Philip Bethge

Tag: cloning

  • The Second Cooing: Raising Passenger Pigeons from the Dead

    The Second Cooing: Raising Passenger Pigeons from the Dead

    The world has been without passenger pigeons since 1914. Now, scientists want to bring them back. Geneticist Ben Novak has embarked on the project and has begun collecting passenger pigeon DNA from natural history museums. His “de-extinction” efforts are not without critics.

    By Philip Bethge

    The eye sockets of the slender pigeon are filled with light-colored cotton. Its neck feathers shimmer in iridescent colors, and it has a russet chest and a slate-blue head. The yellowed paper tag attached to its left leg reads: “Coll. by Capt. Frank Goss, Neosho Falls, Kansas, July 4, 1875.”

    Ben Novak lifts up the stuffed bird to study the tag more closely. Then he returns the pigeon to a group of 11 other specimens of the same species, which are resting on their backs in a wooden drawer. “It’s easy to see just dead birds,” he says. “But imagine them alive, billions of birds. What would they look like in the sky?”

    Novak has an audacious plan. He wants to resurrect the passenger pigeon. Vast numbers of the birds once filled the skies over North America. But in 1914 Martha, the last of her species, died in a zoo in Cincinnati, Ohio.

    Novak, a researcher with the Long Now Foundation, a California think tank, wants to give the species a second chance. At the Museum of Vertebrate Zoology in Berkeley, Novak used a scalpel to slice small tissue samples from the red-painted toes of the passenger pigeons kept there. He hopes to isolate tiny bits of DNA from the samples and use them to assemble an entire genotype. His ultimate goal is the resurrection of the passenger pigeon.

    “It should be possible to reconstruct the entire genome of the passenger pigeon,” says Novak. “The species is one of the most promising candidates for reintroducing an extinct species.”

    The art of breathing new life into long-extinct species is in vogue among biologists. The Tasmanian devil, the wooly rhinoceros, the mammoth, the dodo and the gastric-breeding frog are all on the list of candidates for revival. To recover the genetic makeup of species, experts cut pieces of tissue from stuffed zoological rarities, pulverize pieces of bone or search in the freezers of their institutions for samples of extinct animals.

    The Dream of “De-Extinction”

    The laboratory techniques to create new life with bits of genetic material were pure fantasy in the past. But now scientists believe that the vision could become reality, step by step. Experts in bioengineering, zoologists, ethicists and conservationists recently met in Washington, DC for a public forum on “de-extinction.”

    “Extinct animals are the most endangered species of them all” because “there is hardly anything left but the DNA,” says Stewart Brand of the Long Now Foundation, which co-hosted the meeting with the National Geographic Society. The current showpiece project in bioengineering is the rebirth of the passenger pigeon.

    The story of Ectopistes migratorius is a striking example of human hubris. When the Europeans arrived, the passenger pigeon was probably the most common bird on the American continent. The birds travelled in giant flocks, sometimes several hundred kilometers long. “The air was literally filled with pigeons,” naturalist John Audubon wrote in 1831, after observing the spectacle. “The light of noon-day was obscured as by an eclipse.”

    During their long migrations, the pigeons devastated entire forests. They descended upon their breeding grounds in eastern North America by the millions. There are historical accounts, for example, of a breeding ground in Wisconsin the size of Tokyo, where an estimated 136 million passenger pigeons came to breed. The noise was deafening.

    Living in a flock guaranteed the pigeons safety from predators. But the behavior also sealed their fate. When hunters discovered passenger pigeons as game birds, they were able to kill them with brutal efficiency, either by catching them in nets or shooting them with birdshot. They also placed pots of burning sulfur under trees until the birds, anesthetized by the vapors, dropped to the ground like overripe fruit.

    In some breeding areas, hunters slaughtered up to 50,000 passenger pigeons a day. The birds were shipped by the ton in freight cars and sold to be grilled at a few cents a dozen.

    Sequencing the Pigeon DNA

    By the time the establishment of a closed season for the birds was proposed in the US state of Minnesota in 1897, it was already too late. The last wild passenger pigeon was shot to death in 1900. Then, Pigeon Martha — named after Martha Washington, the country’s first First Lady — finally met her end at around noon on Sept. 1, 1914. She was the last surviving specimen in an unsuccessful program to breed the birds in captivity.

    Novak’s goal is to bring back the species, and he seems perfect for the job. In elementary school, he completed a project on the dodo, the extinct bird species from Mauritius. The passenger pigeon has fascinated him for years. “We caused the extinction of the species,” says the 26-year-old. “Now we have a moral obligation to bring them back.” To that end, the genetic detective is visiting natural history museums to take tissue samples from as many of the roughly 1,500 remaining samples of the skin and bones of the bird as possible.

