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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...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2002
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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. |
format | Text |
id | pubmed-2173107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
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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