Yeast Genetics and Molecular Biology 2002
University of Wisconsin
Madison, Wisconsin USA
July 30 - August 4, 2002


Name: Moffat, Jason
Mailing Address: Department of Medical Genetics, University of Toronto, 8 Taddle Creek Rd, Toronto, on m5s1a8, Canada
Email Address: j.moffat@utoronto.ca
Phone & FAX numbers: 416-978-6113 & 416-978-6885
URL: http://www.utoronto.ca/andrewslab

Abstract #5


Session Title: Signaling Networks
Session Time: Tuesday, July 30 -- 7:00PM - 8:30PM
Presentation: Platform
Topic: Cell Biology

Dynamic regulation of PHO85 G1 cyclins contributes to cell cycle-dependent morphogenesis in budding yeast.
Jason Moffat, Dongqing Huang, Brenda Andrews
Department of Medical Genetics, University of Toronto, 8 Taddle Creek Rd, Toronto, on m5s1a8, Canada

Cyclin-dependent kinases (Cdks) are key regulators of the cell division cycle. Cell cycle progression in budding yeast requires commitment to START and initiation of the G1 transcriptional program in order for bud growth, cell wall construction and DNA replication to occur. The G1 cyclins Pcl1, Pcl2 and Pcl9 are three of ten cyclins that activate the multifunctional Pho85 Cdk, that is involved in aspects of metabolism, cell cycle, cell polarity and gene expression. We uncovered several genetic interactions linking PCL1 and PCL2 to cell wall maintenance/regulation and polarized growth. PCL1 and PCL2 showed strong genetic interactions with effectors of Cdc42 function and components of the cell integrity MAPK pathway; Cdc42 is required for polarity establishment and the cell integrity MAPK pathway is required during periods of polarized growth. The phenotype in these multiple mutants suggests that events in G1 and S that affect cell shape cannot be corrected until the morphogenesis checkpoint in G2-phase. Excitingly, Pcl1, Pcl2 and Pcl9 localized to sites of polarization and to the bud neck. These data are consistent with a suggested role for the Pcls in the cytoplasm. Our study represents the first observation that G1 cyclins can localize in a dynamic fashion to polarization sites within a yeast cell. We suggest that Pcl1 and Pcl2 help to promote normal cell morphology through Cdc42-related functions.


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