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Comparative phylogenomic assessment of mitochondrial introgression among several species of chipmunks (Tamias)

  • Brice A.J. Sarver
  • , John R. Demboski
  • , Jeffrey M. Good
  • , Nicholas Forshee
  • , Samuel S. Hunter
  • , Jack Sullivan

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

Many species are not completely reproductively isolated, resulting in hybridization and genetic introgression. Organellar genomes, such as those derived from mitochondria (mtDNA) and chloroplasts, introgress frequently in natural systems; however, the forces shaping patterns of introgression are not always clear. Here, we investigate extensive mtDNA introgression in western chipmunks, focusing on species in the Tamias quadrivittatus group from the central and southern Rocky Mountains. Specifically, we investigate the role of selection in driving patterns of introgression. We sequenced 51 mtDNA genomes from six species and combine these sequences with other published genomic data to yield annotated mitochondrial reference genomes for nine species of chipmunks. Genomic characterization was performed using a series of molecular evolutionary and phylogenetic analyses to test protein-coding genes for positive selection. We fit a series of maximum likelihood models using a model-averaging approach, assessed deviations from neutral expectations, and performed additional tests to search for codons under the influence of selection. We found no evidence for positive selection among these genomes, suggesting that selection has not been the driving force of introgression in these species. Thus, extensive mtDNA introgression among several species of chipmunks likely reflects genetic drift of introgressed alleles in historically fluctuating populations.

Original languageEnglish
Pages (from-to)7-19
Number of pages13
JournalGenome Biology and Evolution
Volume9
Issue number1
DOIs
StatePublished - Jan 1 2017

Funding

The authors thank the following for assistance in the field over several years: K. Bell, W. Bell, I. Demboski, M. Fraker, D. Good, P. Good, J. Harper, A. Hornsby, S. Poler, A. Runck, and D. Sullivan. We thank B. Martin, J. Gonzalez, and four anonymous reviewers for helpful comments that improved the manuscript. We also thank the Denver Museum of Nature & Science for providing tissue loans. This research was conducted in compliance with University of Idaho Animal Care and Use Committee, under protocol UIACUC-2005-40, and was supported by a seed grant from the University of Idaho Research Foundation, the NSF EPSCoR program (NSF cooperative agreement number EPS-9720634), the Institute for Bioinformatics and Evolutionary Studies (IBEST) at the University of Idaho (by NIH NCRR 1P20RR016454-01; NIH NCRR 1P20RR016448-01; NSF EPS-809935), NSF DEB- 0717426 (JS), NSF DEB-0716200 (JRD), NSF Cooperative Agreement No. DBI-0939454 (JS), and the Denver Museum of Nature & Science. JS and BAJS received funding through BEACON, an NSF-funded Center the Study of Evolution in Action (DBI-0939454). Craig Moritz, Ke Bi, and Tyler Linderoth helped develop exon capture in chipmunks, supported by the University of California, Berkeley VCR-BiGCB and an NSERC Postdoctoral Fellowship to Bi. Additionally, this work was supported by start-up funds from the University of Montana (JMG) and the Gordon and Betty Moore Foundation. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the authors and do not necessarily reflect the views of the National Science Foundation.

FundersFunder number
1P20RR016448-01, DEB- 0717426, 1P20RR016454-01, EPS-809935, DBI-0939454, DEB-0716200
EPS-9720634
P20RR016454
University of Idaho
Denver Museum of Nature & ScienceUIACUC-2005-40

    Keywords

    • Introgression
    • Mitochondrial genomics
    • Molecular evolution
    • Phylogenomics
    • Selection
    • Tamias

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