Scientists continue to speak out against the prospect of producing engineered embryos that could lead to "designer babies."
Leaders of the American Society of Gene and Cell Therapy sent a letter on April 24 to Alex Azar, the secretary of health and human services, adding their voices to the call for a moratorium on experiments that could alter the genes passed down to future generations.
This move follows a widely criticized experiment in China last year that apparently produced children with edited genomes.
The concern is largely ethical. The reality is that biologists probably couldn't produce designer babies even if they wanted to.
It turns out that the genetics underlying desirable traits such as athleticism, intelligence and beauty are so complicated it may not ever be possible to make targeted changes.
Back in the day of Gregor Mendel, the monk who modified the traits of the pea plants in his 19th century garden, it seemed that traits were based on simple elements (later dubbed "genes"). But by the 1920s, it was becoming clear that human traits involved many genes acting in concert.
Still, during the heyday of the Human Genome Project at the end of the 20th century, hopes were high that common diseases might be explained through the interaction of just a handful of genes. You may recall all those stories about scientists hunting "the gene for" various diseases. Hundreds of scientific papers purported to show strong candidates for these critical genes.
British comedian John Cleese poked fun at this idea in a video skit, where he pointed on a chart to "the gene which we scientists now know makes us eat coconut ice cream after a fish dinner."
But the scientific effort to find genes for common conditions was largely a flop (with a few notable exceptions, such as Alzheimer's and breast cancer). For example, hundreds of studies over the years have reportedly found genes associated with schizophrenia.
"When we look at the 20 most studied genes investigated for schizophrenia, we find basically no evidence that any of those are associated at levels greater than we'd expect due to chance," says Matthew Keller at the University of Colorado.
His lab also looked at the early claims for genes linked to depression. Those, too, went nowhere.
"You could have done just as well by throwing a dart at the genome and saying, 'OK, we're going to look at this gene and see if it's associated with depression,' " he says.
Instead, scientists found that thousands upon thousands of genes are associated with common diseases and common traits. And most of them have just a tiny influence on the risk of a disease, often just a small fraction of a percent.
Human traits, like height, follow the same story.
Jonathan Pritchard, a Howard Hughes investigator at Stanford University, has looked into the genetics of height, which is one of the most thoroughly studied traits. "It quickly became clear there's huge numbers of variants that affect height," he says. "We have estimated that it's probably something like 100,000 variants across the genome, so most of the genome affects height by a small amount."
A few years ago, he suggested that height and presumably other common traits are "omnigenetic," meaning they involve all of our genes.
If that's the case, each gene must influence many different traits. A gene linked to height might affect the basic mechanism inside many cells. So editing one gene would affect not only height but who knows what else.
Pritchard and his colleagues published a paper Thursday that reveals the nature of the variants related to complex traits like height. The genetic variation isn't in the genes themselves (the DNA code that tells cells what proteins to produce) but in genetic elements that regulate those genes at the same time they influence other tasks.
His findings suggest our genes work as an interconnected network. It's not a predictable machine as much as it is a flock of starlings, which wheels in the sky based on group dynamics.
That phenomenon makes our biology a challenge to understand, let alone engineer, Pritchard says. "We find nature as it is, not really as we wish it to be," he says, a bit wistfully.
Pritchard's concept of omnigenetics is not wholly accepted by his peers.
The logical conclusion is that genetics is "such a mush that we can't understand it," says Ewan Birney at the European Bioinformatics Institute. "I find that a bit depressing."
Birney still holds out hope that, as we learn more about genetics, clearer mechanisms will emerge.
But in any event, there's no question that complicated traits involve thousands of genes with multiple purposes.
"If anybody thinks we can understand how to change genomes to improve things, they don't have an appreciation for the lack of knowledge that we have," Birney says.
In the case of the rogue Chinese experiment, the scientist attempted to edit a gene to create a variant that apparently protects people from HIV infection, resulting in the birth of genetically engineered twins. But going back to the idea that genes all play multiple roles, it's not clear what else this alteration has done to the children.
Birney also notes there's a big difference between engineering a designer baby with desirable characteristics and fixing a genetic flaw. "We're much better at understanding when things break, and we call those genetic diseases," Birney says.
