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

Bibliographic Collection: 
Publication Type: Journal Article
Authors: Huerta-Sánchez, Emilia; Jin, Xin; Bianba, Zhuoma; Peter, Benjamin M; Vinckenbosch, Nicolas; Liang, Yu; Yi, Xin; He, Mingze; Somel, Mehmet; Ni, Peixiang; Wang, Bo; Ou, Xiaohua; Luosang, Jiangbai; Cuo, Zha Xi Ping; Li, Kui; Gao, Guoyi; Yin, Ye; Wang, Wei; Zhang, Xiuqing; Xu, Xun; Yang, Huanming; Li, Yingrui; Wang, Jian; Wang, Jun; Nielsen, Rasmus
Year of Publication: 2014
Journal: Nature
Volume: 512
Issue: 7513
Pagination: 194-7
Date Published: 2014 Aug 14
Publication Language: eng
ISSN: 1476-4687
Keywords: Adaptation, Physiological, Altitude, Animals, Asian Continental Ancestry Group, Basic Helix-Loop-Helix Transcription Factors, DNA, Gene Frequency, Genetic Variation, Haplotypes, Hominidae, Humans, Polymorphism, Single Nucleotide, Tibet

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.

DOI: 10.1038/nature13408
Alternate Journal: Nature
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