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Annual Review of Genomics and Human Genetics

Volume 21, 2020

The Genomics and Genetics of Oxygen Homeostasis

Abstract

Human survival is dependent upon the continuous delivery of O 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 O supply and demand. The HIFs are negatively regulated by O-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.

Keyword(s): congenital polycythemia, hereditary erythrocytosis, hypoxia-inducible factor, Tibetan highlanders
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/content/journals/10.1146/annurev-genom-111119-073356
2020-08-31
2024-04-18
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/content/journals/10.1146/annurev-genom-111119-073356
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The Genomics and Genetics of Oxygen Homeostasis
Annual Review of Genomics and Human Genetics 21, 183 (2020); https://doi.org/10.1146/annurev-genom-111119-073356
/content/journals/10.1146/annurev-genom-111119-073356
/content/journals/10.1146/annurev-genom-111119-073356
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