There, gene editing could be brought to bear. A broken gene could be edited. But there are other options that carry less risk.
There is already an effective technology, called preimplantation genetic diagnosis, which allows doctors to look for these single-gene flaws in fertilized eggs and select only those that are free of the genetic disease to be implanted in the mother's womb.
This approach is widely regarded as ethical. And the child isn't a "designer baby," but ends up with a natural set of genes.
You can contact NPR science correspondent Richard Harris at email@example.com.
AILSA CHANG, HOST:
The prospect of designer babies is on the agenda this week at the American Society of Gene and Cell Therapy. Leaders of the society are joining calls for a moratorium on engineering of human embryos that could grow into babies. This move follows a widely criticized experiment in China last year that apparently produced children with edited genomes. The concern is, in part, ethical, but as NPR's Richard Harris reports, biologists probably couldn't produce enhanced human beings even if they wanted to.
RICHARD HARRIS, BYLINE: The idea of a designer baby stems from the idea that our genes can be tweaked to produce superior people; that's based on an outdated idea that desirable traits are governed by just a few genes. Biologists have dismissed that idea, certainly for traits like intelligence, athleticism and beauty. Comedian John Cleese even made fun of this idea in a video skit a decade ago. He points to a chart that supposedly shows the location of the God gene, which gives people the impression that there is meaning in the universe.
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JOHN CLEESE: Between the gene which we scientists now know makes us eat coconut ice cream after a fish dinner and this gene here which causes people with weak egos to grasp around desperately for simple explanations.
HARRIS: This idea of a simple connection between genes and traits held up in Gregor Mendel's garden, but the hunt for human genes associated with common traits and common diseases has mostly been a bust. For example, hundreds of studies over the years have reportedly found genes associated with schizophrenia. Matt Keller at the University of Colorado reviewed those claims.
MATTHEW KELLER: When we look at the 20 most-studied genes investigated for schizophrenia, we find basically no evidence that any of those are associated at levels that we'd expect, greater than chance.
HARRIS: Same thing with genes reportedly linked to depression.
KELLER: You could have done just as well by throwing a dart at the genome and saying, OK, we're going to look at this gene, and see if it's associated with depression.
HARRIS: Instead, scientists are finding that thousands upon thousands of genes are associated with common diseases and common traits. Jonathan Pritchard, a Howard Hughes investigator at Stanford University, has looked into one of the most thoroughly studied traits - height.
JONATHAN PRITCHARD: So it quickly became clear there's huge numbers of variance that affect height. And you know, we have estimated there's probably something like 100,000 variants across the genome, so that most of the genome affects height by a small amount.
HARRIS: A few years ago, he suggested this and presumably other common traits are omnigenetic, meaning they involve all of our genes. If true, each gene must influence many different traits. So editing one gene will affect not only height but who knows what else. His findings suggest our genes all work as an interconnected network; that makes our biology a challenge to understand, let alone engineer, Pritchard says.
PRITCHARD: We find nature as it is, not really as we would wish it to be.
EWAN BIRNEY: I find the sort of endpoint of the omnigenetic model, which is, it's all such a mush, we can't understand it - I find that a bit depressing.
PRITCHARD: Ewan Birney at the European Bioinformatics Institute hopes that life is governed by something more comprehensible than a fuzzy cloud of interconnections. But in any event, there's no question that complicated traits involve thousands of genes with multiple purposes.
BIRNEY: If anybody thinks that we can understand how to change genomes to improve things, they do not have an appreciation of the lack of knowledge we have.
HARRIS: That said, Birney adds there is a big difference between creating a designer baby with desirable characteristics and fixing a genetic flaw.
BIRNEY: We're much better at understanding when things break, and we call those genetic diseases.
HARRIS: In principle, those genetic flaws could be fixed through gene editing, but that's actually not necessary, Birney says. There's already an effective technology that's used to avoid these genetic diseases - embryos are created outside the body and one without the worrisome flaw is implanted; that is far less risky than editing embryos and widely regarded as ethical. Richard Harris, NPR News.
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