not something that I was personally involved with. This is a project that's been a collaboration of US Fish and Wildlife, and the San Diego Frozen Zoo, and Revive and Restore, which is a nonprofit conservation organization, I was on their board for a long time, and they're doing really fun work. But the story is interesting. The story is that the prairie dogs, which black-footed ferrets eat, were a real pain in the butt for farmers. And so, they wanted to get rid of prairie dogs, and so they set out all these ways of just trying to kill a whole bunch of prairie dogs. And it killed a couple of prairie dogs, but it killed almost all of the black-footed ferrets, instead. And so, we ended up with a situation where black-footed ferrets were nearly extinct in

• 1:42:10Speaker 00

  the wild. People brought them into captivity, but they could not figure out how to get them to breed in captivity. And eventually, the last captive animal died, and then the last wild animal died. And they thought the species was extinct. It was actually on the, I think it's the class of 1966, the first list of endangered species, when the Endangered Species Act first passed, black-footed ferret was. But then, like a decade later, Shep, the family dog of a family that lived outside of Matizzi, Wyoming, killed a black-footed ferret while it was out one night. And the, the story is that the family took it in to a taxidermist, and they were like, we want this because it's kind of cool. Like, what is this? And the dude was like, uh, uh, I'll be back. And he went back and called somebody and was

• 1:42:54Speaker 00

  like, I think we have a, you know, this extinct species here. And it was proven that it was a black-footed ferret. So there was a population that persisted around Matizzi, Wyoming. People started studying this population again, and they went and they collected a whole bunch more individuals, brought them into captive breeding, and knew more about this. It was a real international push to figure out how to make these animals breed in captivity. But then they noticed that the animals in the wild started to get sick. And in a last ditch effort to save them, they went and collected every individual that they could find in the wild. And I believe one of them was Scarface, who is the one that eventually, like, bred with everybody and ended up having a bunch of

• 1:43:32Andrew D. Huberman?

  Yeah, he's famous.

• 1:43:32Speaker 00

  bunch of diversity. Scarface, he had a scar on his little black-footed ferret. They are so cute. I recommend everyone who's hearing this, look them up. Like, have a picture of

• 1:43:40Andrew D. Huberman?

  Yeah, don't get one as a pet, trust me.

• 1:43:42Speaker 00

  So this is a successful captive breeding program. And every year, they can release about 500 black-footed ferrets into the wild. But there are two problems. The one is what you mentioned, and that is that there's not that much genetic diversity. There were a handful of founders in this population, all of them were from the same population near Matizzi, Wyoming, so they're already closely related to each other. And over time, the amount of diversity in that population is going to decline. So a few years ago, this collaboration of organizations got together and said, there's a solution to this. In the frozen zoo in San Diego, there are tissue samples from that original captive breeding

• 1:44:22Speaker 00

  population, unrelated to the individuals that were in Matizzi, Wyoming, so different genetic diversity. If we could use cloning, the tools that we will use to make mammoth, that we use to make our dire wolves, that most famously was used to make Dolly the Sheep, we can take those skin cells and turn them into a living black-footed ferret.

• 1:44:44Andrew D. Huberman?

  So revert them to stem cells?

• 1:44:46Speaker 00

  Not in this case. You just take an egg that you harvested from another one, and you inject the cell into the egg. And the proteins in the egg itself can do that epigenetic reprogramming, which is kind of like reverting, but you don't need the Yamanaka factors, you just need the egg to do this. So it becomes a cell that starts to divide and become all the different types of cells that make up an animal. So I think in 2020, Elizabeth Ann was born. Elizabeth Ann was the first clone of 40-year-old tissues from an animal that had lived decades earlier. She was not reproductive, unfortunately. She was never able to have offspring.

• 1:45:18Andrew D. Huberman?

  By behavior, or there was some biological wiring issue?

• 1:45:21Speaker 00

  There was some wiring issue. Her ovaries weren't releasing the eggs or something. I can't remember

• 1:45:27Andrew D. Huberman?

  Cause ferrets are, have this induced ovulation thing, too. They have a kind of funny, funny, I mean, to us, it's funny. To them, it's perfectly normal.

• 1:45:34Speaker 00

  But they did make another one, and from the same line. And that animal has reproduced, and there were offspring from that that can be able to be introduced. So, so here we have a solution to introducing genetic diversity into a population that had lost genetic diversity on the path to extinction. But there's another problem, and that is that the thing that's actually killing the black-footed ferrets in the wild is plague.

