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PMID: 16825572 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

A single amino acid mutation contributes to adaptive beach mouse color pattern.

Science (New York, N.Y.) ·Vol. 313 ·No. 5783 ·2006-07-07 ·Pages 101-4

Hoekstra HE, Hirschmann RJ, Bundey RA, Insel PA, Crossland JP

Abstract

Natural populations of beach mice exhibit a characteristic color pattern, relative to their mainland conspecifics, driven by natural selection for crypsis. We identified a derived, charge-changing amino acid mutation in the melanocortin-1 receptor (Mc1r) in beach mice, which decreases receptor function. In genetic crosses, allelic variation at Mc1r explains 9.8% to 36.4% of the variation in seven pigmentation traits determining color pattern. The derived Mc1r allele is present in Florida's Gulf Coast beach mice but not in Atlantic coast mice with similar light coloration, suggesting that different molecular mechanisms are responsible for convergent phenotypic evolution. Here, we link a single mutation in the coding region of a pigmentation gene to adaptive quantitative variation in the wild.

MeSH Terms
Adaptation, Biological Alleles Amino Acid Substitution Animals Cell Line Crosses, Genetic Cyclic AMP/metabolism Female Florida Gene Frequency Genotype Hair Hair Color/genetics Humans Male Molecular Sequence Data Mutation Peromyscus/genetics Phenotype Pigmentation/genetics Polymorphism, Single Nucleotide Principal Component Analysis Receptor, Melanocortin, Type 1/chemistry,genetics,metabolism Sequence Analysis, DNA
Chemicals
Receptor, Melanocortin, Type 1 Cyclic AMP
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Hoekstra Hopi E
Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA. hoekstra@ucsd.edu
Hirschmann Rachel J
Bundey Richard A
Insel Paul A
Crossland Janet P
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
1095-9203
Published
2006-07-07
Pages
101-4
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NCRR NIH HHS · P40-RR14279 · United States
Databases
GENBANK
DQ482848, DQ482850
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