The Rho GTP exchange factor Lfc promotes spindle assembly in early mitosis

被引:52
作者
Bakal, CJ
Finan, D
LaRose, J
Wells, CD
Gish, G
Kulkarni, S
DeSepulveda, P
Wilde, A
Rottapel, R
机构
[1] Univ Toronto, Dept Med Biophys, Toronto, ON M5S 1A8, Canada
[2] Univ Toronto, Dept Med & Immunol, Toronto, ON M5S 1A8, Canada
[3] Univ Toronto, Dept Med Genet & Microbiol, Toronto, ON M5S 1A8, Canada
[4] Princess Margaret Hosp, Ontario Canc Inst, Toronto, ON M5G 2M9, Canada
[5] St Michaels Hosp, Toronto, ON M5B 1WB, Canada
[6] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[7] Inst Natl Sante & Rech Med, U119, F-13009 Marseille, France
关键词
D O I
10.1073/pnas.0504190102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:9529 / 9534
页数:6
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