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Balancing the length of the distal tip by septins is key for stability and signalling function of primary cilia
Primary cilia are antenna‐like organelles required for signalling transduction. How cilia structure is mechanistically maintained at steady‐state to promote signalling is largely unknown. Here, we define that mammalian primary cilia axonemes are formed by proximal segment (PS) and distal segment (DS...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8724769/ https://www.ncbi.nlm.nih.gov/pubmed/34981518 http://dx.doi.org/10.15252/embj.2021108843 |
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author | Kanamaru, Taishi Neuner, Annett Kurtulmus, Bahtiyar Pereira, Gislene |
author_facet | Kanamaru, Taishi Neuner, Annett Kurtulmus, Bahtiyar Pereira, Gislene |
author_sort | Kanamaru, Taishi |
collection | PubMed |
description | Primary cilia are antenna‐like organelles required for signalling transduction. How cilia structure is mechanistically maintained at steady‐state to promote signalling is largely unknown. Here, we define that mammalian primary cilia axonemes are formed by proximal segment (PS) and distal segment (DS) delineated by tubulin polyglutamylation‐rich and ‐poor regions, respectively. The analysis of proximal/distal segmentation indicated that perturbations leading to cilia over‐elongation influenced PS or DS length with a different impact on cilia behaviour. We identified septins as novel repressors of DS growth. We show that septins control the localisation of MKS3 and CEP290 required for a functional transition zone (TZ), and the cilia tip accumulation of the microtubule‐capping kinesin KIF7, a cilia‐growth inhibitor. Live‐cell imaging and analysis of sonic‐hedgehog (SHH) signalling activation established that DS over‐extension increased cilia ectocytosis events and decreased SHH activation. Our data underlines the importance of understanding cilia segmentation for length control and cilia‐dependent signalling. |
format | Online Article Text |
id | pubmed-8724769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87247692022-01-13 Balancing the length of the distal tip by septins is key for stability and signalling function of primary cilia Kanamaru, Taishi Neuner, Annett Kurtulmus, Bahtiyar Pereira, Gislene EMBO J Articles Primary cilia are antenna‐like organelles required for signalling transduction. How cilia structure is mechanistically maintained at steady‐state to promote signalling is largely unknown. Here, we define that mammalian primary cilia axonemes are formed by proximal segment (PS) and distal segment (DS) delineated by tubulin polyglutamylation‐rich and ‐poor regions, respectively. The analysis of proximal/distal segmentation indicated that perturbations leading to cilia over‐elongation influenced PS or DS length with a different impact on cilia behaviour. We identified septins as novel repressors of DS growth. We show that septins control the localisation of MKS3 and CEP290 required for a functional transition zone (TZ), and the cilia tip accumulation of the microtubule‐capping kinesin KIF7, a cilia‐growth inhibitor. Live‐cell imaging and analysis of sonic‐hedgehog (SHH) signalling activation established that DS over‐extension increased cilia ectocytosis events and decreased SHH activation. Our data underlines the importance of understanding cilia segmentation for length control and cilia‐dependent signalling. John Wiley and Sons Inc. 2021-11-22 2022-01-04 /pmc/articles/PMC8724769/ /pubmed/34981518 http://dx.doi.org/10.15252/embj.2021108843 Text en © 2021 The Authors Published under the terms of the CC BY NC ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Articles Kanamaru, Taishi Neuner, Annett Kurtulmus, Bahtiyar Pereira, Gislene Balancing the length of the distal tip by septins is key for stability and signalling function of primary cilia |
title | Balancing the length of the distal tip by septins is key for stability and signalling function of primary cilia |
title_full | Balancing the length of the distal tip by septins is key for stability and signalling function of primary cilia |
title_fullStr | Balancing the length of the distal tip by septins is key for stability and signalling function of primary cilia |
title_full_unstemmed | Balancing the length of the distal tip by septins is key for stability and signalling function of primary cilia |
title_short | Balancing the length of the distal tip by septins is key for stability and signalling function of primary cilia |
title_sort | balancing the length of the distal tip by septins is key for stability and signalling function of primary cilia |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8724769/ https://www.ncbi.nlm.nih.gov/pubmed/34981518 http://dx.doi.org/10.15252/embj.2021108843 |
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