Evidence map›Paper›PMID 21151113›Full record

ArticleNature structural & molecular biology2011

The resistance of DMC1 D-loops to dissociation may account for the DMC1 requirement in meiosis.

Dmitry V Bugreev, Roberto J Pezza, Olga M Mazina, Oleg N Voloshin, R Daniel Camerini-Otero, Alexander V Mazin

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Nature structural & molecular biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

38 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
  2. Frontiers in plant science · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. The Post-Synaptic Function of Brca2.Scientific reports · 2019
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

  • Erratum issued
  • Erratum issued
5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Dmitry V BugreevDepartment of Biochemistry and Molecular Biology, Drexel University College of Medicine, Philadelphia, Pennsylvania, USA.
Roberto J Pezza
Olga M Mazina
Oleg N Voloshin
R Daniel Camerini-Otero
Alexander V Mazin
Drexel University · USNational Institute of Diabetes and Digestive and Kidney Diseases · USNational Institutes of Health · US

Funding

Repair of DNA breaks in human: the role of Rad54 proteinR01CA100839 · NCI · DREXEL UNIVERSITY · PI MAZIN, ALEXANDER V · 2003 to 2013
$2.6M
Proteins and the search for homology in mammalian meiosisZIADK052032 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI CAMERINI-OTERO, RAFAEL · 2009 to 2011
$1.3M
Repair of DNA breaks in humans: the role of Rad54 proteinR56CA100839 · NCI · DREXEL UNIVERSITY · PI MAZIN, ALEXANDER V · 2008 to 2008
$260k
A Screen for Modulators of Human Rad51, a Key DNA Repair ProteinR03MH084119 · NIMH · DREXEL UNIVERSITY · PI MAZIN, ALEXANDER V · 2008 to 2008
$25k
Intramural NIH HHSNCI NIH HHS CA100839NCI NIH HHS R01 CA100839NCI NIH HHS R56 CA100839NIMH NIH HHS MH084119NIMH NIH HHS R03 MH084119
6 · The paper itself

Abstract

The ubiquitously expressed Rad51 recombinase and the meiosis-specific Dmc1 recombinase promote the formation of strand-invasion products (D-loops) between homologous molecules. Strand-invasion products are processed by either the double-strand break repair (DSBR) or synthesis-dependent strand annealing (SDSA) pathway. D-loops destined to be processed by SDSA need to dissociate, producing non-crossovers, and those destined for DSBR should resist dissociation to generate crossovers. The mechanism that channels recombination intermediates into different homologous-recombination pathways is unknown. Here we show that D-loops in a human DMC1-driven reaction are substantially more resistant to dissociation by branch-migration proteins such as RAD54 than those formed by RAD51. We propose that the intrinsic resistance to dissociation of DMC1 strand-invasion intermediates may account for why DMC1 is essential to ensure the proper segregation of chromosomes in meiosis.

Indexed as

Chromosome SegregationMeiosisCell Cycle ProteinsDNA-Binding ProteinsDNA HelicasesDNA RepairHumansModels, GeneticNuclear ProteinsProtein Structure, TertiaryRad51 RecombinaseRecombination, GeneticTrans-ActivatorsCell Cycle ProteinsDMC1 protein, humanDNA-Binding ProteinsDNA HelicasesMND1 protein, humanNuclear ProteinsPSMC3IP protein, humanRAD51 protein, humanRad51 RecombinaseRAD54L protein, humanTrans-Activators

Identifiers

PMID21151113
PMCPMC3058924
OpenAlexW2163539648

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.