Human adaptation to the hypoxia of high altitude: the Tibetan paradigm from the pregenomic to the postgenomic era

J Appl Physiol (1985). 2014 Apr 1;116(7):875-84. doi: 10.1152/japplphysiol.00605.2013. Epub 2013 Nov 7.

Abstract

The Tibetan Plateau is one of the highest regions on Earth. Tibetan highlanders are adapted to life and reproduction in a hypoxic environment and possess a suite of distinctive physiological traits. Recent studies have identified genomic loci that have undergone natural selection in Tibetans. Two of these loci, EGLN1 and EPAS1, encode major components of the hypoxia-inducible factor transcriptional system, which has a central role in oxygen sensing and coordinating an organism's response to hypoxia, as evidenced by studies in humans and mice. An association between genetic variants within these genes and hemoglobin concentration in Tibetans at high altitude was demonstrated in some of the studies (8, 80, 96). Nevertheless, the functional variants within these genes and the underlying mechanisms of action are still not known. Furthermore, there are a number of other possible phenotypic traits, besides hemoglobin concentration, upon which natural selection may have acted. Integration of studies at the genomic level with functional molecular studies and studies in systems physiology has the potential to provide further understanding of human evolution in response to high-altitude hypoxia. The Tibetan paradigm provides further insight on the role of the hypoxia-inducible factor system in humans in relation to oxygen homeostasis.

Keywords: EGLN1; EPAS1; Tibetan; adaptation; evolution; hypoxia-inducible factor.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Acclimatization / genetics*
  • Altitude*
  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Gene Expression Regulation
  • Genetics, Population*
  • Genomics*
  • Genotype
  • Humans
  • Hypoxia / genetics*
  • Hypoxia / metabolism
  • Hypoxia / physiopathology
  • Hypoxia-Inducible Factor-Proline Dioxygenases / genetics
  • Hypoxia-Inducible Factor-Proline Dioxygenases / metabolism
  • Mice
  • Phenotype
  • Selection, Genetic*
  • Tibet
  • Transcription, Genetic

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • endothelial PAS domain-containing protein 1
  • EGLN1 protein, human
  • Hypoxia-Inducible Factor-Proline Dioxygenases