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Paper · 24744239

The Mus81-Mms4 structure-selective endonuclease requires nicked DNA junctions to undergo conformational changes and bend its DNA substrates for cleavage.

Mukherjee S and 3 others. Nucleic Acids Res, 2014. Cited by 17 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. The Mus81-Mms4 structure-selective endonuclease requires nicked DNA junctions to undergo conformational changes and bend its DNA substrates for cleavage. Papers, record 24744239. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/24744239

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
The Mus81-Mms4 structure-selective endonuclease requires nicked DNA junctions to undergo conformational changes and bend its DNA substrates for cleavage.
PubMed
Journal
Nucleic Acids Res
PubMed
Year
2014
PubMed
Publication types
Journal Article, Research Support, N.I.H., Extramural
PubMed
Citations, by iCite
17
iCite
Relative citation ratio, by iCite
0.38
iCite
Revised in PubMed
2021-10-21
PubMed

Authors4

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Mukherjee SSucheta
2Wright WDWilliam Douglass
3Ehmsen KTKirk Tevebaugh
4Heyer WDWolf-Dietrich

Source PubMed

Topics8

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
DNAMajor topic
DNA-Binding ProteinsMajor topic
EndonucleasesMajor topic
Flap EndonucleasesMajor topic
Saccharomyces cerevisiae ProteinsMajor topic
DNA Cleavage
DNA, Cruciform
Protein Conformation

Source PubMed

Grants6

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

Grant, as the record writes itAgencyCountryNIH projectStated bySource
T32 GM007377NIGMS NIH HHSUnited StatesT32GM007377PubMed and NIHNIH RePORTER
CA92276NCI NIH HHSUnited StatesR01CA092276PubMed and NIHNIH RePORTER
R01 CA092276NCI NIH HHSUnited StatesR01CA092276PubMed and NIHNIH RePORTER
GM58015NIGMS NIH HHSUnited StatesR01GM058015PubMed and NIHNIH RePORTER
R01 GM058015NIGMS NIH HHSUnited StatesR01GM058015PubMed and NIHNIH RePORTER
T32 GM099608NIGMS NIH HHSUnited StatesT32GM099608PubMed and NIHNIH RePORTER

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References56

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
122,730,299Cell cycle-dependent regulation of the nuclease activity of Mus81-Eme1/Mms4.Nucleic Acids Res2012https://conductscience.org/library/papers/22730299PubMed
218,054,789Bloom's syndrome helicase and Mus81 are required to induce transient double-strand DNA breaks in response to DNA replication stress.J Mol Biol2008https://conductscience.org/library/papers/18054789PubMed
320,178,992Overlapping roles for Yen1 and Mus81 in cellular Holliday junction processing.J Biol Chem2010https://conductscience.org/library/papers/20178992PubMed
422,123,861Mus81-mediated DNA cleavage resolves replication forks stalled by topoisomerase I-DNA complexes.J Cell Biol2011https://conductscience.org/library/papers/22123861PubMed
521,369,956Processing of joint molecule intermediates by structure-selective endonucleases during homologous recombination in eukaryotes.Chromosoma2011https://conductscience.org/library/papers/21369956PubMed
621,496,641Human flap endonuclease structures, DNA double-base flipping, and a unified understanding of the FEN1 superfamily.Cell2011https://conductscience.org/library/papers/21496641PubMed
721,496,637FEN nucleases: bind, bend, fray, cut.Cell2011https://conductscience.org/library/papers/21496637PubMed
821,660,704Assays for structure-selective DNA endonucleases.Methods Mol Biol2011https://conductscience.org/library/papers/21660704PubMed
911,139,495Requirement for three novel protein complexes in the absence of the Sgs1 DNA helicase in Saccharomyces cerevisiae.Genetics2001https://conductscience.org/library/papers/11139495PubMed
1017,174,892Single Holliday junctions are intermediates of meiotic recombination.Cell2006https://conductscience.org/library/papers/17174892PubMed

Cited by13

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 17 citations.

PMIDTitleJournalYearIn PapersSource
38,832,625Concurrent D-loop cleavage by Mus81 and Yen1 yields half-crossover precursors.Nucleic Acids Res2024https://conductscience.org/library/papers/38832625PubMed
34,804,132Exploring the Structures and Functions of Macromolecular SLX4-Nuclease Complexes in Genome Stability.Front Genet2021https://conductscience.org/library/papers/34804132PubMed
33,967,572Making Choices: DNA Replication Fork Recovery Mechanisms.Semin Cell Dev Biol2021https://conductscience.org/library/papers/33967572PubMed
32,814,343PCNA activates the MutLγ endonuclease to promote meiotic crossing over.Nature2020https://conductscience.org/library/papers/32814343PubMed
30,652,106Guidelines for DNA recombination and repair studies: Mechanistic assays of DNA repair processes.Microb Cell2019https://conductscience.org/library/papers/30652106PubMed
30,590,761Resolution of the Holliday junction recombination intermediate by human GEN1 at the single-molecule level.Nucleic Acids Res2019https://conductscience.org/library/papers/30590761PubMed
28,969,641Role of PCNA and RFC in promoting Mus81-complex activity.BMC Biol2017https://conductscience.org/library/papers/28969641PubMed
28,453,523The mismatch repair and meiotic recombination endonuclease Mlh1-Mlh3 is activated by polymer formation and can cleave DNA substrates in trans.PLoS Biol2017https://conductscience.org/library/papers/28453523PubMed
28,257,701The SMX DNA Repair Tri-nuclease.Mol Cell2017https://conductscience.org/library/papers/28257701PubMed
26,686,657Roles for mismatch repair family proteins in promoting meiotic crossing over.DNA Repair (Amst)2016https://conductscience.org/library/papers/26686657PubMed

1 to 10 of 13

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Genes9

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

Sources 11

  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • HGNCCC0
  • iCiteCC BY 4.0
  • NCBI GenePublic domain (US government)
  • NIH RePORTER's grant and paper linksPublic domain
  • Open TargetsCC0 1.0
  • PMC's ID filePublic domain (US government)
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • HGNCCC0: https://www.genenames.org/about/license/
  • iCiteCC BY 4.0
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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