Prophase-Specific Perinuclear Actin Coordinates Centrosome Separation and Positioning to Ensure Accurate Chromosome Segregation.

Eg5 FHOD1 G2/M transition LINC complex centrosome positioning centrosome separation centrosome tracking mitotic entry perinuclear actin, microtubules

Journal

Cell reports
ISSN: 2211-1247
Titre abrégé: Cell Rep
Pays: United States
ID NLM: 101573691

Informations de publication

Date de publication:
26 05 2020
Historique:
received: 05 03 2019
revised: 11 02 2020
accepted: 01 05 2020
entrez: 28 5 2020
pubmed: 28 5 2020
medline: 22 5 2021
Statut: ppublish

Résumé

Centrosome separation in late G2/ early prophase requires precise spatial coordination that is determined by a balance of forces promoting and antagonizing separation. The major effector of centrosome separation is the kinesin Eg5. However, the identity and regulation of Eg5-antagonizing forces is less well characterized. By manipulating candidate components, we find that centrosome separation is reversible and that separated centrosomes congress toward a central position underneath the flat nucleus. This positioning mechanism requires microtubule polymerization, as well as actin polymerization. We identify perinuclear actin structures that form in late G2/early prophase and interact with microtubules emanating from the centrosomes. Disrupting these structures by breaking the interactions of the linker of nucleoskeleton and cytoskeleton (LINC) complex with perinuclear actin filaments abrogates this centrosome positioning mechanism and causes an increase in subsequent chromosome segregation errors. Our results demonstrate how geometrical cues from the cell nucleus coordinate the orientation of the emanating spindle poles before nuclear envelope breakdown.

Identifiants

pubmed: 32460023
pii: S2211-1247(20)30634-3
doi: 10.1016/j.celrep.2020.107681
pmc: PMC7262599
pii:
doi:

Substances chimiques

Actins 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

107681

Subventions

Organisme : Cancer Research UK
ID : C28206/A14499
Pays : United Kingdom

Informations de copyright

Copyright © 2020 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Interests The authors declare no competing interests.

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Auteurs

Tom Stiff (T)

Genome Damage and Stability Centre, School of Life Sciences, University of Sussex, Brighton BN19RQ, UK.

Fabio R Echegaray-Iturra (FR)

Genome Damage and Stability Centre, School of Life Sciences, University of Sussex, Brighton BN19RQ, UK.

Harry J Pink (HJ)

Genome Damage and Stability Centre, School of Life Sciences, University of Sussex, Brighton BN19RQ, UK.

Alex Herbert (A)

Genome Damage and Stability Centre, School of Life Sciences, University of Sussex, Brighton BN19RQ, UK.

Constantino Carlos Reyes-Aldasoro (CC)

GiCentre, Department of Computer Science, City, University of London, London EC1V 0HB, UK.

Helfrid Hochegger (H)

Genome Damage and Stability Centre, School of Life Sciences, University of Sussex, Brighton BN19RQ, UK. Electronic address: hh65@sussex.ac.uk.

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Classifications MeSH