• 1:45:58Andrew D. Huberman?

  Bubonic plague?

• 1:45:59Speaker 00

  Plague, yes.

• 1:46:00Andrew D. Huberman?

  I know that there's

• 1:46:01Speaker 00

  That's another reason you don't want to have a ferret as a pet.

• 1:46:03Andrew D. Huberman?

  Well, definitely not a black-footed ferret. I mean, the, the European, you don't want to send me off on a thing. I had a pet ferret, I'll leave many years ago, and I don't recommend them.

• 1:46:12Speaker 00

  But you were, you were going exactly where I'm going.

• 1:46:14Andrew D. Huberman?

  It was domesticated ferret. It was not the, it was not the black-footed ferret.

• 1:46:17Speaker 00

  Domestic ferrets are not susceptible to plague. And that susceptibility must have some genetic underpinning. So if we can figure out what that is, and there are several hypotheses that different teams are working on right now, we could use the tools of synthetic biology, genetic engineering, to edit the genome of these black-footed ferrets and make them resistant to plague. So not only use cloning, a form of genetic rescue, but then also synthetic biology to create animals that are able to survive in this habitat, despite that people have mucked with that habitat in a way that makes their survival hard. We can use these same tools for, for lots of different things. We have a project related to our dodo project with the Mauritian pink pigeon, another

• 1:47:02Andrew D. Huberman?

  Is it actually pink?

• 1:47:03Speaker 00

  It's pink. It's very pink.

• 1:47:05Andrew D. Huberman?

  Well, you pick cool animals to where you're like, woolly mammoth, dodo bird, pink pigeon. You're like, you know, you guys know how to, you know,

• 1:47:12Speaker 00

  It's part of, part of it, right?

• 1:47:13Andrew D. Huberman?

  Oh, a dire wolf. And the dire wolf thing, my understanding is that it was also on the heels of like, the Game of Thrones popularity. So that, that was like a piece, if you weren't going to make a dragon, you might as well make a very large wolf, because it has these kind of connotations.

• 1:47:25Speaker 00

  When I was working on the first dire wolf genomes, way before I was involved with Colossal, but the very first time we published dire wolf DNA, we were desperate to sync the publication with some editor in some, you know, science journal to the Game of Thrones coming out. We were like, we can get this genome done. Surely, they'll be, they'll want our paper, because then they can have some press attention to the dire wolf paper. We never got the DNA finished in time to do that. It was so poorly preserved. They lived in warmer parts of the world, and so it was really hard to find samples that had high-quality DNA to be able to get. It was a fun project, though.

• 1:48:00Andrew D. Huberman?

  Were the babies cute?

• 1:48:01Speaker 00

  Yes.

• 1:48:02Andrew D. Huberman?

  Yeah, okay. They didn't come out ferocious? Yeah?

• 1:48:05Speaker 00

  No, they were extremely adorable.

• 1:48:07Andrew D. Huberman?

  Putting a plug in for the dire wolf here.

• 1:48:08Speaker 00

  Extremely adorable, yes.

• 1:48:10Andrew D. Huberman?

  I bet. Everyone loves a baby animal.

• 1:48:12Speaker 00

  Yeah, well, that's how we got dogs, I'm pretty sure. They were hanging around outside, cleaning up after us, giving us a little bit of advantage, because if something scary came, like a giant cave bear or something, they would howl, and we would, our ancestors would know. But I'm pretty sure that that was just commensal. We could have lived for a long time with them living around us and us living around them, but I think their puppies were cute.

• 1:48:33Andrew D. Huberman?

  Yeah. And you make a really good point. I mean, you know, this notion, like, the eyes of the getting rounder, like in the, in dog breeds, you know, because people like them. I mean, all the doodle breeds, the hypoallergenic breeds, they don't have fur.

• 1:48:46Speaker 00

  I think about that sometimes, because I have two Labradors, and so my house is permanently coated in at least one layer of dog shed hair.

• 1:48:53Andrew D. Huberman?

  We're so comfortable as humans to modify species for our immediate convenience. But sometimes, that's obviously detrimental to entire populations. You're talking about reintroducing a species that have not been there in a long time, or, or expanding their numbers. I would like to think that with AI or other modeling tools, that you could make predictions, not perfect, but better predictions about, okay, let's model in the mosquito population, the, where the swamps are, what the seasons are like, what the coal population looks like. And you could put, you could model as many things that you're aware of. There's no graduate student, no matter how brilliant, or professor, no

• 1:49:36Andrew D. Huberman?

  matter how brilliant, that can mathematically model all the different influences of all these different plant and animal species. But my, but AI can run it 24 hours a day, seven days a week.

