Heinrich Melanie, Köhler Tim, Mösch Hans-Ulrich
Department of Biology, Molecular Genetics, Philipps University, D-35032 Marburg, Germany.
Eukaryot Cell. 2007 Feb;6(2):317-27. doi: 10.1128/EC.00102-06. Epub 2006 Dec 22.
In Saccharomyces cerevisiae, the highly conserved Rho-type GTPase Cdc42 is essential for cell division and controls cellular development during mating and invasive growth. The role of Cdc42 in mating has been controversial, but a number of previous studies suggest that the GTPase controls the mitogen-activated protein (MAP) kinase cascade by activating the p21-activated protein kinase (PAK) Ste20. To further explore the role of Cdc42 in pheromone-stimulated signaling, we isolated novel alleles of CDC42 that confer resistance to pheromone. We find that in CDC42(V36A) and CDC42(V36A, I182T) mutant strains, the inability to undergo pheromone-induced cell cycle arrest correlates with reduced phosphorylation of the mating MAP kinases Fus3 and Kss1 and with a decrease in mating efficiency. Furthermore, Cdc42(V36A) and Cdc42(V36A, I182T) proteins show reduced interaction with the PAK Cla4 but not with Ste20. We also show that deletion of CLA4 in a CDC42(V36A, I182T) mutant strain suppresses pheromone resistance and that overexpression of CLA4 interferes with pheromone-induced cell cycle arrest and MAP kinase phosphorylation in CDC42 wild-type strains. Our data indicate that Cla4 has the potential to act as a negative regulator of the mating pathway and that this function of the PAK might be under control of Cdc42. In conclusion, our study suggests that control of pheromone signaling by Cdc42 not only depends on Ste20 but also involves interaction of the GTPase with Cla4.
在酿酒酵母中,高度保守的Rho型GTP酶Cdc42对细胞分裂至关重要,并在交配和侵袭性生长过程中控制细胞发育。Cdc42在交配中的作用一直存在争议,但此前的一些研究表明,这种GTP酶通过激活p21激活蛋白激酶(PAK)Ste20来控制丝裂原活化蛋白(MAP)激酶级联反应。为了进一步探究Cdc42在信息素刺激信号传导中的作用,我们分离出了赋予信息素抗性的CDC42新等位基因。我们发现,在CDC42(V36A)和CDC42(V36A,I182T)突变株中,无法经历信息素诱导的细胞周期停滞与交配MAP激酶Fus3和Kss1的磷酸化减少以及交配效率降低相关。此外,Cdc42(V36A)和Cdc42(V36A,I182T)蛋白与PAK Cla4的相互作用减少,但与Ste20的相互作用未减少。我们还表明,在CDC42(V36A,I182T)突变株中删除CLA4可抑制信息素抗性,而CLA4的过表达会干扰CDC42野生型株中信息素诱导的细胞周期停滞和MAP激酶磷酸化。我们的数据表明,Cla4有可能作为交配途径的负调节因子,并且这种PAK的功能可能受Cdc42控制。总之,我们的研究表明,Cdc42对信息素信号传导的控制不仅取决于Ste20,还涉及该GTP酶与Cla4的相互作用。