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Asymmetrically localized proteins stabilize basal bodies against ciliary beating forces
Basal bodies are radially symmetric, microtubule-rich structures that nucleate and anchor motile cilia. Ciliary beating produces asymmetric mechanical forces that are resisted by basal bodies. To resist these forces, distinct regions within the basal body ultrastructure and the microtubules themselv...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5119938/ https://www.ncbi.nlm.nih.gov/pubmed/27807131 http://dx.doi.org/10.1083/jcb.201604135 |
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author | Bayless, Brian A. Galati, Domenico F. Junker, Anthony D. Backer, Chelsea B. Gaertig, Jacek Pearson, Chad G. |
author_facet | Bayless, Brian A. Galati, Domenico F. Junker, Anthony D. Backer, Chelsea B. Gaertig, Jacek Pearson, Chad G. |
author_sort | Bayless, Brian A. |
collection | PubMed |
description | Basal bodies are radially symmetric, microtubule-rich structures that nucleate and anchor motile cilia. Ciliary beating produces asymmetric mechanical forces that are resisted by basal bodies. To resist these forces, distinct regions within the basal body ultrastructure and the microtubules themselves must be stable. However, the molecular components that stabilize basal bodies remain poorly defined. Here, we determine that Fop1 functionally interacts with the established basal body stability components Bld10 and Poc1. We find that Fop1 and microtubule glutamylation incorporate into basal bodies at distinct stages of assembly, culminating in their asymmetric enrichment at specific triplet microtubule regions that are predicted to experience the greatest mechanical force from ciliary beating. Both Fop1 and microtubule glutamylation are required to stabilize basal bodies against ciliary beating forces. Our studies reveal that microtubule glutamylation and Bld10, Poc1, and Fop1 stabilize basal bodies against the forces produced by ciliary beating via distinct yet interdependent mechanisms. |
format | Online Article Text |
id | pubmed-5119938 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-51199382017-05-21 Asymmetrically localized proteins stabilize basal bodies against ciliary beating forces Bayless, Brian A. Galati, Domenico F. Junker, Anthony D. Backer, Chelsea B. Gaertig, Jacek Pearson, Chad G. J Cell Biol Research Articles Basal bodies are radially symmetric, microtubule-rich structures that nucleate and anchor motile cilia. Ciliary beating produces asymmetric mechanical forces that are resisted by basal bodies. To resist these forces, distinct regions within the basal body ultrastructure and the microtubules themselves must be stable. However, the molecular components that stabilize basal bodies remain poorly defined. Here, we determine that Fop1 functionally interacts with the established basal body stability components Bld10 and Poc1. We find that Fop1 and microtubule glutamylation incorporate into basal bodies at distinct stages of assembly, culminating in their asymmetric enrichment at specific triplet microtubule regions that are predicted to experience the greatest mechanical force from ciliary beating. Both Fop1 and microtubule glutamylation are required to stabilize basal bodies against ciliary beating forces. Our studies reveal that microtubule glutamylation and Bld10, Poc1, and Fop1 stabilize basal bodies against the forces produced by ciliary beating via distinct yet interdependent mechanisms. The Rockefeller University Press 2016-11-21 /pmc/articles/PMC5119938/ /pubmed/27807131 http://dx.doi.org/10.1083/jcb.201604135 Text en © 2016 Bayless et al. 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Bayless, Brian A. Galati, Domenico F. Junker, Anthony D. Backer, Chelsea B. Gaertig, Jacek Pearson, Chad G. Asymmetrically localized proteins stabilize basal bodies against ciliary beating forces |
title | Asymmetrically localized proteins stabilize basal bodies against ciliary beating forces |
title_full | Asymmetrically localized proteins stabilize basal bodies against ciliary beating forces |
title_fullStr | Asymmetrically localized proteins stabilize basal bodies against ciliary beating forces |
title_full_unstemmed | Asymmetrically localized proteins stabilize basal bodies against ciliary beating forces |
title_short | Asymmetrically localized proteins stabilize basal bodies against ciliary beating forces |
title_sort | asymmetrically localized proteins stabilize basal bodies against ciliary beating forces |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5119938/ https://www.ncbi.nlm.nih.gov/pubmed/27807131 http://dx.doi.org/10.1083/jcb.201604135 |
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