Alp7/TACC is a crucial target in Ran-GTPase-dependent spindle formation in fission yeast

被引:56
作者
Sato, Masamitsu [1 ]
Toda, Takashi [1 ]
机构
[1] Canc Res UK, London Res Inst, Lincolns Inn Fields Labs, Lab Cell Regulat, London WC2A 3PX, England
基金
日本学术振兴会;
关键词
D O I
10.1038/nature05773
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
Microtubules are essential intracellular structures involved in several cellular phenomena, including polarity establishment and chromosome segregation(1). Because the nuclear envelope persists during mitosis ( closed mitosis) in fission yeast ( Schizosaccharomyces pombe), cytoplasmic microtubules must be reorganized into the spindle in the compartmentalized nucleus on mitotic entry(2). An ideal mechanism might be to take advantage of an evolutionarily conserved microtubule formation system that uses the Ran-GTPase nuclear transport machinery(3-5), but no targets of Ran for spindle formation have been identified in yeast. Here we show that a microtubule-associated protein, Alp7, which forms a complex with Alp14, is a target of Ran in yeast for spindle formation. The Ran-deficient pim1 mutant (pim1-F201S) failed to show mitosis-specific nuclear accumulation of Alp7. Moreover, this mutant exhibited compromised spindle formation and early mitotic delay. Importantly, these defects were suppressed by Alp7 that was artificially targeted to the nucleus by a Ran-independent and importin-alpha-mediated system. Thus, Ran targets Alp7 - Alp14 to achieve nuclear spindle formation, and might differentiate its targets depending on whether the organism undergoes closed or open mitosis.
引用
收藏
页码:334 / U9
页数:5
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