Evidence map›Paper›PMID 29985428›Full record

ArticleScientific reports2018

Dynamic behavior of DNA topoisomerase IIβ in response to DNA double-strand breaks.

Keiko Morotomi-Yano, Shinta Saito, Noritaka Adachi, Ken-Ichi Yano

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Aclarubicin Reduces the Nuclear Mobility of Human DNA Topoisomerase IIβ.International journal of molecular sciences · 2024
    Article
  5. Article
  6. Article
  7. International journal of molecular sciences · 2023
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. The Role of Topoisomerase II in DNA Repair and Recombination inInternational journal of molecular sciences · 2021
    Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Twist and Turn-Topoisomerase Functions in Mitochondrial DNA Maintenance.International journal of molecular sciences · 2019
    Review
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

4 authors at 3 institutions in 1 country.

Keiko Morotomi-YanoDepartment of Bioelectrics, Institute of Pulsed Power Science, Kumamoto University, Kumamoto, 860-8555, Japan.
Shinta SaitoDepartment of Life and Environmental System Science, Graduate School of Nanobioscience, Yokohama City University, Yokohama, 236-0027, Japan.
Noritaka AdachiDepartment of Life and Environmental System Science, Graduate School of Nanobioscience, Yokohama City University, Yokohama, 236-0027, Japan.
Ken-Ichi YanoDepartment of Bioelectrics, Institute of Pulsed Power Science, Kumamoto University, Kumamoto, 860-8555, Japan. yanoken@kumamoto-u.ac.jp.
Kumamoto University · JPYokohama City University · JPYokohama City University Medical Center · JP

Funding

Japan Society for the Promotion of Science (JSPS) 15H04323Japan Society for the Promotion of Science (JSPS) 16H02311Japan Society for the Promotion of Science (JSPS) 16K01363
6 · The paper itself

Abstract

DNA topoisomerase II (Topo II) is crucial for resolving topological problems of DNA and plays important roles in various cellular processes, such as replication, transcription, and chromosome segregation. Although DNA topology problems may also occur during DNA repair, the possible involvement of Topo II in this process remains to be fully investigated. Here, we show the dynamic behavior of human Topo IIβ in response to DNA double-strand breaks (DSBs), which is the most harmful form of DNA damage. Live cell imaging coupled with site-directed DSB induction by laser microirradiation demonstrated rapid recruitment of EGFP-tagged Topo IIβ to the DSB site. Detergent extraction followed by immunofluorescence showed the tight association of endogenous Topo IIβ with DSB sites. Photobleaching analysis revealed that Topo IIβ is highly mobile in the nucleus. The Topo II catalytic inhibitors ICRF-187 and ICRF-193 reduced the Topo IIβ mobility and thereby prevented Topo IIβ recruitment to DSBs. Furthermore, Topo IIβ knockout cells exhibited increased sensitivity to bleomycin and decreased DSB repair mediated by homologous recombination (HR), implicating the role of Topo IIβ in HR-mediated DSB repair. Taken together, these results highlight a novel aspect of Topo IIβ functions in the cellular response to DSBs.

Indexed as

DNA Breaks, Double-StrandedBleomycinDexrazoxaneDNA RepairDNA Topoisomerases, Type IIHeLa CellsHomologous RecombinationHumansLasersMicroscopy, FluorescenceMutagenesis, Site-DirectedRecombinant Fusion ProteinsBleomycinDexrazoxaneDNA Topoisomerases, Type IIRecombinant Fusion Proteins

Identifiers

PMID29985428
PMCPMC6037730
OpenAlexW2810027625

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.