Barale Sophie, McCusker Derek, Arkowitz Robert A
Institute of Signaling, Developmental Biology, and Cancer, Centre National de la Recherche Scientifique UMR 6543, Université de Nice, Faculté des Sciences-Parc Valrose, 06108 Nice Cedex 2, France.
Mol Biol Cell. 2006 Jun;17(6):2824-38. doi: 10.1091/mbc.e05-11-1040. Epub 2006 Mar 29.
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.
高度保守的小Rho G蛋白Cdc42p在所有真核生物的细胞极性和细胞骨架组织中起着关键作用。在酿酒酵母中,Cdc42p在酵母交配过程中对于细胞极性建立、隔膜环组装以及信息素依赖性丝裂原活化蛋白激酶信号传导很重要。在本研究中,我们通过筛选特定的交配缺陷型cdc42等位基因,进一步研究了Cdc42p在交配过程中的作用。我们鉴定并表征了在营养细胞极性方面未受影响的新型交配缺陷型cdc42等位基因。用Met取代Cdc42p的Val36残基导致了特定的细胞融合缺陷。这个cdc42[V36M]突变体对交配信息素作出反应,但在细胞融合以及细胞融合蛋白Fus1p的定位方面存在缺陷,类似于先前分离出的cdc24(cdc24-m6)突变体。快速循环的Cdc42p突变体的过表达抑制了cdc24-m6的融合缺陷,相反,Cdc24p的过表达抑制了cdc42[V36M]的融合缺陷。综上所述,我们的结果表明Cdc42p的GDP-GTP循环对于有效的细胞融合至关重要。