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Molecular and Cellular Biology, June 2007, p. 3900-3910, Vol. 27, No. 11
0270-7306/07/$08.00+0     doi:10.1128/MCB.00089-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Selective Requirement for SAGA in Hog1-Mediated Gene Expression Depending on the Severity of the External Osmostress Conditions{triangledown}

Meritxell Zapater,1 Marc Sohrmann,2 Matthias Peter,2 Francesc Posas,1* and Eulàlia de Nadal1

Cell Signaling Unit, Departament de Ciències Experimentals i de la Salut, Universitat Pompeu Fabra, Parc de Recerca Biomèdica de Barcelona, E-08003 Barcelona, Spain,1 Swiss Federal Institute of Technology Zurich (ETH), Institute of Biochemistry, Zurich, Switzerland2

Received 16 January 2007/ Returned for modification 14 March 2007/ Accepted 23 March 2007

Regulation of gene expression by the Hog1 stress-activated protein kinase is essential for proper cell adaptation to osmostress. Hog1 coordinates an extensive transcriptional program through the modulation of transcription. To identify systematically novel components of the transcriptional machinery required for osmostress-mediated gene expression, we performed an exhaustive genome-wide genetic screening, searching for mutations that render cells osmosensitive at high osmolarity and that are associated with reduced expression of osmoresponsive genes. The SAGA and Mediator complexes were identified as putative novel regulators of osmostress-mediated transcription. Interestingly, whereas Mediator is essential for osmostress gene expression, the requirement for SAGA is different depending on the strength of the extracellular osmotic conditions. At mild osmolarity, SAGA mutants show only very slight defects on RNA polymerase II (Pol II) recruitment and gene expression, whereas at severe osmotic conditions, SAGA mutants show completely impaired RNA Pol II recruitment and transcription of osmoresponsive genes. Thus, our results define an essential role for Mediator in osmostress gene expression and a selective role for SAGA under severe osmostress. Our results indicate that the requirement for a transcriptional complex to regulate a promoter might be determined by the strength of the stimuli perceived by the cell through the regulation of interactions between transcriptional complexes.


* Corresponding author. Mailing address: Cell Signaling Unit, Departament de Ciències Experimentals i de la Salut, Universitat Pompeu Fabra, Parc de Recerca Biomèdica de Barcelona, Dr. Aiguader 88, E-08003 Barcelona, Spain. Phone: 34-933160849. Fax: 34-933160901. E-mail: francesc.posas{at}upf.edu

{triangledown} Published ahead of print on 2 April 2007.


Molecular and Cellular Biology, June 2007, p. 3900-3910, Vol. 27, No. 11
0270-7306/07/$08.00+0     doi:10.1128/MCB.00089-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.







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