• 1:49:46Speaker 00

  Yeah, this idea of digital twins. Can we create a digital twin of an ecosystem, and then perturb it in lots of different ways and see what happens? I think this is totally within the realm of feasibility. It's a big foundational model. But I know there are groups of people who are working on this for, for smaller systems, like individuals, to think about human medicine, how, what happens in this system, this particular organ system, if you perturb it in this way, and using AI to be able to narrow down the window of what edits might be reasonable to make and what might others. I mean, we're doing other things. We have a completely independent group of people that make what we're calling our care reports, which are deep dives into the ecosystems where we would be releasing any future de-extinct animal. We, we release these when we have them. With

• 1:50:30Speaker 00

  the Blue Buck, we have a Blue Buck care report that people can read to figure out what we've thought about in terms of the impact to the ecosystem over short, medium, and long term. And it involves conversations with local stakeholders, and conservation biologists, and people who are thinking about it from all sorts of different perspectives. So it's absolutely, as you say, critically important to think hard before doing things, but also be willing eventually, after you understand as best you can, what that risk was.

• 1:50:58Andrew D. Huberman?

  Yeah. Along those lines, I predict in probably three to five years, not 10, the technology that we were talking about earlier of, of mutating the HIV receptor, that sort of thing will be very commonplace in the context of fertility. I mean, if we knew a certain constellation of disease genes inevitably led to a disease or a high probability of disease, and there was a, a way to use gene editing to rule those out, once that had been established a, a number of times, I'm willing to bet, even outside the Bay Area, that people would want that. Nobody wants a, a harder life for their child.

• 1:51:32Speaker 00

  Right. You know, it could also come, I, I've thought about this, my, my last book is called Life as We Made It. And it's all about how we've been messing with the species that we encounter for as long as we exist. In the last chapter, I think about How we might turn our editing technology on ourselves, really asking the question, what is it that will push us over that edge?

• 1:51:51Andrew D. Huberman?

  Yeah.

• 1:51:51Speaker 00

  One of the possible scenarios is that we have a pandemic, a crisis, and we learn that there are certain people who have a particular genetic variant that means that they will die. And suddenly, the most morally reprehensible thing that we could imagine doing becomes the actual only ethical solution. And that is the thing that pushes us over the edge.

• 1:52:14Andrew D. Huberman?

  You mean, so you're talking about more people dying or rescuing that through gene editing?

• 1:52:18Speaker 00

  Gene editing ourselves.

• 1:52:19Andrew D. Huberman?

  Uh huh. And now we're talking more about public perception, scientists and implementation, and where those intersect. And I think that one thing that I've learned is that a lot of it is about the delivery method. So when we hear about gene editing and you're taking a cell and you're putting it in a dish, or even ICSI, what you described before, like, you know, in a dish of, you're basically injecting a sperm cell into an egg as opposed to running a sperm race, right? People are a little more comfortable with that than they are like the ICSI. It's like, this one, we're taking this one. Already, because you're biasing an outcome in a strong way, right? You're not letting the system decide.

• 1:52:54Speaker 00

  But people are okay with this if, for example, you have a man with a very low sperm count or with very few healthy sperm, where you can take a healthy sperm and put it in the egg.

• 1:53:05Andrew D. Huberman?

  Yeah, no, I think people are comfortable with it now because it's been around for a while.

• 1:53:09Speaker 00

  Right. It's this every new technology, you have your first, is it scary?

• 1:53:12Andrew D. Huberman?

  Right.

• 1:53:12Speaker 00

  Like, why do I hate this? Before, let me be curious.

• 1:53:15Andrew D. Huberman?

  Yeah, I mean, in a different conversation, but one that is relevant, you know, it's, fortunately, we're not talking about it today, but you know, I get asked about peptides like every five minutes these days, and not the peptides of the GLP sort, but what's happened in the health space is that the GLP drugs have de-stigmatized and taken away needle phobia by putting the, it's still a needle, but it's on a pen. And so now people are like, which peptide should I take? And I'm like, how do you get it? No one's saying like, is there a capsule version anymore? That was a big thing.

• 1:53:44Speaker 00

  Right.

• 1:53:44Andrew D. Huberman?

  And now people are like, because it turns out it's the hypodermic part, not the needle that freaks people out.

• 1:53:49Speaker 00

  Right.

• 1:53:49Andrew D. Huberman?

