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The conversion of centrioles to centrosomes: essential coupling of duplication with segregation
Centrioles are self-reproducing organelles that form the core structure of centrosomes or microtubule-organizing centers (MTOCs). However, whether duplication and MTOC organization reflect innate activities of centrioles or activities acquired conditionally is unclear. In this paper, we show that ne...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166877/ https://www.ncbi.nlm.nih.gov/pubmed/21576395 http://dx.doi.org/10.1083/jcb.201101109 |
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author | Wang, Won-Jing Soni, Rajesh Kumar Uryu, Kunihiro Bryan Tsou, Meng-Fu |
author_facet | Wang, Won-Jing Soni, Rajesh Kumar Uryu, Kunihiro Bryan Tsou, Meng-Fu |
author_sort | Wang, Won-Jing |
collection | PubMed |
description | Centrioles are self-reproducing organelles that form the core structure of centrosomes or microtubule-organizing centers (MTOCs). However, whether duplication and MTOC organization reflect innate activities of centrioles or activities acquired conditionally is unclear. In this paper, we show that newly formed full-length centrioles had no inherent capacity to duplicate or to organize pericentriolar material (PCM) but acquired both after mitosis through a Plk1-dependent modification that occurred in early mitosis. Modified centrioles initiated PCM recruitment in G1 and segregated equally in mitosis through association with spindle poles. Conversely, unmodified centrioles segregated randomly unless passively tethered to modified centrioles. Strikingly, duplication occurred only in centrioles that were both modified and disengaged, whereas unmodified centrioles, engaged or not, were “infertile,” indicating that engagement specifically blocks modified centrioles from reduplication. These two requirements, centriole modification and disengagement, fully exclude unlimited duplication in one cell cycle. We thus uncovered a Plk1-dependent mechanism whereby duplication and segregation are coupled to maintain centriole homeostasis. |
format | Online Article Text |
id | pubmed-3166877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-31668772011-11-16 The conversion of centrioles to centrosomes: essential coupling of duplication with segregation Wang, Won-Jing Soni, Rajesh Kumar Uryu, Kunihiro Bryan Tsou, Meng-Fu J Cell Biol Research Articles Centrioles are self-reproducing organelles that form the core structure of centrosomes or microtubule-organizing centers (MTOCs). However, whether duplication and MTOC organization reflect innate activities of centrioles or activities acquired conditionally is unclear. In this paper, we show that newly formed full-length centrioles had no inherent capacity to duplicate or to organize pericentriolar material (PCM) but acquired both after mitosis through a Plk1-dependent modification that occurred in early mitosis. Modified centrioles initiated PCM recruitment in G1 and segregated equally in mitosis through association with spindle poles. Conversely, unmodified centrioles segregated randomly unless passively tethered to modified centrioles. Strikingly, duplication occurred only in centrioles that were both modified and disengaged, whereas unmodified centrioles, engaged or not, were “infertile,” indicating that engagement specifically blocks modified centrioles from reduplication. These two requirements, centriole modification and disengagement, fully exclude unlimited duplication in one cell cycle. We thus uncovered a Plk1-dependent mechanism whereby duplication and segregation are coupled to maintain centriole homeostasis. The Rockefeller University Press 2011-05-16 /pmc/articles/PMC3166877/ /pubmed/21576395 http://dx.doi.org/10.1083/jcb.201101109 Text en © 2011 Wang 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 Wang, Won-Jing Soni, Rajesh Kumar Uryu, Kunihiro Bryan Tsou, Meng-Fu The conversion of centrioles to centrosomes: essential coupling of duplication with segregation |
title | The conversion of centrioles to centrosomes: essential coupling of duplication with segregation |
title_full | The conversion of centrioles to centrosomes: essential coupling of duplication with segregation |
title_fullStr | The conversion of centrioles to centrosomes: essential coupling of duplication with segregation |
title_full_unstemmed | The conversion of centrioles to centrosomes: essential coupling of duplication with segregation |
title_short | The conversion of centrioles to centrosomes: essential coupling of duplication with segregation |
title_sort | conversion of centrioles to centrosomes: essential coupling of duplication with segregation |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166877/ https://www.ncbi.nlm.nih.gov/pubmed/21576395 http://dx.doi.org/10.1083/jcb.201101109 |
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