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Originally published as MBC in Press, 10.1091/mbc.E03-01-0042 on June 27, 2003

Vol. 14, Issue 10, 4272-4284, October 2003

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Amino Acid Starvation and Gcn4p Regulate Adhesive Growth and FLO11 Gene Expression in Saccharomyces cerevisiae

Gerhard H. Braus *, Olav Grundmann, Stefan Brückner, and Hans-Ulrich Mösch

Institute for Microbiology and Genetics, Georg-August-University, D-37077 Göttingen, Germany

Submitted January 27, 2003; Revised May 22, 2003; Accepted May 27, 2003
Monitoring Editor: Trisha Davis

In baker's yeast Saccharomyces cerevisiae, cell-cell and cell-surface adhesion are required for haploid invasive growth and diploid pseudohyphal development. These morphogenetic events are induced by starvation for glucose or nitrogen and require the cell surface protein Flo11p. We show that amino acid starvation is a nutritional signal that activates adhesive growth and expression of FLO11 in both haploid and diploid strains in the presence of glucose and ammonium, known suppressors of adhesion. Starvation-induced adhesive growth requires Flo11p and is under control of Gcn2p and Gcn4p, elements of the general amino acid control system. Tpk2p and Flo8p, elements of the cAMP pathway, are also required for activation but not Ste12p and Tec1p, known targets of the mitogen-activated protein kinase cascade. Promoter analysis of FLO11 identifies one upstream activation sequence (UASR) and one repression site (URS) that confer regulation by amino acid starvation. Gcn4p is not required for regulation of the UASR by amino acid starvation, but seems to be indirectly required to overcome the negative effects of the URS on FLO11 transcription. In addition, Gcn4p controls expression of FLO11 by affecting two basal upstream activation sequences (UASB). In summary, our study suggests that amino acid starvation is a nutritional signal that triggers a Gcn4p-controlled signaling pathway, which relieves repression of FLO11 gene expression and induces adhesive growth.


Article published online ahead of print. Mol. Biol. Cell 10.1091/mbc.E03–01–0042. Article and publication date are available at www.molbiolcell.org/cgi/doi/10.1091/mbc.E03-01-0042.

* Corresponding author. E-mail address: gbraus{at}gwdg.de.




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