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Synchronizing chromosome segregation by flux-dependent force equalization at kinetochores

The synchronous movement of chromosomes during anaphase ensures their correct inheritance in every cell division. This reflects the uniformity of spindle forces acting on chromosomes and their simultaneous entry into anaphase. Although anaphase onset is controlled by the spindle assembly checkpoint,...

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Detalles Bibliográficos
Autores principales: Matos, Irina, Pereira, António J., Lince-Faria, Mariana, Cameron, Lisa A., Salmon, Edward D., Maiato, Helder
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2712998/
https://www.ncbi.nlm.nih.gov/pubmed/19581410
http://dx.doi.org/10.1083/jcb.200904153
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author Matos, Irina
Pereira, António J.
Lince-Faria, Mariana
Cameron, Lisa A.
Salmon, Edward D.
Maiato, Helder
author_facet Matos, Irina
Pereira, António J.
Lince-Faria, Mariana
Cameron, Lisa A.
Salmon, Edward D.
Maiato, Helder
author_sort Matos, Irina
collection PubMed
description The synchronous movement of chromosomes during anaphase ensures their correct inheritance in every cell division. This reflects the uniformity of spindle forces acting on chromosomes and their simultaneous entry into anaphase. Although anaphase onset is controlled by the spindle assembly checkpoint, it remains unknown how spindle forces are uniformly distributed among different chromosomes. In this paper, we show that tension uniformity at metaphase kinetochores and subsequent anaphase synchrony in Drosophila S2 cells are promoted by spindle microtubule flux. These results can be explained by a mechanical model of the spindle where microtubule poleward translocation events associated with flux reflect relaxation of the kinetochore–microtubule interface, which accounts for the redistribution and convergence of kinetochore tensions in a timescale comparable to typical metaphase duration. As predicted by the model, experimental acceleration of mitosis precludes tension equalization and anaphase synchrony. We propose that flux-dependent equalization of kinetochore tensions ensures a timely and uniform maturation of kinetochore–microtubule interfaces necessary for error-free and coordinated segregation of chromosomes in anaphase.
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spelling pubmed-27129982010-01-13 Synchronizing chromosome segregation by flux-dependent force equalization at kinetochores Matos, Irina Pereira, António J. Lince-Faria, Mariana Cameron, Lisa A. Salmon, Edward D. Maiato, Helder J Cell Biol Research Articles The synchronous movement of chromosomes during anaphase ensures their correct inheritance in every cell division. This reflects the uniformity of spindle forces acting on chromosomes and their simultaneous entry into anaphase. Although anaphase onset is controlled by the spindle assembly checkpoint, it remains unknown how spindle forces are uniformly distributed among different chromosomes. In this paper, we show that tension uniformity at metaphase kinetochores and subsequent anaphase synchrony in Drosophila S2 cells are promoted by spindle microtubule flux. These results can be explained by a mechanical model of the spindle where microtubule poleward translocation events associated with flux reflect relaxation of the kinetochore–microtubule interface, which accounts for the redistribution and convergence of kinetochore tensions in a timescale comparable to typical metaphase duration. As predicted by the model, experimental acceleration of mitosis precludes tension equalization and anaphase synchrony. We propose that flux-dependent equalization of kinetochore tensions ensures a timely and uniform maturation of kinetochore–microtubule interfaces necessary for error-free and coordinated segregation of chromosomes in anaphase. The Rockefeller University Press 2009-07-13 /pmc/articles/PMC2712998/ /pubmed/19581410 http://dx.doi.org/10.1083/jcb.200904153 Text en © 2009 Matos 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
Matos, Irina
Pereira, António J.
Lince-Faria, Mariana
Cameron, Lisa A.
Salmon, Edward D.
Maiato, Helder
Synchronizing chromosome segregation by flux-dependent force equalization at kinetochores
title Synchronizing chromosome segregation by flux-dependent force equalization at kinetochores
title_full Synchronizing chromosome segregation by flux-dependent force equalization at kinetochores
title_fullStr Synchronizing chromosome segregation by flux-dependent force equalization at kinetochores
title_full_unstemmed Synchronizing chromosome segregation by flux-dependent force equalization at kinetochores
title_short Synchronizing chromosome segregation by flux-dependent force equalization at kinetochores
title_sort synchronizing chromosome segregation by flux-dependent force equalization at kinetochores
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2712998/
https://www.ncbi.nlm.nih.gov/pubmed/19581410
http://dx.doi.org/10.1083/jcb.200904153
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