Author:
Fitch Karen R.,McGowan Kelly A.,van Raamsdonk Catherine D.,Fuchs Helmut,Lee Daekee,Puech Anne,Hérault Yann,Threadgill David W.,de Angelis Martin Hrabé,Barsh Gregory S.
Abstract
Chemical mutagenesis in the mouse is a powerful approach for phenotype-driven genetics, but questions remain about the efficiency with which new mutations ascertained by their phenotype can be localized and identified, and that knowledge applied to a specific biological problem. During a global screen for dominant phenotypes in about 30,000 animals, a novel class of pigmentation mutants were identified by dark skin (Dsk). We determined the genetic map location, homozygous phenotype, and histology of 10 newDskand 2 new dark coat (Dcc) mutations, and identified mutations inAgouti(Met1Leu,Dcc4),Sox18(Leu220ter,Dcc1),Keratin 2e(Thr500Pro,Dsk2), andEgfr(Leu863Gln,Dsk5). Cutaneous effects of mostDskmutations are limited to melanocytes, except for theKeratin 2eandEgfrmutations, in which hyperkeratosis and epidermal thickening precede epidermal melanocytosis by 3–6 wk. TheDsk2mutation is likely to impair intermediate filament assembly, leading to cytolysis of suprabasal keratinocytes and secondary hyperkeratosis and melanocytosis. TheDsk5mutation causes increased tyrosine kinase activity and a decrease in steady-state receptor levels in vivo. TheDskmutations represent genes or map locations not implicated previously in pigmentation, and delineate a developmental pathway in which mutations can be classified on the basis of body region, microscopic site, and timing of pigment accumulation.
Publisher
Cold Spring Harbor Laboratory
Subject
Developmental Biology,Genetics