Eccles Institute of Human Genetics, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Hum Genet. 2012 Apr;131(4):527-33. doi: 10.1007/s00439-011-1109-3. Epub 2011 Nov 9.
Some highland populations have genetic adaptations that enable their successful existence in a hypoxic environment. Tibetans are protected against many of the harmful responses exhibited by non-adapted populations upon exposure to severe hypoxia, including elevated hemoglobin concentration (i.e., polycythemia). Recent studies have highlighted several genes subject to natural selection in native high-altitude Tibetans. Three of these genes, EPAS1, EGLN1 and PPARA, regulate or are regulated by hypoxia inducible factor, a principal controller of erythropoiesis and other organismal functions. Uncovering the molecular basis of hypoxic adaptation should have implications for understanding hematological and other adaptations involved in hypoxia tolerance. Because the hypoxia response involves a variety of cardiovascular, pulmonary and metabolic functions, this knowledge would improve our understanding of disease mechanisms and could ultimately be translated into targeted therapies for oxygen deprivation, cardiopulmonary and cerebral pathologies, and metabolic disorders such as diabetes and obesity.
一些高原人群拥有基因适应性,使他们能够在缺氧环境中成功生存。与非适应人群在暴露于严重缺氧时表现出的许多有害反应不同,藏人血红蛋白浓度升高(即红细胞增多症)的情况较少。最近的研究强调了几个在本地高原藏人中受到自然选择的基因。这三个基因,EPAS1、EGLN1 和 PPARA,调节或受缺氧诱导因子调节,缺氧诱导因子是红细胞生成和其他机体功能的主要控制器。揭示低氧适应的分子基础应该有助于理解与低氧耐受相关的血液学和其他适应。由于缺氧反应涉及多种心血管、肺和代谢功能,这方面的知识将有助于我们更好地理解疾病机制,并最终转化为针对缺氧、心肺和脑病理以及代谢紊乱(如糖尿病和肥胖症)的靶向治疗。