Evidence map›Paper›PMID 22704558›Full record

ArticleMolecular cell2012

Polyubiquitinated PCNA recruits the ZRANB3 translocase to maintain genomic integrity after replication stress.

Alberto Ciccia, Amitabh V Nimonkar, Yiduo Hu, Ildiko Hajdu, Yathish Jagadheesh Achar, Lior Izhar, Sarah A Petit, Britt Adamson, John C Yoon, Stephen C Kowalczykowski and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 197 papers.

0numbers the graph read from it
0cells of the map it votes in
197citing papers in PubMed
8.5field-weighted citation impact, top 2% 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

197 citing papers in PubMed, 294 citations in OpenAlex.

  1. Article
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  6. The Zinc Finger Ran-Binding Protein 3 (ZRANB3): An Advanced Perspective.International journal of molecular sciences · 2026
    Review
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137 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 6 institutions in 2 countries.

Alberto CicciaDepartment of Genetics, Harvard University Medical School, Boston, MA 02115, USA.
Amitabh V Nimonkar
Yiduo Hu
Ildiko Hajdu
Yathish Jagadheesh Achar
Lior Izhar
Sarah A Petit
Britt Adamson
John C Yoon
Stephen C Kowalczykowski
David M Livingston
Lajos Haracska
Stephen J Elledge
Brigham and Women's Hospital · USHarvard University · USHoward Hughes Medical Institute · USHungarian Academy of Sciences · HUUniversity of California, Davis · USDana-Farber Cancer Institute · US

Funding

Use of Organotypic and Mammary Gland Models to Investigate the Outcomes of ClonalP01CA080111 · NCI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI DILLON, DEBORAH · 1999 to 2018
$36.0M
Mechanistic Studies of Genetic RecombinationR01GM062653 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KOWALCZYKOWSKI, STEPHEN CHARLES · 2010 to 2018
$4.4M
MECHANISTIC STUDIES OF GENETIC RECOMBINATIONR37GM062653 · NIGMS · UNIVERSITY OF CALIFORNIA DAVIS · PI KOWALCZYKOWSKI, STEPHEN CHARLES · 2000 to 2009
$3.6M
Genetics of Cell Cycle &DNA Damage Regulation in YeastR37GM044664 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI ELLEDGE, STEPHEN J · 2003 to 2012
$3.5M
GENETICS OF CELL CYCLE &DNA DAMAGE REGULATION IN YEASTR01GM044664 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI ELLEDGE, STEPHEN J · 1990 to 2016
$2.0M
Howard Hughes Medical Institute 55005612NCI NIH HHS P01 CA080111NIGMS NIH HHS GM62653NIGMS NIH HHS R01 GM044664NIGMS NIH HHS R01 GM062653NIGMS NIH HHS R37 GM044664NIGMS NIH HHS R37 GM062653
6 · The paper itself

Abstract

Completion of DNA replication after replication stress depends on PCNA, which undergoes monoubiquitination to stimulate direct bypass of DNA lesions by specialized DNA polymerases or is polyubiquitinated to promote recombination-dependent DNA synthesis across DNA lesions by template switching mechanisms. Here we report that the ZRANB3 translocase, a SNF2 family member related to the SIOD disorder SMARCAL1 protein, is recruited by polyubiquitinated PCNA to promote fork restart following replication arrest. ZRANB3 depletion in mammalian cells results in an increased frequency of sister chromatid exchange and DNA damage sensitivity after treatment with agents that cause replication stress. Using in vitro biochemical assays, we show that recombinant ZRANB3 remodels DNA structures mimicking stalled replication forks and disassembles recombination intermediates. We therefore propose that ZRANB3 maintains genomic stability at stalled or collapsed replication forks by facilitating fork restart and limiting inappropriate recombination that could occur during template switching events.

Indexed as

Amino Acid SequenceCell Line, TumorDNA DamageDNA HelicasesDNA ReplicationGenomic InstabilityGreen Fluorescent ProteinsHumansMolecular Sequence DataOsteosarcomaPolyubiquitinProliferating Cell Nuclear AntigenProtein BindingRecombination, GeneticSister Chromatid ExchangeStress, PhysiologicalDNA HelicasesGreen Fluorescent ProteinsPolyubiquitinProliferating Cell Nuclear AntigenSMARCAL1 protein, humanZRANB3 protein, human

Identifiers

PMID22704558
PMCPMC3613862
OpenAlexW2056870028

What OpenQuestion holds

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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.