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Mechanism of transport of IFT particles in C. elegans cilia by the concerted action of kinesin-II and OSM-3 motors
The assembly and function of cilia on Caenorhabditis elegans neurons depends on the action of two kinesin-2 motors, heterotrimeric kinesin-II and homodimeric OSM-3–kinesin, which cooperate to move the same intraflagellar transport (IFT) particles along microtubule (MT) doublets. Using competitive in...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064394/ https://www.ncbi.nlm.nih.gov/pubmed/17000880 http://dx.doi.org/10.1083/jcb.200606003 |
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author | Pan, Xiaoyu Ou, Guangshuo Civelekoglu-Scholey, Gul Blacque, Oliver E. Endres, Nicholas F. Tao, Li Mogilner, Alex Leroux, Michel R. Vale, Ronald D. Scholey, Jonathan M. |
author_facet | Pan, Xiaoyu Ou, Guangshuo Civelekoglu-Scholey, Gul Blacque, Oliver E. Endres, Nicholas F. Tao, Li Mogilner, Alex Leroux, Michel R. Vale, Ronald D. Scholey, Jonathan M. |
author_sort | Pan, Xiaoyu |
collection | PubMed |
description | The assembly and function of cilia on Caenorhabditis elegans neurons depends on the action of two kinesin-2 motors, heterotrimeric kinesin-II and homodimeric OSM-3–kinesin, which cooperate to move the same intraflagellar transport (IFT) particles along microtubule (MT) doublets. Using competitive in vitro MT gliding assays, we show that purified kinesin-II and OSM-3 cooperate to generate movement similar to that seen along the cilium in the absence of any additional regulatory factors. Quantitative modeling suggests that this could reflect an alternating action mechanism, in which the motors take turns to move along MTs, or a mechanical competition, in which the motors function in a concerted fashion to move along MTs with the slow motor exerting drag on the fast motor and vice versa. In vivo transport assays performed in Bardet-Biedl syndrome (BBS) protein and IFT motor mutants favor a mechanical competition model for motor coordination in which the IFT motors exert a BBS protein–dependent tension on IFT particles, which controls the IFT pathway that builds the cilium foundation. |
format | Text |
id | pubmed-2064394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-20643942007-11-29 Mechanism of transport of IFT particles in C. elegans cilia by the concerted action of kinesin-II and OSM-3 motors Pan, Xiaoyu Ou, Guangshuo Civelekoglu-Scholey, Gul Blacque, Oliver E. Endres, Nicholas F. Tao, Li Mogilner, Alex Leroux, Michel R. Vale, Ronald D. Scholey, Jonathan M. J Cell Biol Research Articles The assembly and function of cilia on Caenorhabditis elegans neurons depends on the action of two kinesin-2 motors, heterotrimeric kinesin-II and homodimeric OSM-3–kinesin, which cooperate to move the same intraflagellar transport (IFT) particles along microtubule (MT) doublets. Using competitive in vitro MT gliding assays, we show that purified kinesin-II and OSM-3 cooperate to generate movement similar to that seen along the cilium in the absence of any additional regulatory factors. Quantitative modeling suggests that this could reflect an alternating action mechanism, in which the motors take turns to move along MTs, or a mechanical competition, in which the motors function in a concerted fashion to move along MTs with the slow motor exerting drag on the fast motor and vice versa. In vivo transport assays performed in Bardet-Biedl syndrome (BBS) protein and IFT motor mutants favor a mechanical competition model for motor coordination in which the IFT motors exert a BBS protein–dependent tension on IFT particles, which controls the IFT pathway that builds the cilium foundation. The Rockefeller University Press 2006-09-25 /pmc/articles/PMC2064394/ /pubmed/17000880 http://dx.doi.org/10.1083/jcb.200606003 Text en Copyright © 2006, 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 | Research Articles Pan, Xiaoyu Ou, Guangshuo Civelekoglu-Scholey, Gul Blacque, Oliver E. Endres, Nicholas F. Tao, Li Mogilner, Alex Leroux, Michel R. Vale, Ronald D. Scholey, Jonathan M. Mechanism of transport of IFT particles in C. elegans cilia by the concerted action of kinesin-II and OSM-3 motors |
title | Mechanism of transport of IFT particles in C. elegans cilia by the concerted action of kinesin-II and OSM-3 motors |
title_full | Mechanism of transport of IFT particles in C. elegans cilia by the concerted action of kinesin-II and OSM-3 motors |
title_fullStr | Mechanism of transport of IFT particles in C. elegans cilia by the concerted action of kinesin-II and OSM-3 motors |
title_full_unstemmed | Mechanism of transport of IFT particles in C. elegans cilia by the concerted action of kinesin-II and OSM-3 motors |
title_short | Mechanism of transport of IFT particles in C. elegans cilia by the concerted action of kinesin-II and OSM-3 motors |
title_sort | mechanism of transport of ift particles in c. elegans cilia by the concerted action of kinesin-ii and osm-3 motors |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064394/ https://www.ncbi.nlm.nih.gov/pubmed/17000880 http://dx.doi.org/10.1083/jcb.200606003 |
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