| DOI | Resolve DOI: https://doi.org/10.1128/EC.5.1.192-202.2006 |
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| Author | Search for: Dignard, Daniel1; Search for: Whiteway, Malcolm1 |
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| Affiliation | - National Research Council of Canada. NRC Biotechnology Research Institute
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| Format | Text, Article |
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| Subject | Candida; Candida albicans; Cell Cycle; Cells; Gene Expression; pharmaceutical; Protein; Saccharomyces cerevisiae |
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| Abstract | Candida albicans contains a functional mating response pathway that is similar to the well-studied system of Saccharomyces cerevisiae. We have characterized a regulator of G protein signaling (RGS) homolog in C. albicans with sequence similarity to the SST2 gene of Saccharomyces cerevisiae. Disruption of this gene, which had been designated SST2, causes an opaque MTLa/MTLa derivative of strain SC5314 to show hypersensitivity to the C. albicans alpha-factor. This hypersensitivity generates an enhanced cell cycle arrest detected in halo assays but reduces the overall mating efficiency of the cells. Transcriptional profiling of the pheromone-regulated gene expression in the sst2 mutant shows a pattern of gene induction similar to that observed in wild-type cells, but the responsiveness is heightened. This involvement of an RGS in the sensitivity to pheromone is consistent with the prediction that the mating response pathway in C. albicans requires the activation of a heterotrimeric G protein. |
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| Publication date | 2006-01 |
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| In | |
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| Note | English16400182 |
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| Language | English |
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| NRC number | 47485 |
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| NPARC number | 3538671 |
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| Export citation | Export as RIS |
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| Report a correction | Report a correction (opens in a new tab) |
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| Record identifier | b6bfcf10-c427-44bf-b3fd-cf32dadc924c |
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| Record created | 2009-03-01 |
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| Record modified | 2020-04-22 |
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