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Activation of myosin V–based motility and F-actin–dependent network formation of endoplasmic reticulum during mitosis

It is widely believed that microtubule- and F-actin–based transport of cytoplasmic organelles and membrane fusion is down-regulated during mitosis. Here we show that during the transition of Xenopus egg extracts from interphase to metaphase myosin V–driven movement of small globular vesicles along F...

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Detalles Bibliográficos
Autores principales: Wöllert, Torsten, Weiss, Dieter G., Gerdes, Hans-Hermann, Kuznetsov, Sergei A.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173107/
https://www.ncbi.nlm.nih.gov/pubmed/12438410
http://dx.doi.org/10.1083/jcb.200204065
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author Wöllert, Torsten
Weiss, Dieter G.
Gerdes, Hans-Hermann
Kuznetsov, Sergei A.
author_facet Wöllert, Torsten
Weiss, Dieter G.
Gerdes, Hans-Hermann
Kuznetsov, Sergei A.
author_sort Wöllert, Torsten
collection PubMed
description It is widely believed that microtubule- and F-actin–based transport of cytoplasmic organelles and membrane fusion is down-regulated during mitosis. Here we show that during the transition of Xenopus egg extracts from interphase to metaphase myosin V–driven movement of small globular vesicles along F-actin is strongly inhibited. In contrast, the movement of ER and ER network formation on F-actin is up-regulated in metaphase extracts. Our data demonstrate that myosin V–driven motility of distinct organelles is differently controlled during the cell cycle and suggest an active role of F-actin in partitioning, positioning, and membrane fusion of the ER during cell division.
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spelling pubmed-21731072008-05-01 Activation of myosin V–based motility and F-actin–dependent network formation of endoplasmic reticulum during mitosis Wöllert, Torsten Weiss, Dieter G. Gerdes, Hans-Hermann Kuznetsov, Sergei A. J Cell Biol Report It is widely believed that microtubule- and F-actin–based transport of cytoplasmic organelles and membrane fusion is down-regulated during mitosis. Here we show that during the transition of Xenopus egg extracts from interphase to metaphase myosin V–driven movement of small globular vesicles along F-actin is strongly inhibited. In contrast, the movement of ER and ER network formation on F-actin is up-regulated in metaphase extracts. Our data demonstrate that myosin V–driven motility of distinct organelles is differently controlled during the cell cycle and suggest an active role of F-actin in partitioning, positioning, and membrane fusion of the ER during cell division. The Rockefeller University Press 2002-11-25 /pmc/articles/PMC2173107/ /pubmed/12438410 http://dx.doi.org/10.1083/jcb.200204065 Text en Copyright © 2002, 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 Report
Wöllert, Torsten
Weiss, Dieter G.
Gerdes, Hans-Hermann
Kuznetsov, Sergei A.
Activation of myosin V–based motility and F-actin–dependent network formation of endoplasmic reticulum during mitosis
title Activation of myosin V–based motility and F-actin–dependent network formation of endoplasmic reticulum during mitosis
title_full Activation of myosin V–based motility and F-actin–dependent network formation of endoplasmic reticulum during mitosis
title_fullStr Activation of myosin V–based motility and F-actin–dependent network formation of endoplasmic reticulum during mitosis
title_full_unstemmed Activation of myosin V–based motility and F-actin–dependent network formation of endoplasmic reticulum during mitosis
title_short Activation of myosin V–based motility and F-actin–dependent network formation of endoplasmic reticulum during mitosis
title_sort activation of myosin v–based motility and f-actin–dependent network formation of endoplasmic reticulum during mitosis
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173107/
https://www.ncbi.nlm.nih.gov/pubmed/12438410
http://dx.doi.org/10.1083/jcb.200204065
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