  The needle kind of freaks people out, but people have no problem taking a pen and going, but they don't like using a plunger and a needle.

• 1:53:55Speaker 00

  Right.

• 1:53:55Andrew D. Huberman?

  So now people, needle phobia has plummeted, and people are willing to explore things that, some of which there's good data on, some of which there's like no data, and people are pinning themselves all over the country, right? And so it turns out that something, this couldn't have been predicted, that there was this other thing that was getting in the way. It wasn't really the thing about taking the peptide.

• 1:54:16Speaker 00

  Right.

• 1:54:16Andrew D. Huberman?

  That may or may not have enough data. There are a lot of data on the GLPs, but it really was the delivery method. We saw this with computers, right? They were big clunky things, you had, everyone had to use the same one. Then all of a sudden, you turn it into a phone that's also a camera, and the next thing you know, you kind of forget that it's a computer.

• 1:54:31Speaker 00

  Right.

• 1:54:32Andrew D. Huberman?

  Same thing with brain machine interface. As long as people think you need to drill into the skull or put something, a wire behind the ear, pretty soon this will be non-invasive.

• 1:54:39Speaker 00

  Right.

• 1:54:39Andrew D. Huberman?

  And then people aren't thinking about, oh, it's going to control my brain. So that big fear wall tends to come down to zero through these things that are hard to predict. And it's often a combination of the messaging and kind of like, like maybe everyone should pet a dire wolf just once, just a little bit.

• 1:54:59Speaker 00

  Would you like to pet a dire wolf?

• 1:55:00Andrew D. Huberman?

  I would love to pet a dire wolf, especially the little ones, but you know.

• 1:55:02Speaker 00

  You should come visit us in the lab, and you'll see some of the really cool stuff. We're doing the artificial wombs, our really cool artificial eggs, and there's a.

• 1:55:09Andrew D. Huberman?

  You have artificial wombs?

• 1:55:11Speaker 00

  We have one of our.

• 1:55:12Andrew D. Huberman?

  You realize this is going to terrify people. I'm a biologist, but, okay, so describe to me an artificial womb and what that looks like.

• 1:55:17Speaker 00

  Well, right now, we're thinking about, about mice, right? So the idea is, if we're going to have hundreds of mammoths, we're not going to get there by having 100 Asian elephants pregnant for 22 months with mammoths. We need a way to be able to birth multiple mammoths simultaneously without using elephants. Elephants should be allowed to make elephants, right? And so we'll need to build the technology to do this. But building that technology is also an opportunity to build technology that can really help people and can help other species, but really thinking mostly about people. I have a friend who was diagnosed with breast cancer during her pregnancy, and she had to make a decision about not starting the therapy until she gave birth or taking a

• 1:56:02Speaker 00

  giant risk with the baby. What if we could just take the baby out and be able to put it in a place and have it completely develop? And then she could start the treatment a couple of months earlier. Or if a baby needs surgery, but you can't really do it inside, have a safe way to have that baby come out. These are all technologies that are, will be feasible in the future, that are motivated by de-extinction. How crazy is that?

• 1:56:25Andrew D. Huberman?

  It is wild. One of the most incredible things that I've witnessed is a NICU. It's a different form of what you're describing, but it's incredible. Like, you go in these places and it's room upon room, and it's super quiet, and you know, they're trying to keep it dark. And it's, I mean, like, these are artificial wombs, so to speak, right? These are so preemie babies, and some of which are very preemie. Some have issues and some don't. Some are just early, which is an issue of its own kind. But the NICU technology has come a long, long way. It's, you know, far from perfect, but that's essentially what you're talking about, right?

• 1:56:59Speaker 00

  Yes, a more sophisticated NICU where we've learned so much more because of the complementarity of understanding how genes map to phenotypes and being able to use all of the genetic resources that are available to us from all of the people, and learning about epigenetics, and building this technology that builds on what we understand about the developmental process. I mean, it's a, we are facing a future that I think is really exciting and spectacular, maybe a little bit scary, but I think as long as we keep talking about it and having conversations about it way before it's possible, we can get to a place that people are comfortable with and people are excited about.

• 1:57:38Andrew D. Huberman?

  There seems to be a theme lately in my life where people come on this podcast and they're talking about revolutionizing education. We had someone, the principal of Alpha School, come on here. Kids spend two hours a day on their iPad, learning from an AI tutor that knows exactly what they need to fill every gap in their knowledge.

• 1:57:54Speaker 00

  Cool, I need that.

