Evidence map›Paper›PMID 31590076›Full record

ArticleiScience2019

Long and Repeat-Rich Intronic Sequences Favor Circular RNA Formation under Conditions of Reduced Spliceosome Activity.

Mantian Wang, Jingyi Hou, Michaela Müller-McNicoll, Wei Chen, Erin M Schuman

Open access · goldAbstract read
In one paragraph

Article in iScience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

28 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. AAGGG repeat expansions triggerScience advances · 2024
    Article
  8. Optimal design of synthetic circular RNAs.Experimental & molecular medicine · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Biogenesis and Regulatory Roles of Circular RNAs.Annual review of cell and developmental biology · 2022
    Review
  16. Article
  17. Review
  18. Review
  19. Review
  20. Circular RNAs in the Brain: A Possible Role in Memory?The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2021
    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

5 authors at 4 institutions in 2 countries.

Mantian WangMax Planck Institute for Brain Research, Max-von-Laue-Str.4, 60438 Frankfurt am Main, Germany.
Jingyi HouMax-Delbrueck-Center for Molecular Medicine, 13125 Berlin, Germany.
Michaela Müller-McNicollInstitute for Cell Biology and Neuroscience, Goethe University, 60438 Frankfurt, Germany.
Wei ChenDepartment of Biology, Southern University of Science and Technology, Shenzhen 518055, China.
Erin M SchumanMax Planck Institute for Brain Research, Max-von-Laue-Str.4, 60438 Frankfurt am Main, Germany. Electronic address: erin.schuman@brain.mpg.de.
Max Planck Institute for Brain Research · DEGoethe University Frankfurt · DEMax Delbrück Center · DESouthern University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circular RNAs (circRNAs), an important class of regulatory RNAs, have been shown to be the most prevalent in the brain compared with other tissues. However the processes governing their biogenesis in neurons are still elusive. Moreover, little is known about whether and how different biogenesis factors work in synchrony to generate neuronal circRNAs. To address this question, we pharmacologically inhibited the spliceosome and profiled rat neuronal circRNAs using RNA sequencing. We identified over 100 circRNAs that were up-regulated and a few circRNAs that were down-regulated upon spliceosome inhibition. Bioinformatic analysis revealed that up-regulated circRNAs possess significantly longer flanking introns compared with the un-changed circRNA population. Moreover, the flanking introns of up-regulated circRNAs harbor a higher number of distinct repeat sequences and more reverse complementary motifs compared with the unchanged circRNAs. Taken together, our data demonstrate that the biogenesis of circRNAs containing distinct intronic features becomes favored under conditions of limited spliceosome activity.

Indexed as

Biological SciencesCell BiologyMolecular BiologyOmics

Identifiers

PMID31590076
PMCPMC6817660
OpenAlexW2971913097

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.