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The CP110-interacting proteins Talpid3 and Cep290 play overlapping and distinct roles in cilia assembly
We have identified Talpid3/KIAA0586 as a component of a CP110-containing protein complex important for centrosome and cilia function. Talpid3 assembles a ring-like structure at the extreme distal end of centrioles. Ablation of Talpid3 resulted in an aberrant distribution of centriolar satellites inv...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897186/ https://www.ncbi.nlm.nih.gov/pubmed/24421332 http://dx.doi.org/10.1083/jcb.201304153 |
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author | Kobayashi, Tetsuo Kim, Sehyun Lin, Yu-Chun Inoue, Takanari Dynlacht, Brian David |
author_facet | Kobayashi, Tetsuo Kim, Sehyun Lin, Yu-Chun Inoue, Takanari Dynlacht, Brian David |
author_sort | Kobayashi, Tetsuo |
collection | PubMed |
description | We have identified Talpid3/KIAA0586 as a component of a CP110-containing protein complex important for centrosome and cilia function. Talpid3 assembles a ring-like structure at the extreme distal end of centrioles. Ablation of Talpid3 resulted in an aberrant distribution of centriolar satellites involved in protein trafficking to centrosomes as well as cilia assembly defects, reminiscent of loss of Cep290, another CP110-associated protein. Talpid3 depletion also led to mislocalization of Rab8a, a small GTPase thought to be essential for ciliary vesicle formation. Expression of activated Rab8a suppressed cilia assembly defects provoked by Talpid3 depletion, suggesting that Talpid3 affects cilia formation through Rab8a recruitment and/or activation. Remarkably, ultrastructural analyses showed that Talpid3 is required for centriolar satellite dispersal, which precedes the formation of mature ciliary vesicles, a process requiring Cep290. These studies suggest that Talpid3 and Cep290 play overlapping and distinct roles in ciliary vesicle formation through regulation of centriolar satellite accretion and Rab8a. |
format | Online Article Text |
id | pubmed-3897186 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38971862014-07-20 The CP110-interacting proteins Talpid3 and Cep290 play overlapping and distinct roles in cilia assembly Kobayashi, Tetsuo Kim, Sehyun Lin, Yu-Chun Inoue, Takanari Dynlacht, Brian David J Cell Biol Research Articles We have identified Talpid3/KIAA0586 as a component of a CP110-containing protein complex important for centrosome and cilia function. Talpid3 assembles a ring-like structure at the extreme distal end of centrioles. Ablation of Talpid3 resulted in an aberrant distribution of centriolar satellites involved in protein trafficking to centrosomes as well as cilia assembly defects, reminiscent of loss of Cep290, another CP110-associated protein. Talpid3 depletion also led to mislocalization of Rab8a, a small GTPase thought to be essential for ciliary vesicle formation. Expression of activated Rab8a suppressed cilia assembly defects provoked by Talpid3 depletion, suggesting that Talpid3 affects cilia formation through Rab8a recruitment and/or activation. Remarkably, ultrastructural analyses showed that Talpid3 is required for centriolar satellite dispersal, which precedes the formation of mature ciliary vesicles, a process requiring Cep290. These studies suggest that Talpid3 and Cep290 play overlapping and distinct roles in ciliary vesicle formation through regulation of centriolar satellite accretion and Rab8a. The Rockefeller University Press 2014-01-20 /pmc/articles/PMC3897186/ /pubmed/24421332 http://dx.doi.org/10.1083/jcb.201304153 Text en © 2014 Kobayashi 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 Kobayashi, Tetsuo Kim, Sehyun Lin, Yu-Chun Inoue, Takanari Dynlacht, Brian David The CP110-interacting proteins Talpid3 and Cep290 play overlapping and distinct roles in cilia assembly |
title | The CP110-interacting proteins Talpid3 and Cep290 play overlapping and distinct roles in cilia assembly |
title_full | The CP110-interacting proteins Talpid3 and Cep290 play overlapping and distinct roles in cilia assembly |
title_fullStr | The CP110-interacting proteins Talpid3 and Cep290 play overlapping and distinct roles in cilia assembly |
title_full_unstemmed | The CP110-interacting proteins Talpid3 and Cep290 play overlapping and distinct roles in cilia assembly |
title_short | The CP110-interacting proteins Talpid3 and Cep290 play overlapping and distinct roles in cilia assembly |
title_sort | cp110-interacting proteins talpid3 and cep290 play overlapping and distinct roles in cilia assembly |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897186/ https://www.ncbi.nlm.nih.gov/pubmed/24421332 http://dx.doi.org/10.1083/jcb.201304153 |
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