A role for NuSAP in linking microtubuies to mitotic chromosomes

被引:65
作者
Ribbeck, Katharina
Raemaekers, Tim
Carmeliet, Geert
Mattaj, Iain W.
机构
[1] European Mol Biol Lab, D-69117 Heidelberg, Germany
[2] Katholieke Univ Leuven, Membrane Trafficking Lab, Ctr Human Genet, Flanders Interuniv Inst Biotechnol, B-3000 Louvain, Belgium
[3] Katholieke Univ Leuven, Lab Expt Med & Endocrinol, B-3000 Louvain, Belgium
关键词
D O I
10.1016/j.cub.2006.11.050
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
The spindle apparatus is a microtubule (MT)-based machinery that attaches to and segregates the chromosomes during mitosis and meiosis. Self-organization of the spindle around chromatin involves the assembly of MTs, their attachment to the chromosomes, and their organization into a bipolar array. One regulator of spindle self-organization is RanGTP. RanGTP is generated at chromatin and activates a set of soluble, Ran-regulated spindle factors such as TPX2, NuMA, and NuSAP [1]. How the spindle factors direct and attach MTs to the chromosomes are key open questions. Nucleolar and Spindle-Associated Protein (NuSAP) was recently identified as an essential MT-stabilizing and bundling protein that is enriched at the central part of the spindle [2, 3]. Here, we show by biochemical reconstitution that NuSAP efficiently adsorbs to isolated chromatin and DNA and that it can directly produce and retain high concentrations of MTs in the immediate vicinity of chromatin or DNA. Moreover, our data reveal that NuSAP-chromatin interaction is subject to Ran regulation and can be suppressed by Importin alpha (Imp alpha) and Imp7. We propose that the presence of MT binding agents such as NuSAP, which can be directly immobilized on chromatin, are critical for targeting MT production to vertebrate chromosomes during spindle self-organization.
引用
收藏
页码:230 / 236
页数:7
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