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Fifty years of microtubule sliding in cilia

Motility of cilia (also known as flagella in some eukaryotes) is based on axonemal doublet microtubule sliding that is driven by the dynein molecular motors. Dyneins are organized into intricately patterned inner and outer rows of arms, whose collective activity is to produce inter-microtubule movem...

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Autores principales: King, Stephen M., Sale, Winfield S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003218/
https://www.ncbi.nlm.nih.gov/pubmed/29535180
http://dx.doi.org/10.1091/mbc.E17-07-0483
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author King, Stephen M.
Sale, Winfield S.
author_facet King, Stephen M.
Sale, Winfield S.
author_sort King, Stephen M.
collection PubMed
description Motility of cilia (also known as flagella in some eukaryotes) is based on axonemal doublet microtubule sliding that is driven by the dynein molecular motors. Dyneins are organized into intricately patterned inner and outer rows of arms, whose collective activity is to produce inter-microtubule movement. However, to generate a ciliary bend, not all dyneins can be active simultaneously. The switch point model accounts, in part, for how dynein motors are regulated during ciliary movement. On the basis of this model, supported by key direct experimental observations as well as more recent theoretical and structural studies, we are now poised to understand the mechanics of how ciliary dynein coordination controls axonemal bend formation and propagation.
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spelling pubmed-60032182018-06-20 Fifty years of microtubule sliding in cilia King, Stephen M. Sale, Winfield S. Mol Biol Cell Retrospective Motility of cilia (also known as flagella in some eukaryotes) is based on axonemal doublet microtubule sliding that is driven by the dynein molecular motors. Dyneins are organized into intricately patterned inner and outer rows of arms, whose collective activity is to produce inter-microtubule movement. However, to generate a ciliary bend, not all dyneins can be active simultaneously. The switch point model accounts, in part, for how dynein motors are regulated during ciliary movement. On the basis of this model, supported by key direct experimental observations as well as more recent theoretical and structural studies, we are now poised to understand the mechanics of how ciliary dynein coordination controls axonemal bend formation and propagation. The American Society for Cell Biology 2018-03-15 /pmc/articles/PMC6003218/ /pubmed/29535180 http://dx.doi.org/10.1091/mbc.E17-07-0483 Text en © 2018 King and Sale. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. http://creativecommons.org/licenses/by-nc-sa/3.0/ 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.
spellingShingle Retrospective
King, Stephen M.
Sale, Winfield S.
Fifty years of microtubule sliding in cilia
title Fifty years of microtubule sliding in cilia
title_full Fifty years of microtubule sliding in cilia
title_fullStr Fifty years of microtubule sliding in cilia
title_full_unstemmed Fifty years of microtubule sliding in cilia
title_short Fifty years of microtubule sliding in cilia
title_sort fifty years of microtubule sliding in cilia
topic Retrospective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003218/
https://www.ncbi.nlm.nih.gov/pubmed/29535180
http://dx.doi.org/10.1091/mbc.E17-07-0483
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