4.5 Article

Genetic variation in haemoglobin is associated with evolved changes in breathing in high-altitude deer mice

Journal

JOURNAL OF EXPERIMENTAL BIOLOGY
Volume 225, Issue 2, Pages -

Publisher

COMPANY BIOLOGISTS LTD
DOI: 10.1242/jeb.243595

Keywords

Evolutionary physiology; Hypoxia acclimation; Pulmonary ventilation; Ventilatory acclimatization to hypoxia

Categories

Funding

  1. Natural Sciences and Engineering Research Council of Canada (NSERC) [RGPIN-2018-05707]
  2. National Science Foundation (NSF) [IOS-1354934, IOS-1634219, IOS1755411, OIA-1736249, IOS-1354390, IOS-2114465, OIA1736249]
  3. National Institutes of Health (NIH) [HL087216]
  4. National Science Foundation Postdoc Research Fellowship in Biology [1612859]
  5. National Institutes of Health National Heart, Lung and Blood Institute Research Service Award Fellowship [1F32HL136124-01]
  6. National Science Foundation (DBI) Postdoctoral Fellowship in Biology Award [1612283]
  7. Direct For Biological Sciences
  8. Div Of Biological Infrastructure [1612283] Funding Source: National Science Foundation
  9. Direct For Biological Sciences
  10. Div Of Biological Infrastructure [1612859] Funding Source: National Science Foundation

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Genetic variants in haemoglobin associated with high-altitude adaptation in deer mice were found to also be linked to breathing phenotypes that enhance oxygen uptake in hypoxia, showing unexpected effects of adaptive variation in Hb on physiology beyond its traditional function in oxygen transport.
Physiological systems often have emergent properties but the effects of genetic variation on physiology are often unknown, which presents a major challenge to understanding the mechanisms of phenotypic evolution. We investigated whether genetic variants in haemoglobin (Hb) that contribute to high-altitude adaptation in deer mice (Peromyscus maniculatus) are associated with evolved changes in the control of breathing. We created F-2 inter-population hybrids of highland and lowland deer mice to test for phenotypic associations of alpha- and beta-globin variants on a mixed genetic background. Hb genotype had expected effects on Hb-O-2 affinity that were associated with differences in arterial O-2 saturation in hypoxia. However, high-altitude genotypes were also associated with breathing phenotypes that should contribute to enhancing O-2 uptake in hypoxia. Mice with highland alpha-globin exhibited a more effective breathing pattern, with highland homozygotes breathing deeper but less frequently across a range of inspired O-2, and this difference was comparable to the evolved changes in breathing pattern in deer mouse populations native to high altitude. The ventilatory response to hypoxia was augmented in mice that were homozygous for highland beta-globin. The association of globin variants with variation in breathing phenotypes could not be recapitulated by acute manipulation of Hb-O-2 affinity, because treatment with efaproxiral (a synthetic drug that acutely reduces Hb-O-2 affinity) had no effect on breathing in normoxia or hypoxia. Therefore, adaptive variation in Hb may have unexpected effects on physiology in addition to the canonical function of this protein in circulatory O-2 transport.

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