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Vol. 14, Issue 7, 3013-3026, July 2003
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Department of Biochemistry and Molecular Biology, SUNY Upstate Medical University, Syracuse, New York 13210
Submitted November 19, 2002;
Revised February 27, 2003;
Accepted February 27, 2003
Monitoring Editor: David Drubin 0747
Osmotic stress causes actin cytoskeleton disassembly, a cell cycle arrest,
and activation of the high osmolarity growth mitogen-activated protein kinase
pathway. A previous study showed that Ssk2p, a mitogen-activated protein
kinase kinase kinase of the high osmolarity growth pathway, promotes actin
cytoskeleton recovery to the neck of late cell cycle, osmotically stressed
yeast cells. Data presented herein examined the role of Ssk2p in actin
recovery early in the cell cycle. We found that actin recovery at all stages
of the cell cycle is not controlled by Ssk1p, the known activator of Ssk2p,
but required a polarized distribution of Ssk2p as well as its
actin-interacting and kinase activity. Stress-induced localization of Ssk2p to
the neck required the septin Shs1p, whereas localization to the bud cortex
depended on the polarity scaffold protein Spa2p. spa2
cells,
like ssk2
cells, were defective for actin recovery from
osmotic stress. These spa2
defects could be suppressed by
overexpression of catalytically active Ssk2p. Furthermore, Spa2p could be
precipitated by GST-Ssk2p from extracts of osmotically stressed cells. The
Ssk2p mediated actin recovery pathway seems to be conserved; MTK1, a human
mitogen-activated protein kinase kinase kinase of the p38 stress response
pathway and Ssk2p homolog, was also able to localize at polarized growth
sites, form a complex with actin and Spa2p, and complement actin recovery
defects in osmotically stressed ssk2
and spa2
yeast cells. We hypothesize that osmotic stress-induced actin disassembly
leads to the formation of an Ssk2pactin complex and the polarized
localization of Ssk2p. Polarized Ssk2p associates with the scaffold protein
Spa2p in the bud and Shs1p in the neck, allowing Ssk2p to regulate substrates
involved in polarized actin assembly.
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