Adaptive tail-length evolution in deer mice is associated with differential Hoxd13 expression in early development

Author:

Kingsley Evan P.ORCID,Hager Emily R.ORCID,Lassance Jean-MarcORCID,Turner Kyle M.ORCID,Harringmeyer Olivia S.ORCID,Kirby ChristopherORCID,Neugeboren Beverly I.ORCID,Hoekstra Hopi E.ORCID

Abstract

AbstractVariation in the size and number of axial segments underlies much of the diversity in animal body plans. Here we investigate the evolutionary, genetic and developmental mechanisms driving tail-length differences between forest and prairie ecotypes of deer mice (Peromyscus maniculatus). We first show that long-tailed forest mice perform better in an arboreal locomotion assay, consistent with tails being important for balance during climbing. We then identify six genomic regions that contribute to differences in tail length, three of which associate with caudal vertebra length and the other three with vertebra number. For all six loci, the forest allele increases tail length, indicative of the cumulative effect of natural selection. Two of the genomic regions associated with variation in vertebra number contain Hox gene clusters. Of those, we find an allele-specific decrease in Hoxd13 expression in the embryonic tail bud of long-tailed forest mice, consistent with its role in axial elongation. Additionally, we find that forest embryos have more presomitic mesoderm than prairie embryos and that this correlates with an increase in the number of neuromesodermal progenitors, which are modulated by Hox13 paralogues. Together, these results suggest a role for Hoxd13 in the development of natural variation in adaptive morphology on a microevolutionary timescale.

Funder

Harvard University | Museum of Comparative Zoology, Harvard University

Harvard University | Robert A. Chapman Memorial Scholarships for the study of Vertebrate Locomotion

U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences

Harvard University | Robert A. Chapman Memorial Scholarships for the study of Vertebrate Locomotion Harvard University | Theodore H. Ashford Fellowship

European Molecular Biology Organization

Human Frontier Science Program

National Science Foundation

Harvard University | Quantitative Biology Student Fellowship

Howard Hughes Medical Institute

Publisher

Springer Science and Business Media LLC

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