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Mutations in dopachrome tautomerase (Dct) affect eumelanin/pheomelanin synthesis, but do not affect intracellular trafficking of the mutant protein.
Costin, Gertrude-E; Valencia, Julio C; Wakamatsu, Kazumasa; Ito, Shosuke; Solano, Francisco; Milac, Adina L; Vieira, Wilfred D; Yamaguchi, Yuji; Rouzaud, François; Petrescu, Andrei-J; Lamoreux, M Lynn; Hearing, Vincent J.
Afiliación
  • Costin GE; Pigment Cell Biology Section, Laboratory of Cell Biology, National Cancer Institute, National Institutes of Health (NIH), Bethesda, MD 20892, USA.
Biochem J ; 391(Pt 2): 249-59, 2005 Oct 15.
Article en En | MEDLINE | ID: mdl-15960609
Dopachrome tautomerase (Dct) is a type I membrane protein and an important regulatory enzyme that plays a pivotal role in the biosynthesis of melanin and in the rapid metabolism of its toxic intermediates. Dct-mutant melanocytes carrying the slaty or slaty light mutations were derived from the skin of newborn congenic C57BL/6J non-agouti black mice and were used to study the effect(s) of these mutations on the intracellular trafficking of Dct and on the pigmentation of the cells. Dct activity is 3-fold lower in slaty cells compared with non-agouti black melanocytes, whereas slaty light melanocytes have a surprisingly 28-fold lower Dct activity. Homology modelling of the active site of Dct suggests that the slaty mutation [R194Q (Arg194-->Gln)] is located in the active site and may alter the ability of the enzyme to transform the substrate. Transmembrane prediction methods indicate that the slaty light mutation [G486R (Gly486-->Arg)] may result in the sliding of the transmembrane domain towards the N-terminus, thus interfering with Dct function. Chemical analysis showed that both Dct mutations increase pheomelanin and reduce eumelanin produced by melanocytes in culture. Thus the enzymatic activity of Dct may play a role in determining whether the eumelanin or pheomelanin pathway is preferred for pigment biosynthesis.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oxidorreductasas Intramoleculares / Melaninas / Melanocitos Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Biochem J Año: 2005 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oxidorreductasas Intramoleculares / Melaninas / Melanocitos Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Biochem J Año: 2005 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido