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.
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25 September 2006
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September 21 2006
Mechanism of transport of IFT particles in C. elegans cilia by the concerted action of kinesin-II and OSM-3 motors
Xiaoyu Pan,
Xiaoyu Pan
1Section of Molecular and Cellular Biology, Center for Genetics and Development, University of California, Davis, Davis, CA 95616
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Guangshuo Ou,
Guangshuo Ou
1Section of Molecular and Cellular Biology, Center for Genetics and Development, University of California, Davis, Davis, CA 95616
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Gul Civelekoglu-Scholey,
Gul Civelekoglu-Scholey
1Section of Molecular and Cellular Biology, Center for Genetics and Development, University of California, Davis, Davis, CA 95616
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Oliver E. Blacque,
Oliver E. Blacque
2Department of Molecular Biology and Biochemistry, Simon Fraser University, Burnaby, British Columbia V5A 1S6, Canada
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Nicholas F. Endres,
Nicholas F. Endres
3Howard Hughes Medical Institute
4Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94107
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Li Tao,
Li Tao
1Section of Molecular and Cellular Biology, Center for Genetics and Development, University of California, Davis, Davis, CA 95616
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Alex Mogilner,
Alex Mogilner
1Section of Molecular and Cellular Biology, Center for Genetics and Development, University of California, Davis, Davis, CA 95616
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Michel R. Leroux,
Michel R. Leroux
2Department of Molecular Biology and Biochemistry, Simon Fraser University, Burnaby, British Columbia V5A 1S6, Canada
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Ronald D. Vale,
Ronald D. Vale
3Howard Hughes Medical Institute
4Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94107
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Jonathan M. Scholey
Jonathan M. Scholey
1Section of Molecular and Cellular Biology, Center for Genetics and Development, University of California, Davis, Davis, CA 95616
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Xiaoyu Pan
1Section of Molecular and Cellular Biology, Center for Genetics and Development, University of California, Davis, Davis, CA 95616
Guangshuo Ou
1Section of Molecular and Cellular Biology, Center for Genetics and Development, University of California, Davis, Davis, CA 95616
Gul Civelekoglu-Scholey
1Section of Molecular and Cellular Biology, Center for Genetics and Development, University of California, Davis, Davis, CA 95616
Oliver E. Blacque
2Department of Molecular Biology and Biochemistry, Simon Fraser University, Burnaby, British Columbia V5A 1S6, Canada
Nicholas F. Endres
3Howard Hughes Medical Institute
4Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94107
Li Tao
1Section of Molecular and Cellular Biology, Center for Genetics and Development, University of California, Davis, Davis, CA 95616
Alex Mogilner
1Section of Molecular and Cellular Biology, Center for Genetics and Development, University of California, Davis, Davis, CA 95616
Michel R. Leroux
2Department of Molecular Biology and Biochemistry, Simon Fraser University, Burnaby, British Columbia V5A 1S6, Canada
Ronald D. Vale
3Howard Hughes Medical Institute
4Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94107
Jonathan M. Scholey
1Section of Molecular and Cellular Biology, Center for Genetics and Development, University of California, Davis, Davis, CA 95616
Correspondence to Jonathan M. Scholey: [email protected]
X. Pan and G. Ou contributed equally to this paper.
Abbreviations used in this paper: BBS, Bardet-Biedl syndrome; IFT, intraflagellar transport; MT, microtubule.
Received:
June 01 2006
Accepted:
August 25 2006
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2006
J Cell Biol (2006) 174 (7): 1035–1045.
Article history
Received:
June 01 2006
Accepted:
August 25 2006
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Citation
Xiaoyu Pan, Guangshuo Ou, Gul Civelekoglu-Scholey, Oliver E. Blacque, Nicholas F. Endres, Li Tao, Alex Mogilner, Michel R. Leroux, Ronald D. Vale, Jonathan M. Scholey; Mechanism of transport of IFT particles in C. elegans cilia by the concerted action of kinesin-II and OSM-3 motors . J Cell Biol 25 September 2006; 174 (7): 1035–1045. doi: https://doi.org/10.1083/jcb.200606003
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