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PMID: 25043035 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Altitude adaptation in Tibetans caused by introgression of Denisovan-like DNA.

Nature ·Vol. 512 ·No. 7513 ·2014-08-14 ·Pages 194-7

Huerta-Sánchez E, Jin X, Asan, Bianba Z, Peter BM, Vinckenbosch N, Liang Y, Yi X, He M, Somel M, Ni P, Wang B, Ou X, Huasang, Luosang J, Cuo ZX, Li K, Gao G, Yin Y, Wang W, Zhang X, Xu X, Yang H, Li Y, Wang J, Wang J, Nielsen R

Abstract

As modern humans migrated out of Africa, they encountered many new environmental conditions, including greater temperature extremes, different pathogens and higher altitudes. These diverse environments are likely to have acted as agents of natural selection and to have led to local adaptations. One of the most celebrated examples in humans is the adaptation of Tibetans to the hypoxic environment of the high-altitude Tibetan plateau. A hypoxia pathway gene, EPAS1, was previously identified as having the most extreme signature of positive selection in Tibetans, and was shown to be associated with differences in haemoglobin concentration at high altitude. Re-sequencing the region around EPAS1 in 40 Tibetan and 40 Han individuals, we find that this gene has a highly unusual haplotype structure that can only be convincingly explained by introgression of DNA from Denisovan or Denisovan-related individuals into humans. Scanning a larger set of worldwide populations, we find that the selected haplotype is only found in Denisovans and in Tibetans, and at very low frequency among Han Chinese. Furthermore, the length of the haplotype, and the fact that it is not found in any other populations, makes it unlikely that the haplotype sharing between Tibetans and Denisovans was caused by incomplete ancestral lineage sorting rather than introgression. Our findings illustrate that admixture with other hominin species has provided genetic variation that helped humans to adapt to new environments.

MeSH Terms
Adaptation, Physiological/genetics Altitude Animals Asians/genetics Basic Helix-Loop-Helix Transcription Factors/genetics DNA/genetics Gene Frequency Genetic Variation Haplotypes Hominidae/genetics Humans Polymorphism, Single Nucleotide Tibet
Chemicals
Basic Helix-Loop-Helix Transcription Factors endothelial PAS domain-containing protein 1 DNA
Authors & Affiliations
27 authors, click to expand affiliations / ORCID
Huerta-Sánchez Emilia
1] BGI-Shenzhen, Shenzhen 518083, China [2] Department of Integrative Biology, University of California, Berkeley, California 94720 USA [3] School of Natural Sciences, University of California, Merced, California 95343 USA [4].
Jin Xin
1] BGI-Shenzhen, Shenzhen 518083, China [2] School of Bioscience and Bioengineering, South China University of Technology, Guangzhou 510006, China [3].
Asan
1] BGI-Shenzhen, Shenzhen 518083, China [2] Binhai Genomics Institute, BGI-Tianjin, Tianjin 300308, China [3] Tianjin Translational Genomics Center, BGI-Tianjin, Tianjin 300308, China [4].
Bianba Zhuoma
1] The People's Hospital of Lhasa, Lhasa 850000, China [2].
Peter Benjamin M
Department of Integrative Biology, University of California, Berkeley, California 94720 USA.
Vinckenbosch Nicolas
Department of Integrative Biology, University of California, Berkeley, California 94720 USA.
Liang Yu
1] BGI-Shenzhen, Shenzhen 518083, China [2] Binhai Genomics Institute, BGI-Tianjin, Tianjin 300308, China [3] Tianjin Translational Genomics Center, BGI-Tianjin, Tianjin 300308, China.
Yi Xin
1] BGI-Shenzhen, Shenzhen 518083, China [2] Binhai Genomics Institute, BGI-Tianjin, Tianjin 300308, China [3] Tianjin Translational Genomics Center, BGI-Tianjin, Tianjin 300308, China.
He Mingze
1] BGI-Shenzhen, Shenzhen 518083, China [2] Bioinformatics and Computational Biology Program, Iowa State University, Ames, Iowa 50011, USA.
Somel Mehmet
Department of Biological Sciences, Middle East Technical University, 06800 Ankara, Turkey.
Ni Peixiang
BGI-Shenzhen, Shenzhen 518083, China.
Wang Bo
BGI-Shenzhen, Shenzhen 518083, China.
Ou Xiaohua
BGI-Shenzhen, Shenzhen 518083, China.
Huasang
BGI-Shenzhen, Shenzhen 518083, China.
Luosang Jiangbai
BGI-Shenzhen, Shenzhen 518083, China.
Cuo Zha Xi Ping
The Second People's Hospital of Tibet Autonomous Region, Lhasa 850000, China.
Li Kui
The People's Hospital of the Tibet Autonomous Region, Lhasa 850000, China.
Gao Guoyi
The hospital of XiShuangBanNa Dai Nationalities, Autonomous Jinghong, 666100 Yunnan, China.
Yin Ye
BGI-Shenzhen, Shenzhen 518083, China.
Wang Wei
BGI-Shenzhen, Shenzhen 518083, China.
Zhang Xiuqing
1] BGI-Shenzhen, Shenzhen 518083, China [2] The Guangdong Enterprise Key Laboratory of Human Disease Genomics, BGI-Shenzhen, 518083 Shenzhen, China [3] Shenzhen Key Laboratory of Transomics Biotechnologies, BGI-Shenzhen, 518083 Shenzhen, China.
Xu Xun
BGI-Shenzhen, Shenzhen 518083, China.
Yang Huanming
1] BGI-Shenzhen, Shenzhen 518083, China [2] Princess Al Jawhara Center of Excellence in the Research of Hereditary Disorders, King Abdulaziz University, Jeddah 21589, Saudi Arabia [3] James D. Watson Institute of Genome Science, 310008 Hangzhou, China.
Li Yingrui
BGI-Shenzhen, Shenzhen 518083, China.
Wang Jian
1] BGI-Shenzhen, Shenzhen 518083, China [2] James D. Watson Institute of Genome Science, 310008 Hangzhou, China.
Wang Jun
1] BGI-Shenzhen, Shenzhen 518083, China [2] Princess Al Jawhara Center of Excellence in the Research of Hereditary Disorders, King Abdulaziz University, Jeddah 21589, Saudi Arabia [3] Department of Biology, University of Copenhagen, Ole MaaløesVej 5, 2200 Copenhagen, Denmark [4] Macau University of Science and Technology, AvenidaWai long, Taipa, Macau 999078, China [5] Department of Medicine, University of Hong Kong 999077, Hong Kong.
Nielsen Rasmus
1] BGI-Shenzhen, Shenzhen 518083, China [2] Department of Integrative Biology, University of California, Berkeley, California 94720 USA [3] Department of Statistics, University of California, Berkeley, California 94720, USA [4] Department of Biology, University of Copenhagen, 2200 Copenhagen, Denmark.
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Article Info
Journal
Nature
Abbr.
Nature
ISSN
1476-4687
Published
2014-08-14
Epub
2014-00-02
Pages
194-7
Language
English
Region
England
NLM ID
0410462
PMCID
PMC4134395
Subset
IM
Grants
NHGRI NIH HHS · R01 HG003229 · United States
NHGRI NIH HHS · R01HG003229-08S2 · United States
NHGRI NIH HHS · R01HG003229 · United States
Databases
SRA
Corrections
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