Jonasson Erin M, Rossio Valentina, Hatakeyama Riko, Abe Mitsuhiro, Ohya Yoshikazu, Yoshida Satoshi
Department of Biology and Rosenstiel Basic Biomedical Sciences Research Center, Brandeis University, Waltham, MA 02454.
Graduate School of Frontier Sciences, The University of Tokyo, Kashiwa 277-8561, Japan.
J Cell Biol. 2016 Jan 4;212(1):51-61. doi: 10.1083/jcb.201508119.
Budding yeast Rho1 guanosine triphosphatase (GTPase) plays an essential role in polarized cell growth by regulating cell wall glucan synthesis and actin organization. Upon cell wall damage, Rho1 blocks polarized cell growth and repairs the wounds by activating the cell wall integrity (CWI) Pkc1-mitogen-activated protein kinase (MAPK) pathway. A fundamental question is how active Rho1 promotes distinct signaling outputs under different conditions. Here we identified the Zds1/Zds2-protein phosphatase 2A(Cdc55) (PP2A(Cdc55)) complex as a novel Rho1 effector that regulates Rho1 signaling specificity. Zds1/Zds2-PP2A(Cdc55) promotes polarized growth and cell wall synthesis by inhibiting Rho1 GTPase-activating protein (GAP) Lrg1 but inhibits CWI pathway by stabilizing another Rho1 GAP, Sac7, suggesting that active Rho1 is biased toward cell growth over stress response. Conversely, upon cell wall damage, Pkc1-Mpk1 activity inhibits cortical PP2A(Cdc55), ensuring that Rho1 preferentially activates the CWI pathway for cell wall repair. We propose that PP2A(Cdc55) specifies Rho1 signaling output and that reciprocal antagonism between Rho1-PP2A(Cdc55) and Rho1-Pkc1 explains how only one signaling pathway is robustly activated at a time.
出芽酵母Rho1鸟苷三磷酸酶(GTPase)通过调节细胞壁葡聚糖合成和肌动蛋白组织,在极化细胞生长中发挥重要作用。在细胞壁受损时,Rho1会阻断极化细胞生长,并通过激活细胞壁完整性(CWI)的Pkc1-丝裂原活化蛋白激酶(MAPK)途径来修复伤口。一个基本问题是,活跃的Rho1如何在不同条件下促进不同的信号输出。在这里,我们鉴定出Zds1/Zds2-蛋白磷酸酶2A(Cdc55)(PP2A(Cdc55))复合物是一种新型的Rho1效应物,可调节Rho1信号特异性。Zds1/Zds2-PP2A(Cdc55)通过抑制Rho1 GTP酶激活蛋白(GAP)Lrg1来促进极化生长和细胞壁合成,但通过稳定另一种Rho1 GAP Sac7来抑制CWI途径,这表明活跃的Rho1在细胞生长方面比应激反应更具偏向性。相反,在细胞壁受损时,Pkc1-Mpk1活性会抑制皮质PP2A(Cdc55),确保Rho1优先激活CWI途径进行细胞壁修复。我们提出,PP2A(Cdc55)决定了Rho1的信号输出,并且Rho1-PP2A(Cdc55)和Rho1-Pkc1之间的相互拮抗作用解释了为何一次只有一条信号通路能被强烈激活。