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Mechanosignaling between central apparatus and radial spokes controls axonemal dynein activity
Cilia/flagella are conserved organelles that generate fluid flow in eukaryotes. The bending motion of flagella requires concerted activity of dynein motors. Although it has been reported that the central pair apparatus (CP) and radial spokes (RSs) are important for flagellar motility, the molecular...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941055/ https://www.ncbi.nlm.nih.gov/pubmed/24590175 http://dx.doi.org/10.1083/jcb.201312014 |
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author | Oda, Toshiyuki Yanagisawa, Haruaki Yagi, Toshiki Kikkawa, Masahide |
author_facet | Oda, Toshiyuki Yanagisawa, Haruaki Yagi, Toshiki Kikkawa, Masahide |
author_sort | Oda, Toshiyuki |
collection | PubMed |
description | Cilia/flagella are conserved organelles that generate fluid flow in eukaryotes. The bending motion of flagella requires concerted activity of dynein motors. Although it has been reported that the central pair apparatus (CP) and radial spokes (RSs) are important for flagellar motility, the molecular mechanism underlying CP- and RS-mediated dynein regulation has not been identified. In this paper, we identified nonspecific intermolecular collision between CP and RS as one of the regulatory mechanisms for flagellar motility. By combining cryoelectron tomography and motility analyses of Chlamydomonas reinhardtii flagella, we show that binding of streptavidin to RS heads paralyzed flagella. Moreover, the motility defect in a CP projection mutant could be rescued by the addition of exogenous protein tags on RS heads. Genetic experiments demonstrated that outer dynein arms are the major downstream effectors of CP- and RS-mediated regulation of flagellar motility. These results suggest that mechanosignaling between CP and RS regulates dynein activity in eukaryotic flagella. |
format | Online Article Text |
id | pubmed-3941055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39410552014-09-03 Mechanosignaling between central apparatus and radial spokes controls axonemal dynein activity Oda, Toshiyuki Yanagisawa, Haruaki Yagi, Toshiki Kikkawa, Masahide J Cell Biol Research Articles Cilia/flagella are conserved organelles that generate fluid flow in eukaryotes. The bending motion of flagella requires concerted activity of dynein motors. Although it has been reported that the central pair apparatus (CP) and radial spokes (RSs) are important for flagellar motility, the molecular mechanism underlying CP- and RS-mediated dynein regulation has not been identified. In this paper, we identified nonspecific intermolecular collision between CP and RS as one of the regulatory mechanisms for flagellar motility. By combining cryoelectron tomography and motility analyses of Chlamydomonas reinhardtii flagella, we show that binding of streptavidin to RS heads paralyzed flagella. Moreover, the motility defect in a CP projection mutant could be rescued by the addition of exogenous protein tags on RS heads. Genetic experiments demonstrated that outer dynein arms are the major downstream effectors of CP- and RS-mediated regulation of flagellar motility. These results suggest that mechanosignaling between CP and RS regulates dynein activity in eukaryotic flagella. The Rockefeller University Press 2014-03-03 /pmc/articles/PMC3941055/ /pubmed/24590175 http://dx.doi.org/10.1083/jcb.201312014 Text en © 2014 Oda et al. 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Oda, Toshiyuki Yanagisawa, Haruaki Yagi, Toshiki Kikkawa, Masahide Mechanosignaling between central apparatus and radial spokes controls axonemal dynein activity |
title | Mechanosignaling between central apparatus and radial spokes controls axonemal dynein activity |
title_full | Mechanosignaling between central apparatus and radial spokes controls axonemal dynein activity |
title_fullStr | Mechanosignaling between central apparatus and radial spokes controls axonemal dynein activity |
title_full_unstemmed | Mechanosignaling between central apparatus and radial spokes controls axonemal dynein activity |
title_short | Mechanosignaling between central apparatus and radial spokes controls axonemal dynein activity |
title_sort | mechanosignaling between central apparatus and radial spokes controls axonemal dynein activity |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941055/ https://www.ncbi.nlm.nih.gov/pubmed/24590175 http://dx.doi.org/10.1083/jcb.201312014 |
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