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Dynamics of the IFT machinery at the ciliary tip
Intraflagellar transport (IFT) is essential for the elongation and maintenance of eukaryotic cilia and flagella. Due to the traffic jam of multiple trains at the ciliary tip, how IFT trains are remodeled in these turnaround zones cannot be determined by conventional imaging. Using PhotoGate, we visu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662288/ https://www.ncbi.nlm.nih.gov/pubmed/28930071 http://dx.doi.org/10.7554/eLife.28606 |
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author | Chien, Alexander Shih, Sheng Min Bower, Raqual Tritschler, Douglas Porter, Mary E Yildiz, Ahmet |
author_facet | Chien, Alexander Shih, Sheng Min Bower, Raqual Tritschler, Douglas Porter, Mary E Yildiz, Ahmet |
author_sort | Chien, Alexander |
collection | PubMed |
description | Intraflagellar transport (IFT) is essential for the elongation and maintenance of eukaryotic cilia and flagella. Due to the traffic jam of multiple trains at the ciliary tip, how IFT trains are remodeled in these turnaround zones cannot be determined by conventional imaging. Using PhotoGate, we visualized the full range of movement of single IFT trains and motors in Chlamydomonas flagella. Anterograde trains split apart and IFT complexes mix with each other at the tip to assemble retrograde trains. Dynein-1b is carried to the tip by kinesin-II as inactive cargo on anterograde trains. Unlike dynein-1b, kinesin-II detaches from IFT trains at the tip and diffuses in flagella. As the flagellum grows longer, diffusion delays return of kinesin-II to the basal body, depleting kinesin-II available for anterograde transport. Our results suggest that dissociation of kinesin-II from IFT trains serves as a negative feedback mechanism that facilitates flagellar length control in Chlamydomonas. |
format | Online Article Text |
id | pubmed-5662288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-56622882017-11-01 Dynamics of the IFT machinery at the ciliary tip Chien, Alexander Shih, Sheng Min Bower, Raqual Tritschler, Douglas Porter, Mary E Yildiz, Ahmet eLife Structural Biology and Molecular Biophysics Intraflagellar transport (IFT) is essential for the elongation and maintenance of eukaryotic cilia and flagella. Due to the traffic jam of multiple trains at the ciliary tip, how IFT trains are remodeled in these turnaround zones cannot be determined by conventional imaging. Using PhotoGate, we visualized the full range of movement of single IFT trains and motors in Chlamydomonas flagella. Anterograde trains split apart and IFT complexes mix with each other at the tip to assemble retrograde trains. Dynein-1b is carried to the tip by kinesin-II as inactive cargo on anterograde trains. Unlike dynein-1b, kinesin-II detaches from IFT trains at the tip and diffuses in flagella. As the flagellum grows longer, diffusion delays return of kinesin-II to the basal body, depleting kinesin-II available for anterograde transport. Our results suggest that dissociation of kinesin-II from IFT trains serves as a negative feedback mechanism that facilitates flagellar length control in Chlamydomonas. eLife Sciences Publications, Ltd 2017-09-20 /pmc/articles/PMC5662288/ /pubmed/28930071 http://dx.doi.org/10.7554/eLife.28606 Text en © 2017, Chien et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Structural Biology and Molecular Biophysics Chien, Alexander Shih, Sheng Min Bower, Raqual Tritschler, Douglas Porter, Mary E Yildiz, Ahmet Dynamics of the IFT machinery at the ciliary tip |
title | Dynamics of the IFT machinery at the ciliary tip |
title_full | Dynamics of the IFT machinery at the ciliary tip |
title_fullStr | Dynamics of the IFT machinery at the ciliary tip |
title_full_unstemmed | Dynamics of the IFT machinery at the ciliary tip |
title_short | Dynamics of the IFT machinery at the ciliary tip |
title_sort | dynamics of the ift machinery at the ciliary tip |
topic | Structural Biology and Molecular Biophysics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662288/ https://www.ncbi.nlm.nih.gov/pubmed/28930071 http://dx.doi.org/10.7554/eLife.28606 |
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