Adaptive introgression in Tibetans spans focal and distributed architectures
Shen-Ao LiangiD, Qiong Zhu, Xinyun Gao, Yini Xiao, Kai LiuiD, Zhengwei Xie, Lian DengiD, Xueling Ge, Bing SuiD, Qiaomei Fu, Yuanting ZhengiD, Yaoxi HeiD, Shuhua XuiD, Lu Chen
Abstract
The Denisovan-derived EPAS1 haplotype is a paradigmatic example of adaptive introgression, but whether archaic ancestry contributed beyond such large-effect loci remains unclear. We analyzed genomes from 1,039 Tibetans, Han Chinese, archaic hominins and ancient Tibetan Plateau individuals. Denisovan-derived adaptive variation was highly localized around EPAS1, whereas Neanderthal-derived variation was distributed across the genome; temporal and elevational patterns reinforced this contrast. Despite individual-level heterogeneity, Neanderthal-introgressed gene repertoires repeatedly converged on immune, metabolic and signal-transduction pathways. A Tibetan-enriched Neanderthal PPARGC1A haplotype was associated with lower fasting glucose and showed concordant support from an independent East Asian type 2 diabetes GWAS. These findings reveal that adaptive introgression can contribute to complex human adaptation through functionally convergent combinations of archaic variants, rather than only through shared large-effect haplotypes.
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