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The forces that position a mitotic spindle asymmetrically are tethered until after the time of spindle assembly

Regulation of the mitotic spindle's position is important for cells to divide asymmetrically. Here, we use Caenorhabditis elegans embryos to provide the first analysis of the temporal regulation of forces that asymmetrically position a mitotic spindle. We find that asymmetric pulling forces, re...

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Detalles Bibliográficos
Autores principales: Labbé, Jean-Claude, McCarthy, Erin K., Goldstein, Bob
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172534/
https://www.ncbi.nlm.nih.gov/pubmed/15492042
http://dx.doi.org/10.1083/jcb.200406008
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author Labbé, Jean-Claude
McCarthy, Erin K.
Goldstein, Bob
author_facet Labbé, Jean-Claude
McCarthy, Erin K.
Goldstein, Bob
author_sort Labbé, Jean-Claude
collection PubMed
description Regulation of the mitotic spindle's position is important for cells to divide asymmetrically. Here, we use Caenorhabditis elegans embryos to provide the first analysis of the temporal regulation of forces that asymmetrically position a mitotic spindle. We find that asymmetric pulling forces, regulated by cortical PAR proteins, begin to act as early as prophase and prometaphase, even before the spindle forms and shifts to a posterior position. The spindle does not shift asymmetrically during these early phases due to a tethering force, mediated by astral microtubules that reach the anterior cell cortex. We show that this tether is normally released after spindle assembly and independently of anaphase entry. Monitoring microtubule dynamics by photobleaching segments of microtubules during anaphase revealed that spindle microtubules do not undergo significant poleward flux in C. elegans. Together with the known absence of anaphase A, these data suggest that the major forces contributing to chromosome separation during anaphase originate outside the spindle. We propose that the forces positioning the mitotic spindle asymmetrically are tethered until after the time of spindle assembly and that these same forces are used later to drive chromosome segregation at anaphase.
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spelling pubmed-21725342008-03-05 The forces that position a mitotic spindle asymmetrically are tethered until after the time of spindle assembly Labbé, Jean-Claude McCarthy, Erin K. Goldstein, Bob J Cell Biol Research Articles Regulation of the mitotic spindle's position is important for cells to divide asymmetrically. Here, we use Caenorhabditis elegans embryos to provide the first analysis of the temporal regulation of forces that asymmetrically position a mitotic spindle. We find that asymmetric pulling forces, regulated by cortical PAR proteins, begin to act as early as prophase and prometaphase, even before the spindle forms and shifts to a posterior position. The spindle does not shift asymmetrically during these early phases due to a tethering force, mediated by astral microtubules that reach the anterior cell cortex. We show that this tether is normally released after spindle assembly and independently of anaphase entry. Monitoring microtubule dynamics by photobleaching segments of microtubules during anaphase revealed that spindle microtubules do not undergo significant poleward flux in C. elegans. Together with the known absence of anaphase A, these data suggest that the major forces contributing to chromosome separation during anaphase originate outside the spindle. We propose that the forces positioning the mitotic spindle asymmetrically are tethered until after the time of spindle assembly and that these same forces are used later to drive chromosome segregation at anaphase. The Rockefeller University Press 2004-10-25 /pmc/articles/PMC2172534/ /pubmed/15492042 http://dx.doi.org/10.1083/jcb.200406008 Text en Copyright © 2004, The Rockefeller University Press 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.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Labbé, Jean-Claude
McCarthy, Erin K.
Goldstein, Bob
The forces that position a mitotic spindle asymmetrically are tethered until after the time of spindle assembly
title The forces that position a mitotic spindle asymmetrically are tethered until after the time of spindle assembly
title_full The forces that position a mitotic spindle asymmetrically are tethered until after the time of spindle assembly
title_fullStr The forces that position a mitotic spindle asymmetrically are tethered until after the time of spindle assembly
title_full_unstemmed The forces that position a mitotic spindle asymmetrically are tethered until after the time of spindle assembly
title_short The forces that position a mitotic spindle asymmetrically are tethered until after the time of spindle assembly
title_sort forces that position a mitotic spindle asymmetrically are tethered until after the time of spindle assembly
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172534/
https://www.ncbi.nlm.nih.gov/pubmed/15492042
http://dx.doi.org/10.1083/jcb.200406008
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