CLONING AND CHARACTERIZATION OF A YEAST CYTOCHROME B(5)-ENCODING GENE WHICH SUPPRESSES KETOCONAZOLE HYPERSENSITIVITY IN A NADPH-P-450 REDUCTASE-DEFICIENT STRAIN

被引:57
作者
TRUAN, G
EPINAT, JC
ROUGEULLE, C
CULLIN, C
POMPON, D
机构
[1] CNRS, CTR GENET MOLEC, F-91198 GIF SUR YVETTE, FRANCE
[2] INST PASTEUR, UNITE BIOL MOLEC EXPRESS GEN, F-75015 PARIS, FRANCE
关键词
ANTIFUNGAL; LANOSTEROL-C-14-DEMETHYLASE; RECOMBINANT DNA; SACCHAROMYCES CEREVISIAE; STEROL BIOSYNTHESIS;
D O I
10.1016/0378-1119(94)90366-2
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cytochrome P-450 (Cyp) 51 or lanosterol-C14-demethylase is the main target for antifungal compounds of the triazole family like ketoconazole (Kz). Disruption of the associated NADPH-P-450 reductase-encoding gene (YRED) is not lethal, but decreases by about 20-fold the Kz resistance (Kz(R)) of wild-type (wt) Saccharomyces cerevisiae. Transformation of a YRED-disrupted strain by a yeast genomic library based on a multicopy vector allowed us to identify a suppressor of Kz hypersensitivity. Deletion analysis of the 5-kb cloned fragment indicated that yeast cytochrome b(5)-encoding gene (CYB5), which encodes a 120-amino-acid (aa) protein, is required and sufficient for the suppressor effect. The encoded polypeptide shares about 30% aa identity with mammalian cytochromes b(5) (Cyb5). CYB5 disruption and tetrad analysis demonstrate that yeast Cyb5 is not required for growth in a Yred(+) strain. Determination of the microsomal content of b-type cytochromes by differential spectra indicated the presence of a strongly decreased or null Cyb5 level in the disrupted strain. This confirms that we have cloned the gene encoding the major microsomal form of Cyb5 which appears not to be essential. Minor Cyb5 isoforms could also be present in yeast or other redox proteins could substitute for the pleiotropic roles of Cyb5 in the sterol and lipid biosynthesis pathways.
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页码:123 / 127
页数:5
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