ipsc来源的内皮细胞转录组学分析揭示了能量代谢和炎症对高海拔缺氧的适应。

IF 4 2区 生物学 Q1 GENETICS & HEREDITY
PLoS Genetics Pub Date : 2025-02-10 eCollection Date: 2025-02-01 DOI:10.1371/journal.pgen.1011570
Olivia A Gray, David B Witonsky, Jordan Jousma, Débora R Sobreira, Alexander Van Alstyne, Ru-Ting Huang, Yun Fang, Anna Di Rienzo
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引用次数: 0

摘要

西藏人对高海拔缺氧的适应仍然是人类达尔文选择的一个经典例子。在藏族人群中,EPAS1基因(其蛋白产物HIF-2α是缺氧反应的中心调节因子)的等位基因多次被证明在人类中携带一些最强烈的正向选择信号。然而,单独的选择性扫描信号可能只能解释区分高海拔适应人群与密切相关的低地人的一些表型。因此,迫切需要在基因座特异性和全基因组水平以及跨细胞类型上对适应性等位基因及其影响进行功能探测,以揭示全方位的有益性状。为此,我们建立了一个来自藏族和汉族个体的诱导多能干细胞(iPSCs)文库,这是一个强大的模型系统,可以精确地探索等位基因对转录反应的影响,我们将它们分化成血管内皮。使用该系统,我们首先关注缺氧依赖性增强子(ENH5),它有助于调节EPAS1,以研究其在内皮细胞中的位点特异性作用。然后,为了扩大研究范围,我们利用相同的实验系统来比较缺氧条件下藏族和汉族细胞的转录组,并发现血管生成、能量代谢和免疫途径在这两个具有不同长期居住历史的高海拔人群之间存在差异的证据。再加上针对相同途径的多基因适应的证据,这些结果表明,两个种群之间观察到的转录差异是由自然选择形成的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transcriptomic analysis of iPSC-derived endothelium reveals adaptations to high altitude hypoxia in energy metabolism and inflammation.

Tibetan adaptation to high-altitude hypoxia remains a classic example of Darwinian selection in humans. Amongst Tibetan populations, alleles in the EPAS1 gene - whose protein product, HIF-2α, is a central regulator of the hypoxia response - have repeatedly been shown to carry some of the strongest signals of positive selection in humans. However, selective sweep signals alone may only account for some of the phenotypes that differentiate high-altitude adapted populations from closely related lowlanders. Therefore, there is a pressing need to functionally probe adaptive alleles and their impact at both the locus-specific and genome-wide levels and across cell types to uncover the full range of beneficial traits. To this end, we established a library of induced pluripotent stem cells (iPSCs) derived from Tibetan and Han Chinese individuals, a robust model system allowing precise exploration of allelic effects on transcriptional responses, and we differentiated them into vascular endothelium. Using this system, we focus first on a hypoxia-dependent enhancer (ENH5) that contributes to the regulation of EPAS1 to investigate its locus-specific effects in endothelium. Then, to cast a wider net, we harness the same experimental system to compare the transcriptome of Tibetan and Han Chinese cells in hypoxia and find evidence that angiogenesis, energy metabolism and immune pathways differ between these two populations with different histories of long-term residence at high altitude. Coupled with evidence of polygenic adaptations targeting the same pathways, these results suggests that the observed transcriptional differences between the two populations were shaped by natural selection.

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来源期刊
PLoS Genetics
PLoS Genetics GENETICS & HEREDITY-
自引率
2.20%
发文量
438
期刊介绍: PLOS Genetics is run by an international Editorial Board, headed by the Editors-in-Chief, Greg Barsh (HudsonAlpha Institute of Biotechnology, and Stanford University School of Medicine) and Greg Copenhaver (The University of North Carolina at Chapel Hill). Articles published in PLOS Genetics are archived in PubMed Central and cited in PubMed.
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