High-Altitude Adaptation: Mechanistic Insights from Integrated Genomics and Physiology

Mol Biol Evol. 2021 Jun 25;38(7):2677-2691. doi: 10.1093/molbev/msab064.

Abstract

Population genomic analyses of high-altitude humans and other vertebrates have identified numerous candidate genes for hypoxia adaptation, and the physiological pathways implicated by such analyses suggest testable hypotheses about underlying mechanisms. Studies of highland natives that integrate genomic data with experimental measures of physiological performance capacities and subordinate traits are revealing associations between genotypes (e.g., hypoxia-inducible factor gene variants) and hypoxia-responsive phenotypes. The subsequent search for causal mechanisms is complicated by the fact that observed genotypic associations with hypoxia-induced phenotypes may reflect second-order consequences of selection-mediated changes in other (unmeasured) traits that are coupled with the focal trait via feedback regulation. Manipulative experiments to decipher circuits of feedback control and patterns of phenotypic integration can help identify causal relationships that underlie observed genotype-phenotype associations. Such experiments are critical for correct inferences about phenotypic targets of selection and mechanisms of adaptation.

Keywords: EPAS1; adaptation; altitude; genotype–phenotype association; hypoxia; hypoxia-inducible factor.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Adaptation, Biological / genetics*
  • Altitude*
  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Biological Evolution
  • Female
  • Genetic Fitness
  • Hemoglobins / metabolism
  • Humans
  • Hypoxia*
  • Hypoxia-Inducible Factor-Proline Dioxygenases / genetics
  • Metagenomics
  • Oxygen Consumption
  • Phenotype*
  • Physiology
  • Pregnancy
  • Selection, Genetic*

Substances

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