    The passenger pigeon’s DNA has about 1.3 billion base pairs. Their sequence describes what the bird looks like, what its call sounds like and how it behaves. However, the animal’s genetic material in the museums is shredded into miniscule pieces, degraded by bacteria and contaminated with foreign DNA. But that doesn’t deter Novak. He and Beth Shapiro, an evolutionary biologist at the University of California in Santa Cruz, have begun to decode the bird’s DNA.

    The biologists have an ambitious plan. Bit by bit, they intend to match the DNA sequence of the passenger pigeon with that of its close relative, the band-tailed pigeon. Then they will essentially stamp out the divergent sequences from the band-tailed pigeon genome and replace them with synthesized passenger pigeon genetic material.

    With the help of the genome created in this fashion, the scientists will create primordial germ cells for the passenger pigeon, which will then be implanted into young embryos of an easy-to-breed pigeon species. The scientists hope that once they have grown and mated, the pigeons will lay eggs that will hatch into passenger pigeons.

    Chickens in a Duck’s Egg

    The procedure is not only complicated, but also largely untested. But, says Novak, “all the necessary steps are being studied intensively right now.” For instance, he explains, biologists have already managed to insert primordial germ cells from chickens into duck eggs. The drakes that emerged a short time later actually carried the sperm cells of chickens.

    Novak is already thinking beyond the hatching of the first passenger pigeon. Once a flock of the birds has been created, he plans to release them into the wild. “The passenger pigeon was a keystone species in the forest ecosystems,” says Novak, explaining that the destructive force of the flocks led to a radical rejuvenation of forests. Thick layers of pigeon droppings fertilized the soil, which soon led to new growth. “Passenger pigeons are the dance partners of the forest,” the scientist raves. And the “ballroom” still exists.

    But even if scientists can pull off this feat, does it really make sense to bring a long-extinct species back into the world? “Conservation biology’s priority must remain that of ensuring a future for species (currently) existing on the planet,” retired Professor Stanley Temple of the University of Wisconsin-Madison says critically. He fears that species extinction could be trivialized in the future. “People might say: ‘Can’t we let them go extinct and bring them back later?’”

    Zoologist David Ehrenfeld of Rutgers University also criticizes the species resurrection projects, saying that they are “extremely expensive” and, in light of a global species crisis, downright absurd. “At this very moment, brave conservationists are risking their lives to protect dwindling groups of existing African forest elephants from heavily armed poachers, and here we are talking about bringing back the wooly mammoth,” he says.

    Ehrenfeld also doesn’t believe that revived species would stand much of a chance of survival. “Who will care for the passenger pigeon chicks?” he asks, noting that parental care is “critical” for the development of young birds.

    Darkened Skies

    But Novak rejects the criticism. “Passenger pigeon parents were never incredibly involved in raising their young,” he says. He also plans to teach the chicks the basics of passenger pigeon life by dyeing carrier pigeons and essentially using them as flight controllers for the returning species.

    “We’ll ferry them with homing pigeons down to wintering grounds and back to the breeding area,” he says. “After a few years, we have passenger pigeons that fly the same (routes) as their forefathers.”

    When that happens, clouds of passenger pigeons will darken the skies once again, and another dream could be fulfilled for Novak. “Part of me would really love a passenger pigeon as a pet,” says the scientist. And perhaps, he adds, the pigeon zoo could even be expanded.

    There are 50 extinct pigeon species worldwide, says Novak. He has already earmarked three of them for resurrection: the Japanese silver-banded pigeon, the Choiseul crested pigeon and the thick-billed ground dove.

    “I am a pigeon nut,” says Novak.

    Translated from the German by Christopher Sultan

  • SPIEGEL Blog: Surrogate Mother (Not Yet) Sought for Neanderthal

    An interview published last week by SPIEGEL with American genetic scientist George Church has sparked frenetic media speculation about a supposed plan to bring the Neanderthal back from the dead. Church feels his remarks were mistranslated, but it was other media outlets that twisted his words.

    “Wanted: Surrogate Mother For Neanderthal,” screamed an article in the Berliner Kurier tabloid in the German capital on Tuesday, complete with an image of a grinning, bearded caveman. Britain’s Independent seemed positively creeped out by a Harvard professor who wanted to bring such beings back to life as some kind of “Palaeolithic Park.” Meanwhile, the Daily Telegraph implored: “Spare Neanderthals This Modern Freak Show.”

    Media and websites around the world — in Britain, Italy, Poland, Greece, Hungary, Russia, South Korea and Turkey — expressed interest in the idea of resurrecting the Neanderthal. By Wednesday morning, more than 600 sources on Google News had reported the story, with all citing SPIEGEL as their source. What happened?

    The source of the net furore was an interview SPIEGEL conducted with George Church. The Harvard University genetic researcher then provided an explanation to the Boston Herald for the sudden media fever. He blamed it on an error downstream of SPIEGEL. He said it had been incorrectly reported that he was looking for a surrogate mother to carry a Neanderthal clone.

    The sudden interest in the Neanderthal, our human cousin, may tell us a little bit about the diffuse fear of overly ambitious genetic researchers. But it tells us even more about the laws of tabloid journalism.

