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Eukaryotic Cell, August 2006, p. 1215-1228, Vol. 5, No. 8
1535-9778/06/$08.00+0 doi:10.1128/EC.00037-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Analysis of Mitogen-Activated Protein Kinase Signaling Specificity in Response to Hyperosmotic Stress: Use of an Analog-Sensitive HOG1 Allele
Patrick J. Westfall and
Jeremy Thorner*
Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, California 94720
Received 6 February 2006/
Accepted 23 May 2006
When confronted with a marked increase in external osmolarity, budding yeast (Saccharomyces cerevisiae) cells utilize a conserved mitogen-activated protein kinase (MAPK) signaling cascade (the high-osmolarity glycerol or HOG pathway) to elicit cellular responses necessary to permit continued growth. One input that stimulates the HOG pathway requires the integral membrane protein and putative osmosensor Sho1, which recruits and enables activation of the MAPK kinase kinase Ste11. In mutants that lack the downstream MAPK kinase (pbs2
) or the MAPK (hog1
) of the HOG pathway, Ste11 activated by hyperosmotic stress is able to inappropriately stimulate the pheromone response pathway. This loss of signaling specificity is known as cross talk. To determine whether it is the Hog1 polypeptide per se or its kinase activity that is necessary to prevent cross talk, we constructed a fully functional analog-sensitive allele of HOG1 to permit acute inhibition of this enzyme without other detectable perturbations of the cell. We found that the catalytic activity of Hog1 is required continuously to prevent cross talk between the HOG pathway and both the pheromone response and invasive growth pathways. Moreover, contrary to previous reports, we found that the kinase activity of Hog1 is necessary for its stress-induced nuclear import. Finally, our results demonstrate a role for active Hog1 in maintaining signaling specificity under conditions of persistently high external osmolarity.
* Corresponding author. Mailing address: Department of Molecular and Cell Biology, Room 16, Barker Hall, University of California, Berkeley, Berkeley, CA 94720-3202. Phone: (510) 642-2558. Fax: (510) 642-6420. E-mail:
jthorner{at}berkeley.edu.
Eukaryotic Cell, August 2006, p. 1215-1228, Vol. 5, No. 8
1535-9778/06/$08.00+0 doi:10.1128/EC.00037-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
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