The NLS3 Motif in TPX2 Regulates Spindle Architecture in Xenopus Egg Extracts.

Guadalupe E Pena, Xiao Zhou, Lauren Slevin, Christopher Brownlee, Rebecca Heald
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Abstract

A bipolar spindle composed of microtubules and many associated proteins functions to segregate chromosomes during cell division in all eukaryotes, yet both spindle size and architecture vary dramatically across different species and cell types. Targeting protein for Xklp2 (TPX2) is one candidate factor for modulating spindle microtubule organization through its roles in branching microtubule nucleation, activation of the mitotic kinase Aurora A, and association with the kinesin-5 (Eg5) motor. Here we characterize a conserved nuclear localization sequence (NLS) motif, 123KKLK126 in Xenopus laevis TPX2, which regulates astral microtubule formation and spindle pole morphology in Xenopus egg extracts. Addition of recombinant TPX2 with this sequence mutated to AALA stimulated spontaneous formation of microtubule asters and increased recruitment of phosphorylated Aurora A, pericentrin, and Eg5 to meiotic spindle poles while still binding to the regulatory transport factor importin α. We propose that TPX2 is a linchpin spindle assembly factor whose regulation contributes to the activation of multiple microtubule polymerizing and organizing proteins, generating distinct spindle architectures.

TPX2中的NLS3 Motif调控爪蟾卵提取物的纺锤体结构。
在所有真核生物中,由微管和许多相关蛋白组成的双极性纺锤体在细胞分裂过程中起分离染色体的作用,然而纺锤体的大小和结构在不同的物种和细胞类型中都有很大的不同。靶蛋白Xklp2 (TPX2)是调节纺锤体微管组织的一个候选因子,它在分支微管成核、有丝分裂激酶Aurora A的激活以及与激酶5 (Eg5)马达的关联中发挥作用。我们在非洲爪蟾(Xenopus laevis) TPX2中鉴定了一个保守的核定位序列(NLS)基序123KKLK126,该基序调控爪蟾卵提取物的星状微管形成和纺锤极形态。添加AALA突变序列的重组TPX2刺激了微管母细胞的自发形成,并增加了磷酸化的Aurora A、中心周蛋白和Eg5在减数分裂纺锤极上的募集,同时仍与调节运输因子输入蛋白α结合。我们认为TPX2是一个关键的纺锤体组装因子,其调节有助于激活多种微管聚合和组织蛋白,产生不同的纺锤体结构。
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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