Generation of GTP-bound Ran by RCC1 is required for chromatin-induced mitotic spindle formation

被引:403
作者
Carazo-Salas, RE [1 ]
Guarguaglini, G [1 ]
Gruss, OJ [1 ]
Segref, A [1 ]
Karsenti, E [1 ]
Mattaj, IW [1 ]
机构
[1] European Mol Biol Lab, D-69117 Heidelberg, Germany
关键词
D O I
10.1038/22133
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
Chromosomes are segregated by two antiparallel arrays of microtubules arranged to form the spindle apparatus. During cell division, the nucleation of cytosolic microtubules is prevented and spindle microtubules nucleate from centrosomes (in mitotic animal cells) or around chromosomes (in plants and some meiotic cells)(1,2). The molecular mechanism by which chromosomes induce local microtubule nucleation in the absence of centrosomes is unknown(3-5), but it can be studied by adding chromatin beads to Xenopus egg extracts(6). The beads nucleate microtubules that eventually reorganize into a bipolar spindle. RCC1, the guanine-nucleotide-exchange factor for the GTPase protein Ran, is a component of chromatin. Using the chromatin bead assay, we show here that the activity of chromosome-associated RCC1 protein is required for spindle formation. Ran itself, when in the GTP-bound state (Ran-GTP), induces microtubule nucleation and spindle-like structures in M-phase extract. We propose that RCC1 generates a high local concentration of Ran-GTP around chromatin which in turn induces the local nucleation of microtubules.
引用
收藏
页码:178 / 181
页数:4
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