Evidence map›Paper›PMID 29684182›Full record

ArticleNucleic acids research2018

Visualizing structure-mediated interactions in supercoiled DNA molecules.

Shane Scott, Zhi Ming Xu, Fedor Kouzine, Daniel J Berard, Cynthia Shaheen, Barbara Gravel, Laura Saunders, Alexander Hofkirchner, Catherine Leroux, Jill Laurin and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2018. 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
2.9field-weighted citation impact, top 9% 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, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. A guide RNA repeat checkpoint steers CRISPR-Cas9 catalysis.bioRxiv : the preprint server for biology · 2025
    Article
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  7. Review
  8. Article
  9. Biophysical reviews · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Transcription factor regulation of RNA polymerase's torque generation capacity.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  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

13 authors at 3 institutions in 2 countries.

Shane ScottDepartment of Physics, McGill University, Montreal, Quebec H3A 2T8, Canada.
Zhi Ming XuDepartment of Physics, McGill University, Montreal, Quebec H3A 2T8, Canada.
Fedor KouzineCenter for Cancer Research, National Cancer Institute, Bethesda, MD 20892, USA.
Daniel J BerardDepartment of Physics, McGill University, Montreal, Quebec H3A 2T8, Canada.
Cynthia ShaheenDepartment of Physics, McGill University, Montreal, Quebec H3A 2T8, Canada.
Barbara GravelDepartment of Physics, McGill University, Montreal, Quebec H3A 2T8, Canada.
Laura SaundersDepartment of Physics, McGill University, Montreal, Quebec H3A 2T8, Canada.
Alexander HofkirchnerDepartment of Physics, McGill University, Montreal, Quebec H3A 2T8, Canada.
Catherine LerouxDepartment of Physics, McGill University, Montreal, Quebec H3A 2T8, Canada.
Jill LaurinDepartment of Physics, McGill University, Montreal, Quebec H3A 2T8, Canada.
David LevensCenter for Cancer Research, National Cancer Institute, Bethesda, MD 20892, USA.
Craig J BenhamGenome Center, University of California Davis, Davis, CA 95616, USA.
Sabrina R LeslieDepartment of Physics, McGill University, Montreal, Quebec H3A 2T8, Canada.
McGill University · CANational Cancer Institute · USUniversity of California, Davis · US

Funding

The genome-wide function of supercoiling and alternative DNA conformationsZIABC011011 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LEVENS, DAVID L. · 2009 to 2025
$16.1M
6 · The paper itself

Abstract

We directly visualize the topology-mediated interactions between an unwinding site on a supercoiled DNA plasmid and a specific probe molecule designed to bind to this site, as a function of DNA supercoiling and temperature. The visualization relies on containing the DNA molecules within an enclosed array of glass nanopits using the Convex Lens-induced Confinement (CLiC) imaging method. This method traps molecules within the focal plane while excluding signal from out-of-focus probes. Simultaneously, the molecules can freely diffuse within the nanopits, allowing for accurate measurements of exchange rates, unlike other methods which could introduce an artifactual bias in measurements of binding kinetics. We demonstrate that the plasmid's structure influences the binding of the fluorescent probes to the unwinding site through the presence, or lack, of other secondary structures. With this method, we observe an increase in the binding rate of the fluorescent probe to the unwinding site with increasing temperature and negative supercoiling. This increase in binding is consistent with the results of our numerical simulations of the probability of site-unwinding. The temperature dependence of the binding rate has allowed us to distinguish the effects of competing higher order DNA structures, such as Z-DNA, in modulating local site-unwinding, and therefore binding.

Indexed as

DNA, SuperhelicalDNA Topoisomerases, Type IKineticsMicroscopy, FluorescenceOligonucleotide ProbesPlasmidsTemperatureDNA, SuperhelicalDNA Topoisomerases, Type IOligonucleotide Probes

Identifiers

PMID29684182
PMCPMC5961182
OpenAlexW2949297585

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.