Researchers create the world's most advanced genetic map
Wednesday, July 20, 2011
New biological atlas focuses on African American genomics
A consortium led by scientists at the University of Oxford and Harvard Medical School has constructed the world’s most detailed genetic map.
Karmanos Cancer Institute Executive Vice President/Deputy Director Ann G. Schwartz, Ph.D., MPH, was part of the consortium of scientific researchers. Cathryn H. Bock, Ph.D., assistant professor, Department of Oncology at Karmanos, was one of the authors of the final report.
A genetic map specifies the precise areas in a sperm or egg where the DNA from the mother and father has been reshuffled in order to produce this single reproductive cell. The biological process whereby this reshuffling occurs is known as “recombination.” While almost every genetic map built so far has been developed from people of European ancestry, this new map is the first constructed from African American recombination genomic data.
“This is the world’s best genetic map,” said David Reich, professor of genetics at Harvard Medical School, who co-led the study with Simon Myers, a lecturer in the Department of Statistics at the University of Oxford.
The researchers were surprised to find that positions where recombination occurs in African Americans are significantly different from non-African populations.
“The landscape of recombination has shifted in African Americans compared with Europeans,” said Anjali Hinch, first author and a post-graduate student at Oxford University’s Wellcome Trust Centre for Human Genetics.
Simon Myers added, “Over half of African Americans carry a version of the biological machinery for recombination that is different to that in Europeans. As a result, African Americans experience recombination where it almost never occurs in Europeans.”
The findings will be published in the July 21 edition of Nature.
Scientists have only recently begun to explore the genetic differences between individuals and populations — and the role those differences play in human health. In that respect, the first draft of the human genome, completed a decade ago, was only a starting point for understanding the genetic origins of disease.
As researchers begin to parse those differences, a crucial tool is a genetic map, which reveals where recombination occurs across the genome. Recombination, together with mutation, accounts for all the genetic (and thus physical) variety we see within species. But while mutation refers to the errors introduced into single locations within genomes when cells divide, recombination refers to the process by which huge chunks of chromosomes are stitched together during sexual reproduction.
But this stitching process only occurs at specific locations. In a prior landmark set of papers, Myers and his colleagues identified a DNA code, or motif, that attracted part of the recombination machinery, a gene called PRDM9. Knowing the motif, a string of thirteen DNA letters, researchers could zero in on the locations where recombination typically occurred—the “recombination hotspots.”
“When recombination goes wrong, it can lead to mutations causing congenital diseases, for example diseases like Charcot-Marie-Tooth disease, or certain anemias,” said Myers. “We found the same thirteen base motif marking many of these disease mutation sites.”
Explained Reich, “The places in the genome where there are recombination hotspots can also be disease hotspots. Charting recombination hotspots can thus bring us identify places in the genome that cause disease.”
The researchers discovered that the 13 base-pair motif that is responsible for many of the hotspots in Europeans accounts for only two thirds as much recombination in African Americans. They connected the remaining third to a new motif of 17 base pairs, which is recognized by a version of the recombinational machinery that occurs almost exclusively in people of African ancestry.
These findings are expected to help researchers understand the roots of congenital conditions that occur more often in African Americans (due to mutations at hotspots that are more common in African Americans), and also to help discover new disease genes in all populations, because of the ability to map these genes more precisely.
The new map is so accurate because African American individuals often have a mixture of African and European ancestry from over the last two hundred years. David Reich and Simon Myers are experts in analyzing genetic data to reconstruct the mosaic of regions of African and European genetic ancestry in DNA of African Americans. By applying a computer program they previously wrote, Anjali Hinch identified the places in the genomes of the 30,000 people where the African and European ancestry switches, detecting about 70 per person. The researchers concluded that these areas corresponded to recombination events in the last two hundred years, resulting in the more than two million recombination events that were used to build the map.
The study was only possible because of collaboration from 81 co-authors, using DNA samples from five large studies that have been carried out to study common diseases such as heart disease and cancer, funded by the National Institutes of Health, the Department of Defense, and many private foundations.
Said James Wilson, a professor at the University of Mississippi Medical Center who was responsible for coordinating the collaboration, “All the co-authors worked together in an incredibly collegial way to put together the enormous set of samples and high quality genetic data that made this study a success.”