Evidence map›Paper›PMID 22632967›Full record

ArticleCell2012

Cyclin F-mediated degradation of ribonucleotide reductase M2 controls genome integrity and DNA repair.

Vincenzo D'Angiolella, Valerio Donato, Frances M Forrester, Yeon-Tae Jeong, Claudia Pellacani, Yasusei Kudo, Anita Saraf, Laurence Florens, Michael P Washburn, Michele Pagano

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 250 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
250citing papers in PubMed, 1 pooled it
9.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

250 citing papers in PubMed, 1 synthesis or guideline pooled it, 411 citations in OpenAlex.

  1. Pooled it
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  8. ATR kinase inhibitors induce mitochondrial fission in CD8bioRxiv : the preprint server for biology · 2026
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190 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 2 countries.

Vincenzo D'AngiolellaDepartment of Pathology, NYU Cancer Institute, New York University School of Medicine, 522 First Avenue, SRB 1107, New York, NY 10016, USA.
Valerio Donato
Frances M Forrester
Yeon-Tae Jeong
Claudia Pellacani
Yasusei Kudo
Anita Saraf
Laurence Florens
Michael P Washburn
Michele Pagano
New York University · USStowers Institute for Medical Research · US

Funding

REGULATION OF THE GI PHASE BY THE UBIQUITIN PATHWAYR01GM057587 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI PAGANO, MICHELE · 1998 to 2018
$7.8M
F-box proteins: deregulated cell cycle control and proteolysis in cancerR37CA076584 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI PAGANO, MICHELE · 2006 to 2016
$4.7M
Role of the SCF/Fbxo15 ubiquitin ligase in stem cells and cancer biologyR21CA161108 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI PAGANO, MICHELE · 2011 to 2012
$404k
Howard Hughes Medical InstituteNCI NIH HHS R21 CA161108NCI NIH HHS R21-CA161108NCI NIH HHS R37 CA076584NCI NIH HHS R37-CA076584NIGMS NIH HHS R01 GM057587NIGMS NIH HHS R01-GM057587
6 · The paper itself

Abstract

F-box proteins are the substrate binding subunits of SCF (Skp1-Cul1-F-box protein) ubiquitin ligase complexes. Using affinity purifications and mass spectrometry, we identified RRM2 (the ribonucleotide reductase family member 2) as an interactor of the F-box protein cyclin F. Ribonucleotide reductase (RNR) catalyzes the conversion of ribonucleotides to deoxyribonucleotides (dNTPs), which are necessary for both replicative and repair DNA synthesis. We found that, during G2, following CDK-mediated phosphorylation of Thr33, RRM2 is degraded via SCF(cyclin F) to maintain balanced dNTP pools and genome stability. After DNA damage, cyclin F is downregulated in an ATR-dependent manner to allow accumulation of RRM2. Defective elimination of cyclin F delays DNA repair and sensitizes cells to DNA damage, a phenotype that is reverted by expressing a nondegradable RRM2 mutant. In summary, we have identified a biochemical pathway that controls the abundance of dNTPs and ensures efficient DNA repair in response to genotoxic stress.

Indexed as

DNA RepairAmino Acid MotifsAtaxia Telangiectasia Mutated ProteinsCell Cycle ProteinsCell Line, TumorCell NucleusCyclinsDNA DamageDown-RegulationG2 PhaseGenomic InstabilityHumansProtein Serine-Threonine KinasesRibonucleoside Diphosphate ReductaseAtaxia Telangiectasia Mutated ProteinsATR protein, humanCCNF protein, humanCell Cycle ProteinsCyclinsProtein Serine-Threonine KinasesRibonucleoside Diphosphate Reductaseribonucleotide reductase M2

Identifiers

PMID22632967
PMCPMC3616325
OpenAlexW2142393970

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.