Evidence map›Paper›PMID 33594057›Full record

ArticleNature communications2021

Positioning of nucleosomes containing γ-H2AX precedes active DNA demethylation and transcription initiation.

Stephanie Dobersch, Karla Rubio, Indrabahadur Singh, Stefan Günther, Johannes Graumann, Julio Cordero, Rafael Castillo-Negrete, Minh Bao Huynh, Aditi Mehta, Peter Braubach and 12 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 52 citations in OpenAlex.

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  16. EP300 as a Molecular Integrator of Fibrotic Transcriptional Programs.International journal of molecular sciences · 2023
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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

22 authors at 13 institutions in 7 countries.

Stephanie DoberschUniv Paris Est Creteil, Glycobiology, Cell Growth and Tissue Repair Research Unit (Gly-CRRET), Brain and Lung Epigenetics (BLUE), Creteil, France.ORCID 0000-0002-6633-4228
Karla RubioUniv Paris Est Creteil, Glycobiology, Cell Growth and Tissue Repair Research Unit (Gly-CRRET), Brain and Lung Epigenetics (BLUE), Creteil, France.ORCID 0000-0002-8337-3106
Indrabahadur SinghLung Cancer Epigenetic, Max-Planck-Institute for Heart and Lung Research, Bad Nauheim, Germany.
Stefan GüntherECCPS Bioinformatics and Deep Sequencing Platform, Bad Nauheim, Germany.
Johannes GraumannBiomolecular Mass Spectrometry, Max-Planck-Institute for Heart and Lung Research, Bad Nauheim, Germany.ORCID 0000-0002-3015-5850
Julio CorderoAnatomy and Developmental Biology, CBTM, Mannheim, Germany.
Rafael Castillo-NegreteUniv Paris Est Creteil, Glycobiology, Cell Growth and Tissue Repair Research Unit (Gly-CRRET), Brain and Lung Epigenetics (BLUE), Creteil, France.
Minh Bao HuynhUniv Paris Est Creteil, Glycobiology, Cell Growth and Tissue Repair Research Unit (Gly-CRRET), F-, Creteil, France.
Aditi MehtaLung Cancer Epigenetic, Max-Planck-Institute for Heart and Lung Research, Bad Nauheim, Germany.
Peter BraubachInstitute for Pathology, Hannover Medical School, Hanover, Germany.ORCID 0000-0003-3673-7779
Hector Cabrera-FuentesFaculty of Medicine, Department of Biochemistry, Justus Liebig University, Giessen, Germany.
Jürgen BernhagenChair of Vascular Biology, Institute for Stroke and Dementia Research (ISD), LMU University Hospital, Ludwig-Maximilians-University (LMU) Munich, Munich, Germany.ORCID 0000-0003-2996-2652
Cho-Ming ChaoCardio-Pulmonary Institute, Giessen, Germany.
Saverio BellusciCardio-Pulmonary Institute, Giessen, Germany.
Andreas GüntherMember of the Universities of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany.ORCID 0000-0002-2187-0975
Klaus T PreissnerFaculty of Medicine, Department of Biochemistry, Justus Liebig University, Giessen, Germany.
Sita KugelHuman Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Gergana DobrevaAnatomy and Developmental Biology, CBTM, Mannheim, Germany.ORCID 0000-0002-4814-9416
Malgorzata WygreckaMember of the Universities of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany.ORCID 0000-0002-3656-2932
Thomas BraunDepartment of Cardiac Development, Max-Planck-Institute for Heart and Lung Research, Bad Nauheim, Germany.ORCID 0000-0002-6165-4804
Dulce Papy-GarciaUniv Paris Est Creteil, Glycobiology, Cell Growth and Tissue Repair Research Unit (Gly-CRRET), F-, Creteil, France.
Guillermo BarretoUniv Paris Est Creteil, Glycobiology, Cell Growth and Tissue Repair Research Unit (Gly-CRRET), Brain and Lung Epigenetics (BLUE), Creteil, France. guillermo.barreto@u-pec.fr.ORCID 0000-0002-7777-4712
Max Planck Institute for Heart and Lung Research · DEUniversité Paris-Est Créteil · FRCape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa · ZACentre National de la Recherche Scientifique · FRHeidelberg University · DEJustus-Liebig-Universität Gießen · DEWenzhou University · CNGerman Cancer Research Center · DEGerman Center for Lung Research · DEInstitute of Bioinformatics and Systems Biology · DEMedizinische Hochschule Hannover · DEMunich Cluster for Systems Neurology · DENational University of Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In addition to nucleosomes, chromatin contains non-histone chromatin-associated proteins, of which the high-mobility group proteins are the most abundant. Chromatin-mediated regulation of transcription involves DNA methylation and histone modifications. However, the order of events and the precise function of high-mobility group proteins during transcription initiation remain unclear. Here we show that high-mobility group AT-hook 2 protein (HMGA2) induces DNA nicks at the transcription start site, which are required by the histone chaperone FACT complex to incorporate nucleosomes containing the histone variant H2A.X. Further, phosphorylation of H2A.X at S139 (γ-H2AX) is required for repair-mediated DNA demethylation and transcription activation. The relevance of these findings is demonstrated within the context of TGFB1 signaling and idiopathic pulmonary fibrosis, suggesting therapies against this lethal disease. Our data support the concept that chromatin opening during transcriptional initiation involves intermediates with DNA breaks that subsequently require DNA repair mechanisms to ensure genome integrity.

Indexed as

DNA DemethylationTranscription Initiation, GeneticAnimalsAtaxia Telangiectasia Mutated ProteinsChromatinHEK293 CellsHistonesHMGA2 ProteinHumansIdiopathic Pulmonary FibrosisMiceNucleosomesPhosphorylationPhosphoserineRNA Polymerase IITranscriptional ActivationAtaxia Telangiectasia Mutated ProteinsChromatingamma-H2AX protein, mouseHistonesHMGA2 ProteinNucleosomesPhosphoserineRNA Polymerase IITransforming Growth Factor beta1

Identifiers

PMID33594057
PMCPMC7886895
OpenAlexW3129633320

What OpenQuestion holds

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LicenceCC BY
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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.