    In this case, the entire brouhaha arose in articles written outside of SPIEGEL’s domain. And it is important to us to communicate this because we make a significant effort to ensure that our stories are correctly translated when they appear on our English-language website. Occasionally mistakes slip through — as is inevitable with any site that relies heavily on translation — but when they do we are quick to correct them.

    In addition, we sent Church an English version of our interview the week before it went to print for authorization. This provided him with an opportunity to change any formulations that may have caused any room for misinterpretation. We did make some alterations later without checking, and have since apologized to him for introducing the word “hell,” which he did not say.

    A Storm of Coverage

    It should quickly be obvious to anyone following the hype over the Neanderthal surrogate mother closely that the storm of coverage didn’t break out until a week after the interview was published. Last Friday, we posted the interview, which we had requested from George Church because we had been fascinated by his latest book. The title alone, “Regenisis,” seemed promising.

    And Church didn’t disappoint in his interview. He laid out the great future he believes the still relatively young research field of “synthetic biology” will have. Regardless whether he was discussing the cloning of humans, the genetic optimization of Homo sapiens, the manipulation of the genetic code of all life forms or the re-creation of the Neanderthal, nothing was treated as taboo in his interview. In other words, it offered plenty of fodder for both controversy and thrilling entertainment.

    The interview first appeared in the German-language print edition of SPIEGEL on Monday, Jan. 14, and the raft of outraged reader letters reflected the intense interest the interview generated. Church has always presented himself as a bold and argumentative visionary who won’t hesitate to consider anything that might be scientifically feasible.

    Initially, few media outlets picked up the story. Nor did that change after we posted a short article focusing primarily on Church’s remarks on the potential for resurrecting the Neanderthal on SPIEGEL ONLINE in German. The hype machine got going shortly after that.

    It was only then that the story was given the decisive spin — by other media outlets. Early tweets on the interview, may have helped to set the tone, like one person who tweeted: “My life’s new ambition: Mate with a Neanderthal woman.” A short time later, the first journalist stumbled across the interview’s emotive word: “surrogate.” That’s when headlines like the one that appeared in the Daily Mail — “Harvard professor seeks mother for cloned cave baby” — were born. Subsequent tweets are already discussing the possibility of a film being made of the story.

    The question of whether a surrogate mother could be used for a possible future Neanderthal clone does in fact pop up in the interview. In the question, we cite a passage in Church’s book in which he writes that, “a whole Neanderthal creature itself could be cloned by a surrogate mother chimp — or by an extremely adventurous female human.”

    No Want Ad Implied

    It would have to be clear to anyone who gives that passage in the interview a critical read — and the same applies to both the German and English versions — that it is in no way intended as some kind of want or personal ad. Church didn’t mean it that way and we didn’t understand it to mean that either. Really, what Church was explaining is that he considers the rebirth of the Neanderthal to be technically possible. He also explains the steps that would be necessary to get there. The last step, someday, would be the search for a surrogate mother. He also says that he believes the chances are good that he might experience the birth of the first Neanderthal clone within his lifetime. We thought that statement alone was a bit of a reach, particularly given that Church is 58 years old today.

    We’re sorry that Church, who provided us with such fascinating insights into his research, has now become the victim of media hype. In the course of the past two decades, he told the Boston Herald, he has done perhaps 500 interviews about his research and this is the first one to spiral out of control quite like this.

    What’s perhaps most bizarre about the entire media hysteria over Church’s interview is that potential surrogate mothers are now contacting the geneticist. His concern — at least if things get to that stage — that he will have difficulty finding potential surrogate mothers appears to be unfounded.

    *Editor’s Note: At the request of George Church, five changes have been made to the above text. In particular, he wanted to avoid the impression that he had blamed a translation error on the part of DER SPIEGEL for the confusion that ensued following the interview’s publication.

     

  • Interview with George Church: Can Neanderthals Be Brought Back from the Dead?

    In a SPIEGEL interview, synthetic biology expert George Church of Harvard University explains how DNA will become the building material of the future — one that can help create virus-resistant human beings and possibly bring back lost species like the Neanderthal.

    –> Update: The Interview has sparked frenetic media speculation about a supposed plan to bring the Neanderthal back from the dead. Church feels his remarks were mistranslated, but it was other media outlets that twisted his words.

    George Church, 58, is a pioneer in synthetic biology, a field whose aim is to create synthetic DNA and organisms in the laboratory. During the 1980s, the Harvard University professor of genetics helped initiate the Human Genome Project that created a map of the human genome. In addition to his current work in developing accelerated procedures for sequencing and synthesizing DNA, he has also been involved in the establishing of around two dozen biotech firms. In his new book, “Regenesis: How Synthetic Biology Will Reinvent Nature and Ourselves,” which he has also encoded as strands of DNA and distributed on small DNA chips, Church sketches out a story of a second, man-made Creation.

