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Ubiquitin-proteasome system controls ciliogenesis at the initial step of axoneme extension

Primary cilia are microtubule-based sensory organelles that organize numerous key signals during developments and tissue homeostasis. Ciliary microtubule doublet, named axoneme, is grown directly from the distal end of mother centrioles through a multistep process upon cell cycle exit; however, the...

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Autores principales: Kasahara, Kousuke, Kawakami, Yoshitaka, Kiyono, Tohru, Yonemura, Shigenobu, Kawamura, Yoshifumi, Era, Saho, Matsuzaki, Fumio, Goshima, Naoki, Inagaki, Masaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2014
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4205846/
https://www.ncbi.nlm.nih.gov/pubmed/25270598
http://dx.doi.org/10.1038/ncomms6081
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author Kasahara, Kousuke
Kawakami, Yoshitaka
Kiyono, Tohru
Yonemura, Shigenobu
Kawamura, Yoshifumi
Era, Saho
Matsuzaki, Fumio
Goshima, Naoki
Inagaki, Masaki
author_facet Kasahara, Kousuke
Kawakami, Yoshitaka
Kiyono, Tohru
Yonemura, Shigenobu
Kawamura, Yoshifumi
Era, Saho
Matsuzaki, Fumio
Goshima, Naoki
Inagaki, Masaki
author_sort Kasahara, Kousuke
collection PubMed
description Primary cilia are microtubule-based sensory organelles that organize numerous key signals during developments and tissue homeostasis. Ciliary microtubule doublet, named axoneme, is grown directly from the distal end of mother centrioles through a multistep process upon cell cycle exit; however, the instructive signals that initiate these events are poorly understood. Here we show that ubiquitin-proteasome machinery removes trichoplein, a negative regulator of ciliogenesis, from mother centrioles and thereby causes Aurora-A inactivation, leading to ciliogenesis. Ciliogenesis is blocked if centriolar trichoplein is stabilized by treatment with proteasome inhibitors or by expression of non-ubiquitylatable trichoplein mutant (K50/57R). Started from two-stepped global E3 screening, we have identified KCTD17 as a substrate-adaptor for Cul3-RING E3 ligases (CRL3s) that polyubiquitylates trichoplein. Depletion of KCTD17 specifically arrests ciliogenesis at the initial step of axoneme extension through aberrant trichoplein-Aurora-A activity. Thus, CRL3-KCTD17 targets trichoplein to proteolysis to initiate the axoneme extension during ciliogenesis.
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spelling pubmed-42058462014-10-27 Ubiquitin-proteasome system controls ciliogenesis at the initial step of axoneme extension Kasahara, Kousuke Kawakami, Yoshitaka Kiyono, Tohru Yonemura, Shigenobu Kawamura, Yoshifumi Era, Saho Matsuzaki, Fumio Goshima, Naoki Inagaki, Masaki Nat Commun Article Primary cilia are microtubule-based sensory organelles that organize numerous key signals during developments and tissue homeostasis. Ciliary microtubule doublet, named axoneme, is grown directly from the distal end of mother centrioles through a multistep process upon cell cycle exit; however, the instructive signals that initiate these events are poorly understood. Here we show that ubiquitin-proteasome machinery removes trichoplein, a negative regulator of ciliogenesis, from mother centrioles and thereby causes Aurora-A inactivation, leading to ciliogenesis. Ciliogenesis is blocked if centriolar trichoplein is stabilized by treatment with proteasome inhibitors or by expression of non-ubiquitylatable trichoplein mutant (K50/57R). Started from two-stepped global E3 screening, we have identified KCTD17 as a substrate-adaptor for Cul3-RING E3 ligases (CRL3s) that polyubiquitylates trichoplein. Depletion of KCTD17 specifically arrests ciliogenesis at the initial step of axoneme extension through aberrant trichoplein-Aurora-A activity. Thus, CRL3-KCTD17 targets trichoplein to proteolysis to initiate the axoneme extension during ciliogenesis. Nature Pub. Group 2014-10-01 /pmc/articles/PMC4205846/ /pubmed/25270598 http://dx.doi.org/10.1038/ncomms6081 Text en Copyright © 2014, 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
Kasahara, Kousuke
Kawakami, Yoshitaka
Kiyono, Tohru
Yonemura, Shigenobu
Kawamura, Yoshifumi
Era, Saho
Matsuzaki, Fumio
Goshima, Naoki
Inagaki, Masaki
Ubiquitin-proteasome system controls ciliogenesis at the initial step of axoneme extension
title Ubiquitin-proteasome system controls ciliogenesis at the initial step of axoneme extension
title_full Ubiquitin-proteasome system controls ciliogenesis at the initial step of axoneme extension
title_fullStr Ubiquitin-proteasome system controls ciliogenesis at the initial step of axoneme extension
title_full_unstemmed Ubiquitin-proteasome system controls ciliogenesis at the initial step of axoneme extension
title_short Ubiquitin-proteasome system controls ciliogenesis at the initial step of axoneme extension
title_sort ubiquitin-proteasome system controls ciliogenesis at the initial step of axoneme extension
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4205846/
https://www.ncbi.nlm.nih.gov/pubmed/25270598
http://dx.doi.org/10.1038/ncomms6081
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