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


Name: Kuchin, Sergei
Mailing Address: Institute of Cancer Research, Columbia University, 701 West 168th St., New York, NY 10032, USA
Email Address: svk4@columbia.edu
Phone & FAX numbers: 1-212-305-3851 & 1-212-305-1741

Abstract #44


Session Title: Cell Cycle and Differentiation
Session Time: Friday, August 2 -- 9:00AM - 10:30AM
Presentation: Platform
Topic: Cell Biology

Snf1 kinase and the repressors Nrg1 and Nrg2 regulate FLO11 expression, invasive growth, and pseudohyphal development.
Sergei Kuchin, Valmik K. Vyas, Marian Carlson
Institute of Cancer Research, Columbia University, 701 West 168th St., New York, NY 10032, USA

The Snf1 protein kinase has important roles in cellular responses to glucose limitation, including developmental responses such as haploid invasive growth (Cullen and Sprague, PNAS 97:13619, 2000). We present evidence that the Snf1 kinase positively regulates transcription of FLO11, which encodes a cell-surface glycoprotein required for invasive growth. Nrg1 and Nrg2, two repressor proteins that interact with Snf1, function as repressors of FLO11 and negatively regulate invasive growth. We also examined the role of the Snf1 kinase and the Nrg proteins in two other Flo11-dependent processes. Mutations in the corresponding genes affected adherence to plastic, suggesting a role in biofilm formation. They also affected diploid pseudohyphal differentiation, thereby unexpectedly implicating Snf1 in a response to nitrogen limitation. Deletion of NRG1 and NRG2 suppressed the defects of a snf1 mutant in all of these processes. We propose that the Snf1 kinase positively regulates diverse Flo11-dependent developmental events, at least in part, by antagonizing Nrg-mediated repression of FLO11.


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