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GM130 Regulates Golgi-Derived Spindle Assembly by Activating TPX2 and Capturing Microtubules

机译:GM130通过激活TPX2和捕获微管来调节高尔基衍生的主轴组件。

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Spindle assembly requires the coordinated action of multiple cellular structures to nucleate and organize microtubules in a precise spatiotemporal manner. Amongthem, the contributions of centrosomes, chromosomes, and microtubules have been well studied, yet the involvement of membrane-bound organelles remains largely elusive. Here, we provide mechanistic evidence for a membrane-based, Golgi-derived microtubule assembly pathway in mitosis. Upon mitotic entry, the Golgi matrix protein GM130 interacts with importin alpha via a classical nuclear localization signal that recruits importin alpha to the Golgi membranes. Sequestration of importin alpha by GM130 liberates the spindle assembly factor TPX2, which activates Aurora-A kinase and stimulates local microtubule nucleation. Upon filament assembly, nascent microtubules are further captured by GM130, thus linking Golgi membranes to the spindle. Our results reveal an active role for the Golgi in regulating spindle formation to ensure faithful organelle inheritance.
机译:主轴组装需要多个细胞结构的协同作用,以精确的时空方式成核并组织微管。其中,对中心体,染色体和微管的贡献已进行了充分的研究,但是膜结合细胞器的参与仍然难以捉摸。在这里,我们提供了有丝分裂中基于膜的,高尔基派生的微管组装途径的机械证据。有丝分裂进入后,高尔基体蛋白GM130通过经典的核定位信号与importin alpha相互作用,该信号将importin alpha募集到高尔基体膜上。 GM130螯合importin alpha可释放纺锤体装配因子TPX2,后者激活Aurora-A激酶并刺激局部微管成核。细丝组装后,新生的微管被GM130进一步捕获,从而使高尔基体膜与纺锤体相连。我们的研究结果表明高尔基体在调节纺锤体形成以确保忠实的细胞器遗传中发挥了积极作用。

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