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Genetic Origins and Adaptive Evolution of the Deng People on the Tibetan Plateau

The Tibetan Plateau is populated by diverse ethnic groups, but most of them are underrepresented in genomics studies compared with the Tibetans (TIB). Here, to gain further insight into the genetic diversity and evolutionary history of the people living in the Tibetan Plateau, we sequenced 54 whole...

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Autores principales: Ge, Xueling, Lu, Yan, Chen, Shuanghui, Gao, Yang, Ma, Lifeng, Liu, Lijun, Liu, Jiaojiao, Ma, Xixian, Kang, Longli, Xu, Shuhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584363/
https://www.ncbi.nlm.nih.gov/pubmed/37713634
http://dx.doi.org/10.1093/molbev/msad205
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author Ge, Xueling
Lu, Yan
Chen, Shuanghui
Gao, Yang
Ma, Lifeng
Liu, Lijun
Liu, Jiaojiao
Ma, Xixian
Kang, Longli
Xu, Shuhua
author_facet Ge, Xueling
Lu, Yan
Chen, Shuanghui
Gao, Yang
Ma, Lifeng
Liu, Lijun
Liu, Jiaojiao
Ma, Xixian
Kang, Longli
Xu, Shuhua
author_sort Ge, Xueling
collection PubMed
description The Tibetan Plateau is populated by diverse ethnic groups, but most of them are underrepresented in genomics studies compared with the Tibetans (TIB). Here, to gain further insight into the genetic diversity and evolutionary history of the people living in the Tibetan Plateau, we sequenced 54 whole genomes of the Deng people with high coverage (30–60×) and analyzed the data together with that of TIB and Sherpas, as well as 968 ancient Asian genomes and available archaic and modern human data. We identified 17.74 million novel single-nucleotide variants from the newly sequenced genomes, although the Deng people showed reduced genomic diversity and a relatively small effective population size. Compared with the other Tibetan highlander groups which are highly admixed, the Deng people are dominated by a sole ancestry that could be traced to some ancient northern East Asian populations. The divergence between Deng and Tibetan people (∼4,700–7,200 years) was more recent than that between highlanders and the Han Chinese (Deng-HAN, ∼9,000–14,000 years; TIB-HAN, 7,200–10,000 years). Adaptive genetic variants (AGVs) identified in the Deng are only partially shared with those previously reported in the TIB like HLA-DQB1, whereas others like KLHL12 were not reported in TIB. In contrast, the top candidate genes harboring AGVs as previously identified in TIB, like EPAS1 and EGLN1, do not show strong positive selection signals in Deng. Interestingly, Deng also showed a different archaic introgression scenario from that observed in the TIB. Our results suggest that convergent adaptation might be prevalent on the Tibetan Plateau.
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spelling pubmed-105843632023-10-19 Genetic Origins and Adaptive Evolution of the Deng People on the Tibetan Plateau Ge, Xueling Lu, Yan Chen, Shuanghui Gao, Yang Ma, Lifeng Liu, Lijun Liu, Jiaojiao Ma, Xixian Kang, Longli Xu, Shuhua Mol Biol Evol Discoveries The Tibetan Plateau is populated by diverse ethnic groups, but most of them are underrepresented in genomics studies compared with the Tibetans (TIB). Here, to gain further insight into the genetic diversity and evolutionary history of the people living in the Tibetan Plateau, we sequenced 54 whole genomes of the Deng people with high coverage (30–60×) and analyzed the data together with that of TIB and Sherpas, as well as 968 ancient Asian genomes and available archaic and modern human data. We identified 17.74 million novel single-nucleotide variants from the newly sequenced genomes, although the Deng people showed reduced genomic diversity and a relatively small effective population size. Compared with the other Tibetan highlander groups which are highly admixed, the Deng people are dominated by a sole ancestry that could be traced to some ancient northern East Asian populations. The divergence between Deng and Tibetan people (∼4,700–7,200 years) was more recent than that between highlanders and the Han Chinese (Deng-HAN, ∼9,000–14,000 years; TIB-HAN, 7,200–10,000 years). Adaptive genetic variants (AGVs) identified in the Deng are only partially shared with those previously reported in the TIB like HLA-DQB1, whereas others like KLHL12 were not reported in TIB. In contrast, the top candidate genes harboring AGVs as previously identified in TIB, like EPAS1 and EGLN1, do not show strong positive selection signals in Deng. Interestingly, Deng also showed a different archaic introgression scenario from that observed in the TIB. Our results suggest that convergent adaptation might be prevalent on the Tibetan Plateau. Oxford University Press 2023-09-15 /pmc/articles/PMC10584363/ /pubmed/37713634 http://dx.doi.org/10.1093/molbev/msad205 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Discoveries
Ge, Xueling
Lu, Yan
Chen, Shuanghui
Gao, Yang
Ma, Lifeng
Liu, Lijun
Liu, Jiaojiao
Ma, Xixian
Kang, Longli
Xu, Shuhua
Genetic Origins and Adaptive Evolution of the Deng People on the Tibetan Plateau
title Genetic Origins and Adaptive Evolution of the Deng People on the Tibetan Plateau
title_full Genetic Origins and Adaptive Evolution of the Deng People on the Tibetan Plateau
title_fullStr Genetic Origins and Adaptive Evolution of the Deng People on the Tibetan Plateau
title_full_unstemmed Genetic Origins and Adaptive Evolution of the Deng People on the Tibetan Plateau
title_short Genetic Origins and Adaptive Evolution of the Deng People on the Tibetan Plateau
title_sort genetic origins and adaptive evolution of the deng people on the tibetan plateau
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584363/
https://www.ncbi.nlm.nih.gov/pubmed/37713634
http://dx.doi.org/10.1093/molbev/msad205
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