Centro Andaluz de Biología del Desarrollo, Universidad Pablo de Olavide/Consejo Superior de Investigaciones Cientffícas, Carretera de Utrera Km1, 41013 Sevilla, Spain.
Genetics. 2014 Feb;196(2):455-70. doi: 10.1534/genetics.113.155218. Epub 2013 Dec 13.
In fission yeast, the septation initiation network (SIN) is thought to promote cytokinesis by downstream activation of Rho1, a conserved GTPase that controls cell growth and division. Here we show that Etd1 and PP2A-Pab1, antagonistic regulators of SIN, are Rho1 regulators. Our genetic and biochemical studies indicate that a C-terminal region of Etd1 may activate Rho1 by directly binding it, whereas an N-terminal domain confers its ability to localize at the growing tips and the division site where Rho1 functions. In opposition to Etd1, our results indicate that PP2A-Pab1 inhibits Rho1. The SIN cascade is upstream-regulated by the Spg1 GTPase. In the absence of Etd1, activity of Spg1 drops down prematurely, thereby inactivating SIN. Interestingly, we find that ectopic activation of Rho1 restores Spg1 activity in Etd1-depleted cells. By using a cytokinesis block strategy, we show that Rho1 is essential to feedback-activate Spg1 during actomyosin ring constriction. Therefore, activation of Spg1 by Rho1, which in turn is regulated by Etd1, uncovers a novel feedback loop mechanism that ensures SIN activity while cytokinesis is progressing.
在裂殖酵母中,认为有丝分裂起始网络(SIN)通过下游激活 Rho1 来促进胞质分裂,Rho1 是一种保守的 GTPase,控制细胞生长和分裂。在这里,我们表明,Etd1 和 PP2A-Pab1,SIN 的拮抗调节剂,是 Rho1 的调节剂。我们的遗传和生化研究表明,Etd1 的 C 端区域可能通过直接与其结合来激活 Rho1,而 N 端结构域赋予其在生长尖端和 Rho1 发挥作用的分裂部位定位的能力。与 Etd1 相反,我们的结果表明,PP2A-Pab1 抑制 Rho1。SIN 级联由 Spg1 GTPase 在上游调控。在没有 Etd1 的情况下,Spg1 的活性过早下降,从而使 SIN 失活。有趣的是,我们发现 Rho1 的异位激活可在 Etd1 耗尽的细胞中恢复 Spg1 的活性。通过使用胞质分裂阻断策略,我们表明在肌动球蛋白环收缩期间,Rho1 对于反馈激活 Spg1 是必需的。因此,Rho1 对 Spg1 的激活,反过来又受到 Etd1 的调节,揭示了一种新的反馈环机制,确保了 SIN 活性,同时胞质分裂在进行。