Selective sweep on human amylase genes postdates the split with Neanderthals
Inchley CEPapers in this archive, Larbey CDPapers in this archive, Shwan NAPapers in this archive, Pagani LPapers in this archive, Saag LPapers in this archive, Antão TPapers in this archive, Jacobs GPapers in this archive, Hudjashov GPapers in this archive, Metspalu EPapers in this archive, Mitt MPapers in this archive, Eichstaedt CAPapers in this archive, Malyarchuk BPapers in this archive, Derenko MPapers in this archive, Wee JPapers in this archive, Abdullah SPapers in this archive, Ricaut FXPapers in this archive, Mormina MPapers in this archive, Mägi RPapers in this archive, Villems RPapers in this archive, Metspalu MPapers in this archive, Jones MKPapers in this archive, Armour JAPapers in this archive, Kivisild TPapers in this archive
Abstract
Humans have more copies of amylase genes than other primates. It is still poorly understood, however, when the copy number expansion occurred and whether its spread was enhanced by selection. Here we assess amylase copy numbers in a global sample of 480 high coverage genomes and find that regions flanking the amylase locus show notable depression of genetic diversity both in African and non-African populations. Analysis of genetic variation in these regions supports the model of an early selective sweep in the human lineage after the split of humans from Neanderthals which led to the fixation of multiple copies of AMY1 in place of a single copy. We find evidence of multiple secondary losses of copy number with the highest frequency (52%) of a deletion of AMY2A and associated low copy number of AMY1 in Northeast Siberian populations whose diet has been low in starch content.
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