4.8 Article

An Unexpectedly Complex Architecture for Skin Pigmentation in Africans

期刊

CELL
卷 171, 期 6, 页码 1340-+

出版社

CELL PRESS
DOI: 10.1016/j.cell.2017.11.015

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资金

  1. Stanford University CDEHA seed grant (NIH) [NIA P30 AG017253-12]
  2. Stanford Center for Computational, Evolutionary and Human Genomics
  3. Morrison Institute for Population Studies, Stanford University
  4. NIH Genetics and Developmental Biology Training Program [5T32GM007790]
  5. NIH IRACDA fellowship [NIH K12 GM102778]
  6. Stanford NIH Genome Training Program [5T32HG000044]
  7. South African Medical Research Council
  8. MRC [MR/K013491/1] Funding Source: UKRI
  9. Medical Research Council [MR/K013491/1] Funding Source: researchfish

向作者/读者索取更多资源

Approximately 15 genes have been directly associated with skin pigmentation variation in humans, leading to its characterization as a relatively simple trait. However, by assembling a global survey of quantitative skin pigmentation phenotypes, we demonstrate that pigmentation is more complex than previously assumed, with genetic architecture varying by latitude. We investigate polygenicity in the KhoeSan populations indigenous to southern Africa who have considerably lighter skin than equatorial Africans. We demonstrate that skin pigmentation is highly heritable, butknownpigmentation loci explainonly asmall fraction of the variance. Rather, baseline skin pigmentation is a complex, polygenic trait in the KhoeSan. Despite this, we identify canonical and non-canonical skin pigmentation loci, including near SLC24A5, TYRP1, SMARCA2/VLDLR, and SNX13, using a genome-wide association approach complemented by targeted resequencing. By considering diverse, under-studied African populations, we show how the architecture of skin pigmentation can vary across humans subject to different local evolutionary pressures.

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