Evidence map›Paper›PMID 32369918›Full record

ReviewGenes2020

The Regulation of Homologous Recombination by Helicases.

Eric Huselid, Samuel F Bunting

Open access · goldAbstract readReview
In one paragraph

Review in Genes, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

25 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Neural Tube Defects and Folate Deficiency: Is DNA Repair Defective?International journal of molecular sciences · 2023
    Review
  14. Article
  15. The RecD2 helicase balances RecA activities.Nucleic acids research · 2022
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

2 authors at 1 institution in 1 country.

Eric HuselidDepartment of Molecular Biology and Biochemistry, Rutgers, The State University of New Jersey, Center for Advanced Biochemistry and Medicine, 679 Hoes Lane West, Piscataway, NJ 08854, USA.
Samuel F BuntingDepartment of Molecular Biology and Biochemistry, Rutgers, The State University of New Jersey, Center for Advanced Biochemistry and Medicine, 679 Hoes Lane West, Piscataway, NJ 08854, USA.ORCID 0000-0002-4629-496X
Rutgers, The State University of New Jersey · US

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Tracie Saunders · 1997 to 2026
$94.5M
Control of Commitment Steps in Mammalian Homologous RecombinationR01CA190858 · NCI · RUTGERS, THE STATE UNIV OF N.J. · PI BUNTING, SAMUEL · 2015 to 2021
$2.1M
NCI NIH HHS P30 CA072720NCI NIH HHS R01 CA190858NCI NIH HHS R01CA90858
6 · The paper itself

Abstract

Homologous recombination is essential for DNA repair, replication and the exchange of genetic material between parental chromosomes during meiosis. The stages of recombination involve complex reorganization of DNA structures, and the successful completion of these steps is dependent on the activities of multiple helicase enzymes. Helicases of many different families coordinate the processing of broken DNA ends, and the subsequent formation and disassembly of the recombination intermediates that are necessary for template-based DNA repair. Loss of recombination-associated helicase activities can therefore lead to genomic instability, cell death and increased risk of tumor formation. The efficiency of recombination is also influenced by the 'anti-recombinase' effect of certain helicases, which can direct DNA breaks toward repair by other pathways. Other helicases regulate the crossover versus non-crossover outcomes of repair. The use of recombination is increased when replication forks and the transcription machinery collide, or encounter lesions in the DNA template. Successful completion of recombination in these situations is also regulated by helicases, allowing normal cell growth, and the maintenance of genomic integrity.

Indexed as

DNA DamageDNA HelicasesDNA RepairDNA ReplicationGenomic InstabilityHomologous RecombinationHumansMeiosisDNA Helicasesanti-recombinaseDNA repairhelicaserecombinationreplicationtranscription

Identifiers

PMID32369918
PMCPMC7290689
OpenAlexW3021492972

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.