Evidence map›Paper›PMID 17573434›Full record

ArticleBiophysical journal2007

Probability of the site juxtaposition determines the rate of protein-mediated DNA looping.

Yury S Polikanov, Vladimir A Bondarenko, Vladimir Tchernaenko, Yong I Jiang, Leonard C Lutter, Alexander Vologodskii, Vasily M Studitsky

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

21 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  4. Review
  5. Review
  6. Article
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  8. Article
  9. Article
  10. Quantitation of interactions between two DNA loops demonstrates loop domain insulation in E. coli cells.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  11. Article
  12. DNA supercoiling enhances cooperativity and efficiency of an epigenetic switch.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Simulation of DNA catenanes.Physical chemistry chemical physics : PCCP · 2009
    Review
  19. The why and how of DNA unlinking.Nucleic acids research · 2009
    Review
  20. Analysis of distant communication on defined chromatin templates in vitro.Methods in molecular biology (Clifton, N.J.) · 2009
    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

7 authors at 3 institutions in 1 country.

Yury S PolikanovDepartment of Pharmacology, University of Medicine and Dentistry of New Jersey, Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, and Molecular Biology Research Program, Henry Ford Hospital, Detroit, MI 48202, USA.
Vladimir A Bondarenko
Vladimir Tchernaenko
Yong I Jiang
Leonard C Lutter
Alexander Vologodskii
Vasily M Studitsky
Henry Ford Hospital · USNew York University · USRobert Wood Johnson University Hospital · US

Funding

DNA CATENANES AND TYPE II DNA TOPOISOMERASESR01GM054215 · NIGMS · NEW YORK UNIVERSITY · PI VOLOGODSKII, ALEXANDER V · 1996 to 2010
$2.8M
NIGMS NIH HHS GM54215NIGMS NIH HHS R01 GM054215
6 · The paper itself

Abstract

Numerous biological processes are regulated by DNA elements that communicate with their targets over a distance via formation of protein-bridged DNA loops. One of the first questions arising in studies of DNA looping is whether the rate of loop formation is limited by diffusion of the DNA sites. We addressed this question by comparing the in vitro measured rates of transcription initiation in the NtrC-glnAp2 enhancer-dependent transcription initiation system with predictions of two different theoretical models. The promoter and enhancer were in a 7.6-kb plasmid and separated by 2.5 kb. The measurements were performed for different values of the plasmid superhelix density, from 0 to -0.07. Earlier theoretical analysis, based on the Monte Carlo simulation of DNA conformations, showed that if the rate of loop formation is determined by the equilibrium probability of juxtaposition of the DNA sites, the rate should be approximately 100 times higher in supercoiled than in relaxed DNA. On the other hand, Brownian dynamics simulation showed that if the rate of loop formation is limited by the site diffusion, it should be nearly independent of DNA supercoiling. We found that efficiency of the transcription initiation increases by nearly two orders of magnitude as a result of the corresponding increase of the template supercoiling. This clearly shows that the rate of bridging in the enhancer-promoter system is not limited by diffusion of the DNA sites to one another. We argue that this conclusion derived for the specific system is likely to be valid for the great majority of biological processes involving protein-mediated DNA looping.

Indexed as

Models, ChemicalModels, MolecularBinding SitesComputer SimulationDNADNA-Binding ProteinsModels, StatisticalNucleic Acid ConformationProtein BindingProtein ConformationDNADNA-Binding Proteins

Identifiers

PMID17573434
PMCPMC1989718
OpenAlexW2155996859

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.