Population history and natural selection shape patterns of genetic variation in 132 genes

被引:388
作者
Akey, JM
Eberle, MA
Rieder, MJ
Carlson, CS
Shriver, MD
Nickerson, DA
Kruglyak, L
机构
[1] Fred Hutchinson Canc Res Ctr, Div Human Biol, Seattle, WA 98104 USA
[2] Univ Washington, Dept Genome Sci, Seattle, WA USA
[3] Penn State Univ, Dept Anthropol, University Pk, PA 16802 USA
[4] Howard Hughes Med Inst, Chevy Chase, MD USA
关键词
D O I
10.1371/journal.pbio.0020286
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Identifying regions of the human genome that have been targets of natural selection will provide important insights into human evolutionary history and may facilitate the identification of complex disease genes. Although the signature that natural selection imparts on DNA sequence variation is difficult to disentangle from the effects of neutral processes such as population demographic history, selective and demographic forces can be distinguished by analyzing multiple loci dispersed throughout the genome. We studied the molecular evolution of 132 genes by comprehensively resequencing them in 24 African-Americans and 23 European-Americans. We developed a rigorous computational approach for taking into account multiple hypothesis tests and demographic history and found that while many apparent selective events can instead be explained by demography, there is also strong evidence for positive or balancing selection at eight genes in the European-American population, but none in the African-American population. Our results suggest that the migration of modern humans out of Africa into new environments was accompanied by genetic adaptations to emergent selective forces. In addition, a region containing four contiguous genes on Chromosome 7 showed striking evidence of a recent selective sweep in European-Americans. More generally, our results have important implications for mapping genes underlying complex human diseases.
引用
收藏
页码:1591 / 1599
页数:9
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