Evidence map›Paper›PMID 22203037›Full record

ArticleMolecular and cellular biology2012

Proteins associated with the exon junction complex also control the alternative splicing of apoptotic regulators.

Laetitia Michelle, Alexandre Cloutier, Johanne Toutant, Lulzim Shkreta, Philippe Thibault, Mathieu Durand, Daniel Garneau, Daniel Gendron, Elvy Lapointe, Sonia Couture and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

84 citing papers in PubMed, 133 citations in OpenAlex.

  1. Review
  2. Article
  3. BCL-2 and BCL-xL in Cancer: Regulation, Function, and Therapeutic Targeting.International journal of molecular sciences · 2026
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  6. The oncogenic role of EIF4A3/CDC20 axis in the endometrial cancer.Journal of molecular medicine (Berlin, Germany) · 2024
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  14. Review
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  16. Article
  17. RNPS1 inhibits excessive tumor necrosis factor/tumor necrosis factor receptor signaling to support hematopoiesis in mice.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  18. Review
  19. Article
  20. Article

24 more citing papers are in PubMed but not listed here.

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

15 authors at 2 institutions in 2 countries.

Laetitia MichelleDépartement de Microbiologie et d’Infectiologie, Université de Sherbrooke, Sherbrooke, Québec, Canada.
Alexandre Cloutier
Johanne Toutant
Lulzim Shkreta
Philippe Thibault
Mathieu Durand
Daniel Garneau
Daniel Gendron
Elvy Lapointe
Sonia Couture
Hervé Le Hir
Roscoe Klinck
Sherif Abou Elela
Panagiotis Prinos
Benoit Chabot
Université de Sherbrooke · CACentre National de la Recherche Scientifique · FR

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

Several apoptotic regulators, including Bcl-x, are alternatively spliced to produce isoforms with opposite functions. We have used an RNA interference strategy to map the regulatory landscape controlling the expression of the Bcl-x splice variants in human cells. Depleting proteins known as core (Y14 and eIF4A3) or auxiliary (RNPS1, Acinus, and SAP18) components of the exon junction complex (EJC) improved the production of the proapoptotic Bcl-x(S) splice variant. This effect was not seen when we depleted EJC proteins that typically participate in mRNA export (UAP56, Aly/Ref, and TAP) or that associate with the EJC to enforce nonsense-mediated RNA decay (MNL51, Upf1, Upf2, and Upf3b). Core and auxiliary EJC components modulated Bcl-x splicing through different cis-acting elements, further suggesting that this activity is distinct from the established EJC function. In support of a direct role in splicing control, recombinant eIF4A3, Y14, and Magoh proteins associated preferentially with the endogenous Bcl-x pre-mRNA, interacted with a model Bcl-x pre-mRNA in early splicing complexes, and specifically shifted Bcl-x alternative splicing in nuclear extracts. Finally, the depletion of Y14, eIF4A3, RNPS1, SAP18, and Acinus also encouraged the production of other proapoptotic splice variants, suggesting that EJC-associated components are important regulators of apoptosis acting at the alternative splicing level.

Indexed as

Alternative SplicingExonsApoptosisApoptosis Regulatory Proteinsbcl-X ProteinCarrier ProteinsCo-Repressor ProteinsDEAD-box RNA HelicasesEukaryotic Initiation Factor-4AHEK293 CellsHeLa CellsHumansNuclear ProteinsRibonucleoproteinsRNA-Binding ProteinsRNA InterferenceACIN1 protein, humanApoptosis Regulatory Proteinsbcl-X ProteinCarrier ProteinsCo-Repressor ProteinsDEAD-box RNA HelicasesEIF4A3 protein, humanEukaryotic Initiation Factor-4ANuclear ProteinsRBM8A protein, humanRibonucleoproteinsRNA-Binding ProteinsRNA, MessengerRNPS1 protein, humanSAP18 protein, human

Identifiers

PMID22203037
PMCPMC3295189
OpenAlexW1989930884

What OpenQuestion holds

Textmetadata
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.