• 1:57:55Andrew D. Huberman?

  Two hours a day. Then they go like, learn how to farm, start businesses. It was interesting that public reaction is very divided on that. People who say, great, and then other people say, oh yeah, but it costs a lot, so it's only for rich kids. And it turns out they're starting scholarship programs. But the idea there is to figure out the best way to educate humans and then wicked out to everybody.

• 1:58:15Speaker 00

  Yeah.

• 1:58:15Andrew D. Huberman?

  But there has to be this pioneering spirit, and that's always going to stimulate concern, and there's going to be the haves and have nots things in people's minds. I think, thinking about your work in a different but similar vein, where being a pioneer is hard because you have to tolerate people saying, and a lot, sometimes the assumption that, oh, you're doing this just for your own self-interest, it's all financially driven, and what about the, you know, what about the starlings that, you know, need our help right now? There's always this like, what about the things that need our help right now? Why are we doing this? And I don't have any great solutions for you on this, but I think that public education is clearly a big part of it. And I think the humanizing it at the level of who's doing it, like, it's very clear that you love biology.

• 1:58:59Andrew D. Huberman?

  It's very clear that you like hard problems in biology. And it's very clear that, if I may, it seems like you're not afraid of, but you rather enjoy the fantasy positive outcome part of it. It's not all doom and gloom. I mean, this is similar, this example works for me, hopefully it works for you. You know, like Elon wants to go to Mars, and I have guests on the podcast that say like, no, he should be curing humanity here. And I told that person, that's like telling, you know, the Metallica, they should be the Grateful Dead. We need individuals who are thinking in a different way, steeped in really good ethics, and are excited about the problem, to evolve this thing that we call life on earth.

• 1:59:39Speaker 00

  Sure. And I'm good with that if people say to me, oh, why are you working on this? You should be curing cancer. Those are two different, although, you know, there's things that we're.

• 1:59:48Andrew D. Huberman?

  You know what? Quit this. I don't know you, but quit this and go cure cancer.

• 1:59:52Speaker 00

  Well, I mean, we are learning things from elephants, for example, that we have to know about, and that is actually relevant to curing cancer, but that's not our main, I'm not focusing on curing cancer. But people who say, you should do this instead of saving living species, I just really have to push back on that. We are doing both. There is not enough money in conservation. There just isn't. The idea that we're developing tools that are immediately applicable to existing conservation problems, using new funding, new resources, bringing in new investment ideas, excitement, enthusiasm, excitement from students? I mean, why is this not embraced? Why is it always the, well, you must not be doing that?

• 2:00:32Andrew D. Huberman?

  Right.

• 2:00:32Speaker 00

  We are doing that. The dire wolves, when we announced the dire wolves, we announced that we had cloned red wolves, which is the most endangered species of wolf in North American, endemic wolf that, again, is living in a very small population, captive breeding in the Carolinas. We had colleagues, Brigid von Holt, who works at, is at Princeton, who had discovered a population of coyote-like animals that have a bunch of red wolf ancestry, some on the order of more than 75% red wolf ancestry. And so we've cloned these wolves as a means to introduce new red wolf genetic diversity into the existing red wolf population, using the same toolkit that we used to be able to clone and generate our dire wolves. Have you heard about our red wolves?

• 2:01:15Andrew D. Huberman?

  Hmm.

• 2:01:15Speaker 00

  No, they were announced at the same time, though. So all these people who are like, you should be doing this instead of this. Pay attention, we are.

• 2:01:23Andrew D. Huberman?

  They saved the ginger wolves. I love it. Yeah, there's something that I think people need to understand about scientists and probably technologists, too. But that's not my area, which is the person matters. Like, the person doing the work has to be really, really drawn to, almost obsessed with the project. Because you could sort of ask, like, for any scientist, there are a lot of scientists working on kind of pedestrian stuff, in my opinion. He used to review a lot of grants for NIH and go like, eh, sometimes those get funded, sometimes not. But, but that's the kind of science that certain people do. They want to turn a crank. And then there are certain scientists who really want to be out on that, like, really cutting edge. And they have to be obsessed with the question, otherwise you get nothing.

• 2:02:05Andrew D. Huberman?

