Cdc42p GDP/GTP cycling is necessary for efficient cell fusion during yeast mating

被引:24
作者
Barale, Sophie
McCusker, Derek
Arkowitz, Robert A. [1 ]
机构
[1] Univ Nice, Fac Sci, Inst Signaling, CNRS,UMR 6543, F-06108 Nice 2, France
[2] Univ Calif Santa Cruz, Sinsheimer Labs, Dept Biol, Santa Cruz, CA 95064 USA
关键词
D O I
10.1091/mbc.E05-11-1040
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The highly conserved small Rho G-protein, Cdc42p plays a critical role in cell polarity and cytoskeleton organization in all eukaryotes. In the yeast Saccharomyces cerevisiae, Cdc42p is important for cell polarity establishment, septin ring assembly, and pheromone-dependent MAP-kinase signaling during the yeast mating process. In this study, we further investigated the role of Cdc42p in the mating process by screening for specific mating defective cdc42 alleles. We have identified and characterized novel mating defective cdc42 alleles that are unaffected in vegetative cell polarity. Replacement of the Cdc42p Val36 residue with Met resulted in a specific cell fusion defect. This cdc42[V36M] mutant responded to mating pheromone but was defective in cell fusion and in localization of the cell fusion protein Fus1p, similar to a previously isolated cdc24 (cdc24-m6) mutant. Overexpression of a fast cycling Cdc42p mutant suppressed the cdc24-m6 fusion defect and conversely, overexpression of Cdc24p suppressed the cdc42[V36M] fusion defect. Taken together, our results indicate that Cdc42p GDP-GTP cycling is critical for efficient cell fusion.
引用
收藏
页码:2824 / 2838
页数:15
相关论文
共 70 条
[1]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[2]   A small conserved domain in the yeast Spa2p is necessary and sufficient for its polarized localization [J].
Arkowitz, RA ;
Lowe, N .
JOURNAL OF CELL BIOLOGY, 1997, 138 (01) :17-36
[3]  
BABA M, 1989, J CELL SCI, V94, P207
[4]   The exchange factor Cdc24 is required for cell fusion during yeast mating [J].
Barale, S ;
McCusker, D ;
Arkowitz, RA .
EUKARYOTIC CELL, 2004, 3 (04) :1049-1061
[5]   Assembly of scaffold-mediated complexes containing Cdc42p, the exchange factor Cdc24p and the effector Cla4p required for cell cycle-regulated phosphorylation of Cdc24p [J].
Bose, I ;
Irazoqui, JE ;
Moskow, JJ ;
Bardes, ESG ;
Zyla, TR ;
Lew, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (10) :7176-7186
[6]   Cell fusion during yeast mating requires high levels of a-factor mating pheromone [J].
Brizzio, V ;
Gammie, AE ;
Nijbroek, G ;
Michaelis, S ;
Rose, MD .
JOURNAL OF CELL BIOLOGY, 1996, 135 (06) :1727-1739
[7]   Rvs161p interacts with Fus2p to promote cell fusion in Saccharomyces cerevisiae [J].
Brizzio, V ;
Gammie, AE ;
Rose, MD .
JOURNAL OF CELL BIOLOGY, 1998, 141 (03) :567-584
[8]   The role of Far1p in linking the heterotrimeric G protein to polarity establishment proteins during yeast mating [J].
Butty, AC ;
Pryciak, PM ;
Huang, LS ;
Herskowitz, I ;
Peter, M .
SCIENCE, 1998, 282 (5393) :1511-1516
[9]   The role of Cdc42p GTPase-activating proteins in assembly of the septin ring in yeast [J].
Caviston, JP ;
Longtine, M ;
Pringle, JR ;
Bi, E .
MOLECULAR BIOLOGY OF THE CELL, 2003, 14 (10) :4051-4066
[10]   MULTIFUNCTIONAL YEAST HIGH-COPY-NUMBER SHUTTLE VECTORS [J].
CHRISTIANSON, TW ;
SIKORSKI, RS ;
DANTE, M ;
SHERO, JH ;
HIETER, P .
GENE, 1992, 110 (01) :119-122