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细胞分裂末期的微管组织通过冷冻电子断层扫描技术揭示。

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

机构信息

Department of Life Sciences and the National Institute for Biotechnology in the Negev, Ben Gurion University of the Negev, Beer-Sheva 84105, Israel.

出版信息

J Cell Sci. 2011 Jan 15;124(Pt 2):207-15. doi: 10.1242/jcs.073486.

Abstract

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.

摘要

胞质分裂的完成由中间体主导,这是一个紧密堆积的微管(MT)桥,暂时连接两个子细胞。中间体由浓缩的纺锤体-MT 和许多相关蛋白组装而成,逐渐变窄,直到子细胞在该部位进行分割。尽管中间体多年前就已被描述,但对其分离过程的详细了解仍存在不足。我们应用冷冻电子断层扫描对纯化的中间体进行研究,并结合荧光显微镜,提供了有关中间体内部 MT 组织的新见解。我们发现,中间体在空间上分为穿过电子致密重叠区域的核心 MT 束(连续 MT),被终止于重叠区域内的 MT 包围(极 MT)。残留的连续 MT 直到分离的边缘仍保持完整,而残留的极 MT 在胞质分裂后期失去组织并从重叠区域后退。微管束蛋白 PRC1 的详细定位支持了上述观点。因此,我们的研究提供了对分离过程的详细描述,并表明中间体与之前的中心纺锤体相比,获得了独特的 MT 结构,积极促进了胞质分裂的最后阶段。

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