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The kinesin Eg5 drives poleward microtubule flux in Xenopus laevis egg extract spindles

Although mitotic and meiotic spindles maintain a steady-state length during metaphase, their antiparallel microtubules slide toward spindle poles at a constant rate. This “poleward flux” of microtubules occurs in many organisms and may provide part of the force for chromosome segregation. We use qua...

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Detalles Bibliográficos
Autores principales: Miyamoto, David T., Perlman, Zachary E., Burbank, Kendra S., Groen, Aaron C., Mitchison, Timothy J.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172449/
https://www.ncbi.nlm.nih.gov/pubmed/15583027
http://dx.doi.org/10.1083/jcb.200407126
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author Miyamoto, David T.
Perlman, Zachary E.
Burbank, Kendra S.
Groen, Aaron C.
Mitchison, Timothy J.
author_facet Miyamoto, David T.
Perlman, Zachary E.
Burbank, Kendra S.
Groen, Aaron C.
Mitchison, Timothy J.
author_sort Miyamoto, David T.
collection PubMed
description Although mitotic and meiotic spindles maintain a steady-state length during metaphase, their antiparallel microtubules slide toward spindle poles at a constant rate. This “poleward flux” of microtubules occurs in many organisms and may provide part of the force for chromosome segregation. We use quantitative image analysis to examine the role of the kinesin Eg5 in poleward flux in metaphase Xenopus laevis egg extract spindles. Pharmacological inhibition of Eg5 results in a dose–responsive slowing of flux, and biochemical depletion of Eg5 significantly decreases the flux rate. Our results suggest that ensembles of nonprocessive Eg5 motors drive flux in metaphase Xenopus extract spindles.
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spelling pubmed-21724492008-03-05 The kinesin Eg5 drives poleward microtubule flux in Xenopus laevis egg extract spindles Miyamoto, David T. Perlman, Zachary E. Burbank, Kendra S. Groen, Aaron C. Mitchison, Timothy J. J Cell Biol Research Articles Although mitotic and meiotic spindles maintain a steady-state length during metaphase, their antiparallel microtubules slide toward spindle poles at a constant rate. This “poleward flux” of microtubules occurs in many organisms and may provide part of the force for chromosome segregation. We use quantitative image analysis to examine the role of the kinesin Eg5 in poleward flux in metaphase Xenopus laevis egg extract spindles. Pharmacological inhibition of Eg5 results in a dose–responsive slowing of flux, and biochemical depletion of Eg5 significantly decreases the flux rate. Our results suggest that ensembles of nonprocessive Eg5 motors drive flux in metaphase Xenopus extract spindles. The Rockefeller University Press 2004-12-06 /pmc/articles/PMC2172449/ /pubmed/15583027 http://dx.doi.org/10.1083/jcb.200407126 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
Miyamoto, David T.
Perlman, Zachary E.
Burbank, Kendra S.
Groen, Aaron C.
Mitchison, Timothy J.
The kinesin Eg5 drives poleward microtubule flux in Xenopus laevis egg extract spindles
title The kinesin Eg5 drives poleward microtubule flux in Xenopus laevis egg extract spindles
title_full The kinesin Eg5 drives poleward microtubule flux in Xenopus laevis egg extract spindles
title_fullStr The kinesin Eg5 drives poleward microtubule flux in Xenopus laevis egg extract spindles
title_full_unstemmed The kinesin Eg5 drives poleward microtubule flux in Xenopus laevis egg extract spindles
title_short The kinesin Eg5 drives poleward microtubule flux in Xenopus laevis egg extract spindles
title_sort kinesin eg5 drives poleward microtubule flux in xenopus laevis egg extract spindles
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172449/
https://www.ncbi.nlm.nih.gov/pubmed/15583027
http://dx.doi.org/10.1083/jcb.200407126
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