Evidence map›Paper›PMID 29449903›Full record

ReviewClinical epigenetics2018

Specific or not specific recruitment of DNMTs for DNA methylation, an epigenetic dilemma.

Eric Hervouet, Paul Peixoto, Régis Delage-Mourroux, Michaël Boyer-Guittaut, Pierre-François Cartron

Open access · goldAbstract readReview
In one paragraph

Review in Clinical epigenetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 130 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
130citing papers in PubMed, 1 pooled it
10.5field-weighted citation impact, top 1% 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

130 citing papers in PubMed, 1 synthesis or guideline pooled it, 243 citations in OpenAlex.

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  12. Reversing transgene silencing via targeted chromatin editing.bioRxiv : the preprint server for biology · 2025
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70 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

Eric HervouetINSERM unit 1098, University of Bourgogne Franche-Comté, Besançon, France.
Paul PeixotoINSERM unit 1098, University of Bourgogne Franche-Comté, Besançon, France.
Régis Delage-MourrouxINSERM unit 1098, University of Bourgogne Franche-Comté, Besançon, France.
Michaël Boyer-GuittautINSERM unit 1098, University of Bourgogne Franche-Comté, Besançon, France.
Pierre-François Cartron3INSERM unit S1232, University of Nantes, Nantes, France.
Université Bourgogne Franche-Comté · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our current view of DNA methylation processes is strongly moving: First, even if it was generally admitted that DNMT3A and DNMT3B are associated with de novo methylation and DNMT1 is associated with inheritance DNA methylation, these distinctions are now not so clear. Secondly, since one decade, many partners of DNMTs have been involved in both the regulation of DNA methylation activity and DNMT recruitment on DNA. The high diversity of interactions and the combination of these interactions let us to subclass the different DNMT-including complexes. For example, the DNMT3L/DNMT3A complex is mainly related to de novo DNA methylation in embryonic states, whereas the DNMT1/PCNA/UHRF1 complex is required for maintaining global DNA methylation following DNA replication. On the opposite to these unspecific DNA methylation machineries (no preferential DNA sequence), some recently identified DNMT-including complexes are recruited on specific DNA sequences. The coexistence of both types of DNA methylation (un/specific) suggests a close cooperation and an orchestration between these systems to maintain genome and epigenome integrities. Deregulation of these systems can lead to pathologic disorders.

Indexed as

DNA MethylationAnimalsDNA (Cytosine-5-)-MethyltransferasesDNA ReplicationEmbryonic DevelopmentEpigenesis, GeneticHumansDNA (Cytosine-5-)-MethyltransferasesDNA methylationDNMT1DNMT3ADNMT3BDNMT3LDNMT-including complexesEpigenetics

Identifiers

PMID29449903
PMCPMC5807744
OpenAlexW2794563065

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.