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Ensemble and single-molecule dynamics of IFT dynein in Caenorhabditis elegans cilia
Cytoplasmic dyneins drive microtubule-based, minus-end directed transport in eukaryotic cells. Whereas cytoplasmic dynein 1 has been widely studied, IFT dynein has received far less attention. Here, we use fluorescence microscopy of labelled motors in living Caenorhabditis elegans to investigate IFT...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331336/ https://www.ncbi.nlm.nih.gov/pubmed/28230057 http://dx.doi.org/10.1038/ncomms14591 |
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author | Mijalkovic, Jona Prevo, Bram Oswald, Felix Mangeol, Pierre Peterman, Erwin J. G. |
author_facet | Mijalkovic, Jona Prevo, Bram Oswald, Felix Mangeol, Pierre Peterman, Erwin J. G. |
author_sort | Mijalkovic, Jona |
collection | PubMed |
description | Cytoplasmic dyneins drive microtubule-based, minus-end directed transport in eukaryotic cells. Whereas cytoplasmic dynein 1 has been widely studied, IFT dynein has received far less attention. Here, we use fluorescence microscopy of labelled motors in living Caenorhabditis elegans to investigate IFT-dynein motility at the ensemble and single-molecule level. We find that while the kinesin composition of motor ensembles varies along the track, the amount of dynein remains relatively constant. Remarkably, this does not result in directionality changes of cargo along the track, as has been reported for other opposite-polarity, tug-of-war motility systems. At the single-molecule level, IFT-dynein trajectories reveal unexpected dynamics, including diffusion at the base, and pausing and directional switches along the cilium. Stochastic simulations show that the ensemble IFT-dynein distribution depends upon the probability of single-motor directional switches. Our results provide quantitative insight into IFT-dynein dynamics in vivo, shedding light on the complex functioning of dynein motors in general. |
format | Online Article Text |
id | pubmed-5331336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53313362017-03-21 Ensemble and single-molecule dynamics of IFT dynein in Caenorhabditis elegans cilia Mijalkovic, Jona Prevo, Bram Oswald, Felix Mangeol, Pierre Peterman, Erwin J. G. Nat Commun Article Cytoplasmic dyneins drive microtubule-based, minus-end directed transport in eukaryotic cells. Whereas cytoplasmic dynein 1 has been widely studied, IFT dynein has received far less attention. Here, we use fluorescence microscopy of labelled motors in living Caenorhabditis elegans to investigate IFT-dynein motility at the ensemble and single-molecule level. We find that while the kinesin composition of motor ensembles varies along the track, the amount of dynein remains relatively constant. Remarkably, this does not result in directionality changes of cargo along the track, as has been reported for other opposite-polarity, tug-of-war motility systems. At the single-molecule level, IFT-dynein trajectories reveal unexpected dynamics, including diffusion at the base, and pausing and directional switches along the cilium. Stochastic simulations show that the ensemble IFT-dynein distribution depends upon the probability of single-motor directional switches. Our results provide quantitative insight into IFT-dynein dynamics in vivo, shedding light on the complex functioning of dynein motors in general. Nature Publishing Group 2017-02-23 /pmc/articles/PMC5331336/ /pubmed/28230057 http://dx.doi.org/10.1038/ncomms14591 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Mijalkovic, Jona Prevo, Bram Oswald, Felix Mangeol, Pierre Peterman, Erwin J. G. Ensemble and single-molecule dynamics of IFT dynein in Caenorhabditis elegans cilia |
title | Ensemble and single-molecule dynamics of IFT dynein in Caenorhabditis elegans cilia |
title_full | Ensemble and single-molecule dynamics of IFT dynein in Caenorhabditis elegans cilia |
title_fullStr | Ensemble and single-molecule dynamics of IFT dynein in Caenorhabditis elegans cilia |
title_full_unstemmed | Ensemble and single-molecule dynamics of IFT dynein in Caenorhabditis elegans cilia |
title_short | Ensemble and single-molecule dynamics of IFT dynein in Caenorhabditis elegans cilia |
title_sort | ensemble and single-molecule dynamics of ift dynein in caenorhabditis elegans cilia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331336/ https://www.ncbi.nlm.nih.gov/pubmed/28230057 http://dx.doi.org/10.1038/ncomms14591 |
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