Evidence map›Paper›PMID 25280477›Full record

ArticleJournal of molecular cell biology2015

Hot spots of DNA double-strand breaks and genomic contacts of human rDNA units are involved in epigenetic regulation.

Nickolai A Tchurikov, Daria M Fedoseeva, Dmitri V Sosin, Anastasia V Snezhkina, Nataliya V Melnikova, Anna V Kudryavtseva, Yuri V Kravatsky, Olga V Kretova

Open access · bronzeAbstract read
In one paragraph

Article in Journal of molecular cell biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

52 citing papers in PubMed, 70 citations in OpenAlex.

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  15. Chromosomal Diversification inAnimals : an open access journal from MDPI · 2022
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  17. Unraveling the DNA Methylation in the rDNA Foci in Mutagen-InducedInternational journal of molecular sciences · 2022
    Article
  18. Article
  19. Treacle Sticks the Nucleolar Responses to DNA Damage Together.Frontiers in cell and developmental biology · 2022
    Review
  20. 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 at 1 institution in 1 country.

Nickolai A TchurikovDepartment of Epigenetic Mechanisms of Gene Expression Regulation, Engelhardt Institute of Molecular Biology, Moscow 119334, Russia tchurikov@eimb.ru.
Daria M FedoseevaDepartment of Epigenetic Mechanisms of Gene Expression Regulation, Engelhardt Institute of Molecular Biology, Moscow 119334, Russia.
Dmitri V SosinDepartment of Epigenetic Mechanisms of Gene Expression Regulation, Engelhardt Institute of Molecular Biology, Moscow 119334, Russia.
Anastasia V SnezhkinaGroup of Postgenomic Studies, Engelhardt Institute of Molecular Biology, Moscow 119334, Russia.
Nataliya V MelnikovaGroup of Postgenomic Studies, Engelhardt Institute of Molecular Biology, Moscow 119334, Russia.
Anna V KudryavtsevaGroup of Postgenomic Studies, Engelhardt Institute of Molecular Biology, Moscow 119334, Russia.
Yuri V KravatskyLaboratory of DNA-Protein Interactions, Engelhardt Institute of Molecular Biology, Moscow 119334, Russia.
Olga V KretovaDepartment of Epigenetic Mechanisms of Gene Expression Regulation, Engelhardt Institute of Molecular Biology, Moscow 119334, Russia.
Engelhardt Institute of Molecular Biology · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA double-strand breaks (DSBs) are involved in many cellular mechanisms, including replication, transcription, and genome rearrangements. The recent observation that hot spots of DSBs in human chromosomes delimit DNA domains that possess coordinately expressed genes suggests a strong relationship between the organization of transcription patterns and hot spots of DSBs. In this study, we performed mapping of hot spots of DSBs in a human 43-kb ribosomal DNA (rDNA) repeated unit. We observed that rDNA units corresponded to the most fragile sites in human chromosomes and that these units possessed at least nine specific regions containing clusters of extremely frequently occurring DSBs, which were located exclusively in non-coding intergenic spacer (IGS) regions. The hot spots of DSBs corresponded to only a specific subset of DNase-hypersensitive sites, and coincided with CTCF, PARP1, and HNRNPA2B1 binding sites, and H3K4me3 marks. Our rDNA-4C data indicate that the regions of IGS containing the hot spots of DSBs often form contacts with specific regions in different chromosomes, including the pericentromeric regions, as well as regions that are characterized by H3K27ac and H3K4me3 marks, CTCF binding sites, ChIA-PET and RIP signals, and high levels of DSBs. The data suggest a strong link between chromosome breakage and several different mechanisms of epigenetic regulation of gene expression.

Indexed as

DNA Breaks, Double-StrandedEpigenesis, GeneticGenome, HumanCCCTC-Binding FactorChromatinChromatin ImmunoprecipitationChromosomes, HumanDeoxyribonuclease IDNA MethylationDNA ReplicationDNA, RibosomalHEK293 CellsHeterogeneous-Nuclear Ribonucleoprotein Group A-BHistonesHumansLysineCCCTC-Binding FactorChromatinCTCF protein, humanDeoxyribonuclease IDNA, RibosomalHeterogeneous-Nuclear Ribonucleoprotein Group A-BHistonesLysinePoly(ADP-ribose) PolymerasesRepressor Proteins4Cdouble-strand breaksfragile sitesHNRNPA2B1IGSPARP1rDNA

Identifiers

PMID25280477
PMCPMC4524424
OpenAlexW2102113193

What OpenQuestion holds

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LicenceCC BY-NC
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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.