Cargando…

α-Actinin and fimbrin cooperate with myosin II to organize actomyosin bundles during contractile-ring assembly

The actomyosin contractile ring assembles through the condensation of a broad band of nodes that forms at the cell equator in fission yeast cytokinesis. The condensation process depends on actin filaments that interconnect nodes. By mutating or titrating actin cross-linkers α-actinin Ain1 and fimbri...

Descripción completa

Detalles Bibliográficos
Autores principales: Laporte, Damien, Ojkic, Nikola, Vavylonis, Dimitrios, Wu, Jian-Qiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3418305/
https://www.ncbi.nlm.nih.gov/pubmed/22740629
http://dx.doi.org/10.1091/mbc.E12-02-0123
_version_ 1782240631329914880
author Laporte, Damien
Ojkic, Nikola
Vavylonis, Dimitrios
Wu, Jian-Qiu
author_facet Laporte, Damien
Ojkic, Nikola
Vavylonis, Dimitrios
Wu, Jian-Qiu
author_sort Laporte, Damien
collection PubMed
description The actomyosin contractile ring assembles through the condensation of a broad band of nodes that forms at the cell equator in fission yeast cytokinesis. The condensation process depends on actin filaments that interconnect nodes. By mutating or titrating actin cross-linkers α-actinin Ain1 and fimbrin Fim1 in live cells, we reveal that both proteins are involved in node condensation. Ain1 and Fim1 stabilize the actin cytoskeleton and modulate node movement, which prevents nodes and linear structures from aggregating into clumps and allows normal ring formation. Our computer simulations modeling actin filaments as semiflexible polymers reproduce the experimental observations and provide a model of how actin cross-linkers work with other proteins to regulate actin-filament orientations inside actin bundles and organize the actin network. As predicted by the simulations, doubling myosin II Myo2 level rescues the node condensation defects caused by Ain1 overexpression. Taken together, our work supports a cooperative process of ring self-organization driven by the interaction between actin filaments and myosin II, which is progressively stabilized by the cross-linking proteins.
format Online
Article
Text
id pubmed-3418305
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher The American Society for Cell Biology
record_format MEDLINE/PubMed
spelling pubmed-34183052012-10-30 α-Actinin and fimbrin cooperate with myosin II to organize actomyosin bundles during contractile-ring assembly Laporte, Damien Ojkic, Nikola Vavylonis, Dimitrios Wu, Jian-Qiu Mol Biol Cell Articles The actomyosin contractile ring assembles through the condensation of a broad band of nodes that forms at the cell equator in fission yeast cytokinesis. The condensation process depends on actin filaments that interconnect nodes. By mutating or titrating actin cross-linkers α-actinin Ain1 and fimbrin Fim1 in live cells, we reveal that both proteins are involved in node condensation. Ain1 and Fim1 stabilize the actin cytoskeleton and modulate node movement, which prevents nodes and linear structures from aggregating into clumps and allows normal ring formation. Our computer simulations modeling actin filaments as semiflexible polymers reproduce the experimental observations and provide a model of how actin cross-linkers work with other proteins to regulate actin-filament orientations inside actin bundles and organize the actin network. As predicted by the simulations, doubling myosin II Myo2 level rescues the node condensation defects caused by Ain1 overexpression. Taken together, our work supports a cooperative process of ring self-organization driven by the interaction between actin filaments and myosin II, which is progressively stabilized by the cross-linking proteins. The American Society for Cell Biology 2012-08-15 /pmc/articles/PMC3418305/ /pubmed/22740629 http://dx.doi.org/10.1091/mbc.E12-02-0123 Text en © 2012 Laporte et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell BD; are registered trademarks of The American Society of Cell Biology.
spellingShingle Articles
Laporte, Damien
Ojkic, Nikola
Vavylonis, Dimitrios
Wu, Jian-Qiu
α-Actinin and fimbrin cooperate with myosin II to organize actomyosin bundles during contractile-ring assembly
title α-Actinin and fimbrin cooperate with myosin II to organize actomyosin bundles during contractile-ring assembly
title_full α-Actinin and fimbrin cooperate with myosin II to organize actomyosin bundles during contractile-ring assembly
title_fullStr α-Actinin and fimbrin cooperate with myosin II to organize actomyosin bundles during contractile-ring assembly
title_full_unstemmed α-Actinin and fimbrin cooperate with myosin II to organize actomyosin bundles during contractile-ring assembly
title_short α-Actinin and fimbrin cooperate with myosin II to organize actomyosin bundles during contractile-ring assembly
title_sort α-actinin and fimbrin cooperate with myosin ii to organize actomyosin bundles during contractile-ring assembly
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3418305/
https://www.ncbi.nlm.nih.gov/pubmed/22740629
http://dx.doi.org/10.1091/mbc.E12-02-0123
work_keys_str_mv AT laportedamien aactininandfimbrincooperatewithmyosiniitoorganizeactomyosinbundlesduringcontractileringassembly
AT ojkicnikola aactininandfimbrincooperatewithmyosiniitoorganizeactomyosinbundlesduringcontractileringassembly
AT vavylonisdimitrios aactininandfimbrincooperatewithmyosiniitoorganizeactomyosinbundlesduringcontractileringassembly
AT wujianqiu aactininandfimbrincooperatewithmyosiniitoorganizeactomyosinbundlesduringcontractileringassembly