DNA mutation clock proves tough to set
Geneticists meet to work out why the rate of change in the genome is so hard to pin down.
Mathematicians keep refining ? even though they know it to more than 12 trillion digits; physicists beat themselves up because they cannot pin down the gravitational constant beyond three significant figures. Geneticists, by contrast, are having trouble deciding between one measure of how fast human DNA mutates and another that is half that rate.
The rate is key to calibrating the ‘molecular clock’ that puts DNA-based dates on events in evolutionary history. So at an intimate meeting in Leipzig, Germany, on 25–27 February, a dozen speakers puzzled over why calculations of the rate at which sequence changes pop up in human DNA have been so much lower in recent years than previously. They also pondered why the rate seems to fluctuate over time. The meeting drew not only evolutionary geneticists, but also researchers with an interest in cancer and reproductive biology — fields in which mutations have a central role.
“Mutation is ultimately the source of all heritable diseases and all biological adaptations, so understanding the rate at which mutations evolve is a fundamental question,” says Molly Przeworski, a population geneticist at Columbia University in New York City who attended the Human Mutation Rate Meeting.
Researchers tried to put a number on the human mutation rate even before they knew that genetic information is encoded in DNA. In the 1930s, pioneering geneticist J. B. S. Haldane came up with a good estimate by measuring how the mutations responsible for haemophilia appeared in extended families.
Later estimates of the mutation rate counted the differences between stretches of DNA and protein amino-acid sequences in humans and those in chimpanzees or other apes, and then divided the number of differences by the time that has elapsed since the species’ most recent common ancestor appeared in the fossil record. These estimates were clouded by the patchiness of the fossil record, but researchers eventually settled on a consensus: each DNA letter, on average, mutates once every billion years. That is a “suspiciously round number”, molecular anthropologist Linda Vigilant of the Max Planck Institute for Evolutionary Anthropology in Leipzig told Nature in 2012 (see Nature 489, 343–344; 2012).
In the past six years, more-direct measurements using ‘next-generation’ DNA sequencing have come up with quite different estimates. A number of studies have compared entire genomes of parents and their children — and calculated a mutation rate that consistently comes to about half that of the last-common-ancestor method.
A slower molecular clock worked well to harmonize genetic and archaeological estimates for dates of key events in human evolution, such as migrations out of Africa and around the rest of the world1. But calculations using the slow clock gave nonsensical results when extended further back in time — positing, for example, that the most recent common ancestor of apes and monkeys could have encountered dinosaurs. Reluctant to abandon the older numbers completely, many researchers have started hedging their bets in papers, presenting multiple dates for evolutionary events depending on whether mutation is assumed to be fast, slow or somewhere in between.
Last year, population geneticist David Reich of Harvard Medical School in Boston, Massachusetts, and his colleagues compared the genome of a 45,000-year-old human from Siberia with genomes of modern humans and came up with the lower mutation rate2. Yet just before the Leipzig meeting, which Reich co-organized with Kay Prüfer of the Max Planck Institute for Evolutionary Anthropology, his team published a preprint article3 that calculated an intermediate mutation rate by looking at differences between paired stretches of chromosomes in modern individuals (which, like two separate individuals’ DNA, must ultimately trace back to a common ancestor). Reich is at a loss to explain the discrepancy. “The fact that the clock is so uncertain is very problematic for us,” he says. “It means that the dates we get out of genetics are really quite embarrassingly bad and uncertain.”
Reich hoped that even if the meeting did not reach a consensus on mutation rate, it would highlight the research that is needed to move forward. He and Prüfer kicked off the meeting by polling attendees on their favoured rate, and found that the lower figure had gained popularity, but there was still a wide spread of opinions.
Increasingly, Reich and others conclude that the human mutation rate has fluctuated over millions of years. Much of the discussion at the meeting revolved around when it accelerated and decelerated — and why. Evolutionary changes in metabolism or reproductive biology are both possible causes. Aylwyn Scally, a population geneticist at the University of Cambridge, UK, thinks that the common ancestor of great apes, which lived between 20 million and 12 million years ago, had longer generations than its relatives on the monkey branch of the primate family tree. That would have slowed mutation: a longer generation would lead to fewer mutations per year, on average.
Medical-minded geneticists also fret about mutation rates. Meeting attendee Michael Stratton, director of the Wellcome Trust Sanger Institute in Hinxton, UK, is a cancer geneticist who studies the causes of DNA mutations. Environmental agents such as tobacco smoke trigger some cancers, but others are caused by the normal biochemical operations of cells — through processes that are little-known, says Stratton. Working out what these are could explain fluctuations in the mutation rate.
Reproductive biologists are also interested in the human mutation rate — in part because they have found that some diseases are more common in the children of older men than of younger ones. Sperm are produced throughout a man’s life, whereas women are born with a full array of eggs. The constant division of sperm precursor cells means that men tend to pass on more new mutations to their offspring than women — four times as many, according to a 2012 estimate4 — and older fathers transmit more mutations than young ones. This means that changes in the biology of sperm production or paternal age over evolutionary time could influence mutation rate.
Even though the human mutation rate is still uncertain and unstable, Reich proposed at the meeting that researchers use the slower value for their work, at least until better data come along. Just don’t think of it as a constant, he cautions: “This is not the speed of light. This is not physics.”
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