Diet and the evolution of human amylase gene copy number variation

被引:0
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作者
George H Perry
Nathaniel J Dominy
Katrina G Claw
Arthur S Lee
Heike Fiegler
Richard Redon
John Werner
Fernando A Villanea
Joanna L Mountain
Rajeev Misra
Nigel P Carter
Charles Lee
Anne C Stone
机构
[1] School of Human Evolution and Social Change,Department of Pathology
[2] Arizona State University,Department of Anthropology
[3] Tempe,Department of Anthropological Sciences
[4] Arizona 85287,undefined
[5] USA.,undefined
[6] Brigham and Women's Hospital,undefined
[7] University of California,undefined
[8] School of Life Sciences,undefined
[9] Arizona State University,undefined
[10] The Wellcome Trust Sanger Institute,undefined
[11] The Wellcome Trust Genome Campus,undefined
[12] Stanford University,undefined
[13] Harvard Medical School,undefined
来源
Nature Genetics | 2007年 / 39卷
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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 starch1,2,3. This behavioral variation raises the possibility that different selective pressures have acted on amylase, the enzyme responsible for starch hydrolysis4. 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.
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页码:1256 / 1260
页数:4
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