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Dap1p, a heme-binding protein that regulates the cytochrome P450 protein Erg11p/Cyp51p in Saccharomyces cerevisiae.
Mallory, Julia C; Crudden, Gerard; Johnson, Ben L; Mo, Caiqing; Pierson, Charles A; Bard, Martin; Craven, Rolf J.
Afiliación
  • Mallory JC; Department of Molecular and Biomedical Pharmacology, University of Kentucky, MS-305 UKMC, Lexington, KY 40536, USA.
Mol Cell Biol ; 25(5): 1669-79, 2005 Mar.
Article en En | MEDLINE | ID: mdl-15713626
ABSTRACT
Alkylating agents chemically modify DNA and cause mutations that lead to cancer. In the budding yeast Saccharomyces cerevisiae, resistance to the alkylating agent methyl methanesulfonate (MMS) is mediated in part by Dap1p (damage resistance protein 1). Dap1p is related to cytochrome b5, which activates cytochrome P450 proteins, elevating the metabolism of lipids and xenobiotic compounds. We have found that Dap1p, like cytochrome b5, binds to heme and that Dap1p targets the cytochrome P450 protein Erg11p/Cyp51p. Genetic analysis indicates that Erg11p acts downstream of Dap1p. Furthermore, Dap1p regulates the stability of Erg11p, and Erg11p is stabilized in dap1Delta cells by the addition of heme. Thus, Dap1p utilizes heme to stabilize Erg11p, which in turn regulates ergosterol synthesis and MMS resistance. Dap1p homologues have been identified in numerous eukaryotes, including mammals, suggesting that the Dap1p-cytochrome P450 protein pathway is broadly conserved in eukaryotic species.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Oxidorreductasas / Saccharomyces cerevisiae / Sistema Enzimático del Citocromo P-450 / Proteínas de Saccharomyces cerevisiae / Proteínas de la Membrana Idioma: En Revista: Mol Cell Biol Año: 2005 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Oxidorreductasas / Saccharomyces cerevisiae / Sistema Enzimático del Citocromo P-450 / Proteínas de Saccharomyces cerevisiae / Proteínas de la Membrana Idioma: En Revista: Mol Cell Biol Año: 2005 Tipo del documento: Article País de afiliación: Estados Unidos