Evidence map›Paper›PMID 30713098›Full record

ArticleCell chemical biology2019

Selection of DNA Cleavage Sites by Topoisomerase II Results from Enzyme-Induced Flexibility of DNA.

Yunsu Jang, Heyjin Son, Sang-Wook Lee, Wonseok Hwang, Seung-Ryoung Jung, Jo Ann W Byl, Neil Osheroff, Sanghwa Lee

Abstract read
In one paragraph

Article in Cell chemical biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Target-Mediated Fluoroquinolone Resistance inACS infectious diseases · 2024
    Article
  6. Review
  7. Article
  8. MgProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  9. Review
  10. Article
  11. Article
  12. Length Polymorphism and Methylation Status of UPS29 Minisatellite of theInternational journal of molecular sciences · 2020
    Article
  13. 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

8 authors.

Yunsu JangAdvanced Photonics Research Institute, Gwangju Institute of Science and Technology, Gwangju 61005, South Korea.
Heyjin SonAdvanced Photonics Research Institute, Gwangju Institute of Science and Technology, Gwangju 61005, South Korea.
Sang-Wook LeeDepartment of Physics and Astronomy, National Center for Creative Research Initiatives, Seoul National University, Seoul 08826, South Korea.
Wonseok HwangDepartment of Physics and Astronomy, National Center for Creative Research Initiatives, Seoul National University, Seoul 08826, South Korea.
Seung-Ryoung JungDepartment of Physics and Astronomy, National Center for Creative Research Initiatives, Seoul National University, Seoul 08826, South Korea.
Jo Ann W BylDepartment of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN 37232-0146, USA.
Neil OsheroffDepartment of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN 37232-0146, USA; Department of Medicine (Hematology/Oncology), Vanderbilt University School of Medicine, Nashville, TN 37232-0146, USA; VA Tennessee Valley Healthcare System, Nashville, TN 37212, USA. Electronic address: neil.osheroff@vanderbilt.edu.
Sanghwa LeeAdvanced Photonics Research Institute, Gwangju Institute of Science and Technology, Gwangju 61005, South Korea. Electronic address: sanglee@gist.ac.kr.

Funding

FUNCTION AND BIOLOGY OF EUKARYOTIC DNA TOPOISOMERASESR01GM033944 · NIGMS · VANDERBILT UNIVERSITY · PI OSHEROFF, NEIL · 1985 to 2015
$5.5M
Mechanistic Studies of Type II Topoisomerases and Topoisomerase-Targeted AgentsR01GM126363 · NIGMS · VANDERBILT UNIVERSITY · PI OSHEROFF, NEIL · 2018 to 2025
$2.6M
NIGMS NIH HHS R01 GM033944NIGMS NIH HHS R01 GM126363
6 · The paper itself

Abstract

Topoisomerase II cleaves DNA at preferred sequences with different efficiencies; however, the mechanism of cleavage site selection is not known. Here we used single-molecule fluorescence assays that monitor several critical steps of DNA-topoisomerase II interactions, including binding/dissociation, bending/straightening, and cleavage/religation, and reveal that the cleavage site is selected mainly during the bending step. Furthermore, despite the sensitivity of the bending rate to the DNA sequence, it is not an intrinsic property of the DNA itself. Rather, it is determined by protein-DNA interactions.

Indexed as

DNA CleavageBase SequenceDNA, FungalDNA Topoisomerases, Type IINucleic Acid ConformationProtein BindingSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSubstrate SpecificityDNA, FungalDNA Topoisomerases, Type IISaccharomyces cerevisiae ProteinsDNA bendingDNA cleavageDNA flexibilityG-segment selectionsequence preferencesingle-molecule FRETtopoisomerase IItwo-metal-ion mechanism

Identifiers

PMID30713098
PMCPMC6474810

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Registered trials

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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.