Aurora kinase-A regulates kinetochore/chromatin associated microtubule assembly in human cells

被引:52
作者
Katayama, Hiroshi [1 ]
Sasai, Kaori [1 ]
Kloc, Malgorzata [2 ]
Brinkley, Bill R. [3 ]
Sen, Subrata [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Mol Pathol, Div Pathol & Lab Med, Houston, TX 77054 USA
[2] Methodist Hosp, Res Inst, Immunobiol Lab, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
aurora-A; INCENP; kinetochore associated microtubule formation; centrosome; phosphorylation;
D O I
10.4161/cc.7.17.6460
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Microtubule nucleation and formation from the kinetochore/chromatin have been proposed to contribute to bipolar spindle assembly facilitating equal segregation of chromosomes in mitosis. Although two independent pathways involving the small Ran GTPase-TPX2 proteins and the chromosomal passenger complex proteins have been implicated in the formation of microtubules from the kinetochore/chromatin, detailed molecular mechanisms integrating the pathways and regulating the process have not been well elucidated. This study demonstrates that Aurora kinase-A plays a central role in the kinetochore/chromatin associated microtubule assembly in human cells by integrating the two pathways regulating the process. Silencing by siRNA and overexpression of a kinase inactive mutant revealed involvement of Aurora-A at two critical steps. These include formation of gamma-tubulin foci in the vicinity of kinetochore/ chromatin to create microtubule nucleation sites as well as INCENP and TPX2 mediated activation of Aurora-A facilitating formation and stabilization of microtubules. The findings provide the first evidence of Aurora-A, in association with INCENP and TPX2, being a key regulator of kinetochore/ chromatin associated microtubule formation in human cells.
引用
收藏
页码:2691 / 2704
页数:14
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