Cited by 29Fungal and yeast genetics researchSteroid Chemistry and BiochemistryAntifungal resistance and susceptibility

Cloning and sequencing of the Candida albicans C‐4 sterol methyl oxidase gene (ERG25) and expression of an ERG25 conditional lethal mutation in Saccharomyces cerevisiae

Kennedy, Matthew A., Johnson, Theresa A., Lees, N. Douglas, Barbuch, Robert, Eckstein, James A., Bard, Martin·2000·Lipids

Abstract

The ERG25 gene encoding the Candida albicans C‐4 sterol methyl oxidase was cloned and sequenced by complementing a Saccharomyces cerevisiae erg25 mutant with a C. albicans genomic library. The Erg25p is comprised of 308 amino acids and shows 65 and 38% homology to the enzymes from S. cerevisiae and Homo sapiens, respectively. The protein contains three histidine clusters common to nonheme iron‐binding enzymes and an endoplasmic reticulum retrieval signal as do the proteins from S. cerevisiae and humans. A temperature‐sensitive (ts) conditional lethal mutation of the C. albicans ERG25 was isolated and expressed in S. cerevisiae. Sequence analysis of the ts mutant indicated an amino acid substitution within the region of the protein encompassed by the histidine clusters involved in iron binding. Results indicate that plasmid‐borne conditional lethal mutants of target genes have potential use in the rescue of Candida mutations in genes that are essential for viability.

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Crossref · 10.1007/s11745-000-0521-2

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  • ERG1, ERG7, ERG9, ERG25, ERG26, and ERG27 are essential, while ERG2, ERG3, ERG5, ERG6, and ERG24 are considered non-essential in ergosterol biosynthesis.

    “By using the technology of gene disruption and controlled gene expression, ERG1 , ERG7 , ERG9 , ERG25 , ERG26 , and ERG27 have been proved to be essential, while ERG2 , ERG3 , ERG5 , ERG6 , and ERG24 are considered to be non-essential in ergosterol biosynthesis.”

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References 22 · Cited by 29

Authors
Kennedy, M. A., Johnson, T. A., Lees, N. D., Barbuch, R., Eckstein, J. A., & Bard, M.
Affiliations
  • Indiana University – Purdue University Indianapolis (US)
  • Eli Lilly (United States) (US)
Corresponding author
Lees, N. Douglas
Venue
Lipids
Publisher
Wiley
Published
2000-03
Volume
35
Issue
3
Pages
257-262
ISSN
  • 0024-4201 (ISSN-L)
  • 1558-9307
OpenAlex
W1994381407
Cited by
29
References
22
Citations by year
2024: 4 · 2023: 1 · 2021: 1 · 2020: 2 · 2019: 1 · 2016: 1 · 2015: 1 · 2014: 2 · 2013: 1 · 2012: 2
FWCI
0.24
Type
journal article
Language
en
Open access
closed
Locations
  • Lipids (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Steroid Chemistry and Biochemistry
  • Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
Keywords
Candida albicans, gene cloning, conditional lethal mutations, temperature-sensitive mutants, Saccharomyces cerevisiae complementation, sterol metabolism
MeSH terms
Amino Acid Sequence, Base Sequence, Candida albicans, Cloning, Molecular, Escherichia coli, Genes, Lethal, Humans, Mixed Function Oxygenases, Molecular Sequence Data, Mutation, Recombinant Proteins, Saccharomyces cerevisiae, Sterols, Temperature, Genomic Library, Sequence Alignment, Sequence Homology, Amino Acid

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