CLIP-170 facilitates the formation of kinetochore-microtubule attachments

被引:70
作者
Tanenbaum, ME
Galjart, N
van Vugt, MATM
Medema, RH
机构
[1] Netherlands Canc Inst, Div Mol Biol, NL-1066 CX Amsterdam, Netherlands
[2] Erasmus Med Ctr, Dept Cell Biol & Genet, Rotterdam, Netherlands
关键词
attachment; CLIP170; MAP; spindle;
D O I
10.1038/sj.emboj.7600916
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
CLIP-170 is a microtubule 'plus end tracking' protein involved in several microtubule-dependent processes in interphase. At the onset of mitosis, CLIP-170 localizes to kinetochores, but at metaphase, it is no longer detectable at kinetochores. Although RNA interference (RNAi) experiments have suggested an essential role for CLIP-170 during mitosis, the molecular function of CLIP-170 in mitosis has not yet been revealed. Here, we used a combination of high-resolution microscopy and RNAi-mediated depletion to study the function of CLIP-170 in mitosis. We found that CLIP-170 dynamically localizes to the outer most part of unattached kinetochores and to the ends of growing microtubules. In addition, we provide evidence that a pool of CLIP-170 is transported along kinetochore microtubules by the dynein/dynactin complex. Interference with CLIP-170 expression results in defective chromosome congression and diminished kinetochore microtubule attachments, but does not detectibly affect microtubule dynamics or kinetochore - microtubule stability. Taken together, our results indicate that CLIP-170 facilitates the formation of kinetochore - microtubule attachments, possibly through direct capture of microtubules at the kinetochore.
引用
收藏
页码:45 / 57
页数:13
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