Evidence map›Paper›PMID 25765649›Full record

ArticleNucleic acids research2015

A diverse epigenetic landscape at human exons with implication for expression.

Meromit Singer, Idit Kosti, Lior Pachter, Yael Mandel-Gutfreund

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

33 citing papers in PubMed, 55 citations in OpenAlex.

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  14. Role ofThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  15. Article
  16. Methylation changes at theWorld journal of gastrointestinal oncology · 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

4 authors at 1 institution in 1 country.

Meromit SingerDepartment of Computer Science, University of California at Berkeley, Berkeley, CA 94720 USA.
Idit KostiDepartment of Molecular & Cell Biology, University of California at Berkeley, Berkeley, CA 94720, USA.
Lior PachterDepartment of Computer Science, University of California at Berkeley, Berkeley, CA 94720 USA Department of Mathematics, University of California at Berkeley, Berkeley, CA 94720, USA Department of Molecular & Cell Biology, University of California at Berkeley, Berkeley, CA 94720, USA.
Yael Mandel-GutfreundDepartment of Molecular & Cell Biology, University of California at Berkeley, Berkeley, CA 94720, USA yaelmg@tx.technion.ac.il.
University of California, Berkeley · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA methylation is an important epigenetic marker associated with gene expression regulation in eukaryotes. While promoter methylation is relatively well characterized, the role of intragenic DNA methylation remains unclear. Here, we investigated the relationship of DNA methylation at exons and flanking introns with gene expression and histone modifications generated from a human fibroblast cell-line and primary B cells. Consistent with previous work we found that intragenic methylation is positively correlated with gene expression and that exons are more highly methylated than their neighboring intronic environment. Intriguingly, in this study we identified a unique subset of hypomethylated exons that demonstrate significantly lower methylation levels than their surrounding introns. Furthermore, we observed a negative correlation between exon methylation and the density of the majority of histone modifications. Specifically, we demonstrate that hypo-methylated exons at highly expressed genes are associated with open chromatin and have a characteristic histone code comprised of significantly high levels of histone markings. Overall, our comprehensive analysis of the human exome supports the presence of regulatory hypomethylated exons in protein coding genes. In particular our results reveal a previously unrecognized diverse and complex role of the epigenetic landscape within the gene body.

Indexed as

Epigenesis, GeneticExonsDNADNA MethylationHumansIntronsDNA

Identifiers

PMID25765649
PMCPMC4402514
OpenAlexW2064372674

What OpenQuestion holds

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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.