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Kinetochore-generated pushing forces separate centrosomes during bipolar spindle assembly

机译:线粒体产生的推力在双极纺锤体组装过程中分离中心体

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摘要

In animal somatic cells, bipolar spindle formation requires separation of the centrosome-based spindle poles. Centrosome separation relies on multiple pathways, including cortical forces and antiparallel microtubule (MT) sliding, which are two activities controlled by the protein kinase aurora A. We previously found that depletion of the human kinetochore protein Mcm21RCENP-O results in monopolar spindles, raising the question as to whether kinetochores contribute to centrosome separation. In this study, we demonstrate that kinetochores promote centrosome separation after nuclear envelope breakdown by exerting a pushing force on the kinetochore fibers (k-fibers), which are bundles of MTs that connect kinetochores to centrosomes. This force is based on poleward MT flux, which incorporates new tubulin subunits at the plus ends of k-fibers and requires stable k-fibers to drive centrosomes apart. This kinetochore-dependent force becomes essential for centrosome separation if aurora A is inhibited. We conclude that two mechanisms control centrosome separation during prometaphase: an aurora A–dependent pathway and a kinetochore-dependent pathway that relies on k-fiber–generated pushing forces.
机译:在动物体细胞中,双极纺锤体形成需要分离基于中心体的纺锤体极。中心体分离依赖于多种途径,包括皮层力和反平行微管(MT)滑动,这是蛋白激酶Aurora A控制的两项活动。我们先前发现人类动粒蛋白Mcm21R CENP-O 产生单极纺锤体,提出了有关动植物是否有助于中心体分离的问题。在这项研究中,我们证明了核因子的包膜通过在动粒纤维(k纤维)上施加推力来促进核包膜的分离,所述动粒纤维是将动植物连接到中心体的MT束。此力基于极向MT通量,该通量在k纤维的正端结合了新的微管蛋白亚基,并且需要稳定的k纤维将中心体分开。如果极光A被抑制,则这种依赖于动线粒的力对于中心体分离必不可少。我们得出的结论是,有两种机制可以控制前中期的中心体分离:依赖于k纤维产生的推力的极光A依赖途径和动粒体依赖途径。

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