Olson M F, Ashworth A, Hall A
Department of Biochemistry, University College, London, UK.
Science. 1995 Sep 1;269(5228):1270-2. doi: 10.1126/science.7652575.
Members of the Rho family of small guanosine triphosphatases (GTPases) regulate the organization of the actin cytoskeleton; Rho controls the assembly of actin stress fibers and focal adhesion complexes, Rac regulates actin filament accumulation at the plasma membrane to produce lamellipodia and membrane ruffles, and Cdc42 stimulates the formation of filopodia. When microinjected into quiescent fibroblasts, Rho, Rac, and Cdc42 stimulated cell cycle progression through G1 and subsequent DNA synthesis. Furthermore, microinjection of dominant negative forms of Rac and Cdc42 or of the Rho inhibitor C3 transferase blocked serum-induced DNA synthesis. Unlike Ras, none of the Rho GTPases activated the mitogen-activated protein kinase (MAPK) cascade that contains the protein kinases c-Raf1, MEK (MAPK or ERK kinase), and ERK (extracellular signal-regulated kinase). Instead, Rac and Cdc42, but not Rho, stimulated a distinct MAP kinase, the c-Jun kinase JNK/SAPK (Jun NH2-terminal kinase or stress-activated protein kinase). Rho, Rac, and Cdc42 control signal transduction pathways that are essential for cell growth.
小GTP酶(GTPases)Rho家族的成员调节肌动蛋白细胞骨架的组织;Rho控制肌动蛋白应力纤维和粘着斑复合物的组装,Rac调节质膜上肌动蛋白丝的积累以产生片状伪足和膜皱褶,而Cdc42刺激丝状伪足的形成。当显微注射到静止的成纤维细胞中时,Rho、Rac和Cdc42通过G1期刺激细胞周期进程并随后进行DNA合成。此外,显微注射Rac和Cdc42的显性负性形式或Rho抑制剂C3转移酶可阻断血清诱导的DNA合成。与Ras不同,Rho GTPases均未激活包含蛋白激酶c-Raf1、MEK(丝裂原活化蛋白激酶或细胞外信号调节激酶激酶)和ERK(细胞外信号调节激酶)的丝裂原活化蛋白激酶(MAPK)级联反应。相反,Rac和Cdc42而非Rho刺激了一种独特的MAP激酶,即c-Jun激酶JNK/SAPK(Jun NH2末端激酶或应激激活蛋白激酶)。Rho、Rac和Cdc42控制对细胞生长至关重要的信号转导途径。