Evidence map›Paper›PMID 28712054›Full record

ArticleCell stress & chaperones2018

Alcohol exposure promotes DNA methyltransferase DNMT3A upregulation through reactive oxygen species-dependent mechanisms.

Federico Miozzo, Hélène Arnould, Aurélie de Thonel, Anne-Laure Schang, Délara Sabéran-Djoneidi, Anne Baudry, Benoît Schneider, Valérie Mezger

Open access · greenAbstract read
In one paragraph

Article in Cell stress & chaperones, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 35 citations in OpenAlex.

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  8. Long-term spatial tracking of cells affected by environmental insults.Journal of neurodevelopmental disorders · 2020
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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

8 authors at 3 institutions in 2 countries.

Federico MiozzoCNRS, UMR7216 Épigénétique et Destin Cellulaire, F-75205, Paris Cedex 13, France.
Hélène ArnouldINSERM UMR-S1124, Paris Cedex 6, France.
Aurélie de ThonelCNRS, UMR7216 Épigénétique et Destin Cellulaire, F-75205, Paris Cedex 13, France.
Anne-Laure SchangCNRS, UMR7216 Épigénétique et Destin Cellulaire, F-75205, Paris Cedex 13, France.
Délara Sabéran-DjoneidiCNRS, UMR7216 Épigénétique et Destin Cellulaire, F-75205, Paris Cedex 13, France.
Anne BaudryINSERM UMR-S1124, Paris Cedex 6, France.
Benoît SchneiderINSERM UMR-S1124, Paris Cedex 6, France. benoit.schneider@parisdescartes.fr.
Valérie MezgerCNRS, UMR7216 Épigénétique et Destin Cellulaire, F-75205, Paris Cedex 13, France. valerie.mezger@univ-paris-diderot.fr.ORCID 0000-0003-1623-6213
Délégation Paris 5 · FRCentre National de la Recherche Scientifique · FRUniversity of Geneva · CH

Funding

Agence Nationale de la Recherche Postdoc Fellowship from SAMENTA ANR-13-SAMA-0008-01Agence Nationale de la Recherche Postdoc Fellowship on SAMENTA ANR-13-SAMA-0008-01Agence Nationale de la Recherche SAMENTA ANR-13-SAMA-0008-01Agence Nationale de la Recherche SAMENTA n°13-SAMA-001CNRS (FR) PhD FellowshipFondation Jérôme Lejeune 30RA130012-LEJEUNE-HSFsFondation pour la Recherche en Alcoologie 2014/18Fondation pour la Recherche Médicale PhD FellowshipInstitut de Recherche sur les Boissons 2012/19
6 · The paper itself

Abstract

Abundant evidence has accumulated showing that fetal alcohol exposure broadly modifies DNA methylation profiles in the brain. DNA methyltransferases (DNMTs), the enzymes responsible for DNA methylation, are likely implicated in this process. However, their regulation by ethanol exposure has been poorly addressed. Here, we show that alcohol exposure modulates DNMT protein levels through multiple mechanisms. Using a neural precursor cell line and primary mouse embryonic fibroblasts (MEFs), we found that ethanol exposure augments the levels of Dnmt3a, Dnmt3b, and Dnmt3l transcripts. We also unveil similar elevation of mRNA levels for other epigenetic actors upon ethanol exposure, among which the induction of lysine demethylase Kdm6a shows heat shock factor dependency. Furthermore, we show that ethanol exposure leads to specific increase in DNMT3A protein levels. This elevation not only relies on the upregulation of Dnmt3a mRNA but also depends on posttranscriptional mechanisms that are mediated by NADPH oxidase-dependent production of reactive oxygen species (ROS). Altogether, our work underlines complex regulation of epigenetic actors in response to alcohol exposure at both transcriptional and posttranscriptional levels. Notably, the upregulation of DNMT3A emerges as a prominent molecular event triggered by ethanol, driven by the generation of ROS.

Indexed as

Up-RegulationAnimalsDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3AEmbryo, MammalianEthanolFibroblastsHeat Shock Transcription FactorsMiceNADPH OxidasesNeural Stem CellsReactive Oxygen SpeciesRNA, MessengerDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3ADnmt3a protein, mouseEthanolHeat Shock Transcription FactorsNADPH OxidasesReactive Oxygen SpeciesRNA, MessengerDNA methyltransferasesEpigenetic regulatorsEthanol exposureHeat shock factorsNADPH oxidaseReactive oxygen species (ROS)Transcription

Identifiers

PMID28712054
PMCPMC5741586
OpenAlexW2735864182

What OpenQuestion holds

Textmetadata
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.