Evidence map›Paper›PMID 24395779›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Mismatch repair protein hMSH2-hMSH6 recognizes mismatches and forms sliding clamps within a D-loop recombination intermediate.

Masayoshi Honda, Yusuke Okuno, Sarah R Hengel, Juana V Martín-López, Christopher P Cook, Ravindra Amunugama, Randal J Soukup, Shyamal Subramanyam, Richard Fishel, Maria Spies

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.3field-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

24 citing papers in PubMed, 39 citations in OpenAlex.

  1. Mechanisms That Govern Recombinase Fidelity Control During Eukaryotic Homologous Recombination.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  2. The Role of theGenes · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. RNA-Based Classification of Homologous Recombination Deficiency in Racially Diverse Patients with Breast Cancer.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2022
    Article
  7. Review
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  16. A time for promiscuity in a eukaryotic recombinase.The Journal of biological chemistry · 2017
    Review
  17. Article
  18. Article
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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

10 authors at 4 institutions in 1 country.

Masayoshi HondaDepartment of Biochemistry, University of Iowa, Iowa City, IA 52242.
Yusuke Okuno
Sarah R Hengel
Juana V Martín-López
Christopher P Cook
Ravindra Amunugama
Randal J Soukup
Shyamal Subramanyam
Richard Fishel
Maria Spies
University of Iowa · USThe Ohio State University · USThe Ohio State University Wexner Medical Center · USUniversity of Illinois Urbana-Champaign · US

Funding

The Human Mismatch Repair Proteins and CarcinogenesisR01CA067007 · NCI · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI Richard Fishel · 1995 to 2026
$9.6M
NCI NIH HHS CA67007NCI NIH HHS R01 CA067007
6 · The paper itself

Abstract

High fidelity homologous DNA recombination depends on mismatch repair (MMR), which antagonizes recombination between divergent sequences by rejecting heteroduplex DNA containing excessive nucleotide mismatches. The hMSH2-hMSH6 heterodimer is the first responder in postreplicative MMR and also plays a prominent role in heteroduplex rejection. Whether a similar molecular mechanism underlies its function in these two processes remains enigmatic. We have determined that hMSH2-hMSH6 efficiently recognizes mismatches within a D-loop recombination initiation intermediate. Mismatch recognition by hMSH2-hMSH6 is not abrogated by human replication protein A (HsRPA) bound to the displaced single-stranded DNA (ssDNA) or by HsRAD51. In addition, ATP-bound hMSH2-hMSH6 sliding clamps that are essential for downstream MMR processes are formed and constrained within the heteroduplex region of the D-loop. Moreover, the hMSH2-hMSH6 sliding clamps are stabilized on the D-loop by HsRPA bound to the displaced ssDNA. Our findings reveal similarities and differences in hMSH2-hMSH6 mismatch recognition and sliding-clamp formation between a D-loop recombination intermediate and linear duplex DNA.

Indexed as

DNA Mismatch RepairRecombination, GeneticAdenosine DiphosphateAdenosine TriphosphateBase Pair MismatchBiotinylationDNADNA-Binding ProteinsHumansHydrolysisKineticsMutS Homolog 2 ProteinProtein BindingProtein Structure, TertiaryRad51 RecombinaseReplication Protein AAdenosine DiphosphateAdenosine TriphosphateDNADNA-Binding ProteinsG-T mismatch-binding proteinMSH2 protein, humanMutS Homolog 2 ProteinRAD51 protein, humanRad51 RecombinaseReplication Protein ARPA1 protein, humanhomeologous recombinationhomologous recombinationmismatch DNA repairsingle-moleculetotal internal reflection fluorescence microscopy

Identifiers

PMID24395779
PMCPMC3903253
OpenAlexW1995649118

What OpenQuestion holds

Textmetadata
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.