A β-Defensin Mutation Causes Black Coat Color in Domestic Dogs

Author:

Candille Sophie I.1234,Kaelin Christopher B.1234,Cattanach Bruce M.1234,Yu Bin1234,Thompson Darren A.1234,Nix Matthew A.1234,Kerns Julie A.1234,Schmutz Sheila M.1234,Millhauser Glenn L.1234,Barsh Gregory S.1234

Affiliation:

1. Departments of Genetics and Pediatrics, Stanford University, Stanford, CA, USA.

2. Medical Research Council (MRC) Mammalian Genetics Unit, Harwell, Oxfordshire, OX11 ORD, UK.

3. Departments of Chemistry and Biochemistry, University of California at Santa Cruz (UCSC), Santa Cruz, CA 95064, USA.

4. Department of Animal and Poultry Science, University of Saskatchewan, Saskatoon S7N 5A8, Canada.

Abstract

Genetic analysis of mammalian color variation has provided fundamental insight into human biology and disease. In most vertebrates, two key genes, Agouti and Melanocortin 1 receptor ( Mc1r ), encode a ligand-receptor system that controls pigment type-switching, but in domestic dogs, a third gene is implicated, the K locus, whose genetic characteristics predict a previously unrecognized component of the melanocortin pathway. We identify the K locus as β- defensin 103 ( CBD103 ) and show that its protein product binds with high affinity to the Mc1r and has a simple and strong effect on pigment type-switching in domestic dogs and transgenic mice. These results expand the functional role of β-defensins, a protein family previously implicated in innate immunity, and identify an additional class of ligands for signaling through melanocortin receptors.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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