Evidence map›Paper›PMID 24427299›Full record

ArticlePloS one2014

Alterations of epigenetic signatures in hepatocyte nuclear factor 4α deficient mouse liver determined by improved ChIP-qPCR and (h)MeDIP-qPCR assays.

Qinghao Zhang, Xiaohong Lei, Hong Lu

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Crosstalk of HNF4Acta pharmaceutica Sinica. B · 2016
    Review
  12. Article
  13. 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 at 1 institution in 1 country.

Qinghao ZhangDepartment of Pharmacology, SUNY Upstate Medical University, Syracuse, New York, United States of America.
Xiaohong LeiDepartment of Pharmacology, SUNY Upstate Medical University, Syracuse, New York, United States of America.
Hong LuDepartment of Pharmacology, SUNY Upstate Medical University, Syracuse, New York, United States of America.
SUNY Upstate Medical University · US

Funding

Developmental Regulation of Drug Processing GenesR01ES019487 · NIEHS · UNIVERSITY OF WASHINGTON · PI CUI, JULIA YUE, LU, HONG · 2010 to 2014
$3.0M
Histone methyltransferase EZH2 in liver pathophysiology and carcinogenesisR03CA159350 · NCI · UPSTATE MEDICAL UNIVERSITY · PI LU, HONG · 2011 to 2012
$160k
Histone methyltransferase G9a in liver pathophysiology and carcinogenesisR03CA143656 · NCI · UPSTATE MEDICAL UNIVERSITY · PI LU, HONG · 2010 to 2011
$152k
NCI NIH HHS CA143656NCI NIH HHS CA159350NCI NIH HHS R03 CA143656NCI NIH HHS R03 CA159350NIEHS NIH HHS ES019487NIEHS NIH HHS R01 ES019487
6 · The paper itself

Abstract

Hepatocyte nuclear factor 4α (HNF4α) is a liver-enriched transcription factor essential for liver development and function. In hepatocytes, HNF4α regulates a large number of genes important for nutrient/xenobiotic metabolism and cell differentiation and proliferation. Currently, little is known about the epigenetic mechanism of gene regulation by HNF4α. In this study, the global and specific alterations at the selected gene loci of representative histone modifications and DNA methylations were investigated in Hnf4a-deficient female mouse livers using the improved MeDIP-, hMeDIP- and ChIP-qPCR assay. Hnf4a deficiency significantly increased hepatic total IPed DNA fragments for histone H3 lysine-4 dimethylation (H3K4me2), H3K4me3, H3K9me2, H3K27me3 and H3K4 acetylation, but not for H3K9me3, 5-methylcytosine,or 5-hydroxymethylcytosine. At specific gene loci, the relative enrichments of histone and DNA modifications were changed to different degree in Hnf4a-deficient mouse liver. Among the epigenetic signatures investigated, changes in H3K4me3 correlated the best with mRNA expression. Additionally, Hnf4a-deficient livers had increased mRNA expression of histone H1.2 and H3.3 as well as epigenetic modifiers Dnmt1, Tet3, Setd7, Kmt2c, Ehmt2, and Ezh2. In conclusion, the present study provides convenient improved (h)MeDIP- and ChIP-qPCR assays for epigenetic study. Hnf4a deficiency in young-adult mouse liver markedly alters histone methylation and acetylation, with fewer effects on DNA methylation and 5-hydroxymethylation. The underlying mechanism may be the induction of epigenetic enzymes responsible for the addition/removal of the epigenetic signatures, and/or the loss of HNF4α per se as a key coordinator for epigenetic modifiers.

Indexed as

Epigenesis, GeneticEpigenomicsAnimalsChromatin ImmunoprecipitationDNA MethylationFemaleHepatocyte Nuclear Factor 4HistonesLiverMiceMice, KnockoutReal-Time Polymerase Chain ReactionReproducibility of ResultsRNA, MessengerSensitivity and SpecificityHepatocyte Nuclear Factor 4HistonesHnf4a protein, mouseRNA, Messenger

Identifiers

PMID24427299
PMCPMC3888413
OpenAlexW2058211893

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.