    SPIEGEL recently sat down with Church to discuss his new tome and the prospects for using synthetic biology to bring the Neanderthal back from exctinction as well as the idea of making humans resistant to all viruses.

    SPIEGEL: Mr. Church, you predict that it will soon be possible to clone Neanderthals. What do you mean by “soon”? Will you witness the birth of a Neanderthal baby in your lifetime?

    Church: I think so, but boy there are a lot of parts to that. The reason I would consider it a possibility is that a bunch of technologies are developing faster than ever before. In particular, reading and writing DNA is now about a million times faster than seven or eight years ago. Another technology that the de-extinction of a Neanderthal would require is human cloning. We can clone all kinds of mammals, so it’s very likely that we could clone a human. Why shouldn’t we be able to do so?

    SPIEGEL: Perhaps because it is banned?

    Church: That may be true in Germany, but it’s not banned all over the world. And laws can change, by the way.

    SPIEGEL: Would cloning a Neanderthal be a desirable thing to do?

    Church: Well, that’s another thing. I tend to decide on what is desirable based on societal consensus. My role is to determine what’s technologically feasible. All I can do is reduce the risk and increase the benefits.

    SPIEGEL: So let’s talk about possible benefits of a Neanderthal in this world.

    Church: Well, Neanderthals might think differently than we do. We know that they had a larger cranial size. They could even be more intelligent than us. When the time comes to deal with an epidemic or getting off the planet or whatever, it’s conceivable that their way of thinking could be beneficial.

    SPIEGEL: How do we have to imagine this: You raise Neanderthals in a lab, ask them to solve problems and thereby study how they think?

    Church: No, you would certainly have to create a cohort, so they would have some sense of identity. They could maybe even create a new neo-Neanderthal culture and become a political force.

    SPIEGEL: Wouldn’t it be ethically problematic to create a Neanderthal just for the sake of scientific curiosity?

    Church: Well, curiosity may be part of it, but it’s not the most important driving force. The main goal is to increase diversity. The one thing that is bad for society is low diversity. This is true for culture or evolution, for species and also for whole societies. If you become a monoculture, you are at great risk of perishing. Therefore the recreation of Neanderthals would be mainly a question of societal risk avoidance.

    SPIEGEL: Setting aside all ethical doubts, do you believe it is technically possible to reproduce the Neanderthal?

    Church: The first thing you have to do is to sequence the Neanderthal genome, and that has actually been done. The next step would be to chop this genome up into, say, 10,000 chunks and then synthesize these. Finally, you would introduce these chunks into a human stem cell. If we do that often enough, then we would generate a stem cell line that would get closer and closer to the corresponding sequence of the Neanderthal. We developed the semi-automated procedure required to do that in my lab. Finally, we assemble all the chunks in a human stem cell, which would enable you to finally create a Neanderthal clone.

    SPIEGEL: And the surrogates would be human, right? In your book you write that an “extremely adventurous female human” could serve as the surrogate mother.

    Church: Yes. However, the prerequisite would, of course, be that human cloning is acceptable to society.

    SPIEGEL: Could you also stop the procedure halfway through and build a 50-percent Neanderthal using this technology.

    Church: You could and you might. It could even be that you want just a few mutations from the Neanderthal genome. Suppose you were to realize: Wow, these five mutations might change the neuronal pathways, the skull size, a few key things. They could give us what we want in terms of neural diversity. I doubt that we are going to particularly care about their facial morphology, though (laughs).

    SPIEGEL: Might it one day be possible to descend even deeper into evolutionary history and recreate even older ancestors like Australopithecus or Homo erectus?

    Church: Well, you have got a shot at anything where you have the DNA. The limit for finding DNA fragments is probably around a million years.

    SPIEGEL: So we won’t be seeing the return of the caveman or dinosaurs?

    Church: Probably not. But even if you don’t have the DNA, you can still make something that looks like it. For example, if you wanted to make a dinosaur, you would first consider the ostrich, one of its closest living relatives. You would take an ostrich, which is a large bird, and you would ask: “What’s the difference between birds and dinosaurs? How did the birds lose their hands?” And you would try to identify the mutations and try to back engineer the dinosaur. I think this will be feasible.

    SPIEGEL: Is it also conceivable to create lifeforms that never existed before? What about, for example, rabbits with wings?

    Church: So that’s a further possibility. However, things have to be plausible from an engineering standpoint. There is a bunch of things in birds that make flying possible, not just the wings. They have very lightweight bones, feathers, strong breast muscles, and the list goes on.

    SPIEGEL: Flying rabbits and recreated dinosaurs are pure science fiction today. But on the microbe level, researchers are already creating synthetic life. New bacteria detect arsenic in drinking water. They create synthetic vaccines and diesel fuel. You call these organisms “novel machines”. How do they relate to the machines we know?

    Church: Well, all organisms are mechanical in the sense that they’re made up of moving parts that inter-digitate like gears. The only difference is that they are incredibly intricate. They are atomically precise machines.

