Evidence map›Paper›PMID 23249747›Full record

ArticleRNA (New York, N.Y.)2013

Circular RNAs are abundant, conserved, and associated with ALU repeats.

William R Jeck, Jessica A Sorrentino, Kai Wang, Michael K Slevin, Christin E Burd, Jinze Liu, William F Marzluff, Norman E Sharpless

Erratum issued Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in RNA (New York, N.Y.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT03170830 (Study on CircRNA-Uck2 as a New Diagnostic Marker of Acute Myocardial Infarction), which is not on this map. Cited by 2,669 papers.

0numbers the graph read from it
0cells of the map it votes in
2,669citing papers in PubMed
22.8field-weighted citation impact, top 1% 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.

NCT03170830 naunknown statusnot on this mapstarted 2015, after this paper: background citation

Study on CircRNA-Uck2 as a New Diagnostic Marker of Acute Myocardial Infarction

TypeinterventionalSponsorBeijing Haidian HospitalRan2015 to 2018Enrolled178ConditionsCardiac Disease, Diagnoses Disease, Acute Myocardial InfarctionArmsthe diagnosis value of cUck2 in acute myocardial infarction.
3 · Its place in the literature

Who cites it

2,669 citing papers in PubMed, 4,505 citations in OpenAlex.

  1. Review
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  3. Cell adhesion & migration · 2026
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  8. Circular RNAs in ferroptosis regulation and tumor progression of gynecological and breast cancers: molecular mechanisms and therapeutic potential.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  9. Genome stability disrupted by the circRBM39(4,5,6)-RPA2 axis represses breast tumorigenesis.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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2,609 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

William R JeckDepartment of Genetics, University of North Carolina School of Medicine, Chapel Hill, North Carolina 27599-7295, USA.
Jessica A Sorrentino
Kai Wang
Michael K Slevin
Christin E Burd
Jinze Liu
William F Marzluff
Norman E Sharpless
University of North Carolina at Chapel Hill · USUniversity of Kentucky · US

Funding

TOXICOLOGYT32ES007126 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ILONA JASPERS, Bernard E. Weissman · 1985 to 2026
$13.0M
NRSA IN GENETICST32GM007092 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SEKELSKY, JEFF J. · 1985 to 2019
$5.9M
The Role of p16INK4 in Mammalian AgingR01AG024379 · NIA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HE, SHENGHUI · 2004 to 2019
$4.6M
Unlocking transcript diversity via differential analyses of splice graphsR01HG006272 · NHGRI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LIU, JINZE, PRINS, JAN F · 2012 to 2014
$1.2M
Endogenous Circular RNAs and the Control of Expression of Aging-related GenesF30AG041567 · NIA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI JECK, WILLIAM R · 2011 to 2014
$133k
TUT ase mediated degradation of histone mRNAF32GM087059 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SLEVIN, MICHAEL KEITH · 2009 to 2010
$72k
NHGRI NIH HHS R01 HG006272NIA NIH HHS AG024379NIA NIH HHS AG041567NIA NIH HHS F30 AG041567NIA NIH HHS R01 AG024379NIEHS NIH HHS T32 ES007126NIGMS NIH HHS F32 GM087059NIGMS NIH HHS T32 GM007092
6 · The paper itself

Abstract

Circular RNAs composed of exonic sequence have been described in a small number of genes. Thought to result from splicing errors, circular RNA species possess no known function. To delineate the universe of endogenous circular RNAs, we performed high-throughput sequencing (RNA-seq) of libraries prepared from ribosome-depleted RNA with or without digestion with the RNA exonuclease, RNase R. We identified >25,000 distinct RNA species in human fibroblasts that contained non-colinear exons (a "backsplice") and were reproducibly enriched by exonuclease degradation of linear RNA. These RNAs were validated as circular RNA (ecircRNA), rather than linear RNA, and were more stable than associated linear mRNAs in vivo. In some cases, the abundance of circular molecules exceeded that of associated linear mRNA by >10-fold. By conservative estimate, we identified ecircRNAs from 14.4% of actively transcribed genes in human fibroblasts. Application of this method to murine testis RNA identified 69 ecircRNAs in precisely orthologous locations to human circular RNAs. Of note, paralogous kinases HIPK2 and HIPK3 produce abundant ecircRNA from their second exon in both humans and mice. Though HIPK3 circular RNAs contain an AUG translation start, it and other ecircRNAs were not bound to ribosomes. Circular RNAs could be degraded by siRNAs and, therefore, may act as competing endogenous RNAs. Bioinformatic analysis revealed shared features of circularized exons, including long bordering introns that contained complementary ALU repeats. These data show that ecircRNAs are abundant, stable, conserved and nonrandom products of RNA splicing that could be involved in control of gene expression.

Indexed as

Alu ElementsAnimalsBase SequenceCells, CulturedComputational BiologyConserved SequenceEvolution, MolecularExonsExoribonucleasesGene Expression RegulationHigh-Throughput Nucleotide SequencingHumansMaleMiceMolecular Sequence DataNucleotide MotifsExoribonucleasesPhosphotransferasesribonuclease RRNARNA, CircularRNA, Small Interfering

Identifiers

PMID23249747
PMCPMC3543092
OpenAlexW2147806662

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.