Cyclin F drives proliferation through SCF-dependent degradation of the retinoblastoma-like tumor suppressor p130/RBL2.


Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
01 12 2021
Historique:
received: 26 05 2021
accepted: 19 11 2021
pubmed: 2 12 2021
medline: 27 1 2022
entrez: 1 12 2021
Statut: epublish

Résumé

Cell cycle gene expression programs fuel proliferation and are universally dysregulated in cancer. The retinoblastoma (RB)-family of proteins, RB1, RBL1/p107, and RBL2/p130, coordinately represses cell cycle gene expression, inhibiting proliferation, and suppressing tumorigenesis. Phosphorylation of RB-family proteins by cyclin-dependent kinases is firmly established. Like phosphorylation, ubiquitination is essential to cell cycle control, and numerous proliferative regulators, tumor suppressors, and oncoproteins are ubiquitinated. However, little is known about the role of ubiquitin signaling in controlling RB-family proteins. A systems genetics analysis of CRISPR/Cas9 screens suggested the potential regulation of the RB-network by cyclin F, a substrate recognition receptor for the SCF family of E3 ligases. We demonstrate that RBL2/p130 is a direct substrate of SCF

Identifiants

pubmed: 34851822
doi: 10.7554/eLife.70691
pii: 70691
pmc: PMC8670743
doi:
pii:

Substances chimiques

CCNF protein, human 0
Cyclins 0
KITLG protein, human 0
RBL2 protein, human 0
Retinoblastoma-Like Protein p130 0
Stem Cell Factor 0

Banques de données

Dryad
['10.5061/dryad.69p8cz93d']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIGMS NIH HHS
ID : T32 GM007040
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM120309
Pays : United States
Organisme : NICHD NIH HHS
ID : DP2 HD091800
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA163834
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM128855
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM138834
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM127707
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM134231
Pays : United States

Informations de copyright

© 2021, Enrico et al.

Déclaration de conflit d'intérêts

TE, WS, EW, PN, XW, SR, NB, JP, ME No competing interests declared

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Auteurs

Taylor P Enrico (TP)

Department of Pharmacology. The University of North Carolina at Chapel Hill, Chapel Hill, United States.
Lineberger Comprehensive Cancer Center. The University of North Carolina at Chapel Hill, Chapel Hill, United States.

Wayne Stallaert (W)

Department of Genetics. The University of North Carolina at Chapel Hill, Chapel Hill, United States.

Elizaveta T Wick (ET)

Department of Pharmacology. The University of North Carolina at Chapel Hill, Chapel Hill, United States.
Lineberger Comprehensive Cancer Center. The University of North Carolina at Chapel Hill, Chapel Hill, United States.

Peter Ngoi (P)

Department of Chemistry and Biochemistry. University of California at Santa Cruz, Santa Cruz, United States.

Xianxi Wang (X)

Lineberger Comprehensive Cancer Center. The University of North Carolina at Chapel Hill, Chapel Hill, United States.

Seth M Rubin (SM)

Department of Chemistry and Biochemistry. University of California at Santa Cruz, Santa Cruz, United States.

Nicholas G Brown (NG)

Department of Pharmacology. The University of North Carolina at Chapel Hill, Chapel Hill, United States.
Lineberger Comprehensive Cancer Center. The University of North Carolina at Chapel Hill, Chapel Hill, United States.

Jeremy E Purvis (JE)

Lineberger Comprehensive Cancer Center. The University of North Carolina at Chapel Hill, Chapel Hill, United States.
Department of Genetics. The University of North Carolina at Chapel Hill, Chapel Hill, United States.

Michael J Emanuele (MJ)

Department of Pharmacology. The University of North Carolina at Chapel Hill, Chapel Hill, United States.
Lineberger Comprehensive Cancer Center. The University of North Carolina at Chapel Hill, Chapel Hill, United States.

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Classifications MeSH