Evidence map›Paper›PMID 25114241›Full record

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

Nucleoprotein architectures regulating the directionality of viral integration and excision.

Nicole E Seah, David Warren, Wenjun Tong, Gurunathan Laxmikanthan, Gregory D Van Duyne, Arthur Landy

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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-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

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. DNA binding induces aProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  7. Article
  8. When is a transcription factor a NAP?Current opinion in microbiology · 2020
    Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. 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

6 authors at 2 institutions in 1 country.

Nicole E SeahDepartment of Molecular Biology, Cell Biology, and Biochemistry, Division of Biology and Medicine, Brown University, Providence, RI 02912; and.
David WarrenDepartment of Molecular Biology, Cell Biology, and Biochemistry, Division of Biology and Medicine, Brown University, Providence, RI 02912; and.
Wenjun TongDepartment of Molecular Biology, Cell Biology, and Biochemistry, Division of Biology and Medicine, Brown University, Providence, RI 02912; and.
Gurunathan LaxmikanthanDepartment of Molecular Biology, Cell Biology, and Biochemistry, Division of Biology and Medicine, Brown University, Providence, RI 02912; and.
Gregory D Van DuyneDepartment of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104 vanduyne@mail.med.upenn.edu Arthur_Landy@brown.edu.
Arthur LandyDepartment of Molecular Biology, Cell Biology, and Biochemistry, Division of Biology and Medicine, Brown University, Providence, RI 02912; and vanduyne@mail.med.upenn.edu Arthur_Landy@brown.edu.
Brown University · USUniversity of Pennsylvania · US

Funding

MECHANISMS OF SITE SPECIFIC RECOMBINATIONR01GM062723 · NIGMS · BROWN UNIVERSITY · PI LANDY, ARTHUR · 2000 to 2012
$6.4M
RECOMBINATION INTERMEDIATES-- PROPERTIES &PROCESSINGR01GM033928 · NIGMS · BROWN UNIVERSITY · PI LANDY, ARTHUR · 1985 to 2011
$6.2M
Serine integrase mechanisms and applicationsR01GM108751 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI VAN DUYNE, GREGORY D · 2014 to 2024
$2.5M
NIGMS NIH HHS GM033928NIGMS NIH HHS GM062723NIGMS NIH HHS GM108751NIGMS NIH HHS R01 GM033928NIGMS NIH HHS R01 GM062723NIGMS NIH HHS R01 GM108751
6 · The paper itself

Abstract

The virally encoded site-specific recombinase Int collaborates with its accessory DNA bending proteins IHF, Xis, and Fis to assemble two distinct, very large, nucleoprotein complexes that carry out either integrative or excisive recombination along regulated and essentially unidirectional pathways. The core of each complex consists of a tetramer of Integrase protein (Int), which is a heterobivalent DNA binding protein that binds and bridges a core-type DNA site (where strand cleavage and ligation are executed), and a distal arm-type site, that is brought within range by one or more DNA bending proteins. The recent determination of the patterns of these Int bridges has made it possible to think realistically about the global architecture of the recombinogenic complexes. Here, we combined the previously determined Int bridging patterns with in-gel FRET experiments and in silico modeling to characterize and differentiate the two 400-kDa multiprotein Holiday junction recombination intermediates formed during λ integration and excision. The results lead to architectural models that explain how integration and excision are regulated in λ site-specific recombination. Our confidence in the basic features of these architectures is based on the redundancy and self-consistency of the underlying data from two very different experimental approaches to establish bridging interactions, a set of strategic intracomplex distances from FRET experiments, and the model's ability to explain key aspects of the integrative and excisive recombination pathways, such as topological changes, the mechanism of capturing attB, and the features of asymmetry and flexibility within the complexes.

Indexed as

Bacteriophage lambdaBinding SitesComputer SimulationDNA, BacterialDNA, CruciformEscherichia coliFluorescence Resonance Energy TransferIntegrasesLysogenyModels, MolecularMultiprotein ComplexesNucleic Acid ConformationNucleoproteinsProtein BindingProtein Interaction Domains and MotifsRecombination, GeneticDNA, BacterialDNA, CruciformIntegrasesMultiprotein ComplexesNucleoproteinsViral Proteinsmolecular machinesrecombinogenic architecturesregulation of directionalitytopology

Identifiers

PMID25114241
PMCPMC4151757
OpenAlexW2089859871

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.