Evidence map›Paper›PMID 29934576›Full record

ArticleScientific reports2018

Exon Junction Complexes can have distinct functional flavours to regulate specific splicing events.

Zhen Wang, Lionel Ballut, Isabelle Barbosa, Hervé Le Hir

Abstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
  2. Article
  3. Gene regulation through exon junction complex modularity.Nature structural & molecular biology · 2025
    Review
  4. Article
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  6. Article
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  8. Article
  9. Analysis of the Upregulated Expression Mechanism of Apoptotic Chromatin Condensation Inducer 1 in Hepatocellular Carcinoma Based on Bioinformatics.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2024
    Article
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  11. Article
  12. Article
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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

4 authors.

Zhen WangInstitut de biologie de l'Ecole normale supérieure (IBENS), Ecole normale supérieure, CNRS, INSERM, PSL Research University, Paris, F-75005, France.
Lionel BallutInstitut de Biologie et Chimie des Protéines, CNRS UMR5086, Université de Lyon 1, Lyon, France.
Isabelle BarbosaInstitut de biologie de l'Ecole normale supérieure (IBENS), Ecole normale supérieure, CNRS, INSERM, PSL Research University, Paris, F-75005, France.
Hervé Le HirInstitut de biologie de l'Ecole normale supérieure (IBENS), Ecole normale supérieure, CNRS, INSERM, PSL Research University, Paris, F-75005, France. lehir@ens.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The exon junction complex (EJC) deposited on spliced mRNAs, plays a central role in the post-transcriptional gene regulation and specific gene expression. The EJC core complex is associated with multiple peripheral factors involved in various post-splicing events. Here, using recombinant complex reconstitution and transcriptome-wide analysis, we showed that the EJC peripheral protein complexes ASAP and PSAP form distinct complexes with the EJC core and can confer to EJCs distinct alternative splicing regulatory activities. This study provides the first evidence that different EJCs can have distinct functions, illuminating EJC-dependent gene regulation.

Indexed as

RNA SplicingAlternative SplicingCell Adhesion MoleculesExonsHeLa CellsHumansMicrotubule-Associated ProteinsNuclear ProteinsSaposinsACIN1 protein, humanCell Adhesion MoleculesMAP9 protein, humanMicrotubule-Associated ProteinsNuclear ProteinsPNN protein, humanPSAP protein, humanSaposins

Identifiers

PMID29934576
PMCPMC6015020

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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.