Evidence map›Paper›PMID 26207988›Full record

ArticlePloS one2015

Assessment of mTOR-Dependent Translational Regulation of Interferon Stimulated Genes.

Mark Livingstone, Kristina Sikström, Philippe A Robert, Gilles Uzé, Ola Larsson, Sandra Pellegrini

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Plants (Basel, Switzerland) · 2024
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  2. Inhibiting the P2YJACC. Basic to translational science · 2024
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  8. Molecular therapy oncolytics · 2020
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  12. Article
  13. Palladin Is a Neuron-Specific Translational Target of mTOR Signaling That Regulates Axon Morphogenesis.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  14. Article
  15. Review
  16. Article
  17. 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

6 authors at 3 institutions in 2 countries.

Mark LivingstoneCytokine Signaling Unit, Institut Pasteur, CNRS URA1961, Paris, France.
Kristina SikströmDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Philippe A RobertCytokine Signaling Unit, Institut Pasteur, CNRS URA1961, Paris, France.
Gilles UzéCNRS UMR5235, University of Montpellier II, Montpellier, France.
Ola LarssonDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Sandra PellegriniCytokine Signaling Unit, Institut Pasteur, CNRS URA1961, Paris, France.
Centre National de la Recherche Scientifique · FRKarolinska Institutet · SEInstitut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type-I interferon (IFN)-induced activation of the mammalian target of rapamycin (mTOR) signaling pathway has been implicated in translational control of mRNAs encoding interferon-stimulated genes (ISGs). However, mTOR-sensitive translatomes commonly include mRNAs with a 5' terminal oligopyrimidine tract (TOP), such as those encoding ribosomal proteins, but not ISGs. Because these translatomes were obtained under conditions when ISG expression is not induced, we examined the mTOR-sensitive translatome in human WISH cells stimulated with IFN β. The mTOR inhibitor Torin1 resulted in a repression of global protein synthesis, including that of ISG products, and translation of all but 3 ISG mRNAs (TLR3, NT5C3A, and RNF19B) was not selectively more sensitive to mTOR inhibition. Detailed studies of NT5C3A revealed an IFN-induced change in transcription start site resulting in a switch from a non-TOP to a TOP-like transcript variant and mTOR sensitive translation. Thus, we show that, in the cell model used, translation of the vast majority of ISG mRNAs is not selectively sensitive to mTOR activity and describe an uncharacterized mechanism wherein the 5'-UTR of an mRNA is altered in response to a cytokine, resulting in a shift from mTOR-insensitive to mTOR-sensitive translation.

Indexed as

Cell LineGene Expression RegulationHumansInterferon-betaNaphthyridinesPhosphorylationProtein BiosynthesisTOR Serine-Threonine Kinases1-(4-(4-propionylpiperazin-1-yl)-3-(trifluoromethyl)phenyl)-9-(quinolin-3-yl)benzo(h)(1,6)naphthyridin-2(1H)-oneInterferon-betaNaphthyridinesTOR Serine-Threonine Kinases

Identifiers

PMID26207988
PMCPMC4514843
OpenAlexW935620967

What OpenQuestion holds

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Read underepoch 390

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.