Pena Guadalupe E, Zhou Xiao, Slevin Lauren, Brownlee Christopher, Heald Rebecca
Department of Molecular and Cell Biology, University of California, Berkeley, California, USA.
AbbVie, South San Francisco, California, USA.
Cytoskeleton (Hoboken). 2025 May 6. doi: 10.1002/cm.22034.
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, KKLK 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.
由微管和许多相关蛋白组成的双极纺锤体在所有真核生物的细胞分裂过程中发挥着分离染色体的作用,然而纺锤体的大小和结构在不同物种和细胞类型之间存在显著差异。针对Xklp2的靶向蛋白(TPX2)是通过其在分支微管成核、有丝分裂激酶极光激酶A的激活以及与驱动蛋白-5(Eg5)马达的关联中所起的作用来调节纺锤体微管组织的一个候选因素。在这里,我们鉴定了非洲爪蟾TPX2中一个保守的核定位序列(NLS)基序KKLK,它在非洲爪蟾卵提取物中调节星体微管的形成和纺锤体极形态。添加该序列突变为AALA的重组TPX2会刺激微管星体的自发形成,并增加磷酸化极光激酶A、中心体蛋白和Eg5向减数分裂纺锤体极的募集,同时仍与调节性转运因子输入蛋白α结合。我们提出TPX2是纺锤体组装的关键因子,其调节作用有助于激活多种微管聚合和组织蛋白,从而产生不同的纺锤体结构。