Posttranscriptional regulation of FLO11 upon amino acid starvation in Saccharomyces cerevisiae

2008 | journal article. A publication with affiliation to the University of Göttingen.

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​Posttranscriptional regulation of FLO11 upon amino acid starvation in Saccharomyces cerevisiae​
Fischer, C.; Valerius, O.; Rupprecht, H.; Dumkow, M.; Krappmann, S. & Braus, G. H.​ (2008) 
FEMS Yeast Research8(2) pp. 225​-236​.​ DOI: https://doi.org/10.1111/j.1567-1364.2007.00331.x 

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Authors
Fischer, Claudia; Valerius, Oliver; Rupprecht, Heike; Dumkow, Marc; Krappmann, Sven; Braus, Gerhard H.
Abstract
Various starvation conditions cause adhesive growth of haploid cells or pseudohyphae formation of diploid cells of Saccharomyces cerevisiae. For the genetic Sigma 1278b background, these morphological changes depend on the expression of the gene encoding the cell wall glycoprotein Flo11p, which is increased during nutritional limitations. Deletion of the genes encoding the transcriptional coactivators Rsc1p or Gcn5p impairs FLO11 transcription, which consequently leads to a loss of both haploid invasive growth and diploid pseudohyphae development upon glucose and nitrogen limitation, respectively. In contrast, amino acid starvation induces FLO11-dependent adhesive growth of the rsc1 Delta and gcn5 Delta strains although FLO11 transcription remains very low. The double deletion strain rsc1 Delta flo11 Delta, however, does not grow adhesively, suggesting that the adhesion of the rsc1 Delta strain at amino acid starvation is still FLO11-dependent. The FLO11(prom)-lacZ-encoded beta-galactosidase activities of the rsc1 Delta and gcn5 Delta mutant strains increase manifold upon amino acid starvation. It is therefore concluded that low levels of FLO11 transcripts are essential and sufficient for derepression of FLO11 expression and adhesive growth during amino acid starvation. A posttranscriptional control is assumed to be behind this phenomenon that permits the increased FLO11 expression from low FLO11 transcript abundances.
Issue Date
2008
Status
published
Publisher
Oxford Univ Press
Journal
FEMS Yeast Research 
ISSN
1567-1364; 1567-1356

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