The Genomics and Genetics of Oxygen Homeostasis.

IF 7.7 2区 生物学 Q1 GENETICS & HEREDITY Annual review of genomics and human genetics Pub Date : 2020-08-31 Epub Date: 2020-04-07 DOI:10.1146/annurev-genom-111119-073356
Gregg L Semenza
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引用次数: 50

Abstract

Human survival is dependent upon the continuous delivery of O2 to each cell in the body in sufficient amounts to meet metabolic requirements, primarily for ATP generation by oxidative phosphorylation. Hypoxia-inducible factors (HIFs) regulate the transcription of thousands of genes to balance O2 supply and demand. The HIFs are negatively regulated by O2-dependent hydrox-ylation and ubiquitination by prolyl hydroxylase domain (PHD) proteins and the von Hippel-Lindau (VHL) protein. Germline mutations in the genes encoding VHL, HIF-2α, and PHD2 cause hereditary erythrocytosis, which is characterized by polycythemia and pulmonary hypertension and is caused by increased HIF activity. Evolutionary adaptation to life at high altitude is associated with unique genetic variants in the genes encoding HIF-2α and PHD2 that blunt the erythropoietic and pulmonary vascular responses to hypoxia.

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氧稳态的基因组学和遗传学。
人类的生存依赖于持续向体内每个细胞输送足够量的氧气以满足代谢需求,主要是通过氧化磷酸化产生ATP。缺氧诱导因子(hif)调节数千个基因的转录以平衡氧气供应和需求。hfs受脯氨酸羟化酶结构域(PHD)蛋白和von Hippel-Lindau (VHL)蛋白的o2依赖性氢化和泛素化负调控。编码VHL、HIF-2α和PHD2基因的种系突变引起遗传性红细胞增多症,以红细胞增多症和肺动脉高压为特征,由HIF活性升高引起。对高海拔生活的进化适应与编码HIF-2α和PHD2的基因的独特遗传变异有关,这些基因会减弱红细胞生成和肺血管对缺氧的反应。
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来源期刊
CiteScore
14.90
自引率
1.10%
发文量
29
期刊介绍: Since its inception in 2000, the Annual Review of Genomics and Human Genetics has been dedicated to showcasing significant developments in genomics as they pertain to human genetics and the human genome. The journal emphasizes genomic technology, genome structure and function, genetic modification, human variation and population genetics, human evolution, and various aspects of human genetic diseases, including individualized medicine.
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