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Microtubule organization in the final stages of cytokinesis as revealed by cryo-electron tomography.

机译:冷冻电子断层扫描显示在胞质分裂末期的微管组织。

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The completion of cytokinesis is dominated by the midbody, a tightly-packed microtubule (MT)-based bridge that transiently connects the two daughter cells. Assembled from condensed, spindle-MTs and numerous associated proteins, the midbody gradually narrows down until daughter cell partitioning occurs at this site. Although described many years ago, detailed understanding of the abscission process remains lacking. Applying cryo-electron tomography to purified midbodies, in combination with fluorescence microscopy, we present here new insight into MT organization within the midbody. We find that the midbody is spatially divided into a core bundle of MTs that traverses the electron-dense overlap region (continuous MTs), surrounded by MTs that terminate within the overlap region (polar MTs). Residual continuous MTs remained intact up to the verge of abscission, whereas the residual polar MTs lost their organization and retreated from the overlap region at late cytokinesis stages. A detailed localization of the microtubule-bundling protein PRC1 supports the above notion. Our study thus provides a detailed account of the abscission process and suggests that the midbody, having acquired a distinct MT architecture as compared to the preceding central spindle, actively facilitates the final stage of cytokinesis.
机译:细胞分裂的完成主要由中体决定,中体是紧密连接的基于微管(MT)的桥,该桥瞬时连接两个子细胞。由浓缩的纺锤体MT和许多相关蛋白组装而成,中体逐渐变窄,直到在该部位发生子代细胞分配。尽管已经描述了很多年,但仍缺乏对脱落过程的详细了解。将低温电子层析成像技术应用于纯化的中体,结合荧光显微镜,我们在此介绍中体中MT的新见解。我们发现,中体在空间上被分为MT的核心束,该MT束横穿电子致密的重叠区域(连续的MT),被终止在重叠区域内的MT(极性MT)包围。残留的连续MTs直至脱落前仍保持完整,而残留的极性MTs则失去了组织并在胞质分裂后期从重叠区退缩。微管捆绑蛋白PRC1的详细定位支持上述概念。因此,我们的研究提供了对脱落过程的详细说明,并表明与先前的中心纺锤体相比,获得独特的MT结构的中体积极地促进了胞质分裂的最后阶段。

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