Cep55 promotes cytokinesis of neural progenitors but is dispensable for most mammalian cell divisions.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
08 04 2020
Historique:
received: 01 04 2019
accepted: 27 02 2020
entrez: 10 4 2020
pubmed: 10 4 2020
medline: 28 7 2020
Statut: epublish

Résumé

In mammalian cell lines, the endosomal sorting complex required for transport (ESCRT)-III mediates abscission, the process that physically separates daughter cells and completes cell division. Cep55 protein is regarded as the master regulator of abscission, because it recruits ESCRT-III to the midbody (MB), the site of abscission. However, the importance of this mechanism in a mammalian organism has never been tested. Here we show that Cep55 is dispensable for mouse embryonic development and adult tissue homeostasis. Cep55-knockout offspring show microcephaly and primary neural progenitors require Cep55 and ESCRT for survival and abscission. However, Cep55 is dispensable for cell division in embryonic or adult tissues. In vitro, division of primary fibroblasts occurs without Cep55 and ESCRT-III at the midbody and is not affected by ESCRT depletion. Our work defines Cep55 as an abscission regulator only in specific tissue contexts and necessitates the re-evaluation of an alternative ESCRT-independent cell division mechanism.

Identifiants

pubmed: 32269212
doi: 10.1038/s41467-020-15359-w
pii: 10.1038/s41467-020-15359-w
pmc: PMC7142149
doi:

Substances chimiques

CHMP4B protein, mouse 0
Cell Cycle Proteins 0
Cep55 protein, mouse 0
Endosomal Sorting Complexes Required for Transport 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1746

Subventions

Organisme : Cancer Research UK
ID : FC001039
Pays : United Kingdom
Organisme : Wellcome Trust
ID : FC001039
Pays : United Kingdom
Organisme : Medical Research Council
ID : FC001039
Pays : United Kingdom

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Auteurs

Antonio Tedeschi (A)

Adult Stem Cell Laboratory, The Francis Crick Institute, 1 Midland Road, London, NW1 1AT, UK. antonio.tedeschi@crick.ac.uk.
Cell Division and Aneuploidy Laboratory, Clare Hall Laboratories, Cancer Research UK London Research Institute, London, EN6 3LD, UK. antonio.tedeschi@crick.ac.uk.

Jorge Almagro (J)

Adult Stem Cell Laboratory, The Francis Crick Institute, 1 Midland Road, London, NW1 1AT, UK.

Matthew J Renshaw (MJ)

Advanced Light Microscopy, The Francis Crick Institute, 1 Midland Road, London, NW1 1AT, UK.

Hendrik A Messal (HA)

Adult Stem Cell Laboratory, The Francis Crick Institute, 1 Midland Road, London, NW1 1AT, UK.
Division of Molecular Pathology, Oncode Institute, Netherlands Cancer Institute, Plesmanlaan 121, 1066CX, Amsterdam, The Netherlands.

Axel Behrens (A)

Adult Stem Cell Laboratory, The Francis Crick Institute, 1 Midland Road, London, NW1 1AT, UK.
Faculty of Life Sciences, King's College London, Guy's Campus, London, SE1 1UL, UK.

Mark Petronczki (M)

Cell Division and Aneuploidy Laboratory, Clare Hall Laboratories, Cancer Research UK London Research Institute, London, EN6 3LD, UK.
Boehringer Ingelheim RCV GmbH & Co KG, A-1121, Vienna, Austria.

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