Phospho-signaling couples polar asymmetry and proteolysis within a membraneless microdomain in Caulobacter crescentus.


Journal

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

Informations de publication

Date de publication:
28 Oct 2024
Historique:
received: 16 08 2023
accepted: 09 10 2024
medline: 29 10 2024
pubmed: 29 10 2024
entrez: 29 10 2024
Statut: epublish

Résumé

Asymmetric cell division in bacteria is achieved through cell polarization, where regulatory proteins are directed to specific cell poles. In Caulobacter crescentus, both poles contain a membraneless microdomain, established by the polar assembly hub PopZ, through most of the cell cycle, yet many PopZ clients are unipolar and transiently localized. We find that PopZ's interaction with the response regulator CpdR is controlled by phosphorylation, via the histidine kinase CckA. Phosphorylated CpdR does not interact with PopZ and is not localized to cell poles. At poles where CckA acts as a phosphatase, dephosphorylated CpdR binds directly with PopZ and subsequently recruits ClpX, substrates, and other members of a protease complex to the cell pole. We also find that co-recruitment of protease components and substrates to polar microdomains enhances their coordinated activity. This study connects phospho-signaling with polar assembly and the activity of a protease that triggers cell cycle progression and cell differentiation.

Identifiants

pubmed: 39468040
doi: 10.1038/s41467-024-53395-y
pii: 10.1038/s41467-024-53395-y
doi:

Substances chimiques

Bacterial Proteins 0
Histidine Kinase EC 2.7.13.1
Endopeptidase Clp EC 3.4.21.92

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

9282

Subventions

Organisme : U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS)
ID : R01GM118792
Organisme : U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS)
ID : 2P20GM103432
Organisme : National Science Foundation (NSF)
ID : DBI-1828319

Informations de copyright

© 2024. The Author(s).

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Auteurs

Yasin M Ahmed (YM)

Department of Molecular Biology, University of Wyoming, Laramie, WY, USA.

Logan M Brown (LM)

Department of Molecular, Cellular, and Biomedical Sciences, University of New Hampshire, Durham, NH, USA.

Krisztina Varga (K)

Department of Molecular, Cellular, and Biomedical Sciences, University of New Hampshire, Durham, NH, USA.

Grant R Bowman (GR)

Department of Molecular Biology, University of Wyoming, Laramie, WY, USA. grant.bowman@uwyo.edu.

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