Evidence map›Paper›PMID 21647941›Full record

ReviewJournal of cellular biochemistry2011

Coordination of DNA replication and recombination activities in the maintenance of genome stability.

Robyn L Maher, Amy M Branagan, Scott W Morrical

Open access · greenAbstract readReview
In one paragraph

Review in Journal of cellular biochemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

44 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
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  3. Article
  4. Review
  5. Review
  6. Article
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  8. ORChestra coordinates the replication and repair music.BioEssays : news and reviews in molecular, cellular and developmental biology · 2023
    Article
  9. Review
  10. Article
  11. Article
  12. Review
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  15. Article
  16. The dawn of active genetics.BioEssays : news and reviews in molecular, cellular and developmental biology · 2016
    Review
  17. Article
  18. Review
  19. Article
  20. Article
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

3 authors at 1 institution in 1 country.

Robyn L MaherDepartment of Biochemistry, University of Vermont College of Medicine, Burlington, Vermont 05405, USA.
Amy M Branagan
Scott W Morrical
University of Vermont · US

Funding

SUBSTRATE SPECIFICITY OF THE BER OXIDATIVE DNA GLYCOSYLASESP01CA098993 · NCI · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI DOUBLIE, SYLVIE · 2004 to 2021
$25.9M
ENVIRONMENTAL PATHOLOGY TRAINING PROGRAMT32ES007122 · NIEHS · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI VAN DER VLIET, ALBERT · 1985 to 2012
$4.2M
ASSEMBLY AND ACTIVATION OF ENZYME/SSDNA COMPLEXESR01GM048847 · NIGMS · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI MORRICAL, SCOTT W · 1993 to 2012
$3.1M
Assembly and Activation of Enzyme-ssDNA ComplexesR56GM048847 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI MORRICAL, SCOTT W · 2007 to 2007
$325k
NCI NIH HHS CA98993/P3NCI NIH HHS P01 CA098993NIEHS NIH HHS ES07122NIEHS NIH HHS T32 ES007122NIGMS NIH HHS GM48847NIGMS NIH HHS R01 GM048847NIGMS NIH HHS R56 GM048847
6 · The paper itself

Abstract

Across the evolutionary spectrum, living organisms depend on high-fidelity DNA replication and recombination mechanisms to maintain genome stability and thus to avoid mutation and disease. The repair of severe lesions in the DNA such as double-strand breaks or stalled replication forks requires the coordinated activities of both the homologous recombination (HR) and DNA replication machineries. Growing evidence indicates that so-called "accessory proteins" in both systems are essential for the effective coupling of recombination to replication which is necessary to restore genome integrity following severe DNA damage. In this article we review the major processes of homology-directed DNA repair (HDR), including the double Holliday Junction (dHJ), synthesis-dependent strand annealing (SDSA), break-induced replication (BIR), and error-free lesion bypass pathways. Each of these pathways involves the coupling of a HR event to DNA synthesis. We highlight two major classes of accessory proteins in recombination and replication that facilitate HDR: Recombination mediator proteins exemplified by T4 UvsY, Saccharomyces cerevisiae Rad52, and human BRCA2; and DNA helicases/translocases exemplified by T4 Gp41/Gp59, E. coli DnaB and PriA, and eukaryotic Mcm2-7, Rad54, and Mph1. We illustrate how these factors help to direct the flow of DNA and protein-DNA intermediates on the pathway from a double-strand break or stalled replication fork to a high-fidelity recombination-dependent replication apparatus that can accurately repair the damage.

Indexed as

AnimalsDNA HelicasesDNA RepairDNA ReplicationGenomic InstabilityHumansRecombination, GeneticDNA Helicases

Identifiers

PMID21647941
PMCPMC3178728
OpenAlexW2069507260

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.