Gu Wanjun, Lawrence Elijah S, Evans A Mark, Simonson Tatum S
Department of Medicine, Division of Pulmonary, Crtiical Care, Sleep Medicine, and Physiology, University of California, San Diego, CA, USA.
Department of Neurology, Weill Institute for Neurosciences, University of California, San Francisco, CA, USA.
Philos Trans R Soc Lond B Biol Sci. 2025 Aug 21;380(1933):20240170. doi: 10.1098/rstb.2024.0170.
Advancements in genetic research have greatly enhanced our understanding of human adaptation to high-altitude environments through the identification of genetic markers linked to hypoxia tolerance. Our recent studies identify key genes associated with haematological and ventilatory traits in Andeans. Adaptive variation at , encoding endothelial PAS domain protein 1, a key regulator in the hypoxia-inducible factor (HIF) pathway (the alpha subunit of HIF2), has been associated with relatively low haematocrit at high altitude, which may be linked directly or indirectly to improvements in oxygen transport and/or delivery, while , encoding the AMP-activated protein kinase (AMPK) alpha-1 subunit, has been linked to ventilatory responses during wakefulness that are further associated with sleep phenotypes with metabolic implications. The relevance of these genetic adaptations extends beyond adult physiology; e.g. other studies have associated an adaptive genetic signature at with pregnancy outcomes in Andean populations. Understanding how adaptive genetic variations in and contribute to hypoxia tolerance offers a foundation for investigating broader evolutionary mechanisms of high-altitude adaptation, particularly in the contexts of pregnancy and fetal development, where oxygen availability is crucial. Integrative studies that combine molecular, physiological, and evolutionary perspectives offer promise in revealing the complexities of high-altitude adaptation and its relevance to hypoxia-related health challenges in both highland and lowland populations.This article is part of the discussion meeting issue 'Pregnancy at high altitude: the challenge of hypoxia'.
基因研究的进展通过识别与低氧耐受性相关的基因标记,极大地增进了我们对人类适应高海拔环境的理解。我们最近的研究确定了与安第斯人群血液学和通气特征相关的关键基因。位于 ,编码内皮 PAS 结构域蛋白 1(缺氧诱导因子(HIF)途径中的关键调节因子(HIF2 的α亚基))的适应性变异,与高海拔地区相对较低的血细胞比容有关,这可能直接或间接与氧气运输和/或输送的改善有关,而位于 ,编码 AMP 活化蛋白激酶(AMPK)α-1 亚基的基因,与清醒时的通气反应有关,进一步与具有代谢影响的睡眠表型相关。这些基因适应性的相关性不仅限于成人生理学;例如,其他研究将位于 的适应性基因特征与安第斯人群的妊娠结局联系起来。了解 和 中的适应性基因变异如何促成低氧耐受性,为研究高海拔适应的更广泛进化机制提供了基础,特别是在妊娠和胎儿发育的背景下,其中氧气供应至关重要。结合分子、生理和进化观点的综合研究有望揭示高海拔适应的复杂性及其与高地和低地人群中与低氧相关的健康挑战的相关性。本文是讨论会议议题“高海拔妊娠:低氧挑战”的一部分。