Diet and the evolution of human amylase gene copy number variation

被引:952
作者
Perry, George H.
Dominy, Nathaniel J. [1 ]
Claw, Katrina G.
Lee, Arthur S.
Fiegler, Heike
Redon, Richard
Werner, John
Villanea, Fernando A.
Mountain, Joanna L.
Misra, Rajeev
Carter, Nigel P.
Lee, Charles
Stone, Anne C.
机构
[1] Arizona State Univ, Sch Human Evolut & Social Change, Tempe, AZ 85287 USA
[2] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[3] Univ Calif Santa Cruz, Dept Anthropol, Santa Cruz, CA 95064 USA
[4] Arizona State Univ, Sch Life Sci, Tempe, AZ 85287 USA
[5] Wellcome Trust Sanger Inst, Cambridge CB10 1SA, England
[6] Stanford Univ, Dept Anthropol Sci, Stanford, CA 94305 USA
[7] Harvard Univ, Sch Med, Boston, MA 02115 USA
基金
英国惠康基金;
关键词
D O I
10.1038/ng2123
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Starch consumption is a prominent characteristic of agricultural societies and hunter-gatherers in arid environments. In contrast, rainforest and circum-arctic hunter-gatherers and some pastoralists consume much less starch(1-3). This behavioral variation raises the possibility that different selective pressures have acted on amylase, the enzyme responsible for starch hydrolysis(4). We found that copy number of the salivary amylase gene (AMY1) is correlated positively with salivary amylase protein level and that individuals from populations with high-starch diets have, on average, more AMY1 copies than those with traditionally low-starch diets. Comparisons with other loci in a subset of these populations suggest that the extent of AMY1 copy number differentiation is highly unusual. This example of positive selection on a copy number-variable gene is, to our knowledge, one of the first discovered in the human genome. Higher AMY1 copy numbers and protein levels probably improve the digestion of starchy foods and may buffer against the fitness-reducing effects of intestinal disease.
引用
收藏
页码:1256 / 1260
页数:5
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