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

Author:

Ivy Catherine M.1ORCID,Wearing Oliver H.1ORCID,Natarajan Chandrasekhar2ORCID,Schweizer Rena M.3ORCID,Gutiérrez-Pinto Natalia2ORCID,Velotta Jonathan P.3ORCID,Campbell-Staton Shane C.4ORCID,Petersen Elin E.5,Fago Angela5ORCID,Cheviron Zachary A.3,Storz Jay F.2ORCID,Scott Graham R.1ORCID

Affiliation:

1. Department of Biology, McMaster University, Hamilton, ON, Canada, L8S 4K1

2. School of Biological Sciences, University of Nebraska, Lincoln, NE 68588, USA

3. Divison of Biological Sciences, University of Montana, Missoula, MT 59812, USA

4. Department of Ecology and Evolutionary Biology, University of California, Los Angeles, CA 90095, USA

5. Department of Biology, Aarhus University, 8000 Aarhus C, Denmark

Abstract

ABSTRACT 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 F2 inter-population hybrids of highland and lowland deer mice to test for phenotypic associations of α- and β-globin variants on a mixed genetic background. Hb genotype had expected effects on Hb–O2 affinity that were associated with differences in arterial O2 saturation in hypoxia. However, high-altitude genotypes were also associated with breathing phenotypes that should contribute to enhancing O2 uptake in hypoxia. Mice with highland α-globin exhibited a more effective breathing pattern, with highland homozygotes breathing deeper but less frequently across a range of inspired O2, 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 β-globin. The association of globin variants with variation in breathing phenotypes could not be recapitulated by acute manipulation of Hb–O2 affinity, because treatment with efaproxiral (a synthetic drug that acutely reduces Hb–O2 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 O2 transport.

Funder

Natural Sciences and Engineering Research Council of Canada

National Science Foundation

National Institutes of Health

Ontario Graduate Scholarship

Canada Research Chairs

Publisher

The Company of Biologists

Subject

Insect Science,Molecular Biology,Animal Science and Zoology,Aquatic Science,Physiology,Ecology, Evolution, Behavior and Systematics

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