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Genomic Analysis of Natural Selection and Phenotypic Variation in High-Altitude Mongolians
Deedu (DU) Mongolians, who migrated from the Mongolian steppes to the Qinghai-Tibetan Plateau approximately 500 years ago, are challenged by environmental conditions similar to native Tibetan highlanders. Identification of adaptive genetic factors in this population could provide insight into coordi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715426/ https://www.ncbi.nlm.nih.gov/pubmed/23874230 http://dx.doi.org/10.1371/journal.pgen.1003634 |
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author | Xing, Jinchuan Wuren, Tana Simonson, Tatum S. Watkins, W. Scott Witherspoon, David J. Wu, Wilfred Qin, Ga Huff, Chad D. Jorde, Lynn B. Ge, Ri-Li |
author_facet | Xing, Jinchuan Wuren, Tana Simonson, Tatum S. Watkins, W. Scott Witherspoon, David J. Wu, Wilfred Qin, Ga Huff, Chad D. Jorde, Lynn B. Ge, Ri-Li |
author_sort | Xing, Jinchuan |
collection | PubMed |
description | Deedu (DU) Mongolians, who migrated from the Mongolian steppes to the Qinghai-Tibetan Plateau approximately 500 years ago, are challenged by environmental conditions similar to native Tibetan highlanders. Identification of adaptive genetic factors in this population could provide insight into coordinated physiological responses to this environment. Here we examine genomic and phenotypic variation in this unique population and present the first complete analysis of a Mongolian whole-genome sequence. High-density SNP array data demonstrate that DU Mongolians share genetic ancestry with other Mongolian as well as Tibetan populations, specifically in genomic regions related with adaptation to high altitude. Several selection candidate genes identified in DU Mongolians are shared with other Asian groups (e.g., EDAR), neighboring Tibetan populations (including high-altitude candidates EPAS1, PKLR, and CYP2E1), as well as genes previously hypothesized to be associated with metabolic adaptation (e.g., PPARG). Hemoglobin concentration, a trait associated with high-altitude adaptation in Tibetans, is at an intermediate level in DU Mongolians compared to Tibetans and Han Chinese at comparable altitude. Whole-genome sequence from a DU Mongolian (Tianjiao1) shows that about 2% of the genomic variants, including more than 300 protein-coding changes, are specific to this individual. Our analyses of DU Mongolians and the first Mongolian genome provide valuable insight into genetic adaptation to extreme environments. |
format | Online Article Text |
id | pubmed-3715426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37154262013-07-19 Genomic Analysis of Natural Selection and Phenotypic Variation in High-Altitude Mongolians Xing, Jinchuan Wuren, Tana Simonson, Tatum S. Watkins, W. Scott Witherspoon, David J. Wu, Wilfred Qin, Ga Huff, Chad D. Jorde, Lynn B. Ge, Ri-Li PLoS Genet Research Article Deedu (DU) Mongolians, who migrated from the Mongolian steppes to the Qinghai-Tibetan Plateau approximately 500 years ago, are challenged by environmental conditions similar to native Tibetan highlanders. Identification of adaptive genetic factors in this population could provide insight into coordinated physiological responses to this environment. Here we examine genomic and phenotypic variation in this unique population and present the first complete analysis of a Mongolian whole-genome sequence. High-density SNP array data demonstrate that DU Mongolians share genetic ancestry with other Mongolian as well as Tibetan populations, specifically in genomic regions related with adaptation to high altitude. Several selection candidate genes identified in DU Mongolians are shared with other Asian groups (e.g., EDAR), neighboring Tibetan populations (including high-altitude candidates EPAS1, PKLR, and CYP2E1), as well as genes previously hypothesized to be associated with metabolic adaptation (e.g., PPARG). Hemoglobin concentration, a trait associated with high-altitude adaptation in Tibetans, is at an intermediate level in DU Mongolians compared to Tibetans and Han Chinese at comparable altitude. Whole-genome sequence from a DU Mongolian (Tianjiao1) shows that about 2% of the genomic variants, including more than 300 protein-coding changes, are specific to this individual. Our analyses of DU Mongolians and the first Mongolian genome provide valuable insight into genetic adaptation to extreme environments. Public Library of Science 2013-07-18 /pmc/articles/PMC3715426/ /pubmed/23874230 http://dx.doi.org/10.1371/journal.pgen.1003634 Text en © 2013 Xing et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Xing, Jinchuan Wuren, Tana Simonson, Tatum S. Watkins, W. Scott Witherspoon, David J. Wu, Wilfred Qin, Ga Huff, Chad D. Jorde, Lynn B. Ge, Ri-Li Genomic Analysis of Natural Selection and Phenotypic Variation in High-Altitude Mongolians |
title | Genomic Analysis of Natural Selection and Phenotypic Variation in High-Altitude Mongolians |
title_full | Genomic Analysis of Natural Selection and Phenotypic Variation in High-Altitude Mongolians |
title_fullStr | Genomic Analysis of Natural Selection and Phenotypic Variation in High-Altitude Mongolians |
title_full_unstemmed | Genomic Analysis of Natural Selection and Phenotypic Variation in High-Altitude Mongolians |
title_short | Genomic Analysis of Natural Selection and Phenotypic Variation in High-Altitude Mongolians |
title_sort | genomic analysis of natural selection and phenotypic variation in high-altitude mongolians |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715426/ https://www.ncbi.nlm.nih.gov/pubmed/23874230 http://dx.doi.org/10.1371/journal.pgen.1003634 |
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