Department of Anthropology, University of California, Los Angeles, CA, USA.
Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Mol Biol Evol. 2023 Jul 5;40(7). doi: 10.1093/molbev/msad162.
For over 10,000 years, Andeans have resided at high altitude where the partial pressure of oxygen challenges human survival. Recent studies have provided evidence for positive selection acting in Andeans on the HIF2A (also known as EPAS1) locus, which encodes for a central transcription factor of the hypoxia-inducible factor pathway. However, the precise mechanism by which this allele might lead to altitude-adaptive phenotypes, if any, is unknown. By analyzing whole genome sequencing data from 46 high-coverage Peruvian Andean genomes, we confirm evidence for positive selection acting on HIF2A and a unique pattern of variation surrounding the Andean-specific single nucleotide variant (SNV), rs570553380, which encodes for an H194R amino acid substitution in HIF-2α. Genotyping the Andean-associated SNV rs570553380 in a group of 299 Peruvian Andeans from Cerro de Pasco, Peru (4,338 m), reveals a positive association with increased fraction of exhaled nitric oxide, a marker of nitric oxide biosynthesis. In vitro assays show that the H194R mutation impairs binding of HIF-2α to its heterodimeric partner, aryl hydrocarbon receptor nuclear translocator. A knockin mouse model bearing the H194R mutation in the Hif2a gene displays decreased levels of hypoxia-induced pulmonary Endothelin-1 transcripts and protection against hypoxia-induced pulmonary hypertension. We conclude the Andean H194R HIF2A allele is a hypomorphic (partial loss of function) allele.
一万多年来,安第斯人一直居住在高海拔地区,那里的氧气分压对人类生存构成挑战。最近的研究为在 HIF2A(也称为 EPAS1)基因座上对安第斯人进行积极选择提供了证据,该基因座编码缺氧诱导因子通路的核心转录因子。然而,如果存在任何情况,这种等位基因如何导致适应高海拔的表型的精确机制尚不清楚。通过分析来自 46 个高覆盖率秘鲁安第斯基因组的全基因组测序数据,我们证实了 HIF2A 上存在积极选择的证据,以及围绕安第斯特有的单核苷酸变异(SNV)rs570553380 的独特变异模式,该变异编码 HIF-2α中的 H194R 氨基酸取代。在秘鲁塞罗德帕斯科的 299 名秘鲁安第斯人(海拔 4338 米)中对与安第斯相关的 SNV rs570553380 进行基因分型,结果显示其与呼出的一氧化氮分数增加呈正相关,这是一氧化氮生物合成的标志物。体外测定表明,H194R 突变会损害 HIF-2α与其异二聚体伴侣芳烃受体核转位蛋白的结合。携带 Hif2a 基因中 H194R 突变的基因敲入小鼠模型显示,缺氧诱导的肺内皮素-1 转录物水平降低,并能防止缺氧诱导的肺动脉高压。我们得出结论,安第斯 H194R HIF2A 等位基因是一个低功能(部分功能丧失)等位基因。