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NuSAP在将微管与有丝分裂染色体相连中的作用。

A role for NuSAP in linking microtubules to mitotic chromosomes.

作者信息

Ribbeck Katharina, Raemaekers Tim, Carmeliet Geert, Mattaj Iain W

机构信息

European Molecular Biology Laboratory, Meyerhofstrasse 1, D-69117 Heidelberg, Germany.

出版信息

Curr Biol. 2007 Feb 6;17(3):230-6. doi: 10.1016/j.cub.2006.11.050.

Abstract

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 . 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 . 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 (Impalpha) 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.

摘要

纺锤体是一种基于微管(MT)的机制,在有丝分裂和减数分裂过程中附着并分离染色体。纺锤体围绕染色质的自组织涉及微管的组装、它们与染色体的附着以及它们组织成双极阵列。纺锤体自组织的一个调节因子是RanGTP。RanGTP在染色质处产生,并激活一组可溶性的、受Ran调节的纺锤体因子,如TPX2、NuMA和NuSAP。纺锤体因子如何引导微管并将其附着到染色体上是关键的悬而未决的问题。核仁与纺锤体相关蛋白(NuSAP)最近被鉴定为一种必需的微管稳定和捆绑蛋白,在纺锤体的中央部分富集。在这里,我们通过生化重建表明,NuSAP能有效地吸附到分离的染色质和DNA上,并且它可以在染色质或DNA的紧邻区域直接产生并保留高浓度的微管。此外,我们的数据表明,NuSAP-染色质相互作用受Ran调节,并且可以被输入蛋白α(Impalpha)和Imp7抑制。我们提出,像NuSAP这样可以直接固定在染色质上的微管结合剂的存在,对于在纺锤体自组织过程中将微管产生靶向脊椎动物染色体至关重要。

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