Special type of pheromone-induced invasive growth in Saccharomyces cerevisiae
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Adenosine Triphosphatases genetics metabolism MeSH
- Models, Biological MeSH
- Gene Deletion MeSH
- Genes, Fungal MeSH
- Nuclear Proteins genetics metabolism MeSH
- MAP Kinase Signaling System MeSH
- Mitogen-Activated Protein Kinases genetics metabolism MeSH
- Cell Adhesion Molecules genetics metabolism MeSH
- Protein Precursors genetics metabolism MeSH
- Saccharomyces cerevisiae Proteins genetics metabolism MeSH
- Saccharomyces cerevisiae genetics growth & development metabolism MeSH
- Oligonucleotide Array Sequence Analysis MeSH
- Signal Transduction MeSH
- Transcription Factors genetics metabolism MeSH
- Up-Regulation MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- a-agglutinin protein, S cerevisiae MeSH Browser
- Adenosine Triphosphatases MeSH
- AGA1 protein, S cerevisiae MeSH Browser
- DLS1 protein, S cerevisiae MeSH Browser
- Fig2 protein, S cerevisiae MeSH Browser
- FUS3 protein, S cerevisiae MeSH Browser
- ISWI protein MeSH Browser
- Nuclear Proteins MeSH
- KSS1 protein, S cerevisiae MeSH Browser
- MF(ALPHA)1 protein, S cerevisiae MeSH Browser
- Mitogen-Activated Protein Kinases MeSH
- Cell Adhesion Molecules MeSH
- Protein Precursors MeSH
- Saccharomyces cerevisiae Proteins MeSH
- STE12 protein, S cerevisiae MeSH Browser
- Transcription Factors MeSH
The ability to invade a solid substrate is an important phenomenon due to its connection with pathogenic activity of fungi. We report here on invasion displayed by MATalpha cells of Saccharomyces cerevisiae lacking Isw2p, a subunit of the ISW2 chromatin remodelling complex. We found that on minimal medium, where the isw2Delta MATalpha mutant is not invasive, additional absence of another ISW2 complex subunit, Dls1p or Dpb4p, promoted invasion. Our microarray data showed that derepression of MAT a-specific genes caused by absence of Isw2p is very low. Their expression is increased only by the autocrine activation of the mating pathway. Invasion of isw2Delta MATalpha cells thus resembles the pheromone-induced invasion, including dependence on Fig2p. We show here that another pheromone-induced protein, mating agglutinin Aga1p, can play a role in the agar adhesion necessary for invasion. In contrast with MAT a-cells invading agar under low alpha-pheromone concentration, the invasive growth of isw2Delta cells specifically requires Fus3 kinase. Its function in the invasion of isw2Delta MATalpha cells cannot be completely substituted by Kss1 kinase, which plays a basic role in invasive growth signalling. We suggest that partial dependence of the isw2Delta MATalpha invasion on Fus3p and Aga1p corresponds to a weaker pheromone response of this mutant.
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