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

Nadav Elad, Shahar Abramovitch, Helena Sabanay, Ohad Medalia

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34 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)207-215
Number of pages9
JournalJournal of Cell Science
Volume124
Issue number2
DOIs
Publication statusPublished - 15 Jan 2011

Funding

German-Israeli Cooperation Project [H.2.2]; ERC [243047 INCEL]We thank J. Richard McIntosh for critical discussion and invaluable comments on the manuscript. We thank Benjamin Geiger, Larisa Gheber and Jerry Eichler for critical review, Reinhard Fassler and Alexander Bershadsky for providing plasmids and fruitful discussion, Francis Barr for providing the PRC1 and MKlp1 antibodies, Uri Abdu for providing antibodies, and Alon Monsonego and Shay Abutbul for access to the confocal microscope and assistance with the live imaging. This study was supported by grants from the German-Israeli Cooperation Project (DIP; H.2.2) and by an ERC Starting Grant to O.M. (243047 INCEL).

All Science Journal Classification (ASJC) codes

  • Cell Biology

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