A β-defensin mutation causes black coat color in domestic dogs

被引:267
作者
Candille, Sophie I.
Kaelin, Christopher B.
Cattanach, Bruce M.
Bin Yu
Thompson, Darren A.
Nix, Matthew A.
Kerns, Julie A.
Schmutz, Sheila M.
Millhauser, Glenn L.
Barsh, Gregory S. [1 ]
机构
[1] Stanford Univ, Dept Genet, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Pediat, Stanford, CA 94305 USA
[3] MRC, Mammalian Genet Unit, Harwell OX11 ORD, Oxon, England
[4] Univ Calif Santa Cruz, Dept Chem, Santa Cruz, CA 95064 USA
[5] Univ Calif Santa Cruz, Dept Biochem, Santa Cruz, CA 95064 USA
[6] Univ Saskatchewan, Dept Anim & Poultry Sci, Saskatoon, SK S7N 5A8, Canada
关键词
D O I
10.1126/science.1147880
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 beta-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 beta-defensins, a protein family previously implicated in innate immunity, and identify an additional class of ligands for signaling through melanocortin receptors.
引用
收藏
页码:1418 / 1423
页数:6
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