    SPIEGEL: And what will these machines be used for?

    Church: Oh, life science will co-opt almost every other field of manufacturing. It’s not limited to agriculture and medicine. We can even use biology in ways that biology never has evolved to be used. DNA molecules for example could be used as three-dimensional scaffolding for inorganic materials, and this with atomic precision. You can design almost any structure you want with a computer, then you push a button — and there it is, built-in DNA.

    SPIEGEL: DNA as the building material of the future?

    Church: Exactly. And it’s amazing. Biology is good at making things that are really precise. Take trees for example. Trees are extremely complicated, at least on a molecular basis. However, they are so cheap, that we burn them or convert them into tables. Trees cost about $50 a ton. This means that you can make things that are nearly atomically precise for five cents a kilo.

    SPIEGEL: You are seriously proposing to build all kinds of machines — cars, computers or coffee machines — out of DNA?

    Church: I think it is very likely that this is possible. In fact, computers made of DNA will be better than the current computers, because they will have even smaller processors and be more energy efficient.

    SPIEGEL: Let’s go through a couple of different applications of synthetic biology. How long will it take, for example, until we can fill our tanks with fuel that has been produced using synthentic microbes?

    Church: The fact is that we already have organisms that can produce fuel compatible with current car engines. These organisms convert carbon dioxide and light into fuels by basically using photosynthesis.

    SPIEGEL: And they do so in an economically acceptable way?

    Church: If you consider $1.30 a gallon for fuel a good number, then yeah. And the price will go down. Most of these systems are at least a factor of five away from theoretical limits, maybe even a factor of 10.

    SPIEGEL: So we should urgently include synthetic life in our road map for the future energy supply in Germany?

    Church: Well, I don’t necessarily think it’s a mistake to go slowly. It is not like Germany is losing out to lots of other nations right now, but there should be some sort of engineering and policy planning.

    –> Read original interview at SPIEGEL Online International

    Is Church Playing God?

    SPIEGEL: Germans are traditionally scared of genetically modified organisms.

    Church: But don’t forget: The ones we are talking about won’t be farm GMOs. These will be in containers, and so if there’s a careful planning process, I would predict that Germany would be as good as any country at doing this.

    SPIEGEL: There has been a lot of fierce public opposition to genetic engineering in Germany. How do you experience this? Do you find it annoying?

    Church: Quite to the contrary. I personally think it has been fruitful. And I think there are relatively few examples in which such a debate has slowed down technology. I think we should be quite cautious, but that doesn’t mean that we should put moratoriums on new technologies. It means licensing, surveillance, doing tests. And we actually must make sure the public is educated about them. It would be great if all the politicians in the world were as technologically savvy as the average citizen is politically savvy.

    SPIEGEL: Acceptance is highest for such technology when it is first applied in the medical industry …

    Church: … yes, and the potential of synthetic life is particularly large in pharmaceuticals. The days of classic, small molecule drugs may be numbered. Actually, it is a miracle that they work in the first place. They kind of dose your whole body. They cross-react with other molecules. Now, we are getting better and better at programming cells. So I think cell therapies are going to be the next big thing. If you engineer genomes and cells, you have an incredible amount of sophistication. If you take AIDS virus as an example …

    SPIEGEL: … a disease you also want to beat with cell therapy?

    Church: Yes. All you have to do is take your blood cell precursors out of your body, reengineer them using gene therapy to knock out both copies of your CCR5 gene, which is the AIDS receptor, and then put them back in your body. Then you can’t get AIDS any more, because the virus can’t enter your cells.

    SPIEGEL: Are we correct in assuming you wouldn’t hesitate to use germ cell therapy, as well, if you could improve humans genetically in this way?

    Church: Well, there are stem cell therapies already. There are hematopoietic stem cell transplants that are widely practiced, and skin stem cell transplants. Once you have enough experience with these techniques you can start talking about human cloning. One of the things to do is to engineer our cells so that they have a lower probability of cancer. And then once we have a lower probability of cancer, you can crank up their self-renewal properties, so that they have a lower probability of senescence. We have people who live to be 120 years old. What if we could all live 120 years? That might be considered desirable.

    SPIEGEL: But you haven’t got any idea which genes to change in order to achieve that goal.

    Church: In order to find out, we are now involved in sequencing as many people as possible who have lived for over 110 years. There are only 60 of those people in the world that we know of.

    SPIEGEL: Do you have any results already?

    Church: It’s too early to say. But we collected the DNA of about 20 of them, and the analysis is just beginning.

    SPIEGEL: You expect them all to have the same mutation that guarantees longevity?

    Church: That is one possibility. The other possibility is that they each have their own little advantage over everybody else. What we are looking for is protective alleles. If they each have their own answer, we can look at all of them and ask, what happens if you put them all in one person? Do they cancel each other out, or do they synergize?

    SPIEGEL: You seriously envisage a new era, in which genes are used as anti-aging-cures?

