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A more recent version of this article appeared on April 1, 2008
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Submitted on August 6, 2007
Revised on January 18, 2008
Accepted on January 29, 2008
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115-5730
Monitoring Editor: Tim Stearns
Cell polarization in response to external cues is critical to many eukaryotic cells. During pheromone-induced mating in S. cerevisiae, the MAPK Fus3 induces polarization of the actin cytoskeleton toward a landmark generated by the pheromone receptor. Here we analyze the role of Fus3 activation and cell cycle arrest in mating morphogenesis. The MAPK scaffold Ste5 is initially recruited to the plasma membrane in random patches that polarize before shmoo emergence. Polarized localization of Ste5 is important for shmooing. In fus3 mutants, Ste5 is recruited to significantly more of the plasma membrane whereas recruitment of Bni1 formin, Cdc24 guanine exchange factor and Ste20 PAK are inhibited. In contrast, polarized recruitment still occurs in a far1 mutant that is also defective in G1 arrest. Remarkably, loss of Cln2 or Cdc28 cyclin dependent kinase restores polarized localization of Bni1, Ste5 and Ste20 to a fus3 mutant. These and other findings suggest Fus3 induces polarized growth in G1 phase cells by downregulating Ste5 recruitment and by inhibiting Cln/Cdc28 kinase, which prevents basal recruitment of Ste5, Cdc42-mediated asymmetry, and mating morphogenesis.
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