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


Name: Vyas, Valmik K.
Mailing Address: Institute of Cancer Research, Columbia University, 701 West 168th St., New York, Ny 10032, USA
Email Address: valmik@alum.mit.edu
Phone & FAX numbers: 212-305-3851 & 212-305-1741

Abstract #199


Session Title: Cell Biology: Cell Cycle, Morphogenesis and Differentiation
Presentation: Poster
Topic: Cell Biology

Snf1 kinase complexes containing different beta subunits have distinct roles in invasive growth and filamentation.
Valmik K. Vyas, Sergei Kuchin, Cristin Berkey, Marian Carlson
Institute of Cancer Research, Columbia University, 701 West 168th St., New York, Ny 10032, USA

The Snf1 kinase has a role in regulating haploid invasive growth in response to glucose depletion (Cullen and Sprague, PNAS 97:13619, 2000). S. cerevisiae cells contain three isoforms of the Snf1 kinase, each containing the catalytic alpha subunit Snf1, the activating gamma subunit Snf4, and one of the three beta subunits, Gal83, Sip1 or Sip2. The beta subunits have distinct, although partially overlapping, functions and have roles in regulating the specificity and subcellular localization of the kinase. We present evidence that different beta subunits are required for invasion of agar, as judged by plate washing assays, and for filamentation, as determined by microscopic observation. Thus, the Snf1 kinase affects these different aspects of invasive growth by distinct mechanisms. We show that the isoform of the kinase containing Gal83, which becomes nuclear localized in response to glucose limitation, affects agar invasion by a mechanism involving the repressors Nrg1 and Nrg2 and transcriptional control of FLO11.


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