  In the same way that I think Elon's pretty obsessed, I don't know him, but with this going to Mars thing. And I don't think he's got a bunch of other stuff going on clearly. But you can't really draw him off target by saying, hey, why aren't you working on curing cancer or building? I guess he is building flying cars. So the example of musicians, to me, just works. Like, you can't get Metallica to play the Grateful Dead happily. They're just not going to do it. It's not in their spirit. It's not in their, their soul to do it that way. And so I think that, like, we have to accept this about people. And the people who move things forward, like Howard Hughes, the very Howard Hughes, like, he liked his aircraft, right? He liked, you can't convince people like, oh, you should be saving the coral reefs. Someone else should be saving the coral reefs. But they need to be obsessed with coral reefs.

• 2:02:49Andrew D. Huberman?

  I mean, I'm stating the obvious, but I think from the inside, I relate.

• 2:02:54Speaker 00

  Yeah. Also, people shouldn't feel bad about not being able to do everything. If you think about the amount of time that you have in your life, if you try to do 10 things instead of one thing, you're going to get way less done. You're not going to make an impact, so.

• 2:03:06Andrew D. Huberman?

  It's so interesting. People love to tell other people what to do.

• 2:03:08Speaker 00

  Yeah.

• 2:03:09Andrew D. Huberman?

  But I will say, there are people out there, I know this because of this podcast. There are people out there who are enchanted by biology, that are enchanted by what you've told us today, that are excited about these species and can imagine the positive outcome. And some of them are young and some of them are old, but God bless the young ones because they're the ones. It only takes a few of them in a certain area of science to really move things forward, as you know. So where are the public education efforts outside of podcasting and whatnot? Like, how many people are at Colossal?

• 2:03:40Speaker 00

  There are about 120 scientists and then there's, you know, other, other people involved. We have a huge social media team who put a lot of science bits out for the world, targeting different audiences with different types of information. We work with a lot of podcasters and we work with other teams of people making documentaries and films. We publish papers using the traditional, old-school peer-review process. We post some papers on the archive if we think it's important to get the information out faster before peer-review. So we're trying lots of different methods of communicating. And of course, I go out and talk to people and I'm a National Geographic Explorer. So I do, I take part in the National Geographic Live series.

• 2:04:21Speaker 00

  So I've gone and just talked to communities about, you know, conservation and genetic rescue and de-extinction and a future that can be both biodiverse and filled with people.

• 2:04:31Andrew D. Huberman?

  So in junior high, high school, graduate school, were you sitting there thinking, I'm in a department of zoology at Oxford University and there's a picture of some old dude on the wall. This is how I felt when I went to Cambridge. I'm like, that's Darwin's house. Or like, there are two ways to be in that kind of environment. Like, whoa, that, that's so-and-so and there's this history. Or was it, we can do this all much, much better? Because I get the sense that you like to break the mold, but I don't want to kind of lead the witness here. So what were you like as a kid and in graduate school? Were you thinking, you know, this, this field, this whole zoology thing feels kind of steeped in old stuff and I want to break it open? Or, you know, like, maybe just tell us a little bit about your mindset in, in these kinds of environments?

• 2:05:16Speaker 00

  My, my origin story. I think I always disappoint people with my science origin story. I went to the University of Georgia as a broadcast journalism major. I had worked for the local TV station in the corner of Northwest Georgia where I grew up. I was on air in the mornings. I did local cut-ins on headline news at 24 and 54 after the hour. When I went to the University of Georgia, I was actually the news director of a local radio station that was there, which was not particularly well-aligned with being a freshman at the University of Georgia, we'll just say. I was living in a dorm that had a shared bathroom and we would, I had to be at work at four o'clock in the morning to write and cut the news so I could be on the drive time show. Do you remember these from the 90s, like the, yeah.

• 2:05:56Speaker 00

  So I had an opportunity to take a class after my freshman year. And it was an honors program class and it was geology and archaeology. And it was a nine-week class and we started off on the East Coast and learned about minerals, identifying minerals and the sort of coastal dynamics on the coast, drove across the country, sleeping in national parks, drove up the West Coast, drove back across the country and learned about the formation of the national parks, the landscape that is the US, right? And I thought to myself, as I was watching this, you could see the scars on the landscape from glaciers. And we went to all of these archaeological sites and anthropological sites

• 2:06:39Speaker 00

  and saw the impact of people on the ecosystem and the impact that we had on those people. And I thought, this is the kind of story that I want to tell. Maybe I want to be a science journalist instead of just a regular journalist. The idiocy of people who think they're an expert because they've done something for a few years. I was like, I already know how to be a journalist. I'll just learn how to be a scientist. And so I started taking science classes. I ended up going to Panama, living on a place called Barrow, Colorado Island, and studying parasitoid wasps. And wasn't doing anything related to genetics or really evolution. It was ecology, population ecology. And I met somebody there who was starting up a lab in Edinburgh. And I thought he was really smart and interesting.