    Church: Why not? A lot of things that were once left to luck no longer have to be if we add synthetic biology into the equation. Let’s take an example: virus resistance …

    SPIEGEL: … which is also achievable using synthetic biology?

    Church: Yes, it turns out there are certain ways to make organisms of any kind resistent to any viruses. If you change the genetic code …

    SPIEGEL: … you are talking about the code that all life forms on Earth use to code their genetic information?

    Church: Exactly. You can change that code. We’re testing that out in bacteria and it might well be possible to create completely virus-resistant E. coli, for example. But we won’t know until we get there. And I am not promising anything. I am just laying out a path, so that people can see what possible futures we have.

    SPIEGEL: And if it works in bacteria, you presumably could then move on to plants, animals and even humans? Which means: no more measles, no more rabies, no more influenza?

    Church: Sure. And that would be another argument for cloning, by the way, since cloning is probably going to be recognized as the best way of building such virus resistance into humans. As long as it is safe and tested slowly, it might gain acceptance. And I’m not advocating. I’m just saying, this is the pathway that might happen.

    SPIEGEL: It all sounds so easy and straightforward. Aren’t biological processes far more complicated than you would like to lead us to believe?

    Church: Yes, biology is complicated, but it’s actually simpler than most other technologies we are dealing with. The reason is that we have received a great gift that biology has given to us. We can just take a little bit of DNA and stick it into a human stem cell, and all the rest of it is self-assembled. It just happens. It’s as if a master engineer parked a spacecraft in our back yard with not so many manuals, but lots of goodies in it that are kind of self-explanatory. You pick up something and you pretty much know what it does after a little study.

    SPIEGEL: Do you understand that there will be people who feel rather uncomfortable with the notion of changing the genome of the human species?

    Church: I think the definition of species is about to change anyway. So far, the definition of different species has been that they can’t exchange DNA. But more and more, this species barrier is falling. Humans will probably share genes with all sorts of organisms.

    SPIEGEL: First you propose to change the 3-billion-year-old genetic code. Then you explain how you want to create a new and better man. Is it any wonder to you when people accuse you of playing God?

    Church: I certainly respect other people’s faith. But, in general, in religion you wouldn’t want people to starve. We have 7 billion people living on this planet. If part of the solution to feed those people is to make their crops resistant to viruses, then you have to ask: Is there really anything in the Bible that says you shouldn’t make virus-resistant crops? I don’t think there’s anything fundamentally more religiously problematic about engineering a dog or a cow or a horse the way we have been doing it for 10,000 years versus making a virus-resistant crop.

    SPIEGEL: Virus-resistant crops is one thing. Virus-resistant humans is something altogether different.

    Church: Why? In technology, we generally don’t take leaps. It’s this very slow crawl. We are not going to be making a virus-resistant human before we make a virus-resistant cow. I don’t understand why people should be so deeply hurt by that kind of technology.

    SPIEGEL: Apart from religious opposition, biotechnology also generates very real fears. Artificial lifeforms which might turn out to be dangerous killer-bugs. Don’t we need special precautions?

    Church: We have to be very cautious, I absolutely agree. I almost never vote against caution or regulations. In fact, I requested them for licensing and surveillance of synthetic biology. Yes, I think the risks are high. The risks of doing nothing are also high, if you consider that there are 7 billion people who need food and are polluting the environment.

    SPIEGEL: Mr. Church, do you believe in God?

    Church: I would be blind, if I didn’t see that faith in an overall plan resulted in where we are today. Faith is a very powerful force in the history of humanity. So I greatly respect different kinds of faith. Just as I think diversity is a really good thing genetically, it’s also a good thing societally.

    SPIEGEL: But you’re talking about other people’s faith. What about your own faith?

    Church: I have faith that science is a good thing. Seriously, I’d say that I am very much in awe of nature. In fact, I think to some extent, “awe” was a word that was almost invented for scientists. Not all scientists are in awe, but scientists are in a better position to be in awe than just about anybody else on the planet, because they actually can imagine all the different scales and all the complexity. A poet sees a flower and can go on and on about how beautiful the colors are. But what the poet doesn’t see is the xylem and the phloem and the pollen and the thousands of generations of breeding and the billions of years before that. All of that is only available to the scientists.

    SPIEGEL: Mr. Church, we thank you for this conversation.

    Interview conducted by Philip Bethge and Johann Grolle.

    –> Read original interview at SPIEGEL Online International

  • Preservation in a Petri Dish: Scientists Hope Cloning Will Save Endangered Animals

    Biotechnicians want to use cloning to save endangered species, but they are having only limited success. Critics say that the push toward a new era of wildlife conservation trivializes extinction and funding would be better spent on preserving animal habitats.

    By Philip Bethge

    A number of times each week, Martha Gómez creates new life. Today, she has set out to produce a South African black-footed cat. Using a razor-thin hollow needle under a microscope, the veterinarian injects a body cell from the endangered species into an enucleated egg cell taken from a house cat. Then she applies an electric current.

