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      Effects of G-protein mutations on skin color

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          Abstract

          A new class of dominant dark skin ( Dsk) mutations discovered in a screen of ~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 Gαq 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.

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          Author and article information

          Journal
          9216904
          2419
          Nat Genet
          Nat. Genet.
          Nature genetics
          1061-4036
          1546-1718
          19 June 2020
          22 August 2004
          September 2004
          08 July 2020
          : 36
          : 9
          : 961-968
          Affiliations
          [1 ]Departments of Genetics and Pediatrics, Stanford University School of Medicine, Stanford, California, 94305-5323, USA
          [2 ]Institute of Experimental Genetics, GSF-National Research Center for Environment and Health, Neuherberg, D-85764, Germany
          Author notes
          Correspondence should be addressed to G.S.B. ( gbarsh@ 123456cmgm.stanford.edu ).
          Article
          PMC7341985 PMC7341985 7341985 nihpa1604637
          10.1038/ng1412
          7341985
          15322542
          96920d97-a422-456f-a87d-c62d87e5e767
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