Evidence map›Paper›PMID 30705266›Full record

ArticleNature communications2019

Promoter-proximal pausing mediated by the exon junction complex regulates splicing.

Junaid Akhtar, Nastasja Kreim, Federico Marini, Giriram Mohana, Daniel Brüne, Harald Binder, Jean-Yves Roignant

Abstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
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

27 citing papers in PubMed.

  1. Article
  2. Article
  3. Gene regulation through exon junction complex modularity.Nature structural & molecular biology · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Exon architecture controls mRNA mScience (New York, N.Y.) · 2023
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. mTranscription · 2021
    Review
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

7 authors.

Junaid AkhtarLaboratory of RNA Epigenetics, Institute of Molecular Biology (IMB), 55128, Mainz, Germany.
Nastasja KreimBioinformatics Core Facility, Institute of Molecular Biology (IMB), 55128, Mainz, Germany.
Federico MariniInstitute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), 55101, Mainz, Germany.ORCID http://orcid.org/0000-0003-3252-7758
Giriram MohanaLaboratory of RNA Epigenetics, Institute of Molecular Biology (IMB), 55128, Mainz, Germany.
Daniel BrüneLaboratory of RNA Epigenetics, Institute of Molecular Biology (IMB), 55128, Mainz, Germany.
Harald BinderInstitute of Medical Biometry and Statistics, Faculty of Medicine and Medical Center, University of Freiburg, 79104, Freiburg, Germany.
Jean-Yves RoignantLaboratory of RNA Epigenetics, Institute of Molecular Biology (IMB), 55128, Mainz, Germany. j.roignant@imb-mainz.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Promoter-proximal pausing of RNA polymerase II (Pol II) is a widespread transcriptional regulatory step across metazoans. Here we find that the nuclear exon junction complex (pre-EJC) is a critical and conserved regulator of this process. Depletion of pre-EJC subunits leads to a global decrease in Pol II pausing and to premature entry into elongation. This effect occurs, at least in part, via non-canonical recruitment of pre-EJC components at promoters. Failure to recruit the pre-EJC at promoters results in increased binding of the positive transcription elongation complex (P-TEFb) and in enhanced Pol II release. Notably, restoring pausing is sufficient to rescue exon skipping and the photoreceptor differentiation defect associated with depletion of pre-EJC components in vivo. We propose that the pre-EJC serves as an early transcriptional checkpoint to prevent premature entry into elongation, ensuring proper recruitment of RNA processing components that are necessary for exon definition.

Indexed as

AnimalsCell NucleusExonsGene Expression RegulationHeLa CellsHumansPromoter Regions, GeneticRNA Polymerase IIRNA SplicingRNA Polymerase II

Identifiers

PMID30705266
PMCPMC6355915

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.