Regulated Ran-binding protein 1 activity is required for organization and function of the mitotic spindle in mammalian cells in vivo.

G Guarguaglini, L Renzi, F D'Ottavio, B Di Fiore, M Casenghi, E Cundari, P Lavia
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Abstract

Ran-binding protein (RanBP) 1 is a major regulator of the Ran GTPase and is encoded by a regulatory target gene of E2F factors. The Ran GTPase network controls several cellular processes, including nucleocytoplasmic transport and cell cycle progression, and has recently also been shown to regulate microtubule nucleation and spindle assembly in Xenopus oocyte extracts. Here we report that RanBP1 protein levels are cell cycle regulated in mammalian cells, increase from S phase to M phase, peak in metaphase, and abruptly decline in late telophase. Overexpression of RanBP1 throughout the cell cycle yields abnormal mitoses characterized by severe defects in spindle polarization. In addition, microinjection of anti-RanBP1 antibody in mitotic cells induces mitotic delay and abnormal nuclear division, reflecting an abnormal stabilization of the mitotic spindle. Thus, regulated RanBP1 activity is required for proper execution of mitosis in somatic cells.

调控ran结合蛋白1的活性是哺乳动物细胞有丝分裂纺锤体组织和功能所必需的。
RanBP - 1是rangtpase的主要调控蛋白,由E2F因子的调控靶基因编码。Ran GTPase网络控制着几个细胞过程,包括核胞质运输和细胞周期进程,最近也被证明在爪蟾卵母细胞提取物中调节微管成核和纺锤体组装。在哺乳动物细胞中,RanBP1蛋白水平受细胞周期调控,从S期到M期增加,在中期达到峰值,在末期突然下降。在整个细胞周期中,RanBP1的过表达会产生以纺锤体极化严重缺陷为特征的异常有丝分裂。此外,在有丝分裂细胞中微量注射抗ranbp1抗体会导致有丝分裂延迟和核分裂异常,这反映了有丝分裂纺锤体的异常稳定。因此,调节RanBP1的活性对于体细胞有丝分裂的正常进行是必需的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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