4.8 Article

Genomic diversity and post-admixture adaptation in the Uyghurs

Journal

NATIONAL SCIENCE REVIEW
Volume 9, Issue 3, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nsr/nwab124

Keywords

Uyghur; Eurasian; genetic admixture; genomic diversity; local adaptation

Funding

  1. National Key Research and Development Program of China [2016YFC0906403]
  2. National Natural Science Foundation of China (NSFC) [31771388, 32030020, 31525014, 91731303, 31961130380, 32041008]
  3. Strategic Priority Research Program of the Chinese Academy of Sciences (CAS) [XDB38000000]
  4. Key Research Program of Frontier Sciences of the Chinese Academy of Sciences (CAS) [QYZDJ-SSW-SYS009]
  5. UK Royal Society-Newton Advanced Fellowship [NAF\R1\191094]
  6. Shanghai Municipal Science and Technology Major Project [2017SHZDZX01]

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Population admixture in the Uyghur population in Xinjiang, China has led to increased genetic diversity and phenotypic variation. The study identified functional variants associated with facial morphology and skin pigmentation, as well as genes related to metabolism, digestion, olfactory perception, and immunity that have undergone post-admixture adaptation.
Population admixture results in genome-wide combinations of genetic variants derived from different ancestral populations of distinct ancestry, thus providing a unique opportunity for understanding the genetic determinants of phenotypic variation in humans. Here, we used whole-genome sequencing of 92 individuals with high coverage (30-60x) to systematically investigate genomic diversity in the Uyghurs living in Xinjiang, China (XJU), an admixed population of both European-like and East-Asian-like ancestry. The XJU population shows greater genetic diversity, especially a higher proportion of rare variants, compared with their ancestral source populations, corresponding to greater phenotypic diversity of XJU. Admixture-induced functional variants in EDAR were associated with the diversity of facial morphology in XJU. Interestingly, the interaction of functional variants between SLC24A5 and OCA2 likely influences the diversity of skin pigmentation. Notably, selection has seemingly been relaxed or canceled in several genes with significantly biased ancestry, such as HERC2-OCA2. Moreover, signatures of post-admixture adaptation in XJU were identified, including genes related to metabolism (e.g. CYP2D6), digestion (e.g. COL11A1), olfactory perception (e.g. ANO2) and immunity (e.g. HLA). Our results demonstrated population admixture as a driving force, locally or globally, in shaping human genetic and phenotypic diversity as well as in adaptive evolution.

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