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CEP44 ensures the formation of bona fide centriole wall, a requirement for the centriole-to-centrosome conversion
Centrosomes are essential organelles with functions in microtubule organization that duplicate once per cell cycle. The first step of centrosome duplication is the daughter centriole formation followed by the pericentriolar material recruitment to this centriole. This maturation step was termed cent...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7021698/ https://www.ncbi.nlm.nih.gov/pubmed/32060285 http://dx.doi.org/10.1038/s41467-020-14767-2 |
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author | Atorino, Enrico S. Hata, Shoji Funaya, Charlotta Neuner, Annett Schiebel, Elmar |
author_facet | Atorino, Enrico S. Hata, Shoji Funaya, Charlotta Neuner, Annett Schiebel, Elmar |
author_sort | Atorino, Enrico S. |
collection | PubMed |
description | Centrosomes are essential organelles with functions in microtubule organization that duplicate once per cell cycle. The first step of centrosome duplication is the daughter centriole formation followed by the pericentriolar material recruitment to this centriole. This maturation step was termed centriole-to-centrosome conversion. It was proposed that CEP295-dependent recruitment of pericentriolar proteins drives centriole conversion. Here we show, based on the analysis of proteins that promote centriole biogenesis, that the developing centriole structure helps drive centriole conversion. Depletion of the luminal centriole protein CEP44 that binds to the A-microtubules and interacts with POC1B affecting centriole structure and centriole conversion, despite CEP295 binding to centrioles. Impairment of POC1B, TUBE1 or TUBD1, which disturbs integrity of centriole microtubules, also prevents centriole-to-centrosome conversion. We propose that the CEP295, CEP44, POC1B, TUBE1 and TUBD1 centriole biogenesis pathway that functions in the centriole lumen and on the cytoplasmic side is essential for the centriole-to-centrosome conversion. |
format | Online Article Text |
id | pubmed-7021698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70216982020-02-21 CEP44 ensures the formation of bona fide centriole wall, a requirement for the centriole-to-centrosome conversion Atorino, Enrico S. Hata, Shoji Funaya, Charlotta Neuner, Annett Schiebel, Elmar Nat Commun Article Centrosomes are essential organelles with functions in microtubule organization that duplicate once per cell cycle. The first step of centrosome duplication is the daughter centriole formation followed by the pericentriolar material recruitment to this centriole. This maturation step was termed centriole-to-centrosome conversion. It was proposed that CEP295-dependent recruitment of pericentriolar proteins drives centriole conversion. Here we show, based on the analysis of proteins that promote centriole biogenesis, that the developing centriole structure helps drive centriole conversion. Depletion of the luminal centriole protein CEP44 that binds to the A-microtubules and interacts with POC1B affecting centriole structure and centriole conversion, despite CEP295 binding to centrioles. Impairment of POC1B, TUBE1 or TUBD1, which disturbs integrity of centriole microtubules, also prevents centriole-to-centrosome conversion. We propose that the CEP295, CEP44, POC1B, TUBE1 and TUBD1 centriole biogenesis pathway that functions in the centriole lumen and on the cytoplasmic side is essential for the centriole-to-centrosome conversion. Nature Publishing Group UK 2020-02-14 /pmc/articles/PMC7021698/ /pubmed/32060285 http://dx.doi.org/10.1038/s41467-020-14767-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Atorino, Enrico S. Hata, Shoji Funaya, Charlotta Neuner, Annett Schiebel, Elmar CEP44 ensures the formation of bona fide centriole wall, a requirement for the centriole-to-centrosome conversion |
title | CEP44 ensures the formation of bona fide centriole wall, a requirement for the centriole-to-centrosome conversion |
title_full | CEP44 ensures the formation of bona fide centriole wall, a requirement for the centriole-to-centrosome conversion |
title_fullStr | CEP44 ensures the formation of bona fide centriole wall, a requirement for the centriole-to-centrosome conversion |
title_full_unstemmed | CEP44 ensures the formation of bona fide centriole wall, a requirement for the centriole-to-centrosome conversion |
title_short | CEP44 ensures the formation of bona fide centriole wall, a requirement for the centriole-to-centrosome conversion |
title_sort | cep44 ensures the formation of bona fide centriole wall, a requirement for the centriole-to-centrosome conversion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7021698/ https://www.ncbi.nlm.nih.gov/pubmed/32060285 http://dx.doi.org/10.1038/s41467-020-14767-2 |
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