Bakal Christopher J, Finan Dina, LaRose José, Wells Clark D, Gish Gerald, Kulkarni Sarang, DeSepulveda Paulo, Wilde Andrew, Rottapel Robert
Department of Medical Biophysics, University of Toronto, 1 King's College Circle, Toronto, ON, Canada M5S 1A8.
Proc Natl Acad Sci U S A. 2005 Jul 5;102(27):9529-34. doi: 10.1073/pnas.0504190102. Epub 2005 Jun 23.
Rho GTPases regulate reorganization of actin and microtubule cytoskeletal structures during both interphase and mitosis. The timing and subcellular compartment in which Rho GTPases are activated is controlled by the large family of Rho GTP exchange factors (RhoGEFs). Here, we show that the microtubule-associated RhoGEF Lfc is required for the formation of the mitotic spindle during prophase/prometaphase. The inability of cells to assemble a functioning spindle after Lfc inhibition resulted in a delay in mitosis and an accumulation of prometaphase cells. Inhibition of Lfc's primary target Rho GTPase during prophase/prometaphase, or expression of a catalytically inactive mutant of Lfc, also prevented normal spindle assembly and resulted in delays in mitotic progression. Coinjection of constitutively active Rho GTPase rescued the spindle defects caused by Lfc inhibition, suggesting the requirement of RhoGTP in regulating spindle assembly. Lastly, we implicate mDia1 as an important effector of Lfc signaling. These findings demonstrate a role for Lfc, Rho, and mDia1 during mitosis.
Rho GTP酶在间期和有丝分裂过程中调节肌动蛋白和微管细胞骨架结构的重组。Rho GTP酶激活的时间和亚细胞区室由Rho鸟嘌呤核苷酸交换因子(RhoGEFs)大家族控制。在此,我们表明微管相关的RhoGEF Lfc在前期/前中期有丝分裂纺锤体的形成中是必需的。Lfc抑制后细胞无法组装起功能正常的纺锤体,导致有丝分裂延迟和前中期细胞积累。在前期/前中期抑制Lfc的主要靶标Rho GTP酶,或表达Lfc的催化失活突变体,也会阻止正常的纺锤体组装,并导致有丝分裂进程延迟。共注射组成型激活的Rho GTP酶可挽救由Lfc抑制引起的纺锤体缺陷,表明RhoGTP在调节纺锤体组装中是必需的。最后,我们认为mDia1是Lfc信号的重要效应器。这些发现证明了Lfc、Rho和mDia1在有丝分裂过程中的作用。