• 2:07:21Speaker 00

  We put together this proposal of a project that I could do as a PhD student, where we were going to study the type of wasp that switches back and forth between inbreeding and outbreeding. So the question was, is the switch to inbreeding something that is intended to purge your genome of those deleterious alleles, like the Channel Island foxes? Like, if we inbreed, we'll get rid of all that bad stuff that's accumulated, then we can go back to outbreeding.

• 2:07:44Andrew D. Huberman?

  It's a pressure test.

• 2:07:45Speaker 00

  Yeah. So we designed this experiment. I went back to the University of Georgia. I was like, I'm going to go to Edinburgh. This is going to be great. Help me apply for these scholarships. And they said, cool, because I couldn't afford to go, you know, overseas for grad school. And I said, cool, you can, you can apply, but you have to apply for all of the scholarships that we have for our honors program people together, because it's just one big package. So I applied for the Marshall Scholarship to go to Edinburgh and the Rhodes. And I did not get a first-round interview for the Marshall. So ended up not obviously being able to go to Edinburgh, but I got a Rhodes Scholarship. So I ended up at Oxford.

• 2:08:18Andrew D. Huberman?

  So you are a true, I think you're our first Rhodes Scholar, you know?

• 2:08:22Speaker 00

  I got Rhodes. I ended up at Oxford. I had no idea what I wanted to do or who I was going to work with. And I met on my first few days there, this guy called Alan Cooper, who's a Kiwi. He was setting up an ancient DNA lab. This was one of the few labs at the time that was going to be built to be able to process these old samples. And I was really excited about the idea of ancient DNA because it brought together geology and paleontology and storytelling. If I'm reading DNA sequences from entire ecosystems that used to be alive, I can tell a story about how the environment changed when people first arrived or how the environment changed with rapid warming out of the last ice age.

• 2:09:06Speaker 00

  And I was like, this is the science I want to do. Plus, it was brand new. Nobody was doing it. There were a couple of dinosaur DNA papers that had been published and proven to be false. And it was really an opportunity to bring stuff together that hadn't been done before and just do something entirely new. And he told me that if I joined his lab, I could go to Siberia and that was enough for me. I signed on the line. I was like, I'm in. So that's my origin story. And I think it is because it was new, because it was an opportunity to bring together lots of different disciplines that, you know, otherwise really hadn't been thought of together. I got into de-extinction because everyone who works in ancient DNA is asked as the first question whenever they publish a paper.

• 2:09:49Speaker 00

  This is, you're working in ancient DNA. We're doing stuff that's high profile. We get high profile papers. It's normal in science for this thing to happen. You get interviewed by somebody from the media and the first thing they want to know is, so what does this mean about how close we are to bringing dinosaurs back to life? Every time, every time.

• 2:10:06Andrew D. Huberman?

  I'm more concerned about the black-footed ferrets, frankly.

• 2:10:09Speaker 00

  When I was researching my, my second book, I was using the New York Times Wayback Machine, which is amazing. Love the Wayback Machine. And I was reading the very first article about the very first ancient DNA publication in 1984. Researchers from Berkeley in what was called the Extinct Species Study Group had managed to isolate, using molecular cloning, because this was pre-PCR days, a tiny little fragment of DNA from the skin of a preserved quagga, which is an extinct type of zebra, and show that it was related to a zebra. So the scientific finding was not that illuminating, but the fact that DNA survived after death, this was the first discovery of that. So it was a big deal.

• 2:10:51Speaker 00

  It really set off all of the stuff that became the dinosaur DNA days of ancient DNA.

• 2:10:57Andrew D. Huberman?

  It leads to forensics.

• 2:10:59Speaker 00

  All of the forensic stuff, yeah, all that came, came out of this too. But, but when the journalist interviewed Alan Wilson as the very first ancient DNA researcher, publishing the very first ancient DNA paper, he got to be the first person to ask-

• 2:11:12Andrew D. Huberman?

  The dinosaur question.

• 2:11:14Speaker 00

  The dinosaur question, yes.

• 2:11:15Andrew D. Huberman?

  I mean, it is true that if you walk into the Life Sciences Building at Berkeley, there's a T, full-size T-Rex skeleton there.

• 2:11:20Speaker 00

  It's cool.

• 2:11:21Andrew D. Huberman?

  It's very cool. People love that. I've never been dinosaur obsessed. I, I can think of many more animals and human diseases that to me are more interesting, but this is like the why don't you cure cancer thing, so.

