Isolation from Candida albicans of a functional homolog of the Saccharomyces cerevisiae KRE1 gene, which is involved in cell wall beta-glucan synthesis
- PMID: 1938890
- PMCID: PMC209038
- DOI: 10.1128/jb.173.21.6859-6864.1991
Isolation from Candida albicans of a functional homolog of the Saccharomyces cerevisiae KRE1 gene, which is involved in cell wall beta-glucan synthesis
Abstract
The KRE1 gene of Saccharomyces cerevisiae, sacKRE1, appears to be involved in the synthesis of cell wall beta-glucan. S. cerevisiae strains with mutations in the KRE1 gene produce a structurally altered cell wall (1----6)-beta-glucan, which results in resistance to K1 killer toxin. We isolated the canKRE1 gene from Candida albicans by its ability to complement a kre1 mutation in S. cerevisiae and confer sensitivity to killer toxin. Sequence analysis revealed that the predicted protein encoded by canKRE1 shares an overall structural similarity with that encoded by sacKRE1. The canKRE1 protein is composed of an N-terminal signal sequence, a central domain of 46% identity with the sacKRE1 protein, and a C-terminal hydrophobic tract. These structural and functional similarities imply that the canKRE1 gene carries out a function in C. albicans cell wall assembly similar to that observed for sacKRE1 in S. cerevisiae.
Similar articles
-
Isolation of the Candida albicans homologs of Saccharomyces cerevisiae KRE6 and SKN1: expression and physiological function.J Bacteriol. 1997 Apr;179(7):2363-72. doi: 10.1128/jb.179.7.2363-2372.1997. J Bacteriol. 1997. PMID: 9079924 Free PMC article.
-
The Candida albicans KRE9 gene is required for cell wall beta-1, 6-glucan synthesis and is essential for growth on glucose.Proc Natl Acad Sci U S A. 1998 Aug 18;95(17):9825-30. doi: 10.1073/pnas.95.17.9825. Proc Natl Acad Sci U S A. 1998. PMID: 9707560 Free PMC article.
-
Cloning of the Candida albicans homolog of Saccharomyces cerevisiae GSC1/FKS1 and its involvement in beta-1,3-glucan synthesis.J Bacteriol. 1997 Jul;179(13):4096-105. doi: 10.1128/jb.179.13.4096-4105.1997. J Bacteriol. 1997. PMID: 9209021 Free PMC article.
-
[Isolation and molecular characterization of the CaPHO85 gene: a negative regulator of phosphate metabolism (PHO system) in Candida albicans].Nihon Ishinkin Gakkai Zasshi. 2003;44(2):101-5. doi: 10.3314/jjmm.44.101. Nihon Ishinkin Gakkai Zasshi. 2003. PMID: 12748591 Review. Japanese.
-
Fungal beta(1,3)-D-glucan synthesis.Med Mycol. 2001;39 Suppl 1:55-66. doi: 10.1080/mmy.39.1.55.66. Med Mycol. 2001. PMID: 11800269 Review.
Cited by
-
Candida albicans cell wall proteins.Microbiol Mol Biol Rev. 2008 Sep;72(3):495-544. doi: 10.1128/MMBR.00032-07. Microbiol Mol Biol Rev. 2008. PMID: 18772287 Free PMC article. Review.
-
Covalent association of beta-1,3-glucan with beta-1,6-glucosylated mannoproteins in cell walls of Candida albicans.J Bacteriol. 1995 Jul;177(13):3788-92. doi: 10.1128/jb.177.13.3788-3792.1995. J Bacteriol. 1995. PMID: 7541400 Free PMC article.
-
Genetic Screening of Candida albicans Inactivation Mutants Identifies New Genes Involved in Macrophage-Fungal Cell Interactions.Front Microbiol. 2022 Apr 5;13:833655. doi: 10.3389/fmicb.2022.833655. eCollection 2022. Front Microbiol. 2022. PMID: 35450285 Free PMC article.
-
Signal transduction through homologs of the Ste20p and Ste7p protein kinases can trigger hyphal formation in the pathogenic fungus Candida albicans.Proc Natl Acad Sci U S A. 1996 Nov 12;93(23):13217-22. doi: 10.1073/pnas.93.23.13217. Proc Natl Acad Sci U S A. 1996. PMID: 8917571 Free PMC article.
-
A G-protein alpha subunit from asexual Candida albicans functions in the mating signal transduction pathway of Saccharomyces cerevisiae and is regulated by the a1-alpha 2 repressor.Mol Cell Biol. 1992 May;12(5):1977-85. doi: 10.1128/mcb.12.5.1977-1985.1992. Mol Cell Biol. 1992. PMID: 1569935 Free PMC article.
References
Publication types
MeSH terms
Substances
Associated data
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases