Limited Evidence for Parallel Evolution Among Desert-Adapted Peromyscus Deer Mice.


Journal

The Journal of heredity
ISSN: 1465-7333
Titre abrégé: J Hered
Pays: United States
ID NLM: 0375373

Informations de publication

Date de publication:
24 05 2021
Historique:
received: 25 08 2020
accepted: 27 02 2021
pubmed: 10 3 2021
medline: 15 12 2021
entrez: 9 3 2021
Statut: ppublish

Résumé

Warming climate and increasing desertification urge the identification of genes involved in heat and dehydration tolerance to better inform and target biodiversity conservation efforts. Comparisons among extant desert-adapted species can highlight parallel or convergent patterns of genome evolution through the identification of shared signatures of selection. We generate a chromosome-level genome assembly for the canyon mouse (Peromyscus crinitus) and test for a signature of parallel evolution by comparing signatures of selective sweeps across population-level genomic resequencing data from another congeneric desert specialist (Peromyscus eremicus) and a widely distributed habitat generalist (Peromyscus maniculatus), that may be locally adapted to arid conditions. We identify few shared candidate loci involved in desert adaptation and do not find support for a shared pattern of parallel evolution. Instead, we hypothesize divergent molecular mechanisms of desert adaptation among deer mice, potentially tied to species-specific historical demography, which may limit or enhance adaptation. We identify a number of candidate loci experiencing selective sweeps in the P. crinitus genome that are implicated in osmoregulation (Trypsin, Prostasin) and metabolic tuning (Kallikrein, eIF2-alpha kinase GCN2, APPL1/2), which may be important for accommodating hot and dry environmental conditions.

Identifiants

pubmed: 33686424
pii: 6158454
doi: 10.1093/jhered/esab009
pmc: PMC8141686
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

286-302

Subventions

Organisme : NIGMS NIH HHS
ID : R35 GM128843
Pays : United States

Informations de copyright

© The American Genetic Association. 2021.

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Auteurs

Jocelyn P Colella (JP)

Department of Molecular, Cellular, and Biomedical Sciences, University of New Hampshire, Durham, NH.
Hubbard Genome Center, University of New Hampshire, Durham, NH.
Biodiversity Institute, University of Kansas, Lawrence, KS.

Anna Tigano (A)

Department of Molecular, Cellular, and Biomedical Sciences, University of New Hampshire, Durham, NH.
Hubbard Genome Center, University of New Hampshire, Durham, NH.

Olga Dudchenko (O)

Center for Genome Architecture, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX.
Center for Theoretical and Biological Physics, Rice University, Houston, TX.
Department of Computer Science, Department of Computational and Applied Mathematics, Rice University, Houston, TX.

Arina D Omer (AD)

Center for Genome Architecture, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX.

Ruqayya Khan (R)

Center for Genome Architecture, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX.
Department of Computer Science, Department of Computational and Applied Mathematics, Rice University, Houston, TX.

Ivan D Bochkov (ID)

Center for Genome Architecture, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX.
Department of Computer Science, Department of Computational and Applied Mathematics, Rice University, Houston, TX.

Erez L Aiden (EL)

Center for Genome Architecture, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX.
Center for Theoretical and Biological Physics, Rice University, Houston, TX.
Department of Computer Science, Department of Computational and Applied Mathematics, Rice University, Houston, TX.
Shanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai 201210, China.
School of Agriculture and Environment, University of Western Australia, Perth, WA, Australia.

Matthew D MacManes (MD)

Department of Molecular, Cellular, and Biomedical Sciences, University of New Hampshire, Durham, NH.
Hubbard Genome Center, University of New Hampshire, Durham, NH.

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