Evidence map›Paper›PMID 23161012›Full record

ArticleAdvances in experimental medicine and biology2013

Roles of DNA helicases in the mediation and regulation of homologous recombination.

James M Daley, Hengyao Niu, Patrick Sung

Open access · greenAbstract read
In one paragraph

Article in Advances in experimental medicine and biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. The Srs2 helicase dampens DNA damage checkpoint by recycling RPA from chromatin.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Regulation of DNA pairing in homologous recombination.Cold Spring Harbor perspectives in biology · 2014
    Review
  14. Review
  15. 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.

James M DaleyMolecular Biophysics and Biochemistry, Yale University School of Medicine, New Haven, CT, USA.
Hengyao Niu
Patrick Sung
Yale University · US

Funding

Transcription-Coupled & Replication-Associated Excision RepairP01CA092584 · NCI · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI John A. Tainer · 2001 to 2026
$89.6M
YEAST DNA REPAIR GENES AND PROTEINS OF THE RAD52 GROUPR01ES007061 · NIEHS · YALE UNIVERSITY · PI Patrick Sung · 1995 to 2026
$9.4M
TUMOR SELECTIVE INACTIVATION OF THE REPAIR PROTEIN AGTP01CA129186 · NCI · YALE UNIVERSITY · PI GLAZER, PETER M · 2007 to 2012
$8.5M
Mechanisms of DNA Motor Proteins in Genome MaintenanceR01CA146940 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI KLEIN, HANNAH L. · 2009 to 2019
$5.9M
MODULATION OF DNA REPAIR MACHINERY BY ATAXIA TELANGIECTASIA SIGNALING PATHWAYSP01CA081020 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI LEE, WEN-HWA · 2000 to 2003
$4.9M
FORMATION AND RESOLUTION OF RECOMBINATION INTERMEDIATESR01GM057814 · NIGMS · YALE UNIVERSITY · PI SUNG, PATRICK · 1999 to 2016
$4.2M
Roles of the RecQ Helicases BLM and RECQ5 in Genome MaintenanceR01ES015632 · NIEHS · YALE UNIVERSITY · PI SUNG, PATRICK · 2007 to 2017
$3.9M
Molecular Basis of BRCA2-mediated DNA Repair and Cancer AvoidanceR01ES015252 · NIEHS · YALE UNIVERSITY · PI SUNG, PATRICK · 2007 to 2016
$3.8M
Homology-directed Repair of DNA Breaks in HumansR01CA110415 · NCI · YALE UNIVERSITY · PI SUNG, PATRICK · 2004 to 2008
$1.6M
Role of Rad51 Paralogs in Mammalian DNA RepairR01CA096593 · NCI · YALE UNIVERSITY · PI SUNG, PATRICK · 2002 to 2006
$1.4M
NCI NIH HHS P01 CA081020NCI NIH HHS P01 CA092584NCI NIH HHS P01 CA129186NCI NIH HHS R01 CA096593NCI NIH HHS R01 CA110415NCI NIH HHS R01 CA146940NIEHS NIH HHS R01 ES007061NIEHS NIH HHS R01 ES015252NIEHS NIH HHS R01 ES015632NIGMS NIH HHS R01 GM057814
6 · The paper itself

Abstract

Homologous recombination (HR) is an evolutionarily conserved process that eliminates DNA double-strand breaks from chromosomes, repairs injured DNA replication forks, and helps orchestrate meiotic chromosome segregation. Recent studies have shown that DNA helicases play multifaceted roles in HR mediation and regulation. In particular, the S. cerevisiae Sgs1 helicase and its human ortholog BLM helicase are involved in not only the resection of the primary lesion to generate single-stranded DNA to prompt the assembly of the HR machinery, but they also function in somatic cells to suppress the formation of chromosome arm crossovers during HR. On the other hand, the S. cerevisiae Mph1 and Srs2 helicases, and their respective functional equivalents in other eukaryotes, suppress spurious HR events and favor the formation of noncrossovers via distinct mechanisms. Thus, the functional integrity of the HR process and HR outcomes are dependent upon these helicase enzymes. Since mutations in some of these helicases lead to cancer predisposition in humans and mice, studies on them have clear relevance to human health and disease.

Indexed as

DNA HelicasesSaccharomyces cerevisiaeAnimalsDNA RepairHomologous RecombinationHumansNegotiatingRecombination, GeneticRecQ HelicasesSaccharomyces cerevisiae ProteinsDNA HelicasesRecQ HelicasesSaccharomyces cerevisiae Proteins

Identifiers

PMID23161012
PMCPMC3648520
OpenAlexW160692353

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.