Abstract
Evolutionary adaptation to extreme environments often requires coordinated changes in multiple intersecting physiological pathways, but how such multi-trait adaptation occurs remains unresolved. Transcription factors, which regulate the expression of many genes and can simultaneously alter multiple phenotypes, may be common targets of selection if the benefits of induced changes outweigh the costs of negative pleiotropic effects. We combined complimentary population genetic analyses and physiological experiments in North American deer mice (Peromyscus maniculatus) to examine links between genetic variation in transcription factors that coordinate physiological responses to hypoxia (hypoxia-inducible factors, HIFs) and multiple physiological traits that potentially contribute to high-altitude adaptation. First, we sequenced the exomes of 100 mice sampled from different elevations and discovered that several SNPs in the gene Epas1, which encodes the oxygen sensitive subunit of HIF-2α, exhibited extreme allele frequency differences between highland and lowland populations. Broader geographic sampling confirmed that Epas1 genotype varied predictably with altitude throughout the western US. We then discovered that Epas1 genotype influences heart rate in hypoxia, and the transcriptomic responses to hypoxia (including HIF targets and genes involved in catecholamine signaling) in the heart and adrenal gland. Finally, we used a demographically-informed selection scan to show that Epas1 variants have experienced a history of spatially varying selection, suggesting that differences in cardiovascular function and gene regulation contribute to high-altitude adaptation. Our results suggest a mechanism by which Epas1 may aid long-term survival of high-altitude deer mice and provide general insights into the role that highly pleiotropic transcription factors may play in the process of environmental adaptation.
| Original language | English |
|---|---|
| Article number | e1008420 |
| Journal | PLoS Genetics |
| Volume | 15 |
| Issue number | 11 |
| DOIs | |
| State | Published - 2019 |
Funding
Funding support was provided by the National Science Foundation (https://nsf.gov/; OIA 1736249 to ZAC and JFS; IOS 1755411 to ZAC and GRS; Postdoctoral Research Fellowship in Biology 1612859 to RMS), the National Heart, Lung, and Blood Institute of the National Institutes of Health (https://www.nhlbi.nih.gov/; HL087216 to JFS; Research Service Award Fellow to JPV, Grant Number 1F32HL136124-01), and the Natural Sciences and Engineering Research Council of Canada (http://www.nserc-crsng.gc.ca/index_eng. asp; Discovery Grant 418202-2012 to GRS; Postgraduate Scholarship to CMI). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We thank Kamilla Bentsen for help extracting RNA, and Jean-Marc Lassance and Hopi Hoekstra for providing access to Peromyscus maniculatus genome liftover files. We thank Michael Nachman and Erica Rosenblum for sharing previously unpublished data. Tissue samples were kindly loaned by the Museum of Southwestern Biology (2017.044.Mamm), Museum of Comparative Zoology (2017-56-Cryo), and the Museum of Vertebrate Zoology.
| Funder number |
|---|
| 2017.044 |
| 1612859, OIA 1736249, IOS 1755411 |
| HL087216 |
| F32HL136124 |
| 2017-56-Cryo |
| 418202-2012 |