Evidence map›Paper›PMID 27824289›Full record

ArticleEpigenetics2016

PEG3 binds to H19-ICR as a transcriptional repressor.

An Ye, Hongzhi He, Joomyeong Kim

Abstract read
In one paragraph

Article in Epigenetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Long noncoding RNA H19 - a new player in the pathogenesis of liver diseases.Translational research : the journal of laboratory and clinical medicine · 2021
    Review
  4. Article
  5. Long Noncoding RNA H19: A Novel Therapeutic Target Emerging in OncologyFrontiers in cell and developmental biology · 2021
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

3 authors.

An Yea Department of Biological Sciences , Louisiana State University , Baton Rouge , LA , USA.
Hongzhi Hea Department of Biological Sciences , Louisiana State University , Baton Rouge , LA , USA.
Joomyeong Kima Department of Biological Sciences , Louisiana State University , Baton Rouge , LA , USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paternally expressed gene 3 (Peg3) encodes a DNA-binding protein with 12 C2H2 zinc finger motifs. In the current study, we performed ChIP-seq using mouse embryonic fibroblast (MEF) cells. This experiment identified a set of 16 PEG3 genomic targets, the majority of which overlapped with the promoter regions of genes with oocyte expression. These potential downstream genes were upregulated in MEF cells lacking PEG3 protein, suggesting a potential repressor role for PEG3. Our study also identified the imprinting control region (ICR) of H19 as a genomic target. According to the results, PEG3 binds to a specific sequence motif located between the 3

Indexed as

AnimalsBinding SitesCCCTC-Binding FactorDNA-Binding ProteinsDNA MethylationFemaleGene Expression Regulation, DevelopmentalGenomic ImprintingHumansKruppel-Like Transcription FactorsMiceOocytesPromoter Regions, GeneticProtein BindingRepressor ProteinsRNA, Long NoncodingCCCTC-Binding FactorCTCF protein, humanCtcf protein, mouseDNA-Binding ProteinsH19 long non-coding RNAKruppel-Like Transcription FactorsPeg3 protein, mouseRepressor ProteinsRNA, Long NoncodingChIP-seqCTCFH19imprinting control regionPeg3transcriptional factor

Identifiers

PMID27824289
PMCPMC5193492

What OpenQuestion holds

Textmetadata
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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.