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Tibetan natives have lived on the Tibetan plateau (altitude ∼ 4,000 m) for at least 25,000 years, and as such they are adapted to life and reproduction in a hypoxic environment. Recent studies have identified two genetic loci, EGLN1 and EPAS1, that have undergone natural selection in Tibetans, and further demonstrated an association of EGLN1/EPAS1 genotype with hemoglobin concentration. Both genes encode major components of the hypoxia-inducible factor (HIF) transcriptional pathway, which coordinates an organism's response to hypoxia. Patients living at sea level with genetic disease of the HIF pathway have characteristic phenotypes at both the integrative-physiology and cellular level. We sought to test the hypothesis that natural selection to hypoxia within Tibetans results in related phenotypic differences. We compared Tibetans living at sea level with Han Chinese, who are Tibetans' most closely related major ethnic group. We found that Tibetans had a lower hemoglobin concentration, a higher pulmonary ventilation relative to metabolism, and blunted pulmonary vascular responses to both acute (minutes) and sustained (8 h) hypoxia. At the cellular level, the relative expression and hypoxic induction of HIF-regulated genes were significantly lower in peripheral blood lymphocytes from Tibetans compared with Han Chinese. Within the Tibetans, we found a significant correlation between both EPAS1 and EGLN1 genotype and the induction of erythropoietin by hypoxia. In conclusion, this study provides further evidence that Tibetans respond less vigorously to hypoxic challenge. This is evident at sea level and, at least in part, appears to arise from a hyporesponsive HIF transcriptional system.

Original publication

DOI

10.1152/japplphysiol.00535.2013

Type

Journal article

Journal

J Appl Physiol (1985)

Publication Date

01/04/2014

Volume

116

Pages

893 - 904

Keywords

EGLN1, EPAS1, erythropoietin, high altitude, hypoxic pulmonary vasoconstriction, Acclimatization, Adult, Altitude, Anoxia, Asian Continental Ancestry Group, Basic Helix-Loop-Helix Transcription Factors, Cells, Cultured, China, Erythropoietin, Gene Expression Regulation, Haplotypes, Hemoglobins, Humans, Hypoxia-Inducible Factor-Proline Dioxygenases, Male, Oxygen, Phenotype, Pulmonary Artery, Pulmonary Ventilation, Selection, Genetic, Tibet, Time Factors, Transcription, Genetic, Vasoconstriction, Young Adult