Evidence map›Paper›PMID 34728715›Full record

ArticleScientific reports2021

Nucleolar translocation of human DNA topoisomerase II by ATP depletion and its disruption by the RNA polymerase I inhibitor BMH-21.

Keiko Morotomi-Yano, Ken-Ichi Yano

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. 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
1.1field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  7. Aclarubicin Reduces the Nuclear Mobility of Human DNA Topoisomerase IIβ.International journal of molecular sciences · 2024
    Article
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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

2 authors at 2 institutions in 1 country.

Keiko Morotomi-YanoInstitute of Industrial Nanomaterials, Kumamoto University, Kumamoto, Japan.
Ken-Ichi YanoInstitute of Industrial Nanomaterials, Kumamoto University, Kumamoto, Japan. yanoken@kumamoto-u.ac.jp.
Kumamoto Industrial Research Institute · JPKumamoto University · JP

Funding

Japan Society for the Promotion of Science 19H04271
6 · The paper itself

Abstract

DNA topoisomerase II (TOP2) is a nuclear protein that resolves DNA topological problems and plays critical roles in multiple nuclear processes. Human cells have two TOP2 proteins, TOP2A and TOP2B, that are localized in both the nucleoplasm and nucleolus. Previously, ATP depletion was shown to augment the nucleolar localization of TOP2B, but the molecular details of subnuclear distributions, particularly of TOP2A, remained to be fully elucidated in relation to the status of cellular ATP. Here, we analyzed the nuclear dynamics of human TOP2A and TOP2B in ATP-depleted cells. Both proteins rapidly translocated from the nucleoplasm to the nucleolus in response to ATP depletion. FRAP analysis demonstrated that they were highly mobile in the nucleoplasm and nucleolus. The nucleolar retention of both proteins was sensitive to the RNA polymerase I inhibitor BMH-21, and the TOP2 proteins in the nucleolus were immediately dispersed into the nucleoplasm by BMH-21. Under ATP-depleted conditions, the TOP2 poison etoposide was less effective, indicating the therapeutic relevance of TOP2 subnuclear distributions. These results give novel insights into the subnuclear dynamics of TOP2 in relation to cellular ATP levels and also provide discussions about its possible mechanisms and biological significance.

Indexed as

Adenosine TriphosphateCell NucleolusDNA Topoisomerases, Type IIEnzyme InhibitorsEtoposideHeLa CellsHeterocyclic Compounds, 4 or More RingsHumansPoly-ADP-Ribose Binding ProteinsRNA Polymerase ITopoisomerase II InhibitorsTranslocation, GeneticAdenosine TriphosphateBMH-21DNA Topoisomerases, Type IIEnzyme InhibitorsEtoposideHeterocyclic Compounds, 4 or More RingsPoly-ADP-Ribose Binding ProteinsRNA Polymerase ITOP2A protein, humanTOP2B protein, humanTopoisomerase II Inhibitors

Identifiers

PMID34728715
PMCPMC8563764
OpenAlexW3209991777

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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.