Evidence map›Paper›PMID 26239807›Full record

ArticleScientific reports2015

Genome-wide hydroxymethylcytosine pattern changes in response to oxidative stress.

Benjamin Delatte, Jana Jeschke, Matthieu Defrance, Martin Bachman, Catherine Creppe, Emilie Calonne, Martin Bizet, Rachel Deplus, Laura Marroquí, Myriam Libin and 6 more

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–field-weighted citation impact
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

35 citing papers in PubMed.

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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

16 authors.

Benjamin DelatteLaboratory of Cancer Epigenetics, Faculty of Medicine, ULB, 1070 Brussels, Belgium.
Jana JeschkeLaboratory of Cancer Epigenetics, Faculty of Medicine, ULB, 1070 Brussels, Belgium.
Matthieu DefranceLaboratory of Cancer Epigenetics, Faculty of Medicine, ULB, 1070 Brussels, Belgium.
Martin BachmanCRUK Cambridge Institute, University of Cambridge, Cambridge CB2 0RE, United Kingdom.
Catherine CreppeLaboratory of Cancer Epigenetics, Faculty of Medicine, ULB, 1070 Brussels, Belgium.
Emilie CalonneLaboratory of Cancer Epigenetics, Faculty of Medicine, ULB, 1070 Brussels, Belgium.
Martin BizetLaboratory of Cancer Epigenetics, Faculty of Medicine, ULB, 1070 Brussels, Belgium.
Rachel DeplusLaboratory of Cancer Epigenetics, Faculty of Medicine, ULB, 1070 Brussels, Belgium.
Laura MarroquíULB, Center for Diabetes Research, Faculty of Medicine, ULB, 1070 Brussels, Belgium.
Myriam LibinLaboratory of Vaccinology and Mucosal Immunity, Faculty of Medicine, ULB, 1070 Brussels, Belgium.
Mirunalini RavichandranInstitute of Biochemistry, Stuttgart University, 70569 Stuttgart, Germany.
Françoise MascartLaboratory of Vaccinology and Mucosal Immunity, Faculty of Medicine, ULB, 1070 Brussels, Belgium.
Decio L EizirikULB, Center for Diabetes Research, Faculty of Medicine, ULB, 1070 Brussels, Belgium.
Adele MurrellCRUK Cambridge Institute, University of Cambridge, Cambridge CB2 0RE, United Kingdom.
Tomasz P JurkowskiInstitute of Biochemistry, Stuttgart University, 70569 Stuttgart, Germany.
François FuksLaboratory of Cancer Epigenetics, Faculty of Medicine, ULB, 1070 Brussels, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The TET enzymes convert methylcytosine to the newly discovered base hydroxymethylcytosine. While recent reports suggest that TETs may play a role in response to oxidative stress, this role remains uncertain, and results lack in vivo models. Here we show a global decrease of hydroxymethylcytosine in cells treated with buthionine sulfoximine, and in mice depleted for the major antioxidant enzymes GPx1 and 2. Furthermore, genome-wide profiling revealed differentially hydroxymethylated regions in coding genes, and intriguingly in microRNA genes, both involved in response to oxidative stress. These results thus suggest a profound effect of in vivo oxidative stress on the global hydroxymethylome.

Indexed as

Genome5-MethylcytosineAnimalsAntimetabolitesButhionine SulfoximineCell Line, TumorDioxygenasesDNA-Binding ProteinsGene Expression ProfilingGene Expression RegulationGenome-Wide Association StudyGlutathioneGlutathione PeroxidaseGlutathione Peroxidase GPX1MiceMice, Knockout5-MethylcytosineAntimetabolitesButhionine SulfoximineDioxygenasesDNA-Binding ProteinsGlutathioneGlutathione PeroxidaseGlutathione Peroxidase GPX1Gpx1 protein, mouseGpx2 protein, mouseMicroRNAsProto-Oncogene ProteinsTET1 protein, mouseTet2 protein, mouse

Identifiers

PMID26239807
PMCPMC4523844

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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.