Molecular Biology of the Cell click for CBE Life Science Education Page

Home Help [Feedback] [For Subscribers] [Archive] [Search] --
 QUICK SEARCH:   [advanced]


     


MBC in Press, published online ahead of print February 6, 2008
Mol. Biol. Cell 10.1091/mbc.E07-08-0757

A more recent version of this article appeared on April 1, 2008
This Article
Right arrow Full Text (PDF)
Right arrow Supplemental Materials
Right arrow All Versions of this Article:
E07-08-0757v1
19/4/1739    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Yu, L.
Right arrow Articles by Elion, E. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Yu, L.
Right arrow Articles by Elion, E. A.

Submitted on August 6, 2007
Revised on January 18, 2008
Accepted on January 29, 2008

Counteractive Control of Polarized Morphogenesis during Mating by MAPK Fus3 and G1 Cyclin-dependent Kinase

Lu Yu, Maosong Qi, Mark A. Sheff, and Elaine A. Elion

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.


Address correspondence to: Elaine A. Elion (elaine_elion{at}hms.harvard.edu)




This article has been cited by other articles:


Home page
Cold Spring Harb. Perspect. Biol.Home page
R. A. Arkowitz
Chemical Gradients and Chemotropism in Yeast
Cold Spring Harb Perspect Biol, August 1, 2009; 1(2): a001958 - a001958.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
L. S. Garrenton, A. Braunwarth, S. Irniger, E. Hurt, M. Kunzler, and J. Thorner
Nucleus-Specific and Cell Cycle-Regulated Degradation of Mitogen-Activated Protein Kinase Scaffold Protein Ste5 Contributes to the Control of Signaling Competence
Mol. Cell. Biol., January 15, 2009; 29(2): 582 - 601.
[Abstract] [Full Text] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] --
Copyright © 2008 by The American Society for Cell Biology. Terms of copyright protection, warranties, and disclaimers.