    “Nine volts of alternating current for five microseconds, then 21 volts of direct current for 35 microseconds,” says Gómez. Zap! The egg cell rapidly flexes from the electric surges. It bubbles inside the cell. Then everything is calm.

    “I will check in half an hour if the cells have fused properly,” says the researcher from the Audubon Center for Research of Endangered Species in New Orleans. The very next day, the cloned embryos will be implanted into the uterus of a common domestic house cat, which will serve as a surrogate mother for a foreign species.

    Biotechnicians like Gómez are hoping for a new era of wildlife conservation. In a bid to save endangered species, they tear down biological barriers and create embryos that contain cell material from two different species of mammals. Iberian lynxes, tigers, Ethiopian wolves and panda bears could all soon be carried to term by related surrogate mothers, and thus saved for future generations.

    “Interspecies cloning is an amazing tool to ensure that an endangered species carries on,” says Gómez. “We can’t wait until those species have disappeared.”

    High Mortality Rate

    The world’s first surrogate mother of a cloned animal from another species had udders and was named Bessie. In early 2001, the cow delivered a gaur via cesarean section in the United States. The endangered wild ox calf, native to Southeast Asia, had been cloned by the US company Advanced Cell Technology. But the gaur lived only briefly, dying of common dysentery within 48 hours of birth.

    Since then, researchers have made dozens of attempts at interspecies cloning — but with limited success. Whenever animals were brought into the world alive, they usually died shortly thereafter.

    In 2009, for instance, biotechnicians managed to clone a Pyrenean ibex. The egg was donated by a common domesticated goat. After the birth, the kid desperately gasped for air. Seven minutes later, it was dead.

    Many cloning experiments end this way. Geneticists have so far only been able to speculate on the reasons, but the string of failures actually tends to spur researchers to continue. Gómez, for instance, has specialized in cloning wildcats — and has been quite successful. Cloned African wildcats Ditteaux, Miles and Otis are living in enclosures at the Audubon Center animal facility, and snarl at anyone who approaches them. “They are doing perfectly fine,” says Gómez.

    In addition to African wildcats, the researcher has created embryos for sand cats, black-footed cats and rusty-spotted cats. The surrogate mothers and egg cell donors are domestic house cats, which are both easy to keep and have a reproductive biology that has been thoroughly studied. The animals in Gómez’s research department come under the knife a number of times each week.

    –> Read original article at DER SPIEGEL International

    Saving Genetic Material for the Future

    Today, for example, Olivia the cat is lying on her back on the operating table with her legs spread out. Using a scalpel, research assistant Michal Soosaar makes small incisions in the anesthetized cat’s smoothly shaved abdomen, inserting operating instruments and a miniature camera.

    A monitor immediately provides a view of Olivia’s insides. Soosaar uses tiny forceps to take hold of one of her ovaries. Surgeon Earle Pope then uses a needle to puncture one of the mature follicles. A bloody liquid flows from the cat’s body through a plastic hose and into a test tube.

    The liquid contains mature egg cells from Olivia. In an adjoining room, these circular cells are fished out of the liquid. Now, cell researcher Gómez takes over. Gazing through a microscope, she draws the genetic material from the egg cell and inserts a skin cell from a wildcat. As soon as the cells have merged and embryos have started to grow, they are implanted into the uterus of a surrogate mother.

    “This technology is a viable way to preserve genetic material for the future,” says Gómez. It’s very difficult to collect egg cells and sperm from rare wildcats, she explains, but much easier to obtain skin samples. She goes on to explain that embryos cloned in this manner could be stored for decades in liquid nitrogen and reactivated when needed.

    “By bringing cloning into the set of public policy instruments, we can protect more species, reduce economic costs of protection, or both,” writes US economist Casey Mulligan in a commentary in the New York Times. Mulligan argues that it’s now necessary to freeze the cell material of endangered species and develop technologies that will make it possible to bring the animals back to life after they have become extinct. “In some cases, it may be cheaper to save some DNA, and let a future, richer and perhaps more enthusiastic generation make its own copy of the species,” Mulligan writes.

    Critics Prefer Habitat Conservation

    Other researchers remain unconvinced, though. “The idea of cloning endangered species trivializes what extinction really is,” says zoologist Robert DeSalle from the American Museum of Natural History in New York. He argues that the suggestion is a sign of today’s “Western throwaway society,” and says that “technology can’t solve the problem of large-scale extinction.”

    The World Wildlife Fund (WWF) also opposes cloning as a quick-fix solution. “Habitats cannot be cloned,” says WWF wildlife expert Sybille Klenzendorf. She says that a species is more than just the sum of its genes. “What use is a cloned animal if we have no more space where the species can live?” asks Klenzendorf. She also argues that cloning is far too expensive. “The money would be better invested on direct aid to maintain habitats,” she says.

