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Control of cytoplasmic dynein force production and processivity by its C-terminal domain
Cytoplasmic dynein is a microtubule motor involved in cargo transport, nuclear migration and cell division. Despite structural conservation of the dynein motor domain from yeast to higher eukaryotes, the extensively studied S. cerevisiae dynein behaves distinctly from mammalian dyneins, which produc...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339881/ https://www.ncbi.nlm.nih.gov/pubmed/25670086 http://dx.doi.org/10.1038/ncomms7206 |
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author | Nicholas, Matthew P. Höök, Peter Brenner, Sibylle Wynne, Caitlin L. Vallee, Richard B. Gennerich, Arne |
author_facet | Nicholas, Matthew P. Höök, Peter Brenner, Sibylle Wynne, Caitlin L. Vallee, Richard B. Gennerich, Arne |
author_sort | Nicholas, Matthew P. |
collection | PubMed |
description | Cytoplasmic dynein is a microtubule motor involved in cargo transport, nuclear migration and cell division. Despite structural conservation of the dynein motor domain from yeast to higher eukaryotes, the extensively studied S. cerevisiae dynein behaves distinctly from mammalian dyneins, which produce far less force and travel over shorter distances. However, isolated reports of yeast-like force production by mammalian dynein have called interspecies differences into question. We report that functional differences between yeast and mammalian dynein are real and attributable to a C-terminal motor element absent in yeast, which resembles a ‘cap’ over the central pore of the mammalian dynein motor domain. Removal of this cap increases the force generation of rat dynein from 1 pN to a yeast-like 6 pN and greatly increases its travel distance. Our findings identify the CT-cap as a novel regulator of dynein function. |
format | Online Article Text |
id | pubmed-4339881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43398812015-03-02 Control of cytoplasmic dynein force production and processivity by its C-terminal domain Nicholas, Matthew P. Höök, Peter Brenner, Sibylle Wynne, Caitlin L. Vallee, Richard B. Gennerich, Arne Nat Commun Article Cytoplasmic dynein is a microtubule motor involved in cargo transport, nuclear migration and cell division. Despite structural conservation of the dynein motor domain from yeast to higher eukaryotes, the extensively studied S. cerevisiae dynein behaves distinctly from mammalian dyneins, which produce far less force and travel over shorter distances. However, isolated reports of yeast-like force production by mammalian dynein have called interspecies differences into question. We report that functional differences between yeast and mammalian dynein are real and attributable to a C-terminal motor element absent in yeast, which resembles a ‘cap’ over the central pore of the mammalian dynein motor domain. Removal of this cap increases the force generation of rat dynein from 1 pN to a yeast-like 6 pN and greatly increases its travel distance. Our findings identify the CT-cap as a novel regulator of dynein function. Nature Pub. Group 2015-02-11 /pmc/articles/PMC4339881/ /pubmed/25670086 http://dx.doi.org/10.1038/ncomms7206 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 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 Nicholas, Matthew P. Höök, Peter Brenner, Sibylle Wynne, Caitlin L. Vallee, Richard B. Gennerich, Arne Control of cytoplasmic dynein force production and processivity by its C-terminal domain |
title | Control of cytoplasmic dynein force production and processivity by its C-terminal domain |
title_full | Control of cytoplasmic dynein force production and processivity by its C-terminal domain |
title_fullStr | Control of cytoplasmic dynein force production and processivity by its C-terminal domain |
title_full_unstemmed | Control of cytoplasmic dynein force production and processivity by its C-terminal domain |
title_short | Control of cytoplasmic dynein force production and processivity by its C-terminal domain |
title_sort | control of cytoplasmic dynein force production and processivity by its c-terminal domain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339881/ https://www.ncbi.nlm.nih.gov/pubmed/25670086 http://dx.doi.org/10.1038/ncomms7206 |
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