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Visualization of dynein-dependent microtubule gliding at the cell cortex: implications for spindle positioning

Dynein motors move along the microtubule (MT) lattice in a processive “walking” manner. In the one-cell Caenorhabditis elegans embryo, dynein is required for spindle-pulling forces during mitosis. Posteriorly directed spindle-pulling forces are higher than anteriorly directed forces, and this imbala...

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Detalles Bibliográficos
Autores principales: Gusnowski, Eva M., Srayko, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3153651/
https://www.ncbi.nlm.nih.gov/pubmed/21825072
http://dx.doi.org/10.1083/jcb.201103128
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author Gusnowski, Eva M.
Srayko, Martin
author_facet Gusnowski, Eva M.
Srayko, Martin
author_sort Gusnowski, Eva M.
collection PubMed
description Dynein motors move along the microtubule (MT) lattice in a processive “walking” manner. In the one-cell Caenorhabditis elegans embryo, dynein is required for spindle-pulling forces during mitosis. Posteriorly directed spindle-pulling forces are higher than anteriorly directed forces, and this imbalance results in posterior spindle displacement during anaphase and an asymmetric division. To address how dynein could be asymmetrically activated to achieve posterior spindle displacement, we developed an assay to measure dynein’s activity on individual MTs at the embryo cortex. Our study reveals that cortical dynein motors maintain a basal level of activity that propels MTs along the cortex, even under experimental conditions that drastically reduce anaphase spindle forces. This suggests that dynein-based MT gliding is not sufficient for anaphase spindle-pulling force. Instead, we find that this form of dynein activity is most prominent during spindle centering in early prophase. We propose a model whereby different dynein–MT interactions are used for specific spindle-positioning tasks in the one-cell embryo.
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spelling pubmed-31536512012-02-08 Visualization of dynein-dependent microtubule gliding at the cell cortex: implications for spindle positioning Gusnowski, Eva M. Srayko, Martin J Cell Biol Research Articles Dynein motors move along the microtubule (MT) lattice in a processive “walking” manner. In the one-cell Caenorhabditis elegans embryo, dynein is required for spindle-pulling forces during mitosis. Posteriorly directed spindle-pulling forces are higher than anteriorly directed forces, and this imbalance results in posterior spindle displacement during anaphase and an asymmetric division. To address how dynein could be asymmetrically activated to achieve posterior spindle displacement, we developed an assay to measure dynein’s activity on individual MTs at the embryo cortex. Our study reveals that cortical dynein motors maintain a basal level of activity that propels MTs along the cortex, even under experimental conditions that drastically reduce anaphase spindle forces. This suggests that dynein-based MT gliding is not sufficient for anaphase spindle-pulling force. Instead, we find that this form of dynein activity is most prominent during spindle centering in early prophase. We propose a model whereby different dynein–MT interactions are used for specific spindle-positioning tasks in the one-cell embryo. The Rockefeller University Press 2011-08-08 /pmc/articles/PMC3153651/ /pubmed/21825072 http://dx.doi.org/10.1083/jcb.201103128 Text en © 2011 Gusnowski and Srayko 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Gusnowski, Eva M.
Srayko, Martin
Visualization of dynein-dependent microtubule gliding at the cell cortex: implications for spindle positioning
title Visualization of dynein-dependent microtubule gliding at the cell cortex: implications for spindle positioning
title_full Visualization of dynein-dependent microtubule gliding at the cell cortex: implications for spindle positioning
title_fullStr Visualization of dynein-dependent microtubule gliding at the cell cortex: implications for spindle positioning
title_full_unstemmed Visualization of dynein-dependent microtubule gliding at the cell cortex: implications for spindle positioning
title_short Visualization of dynein-dependent microtubule gliding at the cell cortex: implications for spindle positioning
title_sort visualization of dynein-dependent microtubule gliding at the cell cortex: implications for spindle positioning
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3153651/
https://www.ncbi.nlm.nih.gov/pubmed/21825072
http://dx.doi.org/10.1083/jcb.201103128
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