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Tektin 2 is required for central spindle microtubule organization and the completion of cytokinesis
During anaphase, the nonkinetochore microtubules in the spindle midzone become compacted into the central spindle, a structure which is required to both initiate and complete cytokinesis. We show that Tektin 2 (Tek2) associates with the spindle poles throughout mitosis, organizes the spindle midzone...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386100/ https://www.ncbi.nlm.nih.gov/pubmed/18474621 http://dx.doi.org/10.1083/jcb.200711160 |
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author | Durcan, Thomas M. Halpin, Elizabeth S. Rao, Trisha Collins, Nicholas S. Tribble, Emily K. Hornick, Jessica E. Hinchcliffe, Edward H. |
author_facet | Durcan, Thomas M. Halpin, Elizabeth S. Rao, Trisha Collins, Nicholas S. Tribble, Emily K. Hornick, Jessica E. Hinchcliffe, Edward H. |
author_sort | Durcan, Thomas M. |
collection | PubMed |
description | During anaphase, the nonkinetochore microtubules in the spindle midzone become compacted into the central spindle, a structure which is required to both initiate and complete cytokinesis. We show that Tektin 2 (Tek2) associates with the spindle poles throughout mitosis, organizes the spindle midzone microtubules during anaphase, and assembles into the midbody matrix surrounding the compacted midzone microtubules during cytokinesis. Tek2 small interfering RNA (siRNA) disrupts central spindle organization and proper localization of MKLP1, PRC1, and Aurora B to the midzone and prevents the formation of a midbody matrix. Video microscopy revealed that loss of Tek2 results in binucleate cell formation by aberrant fusion of daughter cells after cytokinesis. Although a myosin II inhibitor, blebbistatin, prevents actin-myosin contractility, the microtubules of the central spindle are compacted. Strikingly, Tek2 siRNA abolishes this actin-myosin–independent midzone microtubule compaction. Thus, Tek2-dependent organization of the central spindle during anaphase is essential for proper midbody formation and the segregation of daughter cells after cytokinesis. |
format | Text |
id | pubmed-2386100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-23861002008-11-19 Tektin 2 is required for central spindle microtubule organization and the completion of cytokinesis Durcan, Thomas M. Halpin, Elizabeth S. Rao, Trisha Collins, Nicholas S. Tribble, Emily K. Hornick, Jessica E. Hinchcliffe, Edward H. J Cell Biol Research Articles During anaphase, the nonkinetochore microtubules in the spindle midzone become compacted into the central spindle, a structure which is required to both initiate and complete cytokinesis. We show that Tektin 2 (Tek2) associates with the spindle poles throughout mitosis, organizes the spindle midzone microtubules during anaphase, and assembles into the midbody matrix surrounding the compacted midzone microtubules during cytokinesis. Tek2 small interfering RNA (siRNA) disrupts central spindle organization and proper localization of MKLP1, PRC1, and Aurora B to the midzone and prevents the formation of a midbody matrix. Video microscopy revealed that loss of Tek2 results in binucleate cell formation by aberrant fusion of daughter cells after cytokinesis. Although a myosin II inhibitor, blebbistatin, prevents actin-myosin contractility, the microtubules of the central spindle are compacted. Strikingly, Tek2 siRNA abolishes this actin-myosin–independent midzone microtubule compaction. Thus, Tek2-dependent organization of the central spindle during anaphase is essential for proper midbody formation and the segregation of daughter cells after cytokinesis. The Rockefeller University Press 2008-05-19 /pmc/articles/PMC2386100/ /pubmed/18474621 http://dx.doi.org/10.1083/jcb.200711160 Text en © 2008 Durcan et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Durcan, Thomas M. Halpin, Elizabeth S. Rao, Trisha Collins, Nicholas S. Tribble, Emily K. Hornick, Jessica E. Hinchcliffe, Edward H. Tektin 2 is required for central spindle microtubule organization and the completion of cytokinesis |
title | Tektin 2 is required for central spindle microtubule organization and the completion of cytokinesis |
title_full | Tektin 2 is required for central spindle microtubule organization and the completion of cytokinesis |
title_fullStr | Tektin 2 is required for central spindle microtubule organization and the completion of cytokinesis |
title_full_unstemmed | Tektin 2 is required for central spindle microtubule organization and the completion of cytokinesis |
title_short | Tektin 2 is required for central spindle microtubule organization and the completion of cytokinesis |
title_sort | tektin 2 is required for central spindle microtubule organization and the completion of cytokinesis |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386100/ https://www.ncbi.nlm.nih.gov/pubmed/18474621 http://dx.doi.org/10.1083/jcb.200711160 |
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