Cytoplasmic division cycles without the nucleus and mitotic CDK/cyclin complexes.

Cdk Drosophila embryo autonomous clocks cell cycle centrosome cyclin cytokinesis epithelial homeostasis microtubules mitosis

Journal

Cell
ISSN: 1097-4172
Titre abrégé: Cell
Pays: United States
ID NLM: 0413066

Informations de publication

Date de publication:
12 10 2023
Historique:
received: 05 06 2022
revised: 11 05 2023
accepted: 12 09 2023
medline: 2 11 2023
pubmed: 14 10 2023
entrez: 13 10 2023
Statut: ppublish

Résumé

Cytoplasmic divisions are thought to rely on nuclear divisions and mitotic signals. We demonstrate in Drosophila embryos that cytoplasm can divide repeatedly without nuclei and mitotic CDK/cyclin complexes. Cdk1 normally slows an otherwise faster cytoplasmic division cycle, coupling it with nuclear divisions, and when uncoupled, cytoplasm starts dividing before mitosis. In developing embryos where CDK/cyclin activity can license mitotic microtubule (MT) organizers like the spindle, cytoplasmic divisions can occur without the centrosome, a principal organizer of interphase MTs. However, centrosomes become essential in the absence of CDK/cyclin activity, implying that the cytoplasm can employ either the centrosome-based interphase or CDK/cyclin-dependent mitotic MTs to facilitate its divisions. Finally, we present evidence that autonomous cytoplasmic divisions occur during unperturbed fly embryogenesis and that they may help extrude mitotically stalled nuclei during blastoderm formation. We postulate that cytoplasmic divisions occur in cycles governed by a yet-to-be-uncovered clock mechanism autonomous from CDK/cyclin complexes.

Identifiants

pubmed: 37832525
pii: S0092-8674(23)01031-0
doi: 10.1016/j.cell.2023.09.010
pmc: PMC10659773
mid: NIHMS1937362
pii:
doi:

Substances chimiques

Cyclins 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S. Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4694-4709.e16

Subventions

Organisme : NIGMS NIH HHS
ID : DP2 GM154328
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM136420
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM149436
Pays : United States

Informations de copyright

Copyright © 2023 The Authors. 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

Anand Bakshi (A)

Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA 94158, USA.

Fabio Echegaray Iturra (FE)

Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA 94158, USA.

Andrew Alamban (A)

Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA 94158, USA; Biophysics Graduate Program, University of California, San Francisco, San Francisco, CA 94158, USA.

Miquel Rosas-Salvans (M)

Department of Bioengineering and Therapeutic Science, University of California, San Francisco, San Francisco, CA 94158, USA.

Sophie Dumont (S)

Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA 94158, USA; Chan Zuckerberg Biohub, San Francisco, CA 94158, USA.

Mustafa G Aydogan (MG)

Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA 94158, USA; Biophysics Graduate Program, University of California, San Francisco, San Francisco, CA 94158, USA. Electronic address: mustafa.aydogan@ucsf.edu.

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