Mallory Julia C, Crudden Gerard, Johnson Ben L, Mo Caiqing, Pierson Charles A, Bard Martin, Craven Rolf J
Department of Molecular and Biomedical Pharmacology, University of Kentucky, MS-305 UKMC, Lexington, KY 40536, USA.
Mol Cell Biol. 2005 Mar;25(5):1669-79. doi: 10.1128/MCB.25.5.1669-1679.2005.
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.
烷化剂通过化学方式修饰DNA并引发导致癌症的突变。在芽殖酵母酿酒酵母中,对烷化剂甲磺酸甲酯(MMS)的抗性部分由Dap1p(抗损伤蛋白1)介导。Dap1p与细胞色素b5相关,细胞色素b5可激活细胞色素P450蛋白,提高脂质和外源性化合物的代谢水平。我们发现,Dap1p与细胞色素b5一样,能结合血红素,且Dap1p靶向细胞色素P450蛋白Erg11p/Cyp51p。遗传分析表明,Erg11p在Dap1p的下游起作用。此外,Dap1p调节Erg11p的稳定性,通过添加血红素可使Erg11p在dap1Δ细胞中稳定。因此,Dap1p利用血红素来稳定Erg11p,而Erg11p反过来调节麦角固醇的合成和对MMS的抗性。在包括哺乳动物在内的众多真核生物中都已鉴定出Dap1p的同源物,这表明Dap1p - 细胞色素P450蛋白途径在真核生物物种中广泛保守。