Department of Pharmacology and Cancer Biology, Duke University Medical Center, , Durham, NC 27710, USA.
Philos Trans R Soc Lond B Biol Sci. 2013 Sep 23;368(1629):20130006. doi: 10.1098/rstb.2013.0006. Print 2013.
Saccharomyces cerevisiae yeast cells polarize in order to form a single bud in each cell cycle. Distinct patterns of bud-site selection are observed in haploid and diploid cells. Genetic approaches have identified the molecular machinery responsible for positioning the bud site: during bud formation, specific locations are marked with immobile landmark proteins. In the next cell cycle, landmarks act through the Ras-family GTPase Rsr1 to promote local activation of the conserved Rho-family GTPase, Cdc42. Additional Cdc42 accumulates by positive feedback, creating a concentrated patch of GTP-Cdc42, which polarizes the cytoskeleton to promote bud emergence. Using time-lapse imaging and mathematical modelling, we examined the process of bud-site establishment. Imaging reveals unexpected effects of the bud-site-selection system on the dynamics of polarity establishment, raising new questions about how that system may operate. We found that polarity factors sometimes accumulate at more than one site among the landmark-specified locations, and we suggest that competition between clusters of polarity factors determines the final location of the Cdc42 cluster. Modelling indicated that temporally constant landmark-localized Rsr1 would weaken or block competition, yielding more than one polarity site. Instead, we suggest that polarity factors recruit Rsr1, effectively sequestering it from other locations and thereby terminating landmark activity.
酿酒酵母细胞在每个细胞周期中都会极化,以形成一个单芽。在单倍体和二倍体细胞中观察到不同的芽位点选择模式。遗传方法已经确定了负责定位芽位点的分子机制:在芽形成过程中,特定位置会被固定的地标蛋白标记。在下一个细胞周期中,地标蛋白通过 Ras 家族 GTP 酶 Rsr1 起作用,促进保守的 Rho 家族 GTP 酶 Cdc42 的局部激活。通过正反馈,更多的 Cdc42 积累,形成一个集中的 GTP-Cdc42 斑点,从而使细胞骨架极化,促进芽的出现。我们使用延时成像和数学建模研究了芽位点建立的过程。成像揭示了芽位点选择系统对极性建立动力学的意外影响,提出了关于该系统如何运作的新问题。我们发现,有时在地标指定的位置之外,极性因子会在多个位点积累,我们认为,极性因子簇之间的竞争决定了 Cdc42 簇的最终位置。模型表明,地标局部定位的 Rsr1 时间不变会削弱或阻止竞争,从而产生多个极性位点。相反,我们认为极性因子招募 Rsr1,有效地将其与其他位置隔离开来,从而终止地标活性。