| Literature DB >> 15322542 |
Catherine D Van Raamsdonk1, Karen R Fitch, Helmut Fuchs, Martin Hrabé de Angelis, Gregory S Barsh.
Abstract
A new class of dominant dark skin (Dsk) mutations discovered in a screen of approximately 30,000 mice is caused by increased dermal melanin. We identified three of four such mutations as hypermorphic alleles of Gnaq and Gna11, which encode widely expressed Galphaq subunits, act in an additive and quantitative manner, and require Ednrb. Interactions between Gq and Kit receptor tyrosine kinase signaling can mediate coordinate or independent control of skin and hair color. Our results provide a mechanism that can explain several aspects of human pigmentary variation and show how polymorphism of essential proteins and signaling pathways can affect a single physiologic system.Entities:
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Year: 2004 PMID: 15322542 PMCID: PMC7341985 DOI: 10.1038/ng1412
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330