Cloning and characterization of a yeast cytochrome b5-encoding gene which suppresses ketoconazole hypersensitivity in a NADPH-P-450 reductase-deficient strain.

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 (KzR) 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 b5-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 b5 (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.

[1]  T. Sutter,et al.  Primary structure of the P450 lanosterol demethylase gene from Saccharomyces cerevisiae. , 1987, DNA.

[2]  P. Reisdorf,et al.  Enhanced in vivo monooxygenase activities of mammalian P450s in engineered yeast cells producing high levels of NADPH-P450 reductase and human cytochrome b5. , 1993, Gene.

[3]  J. Devereux,et al.  A comprehensive set of sequence analysis programs for the VAX , 1984, Nucleic Acids Res..

[4]  P. Janssen,et al.  Mutation in cytochrome P-450-dependent 14 alpha-demethylase results in decreased affinity for azole antifungals. , 1990, Biochemical Society transactions.

[5]  H. Ruis,et al.  Involvement of cytochrome b5 and a cyanide-sensitive monooxygenase in the 4-demethylation of 4,4-dimethylzymosterol by yeast microsomes. , 1981, Biochimica et biophysica acta.

[6]  T. Sutter,et al.  Disruption of the Saccharomyces cerevisiae gene for NADPH-cytochrome P450 reductase causes increased sensitivity to ketoconazole. , 1989, Biochemical and biophysical research communications.

[7]  L. Waskell,et al.  Expression of cytochrome b5 in yeast and characterization of mutants of the membrane-anchoring domain. , 1992, The Journal of biological chemistry.

[8]  K. Bloch,et al.  Sterol synergism in yeast. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[9]  Y. Yoshida,et al.  Sterol 14α-demethylase and its inhibition : structural considerations on interaction of azole antifungal agents with lanosterol 14α-demethylase (P-45014DM) of yeast , 1991 .

[10]  P. Strittmatter,et al.  Purification and properties of rat liver microsomal stearyl coenzyme A desaturase. , 1974, Proceedings of the National Academy of Sciences of the United States of America.

[11]  A. Ito,et al.  The carboxy‐terminal 10 amino acid residues of cytochrome b5 are necessary for its targeting to the endoplasmic reticulum. , 1992, The EMBO journal.

[12]  W. D. Nes,et al.  The structural requirements of sterols for membrane function in Saccharomyces cerevisiae. , 1993, Archives of biochemistry and biophysics.

[13]  L. W. Parks,et al.  Multiple functions for sterols in Saccharomyces cerevisiae. , 1985, Biochimica et Biophysica Acta.

[14]  M. Labouesse,et al.  A family of low and high copy replicative, integrative and single‐stranded S. cerevisiae/E. coli shuttle vectors , 1991, Yeast.

[15]  E. Caspi,et al.  Mechanism of C-5 double bond introduction in the biosynthesis of cholesterol by rat liver microsomes. , 1976, The Journal of biological chemistry.

[16]  Yoshida Yuzo,et al.  Interaction of azole antifungal agents with cytochrome P-45014DM purified from Saccharomyces cerevisiae microsomes. , 1987 .

[17]  D. Lane,et al.  p68 RNA helicase: identification of a nucleolar form and cloning of related genes containing a conserved intron in yeasts , 1991, Molecular and cellular biology.

[18]  A. Myers,et al.  Yeast/E. coli shuttle vectors with multiple unique restriction sites , 1986, Yeast.

[19]  F. Guengerich Reactions and significance of cytochrome P-450 enzymes. , 1991, The Journal of biological chemistry.

[20]  P. Janssen,et al.  From 14 alpha-demethylase inhibitors in fungal cells to androgen and oestrogen biosynthesis inhibitors in mammalian cells. , 1990, Biochemical Society transactions.

[21]  D. Lipman,et al.  Improved tools for biological sequence comparison. , 1988, Proceedings of the National Academy of Sciences of the United States of America.