Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27710, USA.
Mol Biol Cell. 2013 Apr;24(7):914-22. doi: 10.1091/mbc.E12-11-0812. Epub 2013 Feb 6.
Saccharomyces cerevisiae cells exposed to a variety of physiological stresses transiently delay bud emergence or bud growth. To maintain coordination between bud formation and the cell cycle in such circumstances, the morphogenesis checkpoint delays nuclear division via the mitosis-inhibitory Wee1-family kinase, Swe1p. Swe1p is degraded during G2 in unstressed cells but is stabilized and accumulates following stress. Degradation of Swe1p is preceded by its recruitment to the septin scaffold at the mother-bud neck, mediated by the Swe1p-binding protein Hsl7p. Following osmotic shock or actin depolymerization, Swe1p is stabilized, and previous studies suggested that this was because Hsl7p was no longer recruited to the septin scaffold following stress. However, we now show that Hsl7p is in fact recruited to the septin scaffold in stressed cells. Using a cyclin-dependent kinase (CDK) mutant that is immune to checkpoint-mediated inhibition, we show that Swe1p stabilization following stress is an indirect effect of CDK inhibition. These findings demonstrate the physiological importance of a positive-feedback loop in which Swe1p activity inhibits the CDK, which then ceases to target Swe1p for degradation. They also highlight the difficulty in disentangling direct checkpoint pathways from the effects of positive-feedback loops active at the G2/M transition.
酵母细胞暴露于各种生理压力下会短暂地延迟芽的出现或芽的生长。为了在这种情况下维持芽形成和细胞周期之间的协调,形态发生检查点通过有丝分裂抑制的 Wee1 家族激酶 Swe1p 延迟核分裂。在未受压力的细胞中,Swe1p 在 G2 期间被降解,但在受到压力后会稳定并积累。Swe1p 的降解先于其被募集到母-芽颈的隔膜支架上,这是由 Swe1p 结合蛋白 Hsl7p 介导的。在渗透压冲击或肌动蛋白解聚后,Swe1p 被稳定,之前的研究表明,这是因为 Hsl7p 在受到压力后不再被募集到隔膜支架上。然而,我们现在表明,Hsl7p 实际上在受压细胞中被募集到隔膜支架上。使用对检查点介导的抑制具有免疫性的细胞周期蛋白依赖性激酶 (CDK) 突变体,我们表明,应激后 Swe1p 的稳定是 CDK 抑制的间接效应。这些发现证明了 Swe1p 活性抑制 CDK 的正反馈回路在其中的生理重要性,而 CDK 随后不再将 Swe1p 作为降解的靶标。它们还突出了从 G2/M 转换时的正反馈回路的影响中分离直接检查点途径的困难。