Evidence map›Paper›PMID 26338775›Full record

ArticleNucleic acids research2015

Cell type-selective disease-association of genes under high regulatory load.

Mafalda Galhardo, Philipp Berninger, Thanh-Phuong Nguyen, Thomas Sauter, Lasse Sinkkonen

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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

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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

5 authors at 2 institutions in 2 countries.

Mafalda GalhardoLife Sciences Research Unit, University of Luxembourg, L-1511 Luxembourg, Luxembourg.
Philipp BerningerBiozentrum, University of Basel and Swiss Institute of Bioinformatics, 4056 Basel, Switzerland.
Thanh-Phuong NguyenLife Sciences Research Unit, University of Luxembourg, L-1511 Luxembourg, Luxembourg.
Thomas SauterLife Sciences Research Unit, University of Luxembourg, L-1511 Luxembourg, Luxembourg.
Lasse SinkkonenLife Sciences Research Unit, University of Luxembourg, L-1511 Luxembourg, Luxembourg lasse.sinkkonen@uni.lu.
University of Luxembourg · LUUniversity of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We previously showed that disease-linked metabolic genes are often under combinatorial regulation. Using the genome-wide ChIP-Seq binding profiles for 93 transcription factors in nine different cell lines, we show that genes under high regulatory load are significantly enriched for disease-association across cell types. We find that transcription factor load correlates with the enhancer load of the genes and thereby allows the identification of genes under high regulatory load by epigenomic mapping of active enhancers. Identification of the high enhancer load genes across 139 samples from 96 different cell and tissue types reveals a consistent enrichment for disease-associated genes in a cell type-selective manner. The underlying genes are not limited to super-enhancer genes and show several types of disease-association evidence beyond genetic variation (such as biomarkers). Interestingly, the high regulatory load genes are involved in more KEGG pathways than expected by chance, exhibit increased betweenness centrality in the interaction network of liver disease genes, and carry longer 3' UTRs with more microRNA (miRNA) binding sites than genes on average, suggesting a role as hubs integrating signals within regulatory networks. In summary, epigenetic mapping of active enhancers presents a promising and unbiased approach for identification of novel disease genes in a cell type-selective manner.

Indexed as

Enhancer Elements, GeneticGene Expression Regulation3' Untranslated RegionsCell LineChromatin ImmunoprecipitationDiseaseEpigenesis, GeneticGene Regulatory NetworksGenetic VariationHigh-Throughput Nucleotide SequencingHumansLiverLiver DiseasesMicroRNAsMonocytesSequence Analysis, DNA3' Untranslated RegionsMicroRNAsTranscription Factors

Identifiers

PMID26338775
PMCPMC4605313
OpenAlexW2118466722

What OpenQuestion holds

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LicenceCC BY
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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.