• 2:11:31Speaker 00

  Yes. Well, but I think we get to mammoth because as soon as people hear that and understand that we can't have dinosaurs because there's no dinosaur DNA, they, they tend to settle on mammoth, either mammoth or saber-toothed cat. Those are the two things that, that we get after that. But I think it's just because they're big. You know, it's, it's this big thing. We know they're extinct because our ancestors hunted them. We know they're relatively recent. We can imagine what they looked like. They're in popular culture a bit. And so it's a matter of awe, of interest.

• 2:11:59Andrew D. Huberman?

  I think it's the size and scope that is, they make us feel small.

• 2:12:03Speaker 00

  Yeah. People don't like to feel small, but mammoths make us feel small too, I think, but in a way that we, we can appreciate.

• 2:12:10Andrew D. Huberman?

  Yeah, there's something about the psychology around this in terms of public perception and the dinosaur thing. I'm going to go with that people want the best for our species and other species on average. They're a little scared based on, for reasons that make perfect sense to me, based on what they know and, and what they don't know. For that reason and many other reasons, I'm just grateful that you'd come out here and talk about this stuff today and that you're doing what you do. I thought the dire wolf thing was super cool. I still do.

• 2:12:35Speaker 00

  You should come see them.

• 2:12:36Andrew D. Huberman?

  I got it. I'm not saying that, you know, as a biologist, I got it. You know, developmental biologist, I was like, I got it. This is not like taking some human cells from the cortex and putting them into a mouse cortex. Like, those are cutesy experiments, frankly. I thought those experiments were more like cutesy derivative. They didn't really inform or anything, in my opinion. But what you guys did, I thought was really cool. And then as I started learning more about what you're trying to accomplish, like repair ecosystems, make better ecosystems, I'm all for progress. So thank you for doing what you do, for continuing to do what you do. I didn't even get into the fact that you walked away from a fully thriving lab in academia, Howard Hughes Investigator, which is this thing that very few attain.

• 2:13:19Andrew D. Huberman?

  And so to do this, so clearly you're on a mission and I have every anticipation that it's going to work out and work out for the best for animals and for people. I'm excited to see what you guys do.

• 2:13:29Speaker 00

  Thank you for the opportunity to have this conversation.

• 2:13:31Andrew D. Huberman?

  Yeah, it's a lot of fun for me. I rarely come and talk about ferrets, woolly mammoths, dinosaurs, and human gene editing all in one conversation. Thanks so much.

• 2:13:41Speaker 00

  Thank you.

• 2:13:41Andrew D. Huberman?

  Appreciate you. Thank you for joining me for today's discussion with Dr. Beth Shapiro. To learn more about her work, please see the links in the show note caption. If you're learning from and/or enjoying this podcast, please subscribe to our YouTube channel. That's a terrific, zero-cost way to support us. In addition, please follow the podcast by clicking the follow button on both Spotify and Apple. And on both Spotify and Apple, you can leave us up to a five-star review. And you can now leave us comments at both Spotify and Apple. Please also check out the sponsors mentioned at the beginning and throughout today's episode. That's the best way to support this podcast. If you have questions for me or comments about the podcast, or guests or topics that you'd like me to consider for the Huberman Lab podcast, please put those in the comments section on YouTube. I do read all the comments.

• 2:14:24Andrew D. Huberman?

  And if you're not already following me on social media, I am Huberman Lab on all social media platforms. So that's Instagram, X, Threads, Facebook, and LinkedIn. And on all those platforms, I discuss science and science-related tools, some of which overlaps with the content of the Huberman Lab podcast, but much of which is distinct from the information on the Huberman Lab podcast. Again, it's Huberman Lab on all social media platforms. And if you haven't already subscribed to our Neural Network Newsletter, the Neural Network Newsletter is a zero-cost monthly newsletter that includes podcast summaries as well as what we call protocols in the form of one-to-three-page PDFs that cover everything from how to optimize your sleep, how to optimize dopamine, deliberate cold exposure. We have a foundational fitness protocol that covers cardiovascular training and resistance training.

• 2:15:08Andrew D. Huberman?

  All of that is available completely zero cost. You simply go to hubermanlab.com, go to the menu tab in the top right corner, scroll down to newsletter, and enter your email. And I should emphasize that we do not share your email with anybody. Thank you once again for joining me for today's discussion with Dr. Beth Shapiro. And last, but certainly not least, thank you for your interest in science.