Evidence map›Paper›PMID 29138457›Full record

ArticleScientific reports2017

Functional annotation of structural ncRNAs within enhancer RNAs in the human genome: implications for human disease.

Chao Ren, Feng Liu, Zhangyi Ouyang, Gaole An, Chenghui Zhao, Jun Shuai, Shuhong Cai, Xiaochen Bo, Wenjie Shu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-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

18 citing papers in PubMed, 29 citations in OpenAlex.

  1. Role of eRNAs in Cardiovascular Diseases.Current cardiology reviews · 2026
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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

9 authors at 3 institutions in 1 country.

Chao RenDepartment of Biotechnology, Beijing Institute of Radiation Medicine, Beijing, China.
Feng LiuDepartment of Biotechnology, Beijing Institute of Radiation Medicine, Beijing, China.
Zhangyi OuyangDepartment of Biotechnology, Beijing Institute of Radiation Medicine, Beijing, China.
Gaole AnDepartment of Biotechnology, Beijing Institute of Radiation Medicine, Beijing, China.
Chenghui ZhaoDepartment of Biotechnology, Beijing Institute of Radiation Medicine, Beijing, China.
Jun ShuaiDepartment of Information, The 188th Hospital of ChaoZhou, ChaoZhou, China.
Shuhong CaiDepartment of Information, The 188th Hospital of ChaoZhou, ChaoZhou, China.
Xiaochen BoDepartment of Biotechnology, Beijing Institute of Radiation Medicine, Beijing, China. boxc@bmi.ac.cn.
Wenjie ShuDepartment of Biotechnology, Beijing Institute of Radiation Medicine, Beijing, China. shuwj@bmi.ac.cn.ORCID 0000-0001-9044-2352
Beijing Radiation Center · CNChaozhou Central Hospital · CNBeijing VDJBio (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Enhancer RNAs (eRNAs) are a novel class of non-coding RNA (ncRNA) molecules transcribed from the DNA sequences of enhancer regions. Despite extensive efforts devoted to revealing the potential functions and underlying mechanisms of eRNAs, it remains an open question whether eRNAs are mere transcriptional noise or relevant biologically functional species. Here, we identified a catalogue of eRNAs in a broad range of human cell/tissue types and extended our understanding of eRNAs by demonstrating their multi-omic signatures. Gene Ontology (GO) analysis revealed that eRNAs play key roles in human cell identity. Furthermore, we detected numerous known and novel functional RNA structures within eRNA regions. To better characterize the cis-regulatory effects of non-coding variation in these structural ncRNAs, we performed a comprehensive analysis of the genetic variants of structural ncRNAs in eRNA regions that are associated with inflammatory autoimmune diseases. Disease-associated variants of the structural ncRNAs were disproportionately enriched in immune-specific cell types. We also identified riboSNitches in lymphoid eRNAs and investigated the potential pathogenic mechanisms by which eRNAs might function in autoimmune diseases. Collectively, our findings offer valuable insights into the function of eRNAs and suggest that eRNAs might be effective diagnostic and therapeutic targets for human diseases.

Indexed as

Autoimmune DiseasesBase PairingComputational BiologyDatabases, GeneticDatasets as TopicEnhancer Elements, GeneticGene OntologyGenome, HumanHumansLymphocytesMolecular Sequence AnnotationNucleic Acid ConformationPromoter Regions, GeneticRNA, UntranslatedTranscriptional ActivationTranscription, GeneticRNA, Untranslated

Identifiers

PMID29138457
PMCPMC5686184
OpenAlexW2767904963

What OpenQuestion holds

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LicenceCC BY
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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.