European Molecular Biology Laboratory, Heidelberg 69117, Germany.
J Cell Biol. 2009 Dec 14;187(6):813-29. doi: 10.1083/jcb.200906020.
Production of RanGTP around chromosomes induces spindle assembly by activating nuclear localization signal (NLS)-containing factors. Here, we show that the NLS protein ISWI, a known chromatin-remodeling ATPase, is a RanGTP-dependent microtubule (MT)-associated protein. Recombinant ISWI induces MT nucleation, stabilization, and bundling in vitro. In Xenopus culture cells and egg extract, ISWI localizes within the nucleus in interphase and on spindles during mitosis. Depletion of ISWI in egg extracts does not affect spindle assembly, but in anaphase spindle MTs disappear and chromosomes do not segregate. We show directly that ISWI is required for the RanGTP-dependent stabilization of MTs during anaphase independently of its effect on chromosomes. ISWI depletion in Drosophila S2 cells induces defects in spindle MTs and chromosome segregation in anaphase, and the cells eventually stop growing. Our results demonstrate that distinctly from its role in spindle assembly, RanGTP maintains spindle MTs in anaphase through the local activation of ISWI and that this is essential for proper chromosome segregation.
RanGTP 在染色体周围的产生通过激活含有核定位信号 (NLS) 的因子来诱导纺锤体组装。在这里,我们表明 NLS 蛋白 ISWI 是一种已知的染色质重塑 ATP 酶,它是 RanGTP 依赖性微管 (MT) 相关蛋白。重组 ISWI 在体外诱导 MT 成核、稳定和聚集。在非洲爪蟾培养细胞和卵提取物中,ISWI 在有丝分裂间期定位于核内,在有丝分裂纺锤体上。在卵提取物中耗尽 ISWI 不会影响纺锤体组装,但在后期纺锤体 MT 消失,染色体不能分离。我们直接表明,ISWI 对于 RanGTP 依赖性的 MT 在后期的稳定是必需的,与它对染色体的影响无关。在 Drosophila S2 细胞中耗尽 ISWI 会导致后期纺锤体 MT 和染色体分离缺陷,细胞最终停止生长。我们的结果表明,与在纺锤体组装中的作用明显不同,RanGTP 通过局部激活 ISWI 在后期维持纺锤体 MT,这对于正确的染色体分离是必不可少的。