ScienceDaily (July 20, 2011) A group of researchers from the University of Oxford, Harvard Medical School and the University of Mississippi Medical Center has constructed the world’s most detailed genetic map, a tool scientists can use to better understand the roots of disease and how DNA is passed generationally to create diversity in the human species.
About 5,000 Jackson-area volunteers were included in a group of nearly 30,000 African-Americans whose genetic information the scientists used to create the map.
The map pinpoints genome locations where people splice together DNA from their mothers and fathers to produce sperm or eggs. That process, known as recombination, mixes DNA from the person’s parents and passes it on to his or her children.
Almost every prior genetic map was developed in people of European ancestry. The new map is the first built in African-Americans.
“The world’s best genetic map is now built in African-Americans,” said David Reich, professor of genetics at Harvard Medical School, who co-led the study with Simon Myers, a lecturer in statistics at the University of Oxford. “This map, built in 30,000 African-Americans who are from studies of heart disease and cancer, has a resolution so high it is now the world’s most accurate map.”
The findings will be published in the July 21 edition of Nature.
Dr. James Wilson, UMMC professor of medicine and the study’s coordinator, said the map holds promise for both broad, genome-wide applications and narrowly focused, single-disease research.
“The map will be helpful in finding the genetic roots of any disease that’s affected by inheritance — which is virtually every disease,” he said.
For example, studies have shown certain diseases, such as hypertension, affect African-Americans at greater rates than whites, even with other variables like age, weight and socioeconomic level accounted for. The map could be used to better understand why.
A surprise was that the map turned out to be different than those based on people of European and other non-African ancestries.
“The landscape of recombination has shifted in African-Americans compared with Europeans,” said Anjali Hinch, the study’s first author and a post-graduate student at the Oxford University’s Wellcome Trust Centrefor Human Genetics.
Wilson said the African-American genome has become distinct because of recombination in the U.S. during the past two to three centuries.
“African-Americans are a genetically distinguishable group from other continental populations,” he said. “African-Americans differ from their African ancestors in that most of them also have genes from European ancestors.”
The researchers knew that going into the project. But once they analyzed the breakpoints where recombination occurs in African-American genomes, an unexpected difference appeared.
“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,” Myers said.
Scientists have only recently begun to explore the genetic differences between individuals and populations — and the roles 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, as it determines how some groups of genetic differences tend to be inherited together. 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.
A key to the success of genetic maps is that this stitching occurs only at specific locations in the genome. In a landmark set of papers, Myers and his colleagues previously identified a particular DNA code, or motif, that attracted the recombination machinery. Knowing the motif, a string of 13 DNA letters, researchers could zero in on the exact locations where recombination typically occurred — the “recombination hotspots.”
“When recombination goes wrong, it’s known that this can lead to mutations causing congenital diseases, for example diseases like Charcot-Marie-Tooth disease, or certain anemias. We found the same 13-base motif marking many of these disease-mutation sites,” said Myers.
Reich, who is also a senior associate member of the Broad Institute, said the places in the genome where there are recombination hotspots can also be disease hotspots.
“Charting recombination hotspots can thus bring us to the places in the genome that cause disease,” he said.
The researchers discovered that the 13 base-pair motif responsible for many 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 the 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 specifically because so many African-Americans have both African and European genes, due to racial mixing during the last couple of hundred years. Reich and Myers are experts in analyzing genetic data to reconstruct the mosaic of regions of African and European genetic ancestry in DNA of modern African-Americans.
Using a computer program Reich and Myers wrote specifically to sort the massive amounts of data, Hinch identified places in the genomes of the 30,000 people where switches occurred between African and European ancestry, detecting about 70 per person. These switches correspond to recombination events in the last couple of hundred years, resulting in the more than 2 million recombination events that the researchers used to build the map.
The study was only possible because of collaboration from 81 co-authors from many institutions, using DNA samples from five large studies that had previously 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.
“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,” Wilson said.
The analytic work for this study was supported by a nearly $1 million grant to Wilson at UMMC from the National Institute of General Medicine through the American Recovery and Reinvestment Act.
The recombination map is available at http://www.well.ox.ac.uk/~anjali/AAmap/
The almost 30,000 African-Americans whose DNA was analyzed for this project were participants in five large studies:
The Candidate Gene Association Resource (CARe) is a consortium of nine observational studies of cardiovascular disease and related traits. The consortium includes two Mississippi-based population studies: Atherosclerosis Risk in Communities (ARIC) Study and the Jackson Heart Study. The CARe consortium is supported by the National Heart, Lung, and Blood Institute and diverse other grants.
The African American Breast Cancer Consortium (AABCC) is a consortium of 8 studies of women with and without breast cancer, supported by the National Cancer Institute and diverse other grants.
The African American Prostate Cancer Consortium (AAPCC) is a consortium of 10 studies of men with and without prostate cancer, supported by the National Cancer Institute and diverse other grants.
The African American Lung Cancer Consortium (AALCC) is a consortium of 7 studies of people with and without lung cancer, supported by the National Cancer Institute and diverse other grants.
Many samples also come from the Children’s Hospital of Philadelphia (CHOP), which has established a biobank for Philadelphia children to facilitate disease gene discovery.
The above story is reprinted (with editorial adaptations by ScienceDaily staff) from materials provided by University of Mississippi Medical Center. The original article was written by Jack Mazurak.
- Anjali G. Hinch, Arti Tandon, Nick Patterson, Yunli Song, Nadin Rohland, Cameron D. Palmer, Gary K. Chen, Kai Wang, Sarah G. Buxbaum, Ermeg L. Akylbekova, Melinda C. Aldrich, Christine B. Ambrosone, Christopher Amos, Elisa V. Bandera, Sonja I. Berndt, Leslie Bernstein, William J. Blot, Cathryn H. Bock, Eric Boerwinkle, Qiuyin Cai, Neil Caporaso, Graham Casey, L. Adrienne Cupples, Sandra L. Deming, W. Ryan Diver, Jasmin Divers, Myriam Fornage, Elizabeth M. Gillanders, Joseph Glessner, Curtis C. Harris, Jennifer J. Hu, Sue A. Ingles, William Isaacs, Esther M. John, W. H. Linda Kao, Brendan Keating, Rick A. Kittles, Laurence N. Kolonel, Emma Larkin, Loic Le Marchand, Lorna H. McNeill, Robert C. Millikan, Murphy, Solomon Musani, Christine Neslund-Dudas, Sarah Nyante, George J. Papanicolaou, Michael F. Press, Bruce M. Psaty, Alex P. Reiner, Stephen S. Rich, Jorge L. Rodriguez-Gil, Jerome I. Rotter, Benjamin A. Rybicki, Ann G. Schwartz, Lisa B. Signorello, Margaret Spitz, Sara S. Strom, Michael J. Thun, Margaret A. Tucker, Zhaoming Wang, John K. Wiencke, John S. Witte, Margaret Wrensch, Xifeng Wu, Yuko Yamamura, Krista A. Zanetti, Wei Zheng, Regina G. Ziegler, Xiaofeng Zhu, Susan Redline, Joel N. Hirschhorn, Brian E. Henderson, Herman A. Taylor Jr, Alkes L. Price, Hakon Hakonarson, Stephen J. Chanock, Christopher A. Haiman, James G. Wilson, David Reich, Simon R. Myers. The landscape of recombination in African Americans. Nature, 2011; DOI: 10.1038/nature10336
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