Cargando…
PPP1R35 ensures centriole homeostasis by promoting centriole-to-centrosome conversion
Centriole-to-centrosome conversion (CCC) safeguards centriole homeostasis by coupling centriole duplication with segregation, and is essential for stabilization of mature vertebrate centrioles naturally devoid of the geometric scaffold or the cartwheel. Here we identified PPP1R35, a putative regulat...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249868/ https://www.ncbi.nlm.nih.gov/pubmed/30230954 http://dx.doi.org/10.1091/mbc.E18-08-0525 |
_version_ | 1783372837711511552 |
---|---|
author | Fong, Chii Shyang Ozaki, Kanako Tsou, Meng-Fu Bryan |
author_facet | Fong, Chii Shyang Ozaki, Kanako Tsou, Meng-Fu Bryan |
author_sort | Fong, Chii Shyang |
collection | PubMed |
description | Centriole-to-centrosome conversion (CCC) safeguards centriole homeostasis by coupling centriole duplication with segregation, and is essential for stabilization of mature vertebrate centrioles naturally devoid of the geometric scaffold or the cartwheel. Here we identified PPP1R35, a putative regulator of the protein phosphatase PP1, as a novel centriolar protein required for CCC. We found that PPP1R35 is enriched at newborn daughter centrioles in S or G2 phase. In the absence of PPP1R35, centriole assembly initiates normally in S phase, but none of the nascent centrioles can form active centrosomes or recruit CEP295, an essential factor for CCC. Instead, all PPP1R35-null centrioles, although stable during their birth in interphase, become disintegrated after mitosis upon cartwheel removal. Surprisingly, we found that neither the centriolar localization nor the function of PPP1R35 in CCC requires the putative PP1-interacting motif. PPP1R35 is thus acting upstream of CEP295 to induce CCC for proper centriole maintenance. |
format | Online Article Text |
id | pubmed-6249868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-62498682019-01-30 PPP1R35 ensures centriole homeostasis by promoting centriole-to-centrosome conversion Fong, Chii Shyang Ozaki, Kanako Tsou, Meng-Fu Bryan Mol Biol Cell Brief Report Centriole-to-centrosome conversion (CCC) safeguards centriole homeostasis by coupling centriole duplication with segregation, and is essential for stabilization of mature vertebrate centrioles naturally devoid of the geometric scaffold or the cartwheel. Here we identified PPP1R35, a putative regulator of the protein phosphatase PP1, as a novel centriolar protein required for CCC. We found that PPP1R35 is enriched at newborn daughter centrioles in S or G2 phase. In the absence of PPP1R35, centriole assembly initiates normally in S phase, but none of the nascent centrioles can form active centrosomes or recruit CEP295, an essential factor for CCC. Instead, all PPP1R35-null centrioles, although stable during their birth in interphase, become disintegrated after mitosis upon cartwheel removal. Surprisingly, we found that neither the centriolar localization nor the function of PPP1R35 in CCC requires the putative PP1-interacting motif. PPP1R35 is thus acting upstream of CEP295 to induce CCC for proper centriole maintenance. The American Society for Cell Biology 2018-11-15 /pmc/articles/PMC6249868/ /pubmed/30230954 http://dx.doi.org/10.1091/mbc.E18-08-0525 Text en © 2018 Fong et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. http://creativecommons.org/licenses/by-nc-sa/3.0 This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License. |
spellingShingle | Brief Report Fong, Chii Shyang Ozaki, Kanako Tsou, Meng-Fu Bryan PPP1R35 ensures centriole homeostasis by promoting centriole-to-centrosome conversion |
title | PPP1R35 ensures centriole homeostasis by promoting centriole-to-centrosome conversion |
title_full | PPP1R35 ensures centriole homeostasis by promoting centriole-to-centrosome conversion |
title_fullStr | PPP1R35 ensures centriole homeostasis by promoting centriole-to-centrosome conversion |
title_full_unstemmed | PPP1R35 ensures centriole homeostasis by promoting centriole-to-centrosome conversion |
title_short | PPP1R35 ensures centriole homeostasis by promoting centriole-to-centrosome conversion |
title_sort | ppp1r35 ensures centriole homeostasis by promoting centriole-to-centrosome conversion |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249868/ https://www.ncbi.nlm.nih.gov/pubmed/30230954 http://dx.doi.org/10.1091/mbc.E18-08-0525 |
work_keys_str_mv | AT fongchiishyang ppp1r35ensurescentriolehomeostasisbypromotingcentrioletocentrosomeconversion AT ozakikanako ppp1r35ensurescentriolehomeostasisbypromotingcentrioletocentrosomeconversion AT tsoumengfubryan ppp1r35ensurescentriolehomeostasisbypromotingcentrioletocentrosomeconversion |