Cargando…

Gradual centriole maturation associates with the mitotic surveillance pathway in mouse development

Centrosomes, composed of two centrioles and pericentriolar material, organize mitotic spindles during cell division and template cilia during interphase. The first few divisions during mouse development occur without centrioles, which form around embryonic day (E) 3. However, disruption of centriole...

Descripción completa

Detalles Bibliográficos
Autores principales: Xiao, Cally, Grzonka, Marta, Meyer‐Gerards, Charlotte, Mack, Miriam, Figge, Rebecca, Bazzi, Hisham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7857428/
https://www.ncbi.nlm.nih.gov/pubmed/33410253
http://dx.doi.org/10.15252/embr.202051127
_version_ 1783646443936940032
author Xiao, Cally
Grzonka, Marta
Meyer‐Gerards, Charlotte
Mack, Miriam
Figge, Rebecca
Bazzi, Hisham
author_facet Xiao, Cally
Grzonka, Marta
Meyer‐Gerards, Charlotte
Mack, Miriam
Figge, Rebecca
Bazzi, Hisham
author_sort Xiao, Cally
collection PubMed
description Centrosomes, composed of two centrioles and pericentriolar material, organize mitotic spindles during cell division and template cilia during interphase. The first few divisions during mouse development occur without centrioles, which form around embryonic day (E) 3. However, disruption of centriole biogenesis in Sas‐4 null mice leads to embryonic arrest around E9. Centriole loss in Sas‐4 (−/−) embryos causes prolonged mitosis and p53‐dependent cell death. Studies in vitro discovered a similar USP28‐, 53BP1‐, and p53‐dependent mitotic surveillance pathway that leads to cell cycle arrest. In this study, we show that an analogous pathway is conserved in vivo where 53BP1 and USP28 are upstream of p53 in Sas‐4 (−/−) embryos. The data indicate that the pathway is established around E7 of development, four days after the centrioles appear. Our data suggest that the newly formed centrioles gradually mature to participate in mitosis and cilia formation around the beginning of gastrulation, coinciding with the activation of mitotic surveillance pathway upon centriole loss.
format Online
Article
Text
id pubmed-7857428
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-78574282021-02-05 Gradual centriole maturation associates with the mitotic surveillance pathway in mouse development Xiao, Cally Grzonka, Marta Meyer‐Gerards, Charlotte Mack, Miriam Figge, Rebecca Bazzi, Hisham EMBO Rep Reports Centrosomes, composed of two centrioles and pericentriolar material, organize mitotic spindles during cell division and template cilia during interphase. The first few divisions during mouse development occur without centrioles, which form around embryonic day (E) 3. However, disruption of centriole biogenesis in Sas‐4 null mice leads to embryonic arrest around E9. Centriole loss in Sas‐4 (−/−) embryos causes prolonged mitosis and p53‐dependent cell death. Studies in vitro discovered a similar USP28‐, 53BP1‐, and p53‐dependent mitotic surveillance pathway that leads to cell cycle arrest. In this study, we show that an analogous pathway is conserved in vivo where 53BP1 and USP28 are upstream of p53 in Sas‐4 (−/−) embryos. The data indicate that the pathway is established around E7 of development, four days after the centrioles appear. Our data suggest that the newly formed centrioles gradually mature to participate in mitosis and cilia formation around the beginning of gastrulation, coinciding with the activation of mitotic surveillance pathway upon centriole loss. John Wiley and Sons Inc. 2021-01-07 2021-02-03 /pmc/articles/PMC7857428/ /pubmed/33410253 http://dx.doi.org/10.15252/embr.202051127 Text en © 2021 The Authors. Published under the terms of the CC BY NC ND 4.0 license This is an open access article under the terms of the http://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 Reports
Xiao, Cally
Grzonka, Marta
Meyer‐Gerards, Charlotte
Mack, Miriam
Figge, Rebecca
Bazzi, Hisham
Gradual centriole maturation associates with the mitotic surveillance pathway in mouse development
title Gradual centriole maturation associates with the mitotic surveillance pathway in mouse development
title_full Gradual centriole maturation associates with the mitotic surveillance pathway in mouse development
title_fullStr Gradual centriole maturation associates with the mitotic surveillance pathway in mouse development
title_full_unstemmed Gradual centriole maturation associates with the mitotic surveillance pathway in mouse development
title_short Gradual centriole maturation associates with the mitotic surveillance pathway in mouse development
title_sort gradual centriole maturation associates with the mitotic surveillance pathway in mouse development
topic Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7857428/
https://www.ncbi.nlm.nih.gov/pubmed/33410253
http://dx.doi.org/10.15252/embr.202051127
work_keys_str_mv AT xiaocally gradualcentriolematurationassociateswiththemitoticsurveillancepathwayinmousedevelopment
AT grzonkamarta gradualcentriolematurationassociateswiththemitoticsurveillancepathwayinmousedevelopment
AT meyergerardscharlotte gradualcentriolematurationassociateswiththemitoticsurveillancepathwayinmousedevelopment
AT mackmiriam gradualcentriolematurationassociateswiththemitoticsurveillancepathwayinmousedevelopment
AT figgerebecca gradualcentriolematurationassociateswiththemitoticsurveillancepathwayinmousedevelopment
AT bazzihisham gradualcentriolematurationassociateswiththemitoticsurveillancepathwayinmousedevelopment