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Regulation of Thermotolerance by Stress-induced Transcription Factors in Saccharomyces Cerevisiae

Overview
Journal Eukaryot Cell
Specialty Molecular Biology
Date 2008 Mar 25
PMID 18359875
Citations 26
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Abstract

The heat shock transcription factor Hsf1 and the general stress transcription factors Msn2 and Msn4 (Msn2/4) are major regulators of the heat shock response in Saccharomyces cerevisiae. Here, we show that transcriptional activation of their target genes, including HSP104, an antistress chaperone gene, is obligatory for thermotolerance. Although Hsf1 activity might be necessary before the exposure of cells to high temperature, severe heat shock induced the binding of hyperphosphorylated Hsf1 to its target promoters. However, promoter-bound, phosphorylated Hsf1 was inactive for transcription because RNA polymerase II was inactive at high temperatures. Rather, our results suggest that Hsf1 activates the transcription of most of its target genes during the recovery period following severe heat shock. This delayed upregulation by Hsf1, which would be induced by misfolded proteins that accumulate in severely heat-shocked cells, is required for the resumption of normal cell growth. In contrast, the factors Msn2/4 were not involved in the delayed upregulation of genes and were dispensable for cell growth during the recovery period, suggesting that they play a role before the exposure to high temperature. These results show that Hsf1 and Msn2/4 act differentially before and after exposure to extreme temperatures to ensure cell survival and growth.

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References
1.
Smith B, Yaffe M . Uncoupling thermotolerance from the induction of heat shock proteins. Proc Natl Acad Sci U S A. 1991; 88(24):11091-4. PMC: 53079. DOI: 10.1073/pnas.88.24.11091. View

2.
Estruch F . Stress-controlled transcription factors, stress-induced genes and stress tolerance in budding yeast. FEMS Microbiol Rev. 2000; 24(4):469-86. DOI: 10.1111/j.1574-6976.2000.tb00551.x. View

3.
Mori K, Sant A, Kohno K, Normington K, Gething M, Sambrook J . A 22 bp cis-acting element is necessary and sufficient for the induction of the yeast KAR2 (BiP) gene by unfolded proteins. EMBO J. 1992; 11(7):2583-93. PMC: 556733. DOI: 10.1002/j.1460-2075.1992.tb05323.x. View

4.
Yamamoto A, Sakurai H . The DNA-binding domain of yeast Hsf1 regulates both DNA-binding and transcriptional activities. Biochem Biophys Res Commun. 2006; 346(4):1324-9. DOI: 10.1016/j.bbrc.2006.06.057. View

5.
Hahn J, Neef D, Thiele D . A stress regulatory network for co-ordinated activation of proteasome expression mediated by yeast heat shock transcription factor. Mol Microbiol. 2006; 60(1):240-51. DOI: 10.1111/j.1365-2958.2006.05097.x. View