    The poor success rate of less than seven percent is also an indication that the Petri dish is not about to become Noah’s ark, though. It takes hundreds of egg cells and dozens of surrogate mothers to create a single viable clone.

    Gómez admits that there are problems. Fusing cells from two different species often leads to huge mix-ups. Genes are activated or deactivated at the wrong time, and developmental stages become delayed.

    In the case of the black-footed cat, for instance, Gómez has so far had no success. “We were able to insert embryos into the uterus of a house cat,” she says. “But unfortunately, they didn’t develop.”

    No Limits

    But the researcher remains optimistic. She hopes that she will soon be able to transform body cells from her wildcats into pluripotent stem cells. Cells of this type could considerably simplify the cloning process because they can be used to create any type of body cell and can be easily multiplied. Other researchers have already succeeded in producing such stem cells from snow leopards and northern white rhinoceroses, which are both endangered species.

    There are in fact virtually no limits to the creative experimentation of today’s biotechnicians. Chinese researchers have fused body cells from panda bears with eggs cells taken from rabbits. But the resulting embryos died shortly thereafter — in the uteruses of house cats. Meanwhile, Japanese researchers have implanted skin cells from an unborn baby sei whale in enucleated egg cells taken from cattle and pigs.

    Other Japanese scientists are even trying to clone the woolly mammoth. Three years ago, cell nuclei from these hairy, tusked ice-age beasts were discovered in mammoth legs that have been frozen in the permafrost of Northeast Siberia for the past 15,000 years.

    In the laboratory, a team led by geneticist Akira Iritani injected cell nuclei from the prehistoric animal into enucleated egg cells from mice. The cell constructs only survived for a few hours, but Iritani remains optimistic that an elephant surrogate mother will soon bring to term the first mammoth clone.

    “From a scientific point of view it is possible,” says geneticist Gómez. But is there any point in doing it?

    The 51-year-old professor hesitates briefly. “I wouldn’t do it,” she admits. “I would prefer spending all the money on those species that haven’t completely vanished from the earth.”

    Translated from the German by Paul Cohen

    –> Read original article at DER SPIEGEL International

  • Cloned Meat Soon to Hit European Supermarkets

    Cattle cloning has long been standard practice in the United States. Now EU agriculture ministers have decided that cloned meat and milk should be allowed onto the European market. Not everyone is pleased.

    By Philip Bethge

    Anyone who considers creation sacred should make sure they never talk to a cattle breeder. In-vitro fertilization, artificial insemination and embryo transfer are the terms of their trade. And now another word from the lexicon of reproductive medicine has joined the breeder’s jargon: cloning.

    The European Union’s agricultural ministers decided on Monday of last week that in the future, the meat and milk of the offspring of cloned animals should be allowed on the European market. The European Parliament still needs to approve the proposal. However environmental and animal protection organizations responded immediately to the news and condemned the decision. They consider cloning to be unethical and cruel, and warn that the risks of cloned meat for human health have not been adequately researched.

    The ministers’ decision was long overdue. In the US and South America, cloning has long been standard practice among breeders. German experts like Heiner Niemann from the Institute for Animal Breeding at the Friedrich Loeffler Institute also have high expectations of the technique. “In the future, cloning will be one of the standard cattle-breeding techniques,” says Niemann.

    The technology is already widely used in the US. Companies like ViaGen, Cyagra or Trans Ova Genetics offer cattle clones for between $10,000 and $20,000. The benefits are obvious: Multiple copies can be made of a bull with particularly desirable characteristics. And multiple “superbulls” naturally have more offspring than just one — meaning more premium meat for the breeder.

    “With elite animals, cloning can quickly pay for itself,” says Mark Walton of ViaGen. Karen Batra from the Biotechnology Industry Organization estimates there are already about 600 cloned super cattle in the US. The meat of their offspring is already on sale in supermarkets, she says, explaining that it doesn’t need to be specially labeled. “For breeders, cloning is just another reproductive technique, much like in-vitro fertilization,” says Batra.

    But critics see significant differences. Cloning is said to produce deformed animals with short life expectancies. The cloned sheep Dolly is known to have met a painful end. But genetics expert Heiner Niemann claims that “major progress” has been made since then. Far fewer embryos die and “defects” are much more seldom.

    The meat of the cloned animal itself doesn’t end up in supermarkets, however: Both the US and Europe prohibit its sale. What ends up in the store freezers are the steaks from the clone’s offspring. Its quality is indisputable — and these animals are not even clones. Both the European Food Safety Authority (EFSA) and the American Food and Drug Administration (FDA) announced last year that the milk and meat of the offspring of cloned animals pose no health risks.

    So is it only a matter of time before “cloned” meat is to be found on European supermarket shelves too? After all, it can’t be distinguished from normal steaks. The European Parliament needs to decide soon, before American products start landing on the European market unnoticed.

    According to an EFSA report, the technology “is on the verge of widespread commercial use.” The institution’s experts expect the technique will be used around the world “before 2010.”

    –> read original article at SPIEGEL Online International