Evidence map›Paper›PMID 24992036›Full record

ArticlePLoS pathogens2014

G3BP1, G3BP2 and CAPRIN1 are required for translation of interferon stimulated mRNAs and are targeted by a dengue virus non-coding RNA.

Katell Bidet, Dhivya Dadlani, Mariano A Garcia-Blanco

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 187 papers.

0numbers the graph read from it
0cells of the map it votes in
187citing papers in PubMed
20.6field-weighted citation impact, top 1% 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

187 citing papers in PubMed, 279 citations in OpenAlex.

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    Review
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  14. Y-box binding proteins in immunity and RNA virus infection.Microbiology and molecular biology reviews : MMBR · 2025
    Review
  15. Article
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  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 2 countries.

Katell BidetProgram in Emerging Infectious Diseases, Duke-NUS Graduate Medical School, Singapore; NUS Graduate School for Integrative Sciences and Engineering, National University of Singapore, Singapore.
Dhivya DadlaniProgram in Emerging Infectious Diseases, Duke-NUS Graduate Medical School, Singapore.
Mariano A Garcia-BlancoProgram in Emerging Infectious Diseases, Duke-NUS Graduate Medical School, Singapore; NUS Graduate School for Integrative Sciences and Engineering, National University of Singapore, Singapore; Center for RNA Biology, Duke University Medical Center, Durham, North Carolina, United States of America; Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina, United States of America; Department of Medicine, Duke University Medical Center, Durham, North Carolina, United States of America.
Duke-NUS Medical School · SGNational University of Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Viral RNA-host protein interactions are critical for replication of flaviviruses, a genus of positive-strand RNA viruses comprising major vector-borne human pathogens including dengue viruses (DENV). We examined three conserved host RNA-binding proteins (RBPs) G3BP1, G3BP2 and CAPRIN1 in dengue virus (DENV-2) infection and found them to be novel regulators of the interferon (IFN) response against DENV-2. The three RBPs were required for the accumulation of the protein products of several interferon stimulated genes (ISGs), and for efficient translation of PKR and IFITM2 mRNAs. This identifies G3BP1, G3BP2 and CAPRIN1 as novel regulators of the antiviral state. Their antiviral activity was antagonized by the abundant DENV-2 non-coding subgenomic flaviviral RNA (sfRNA), which bound to G3BP1, G3BP2 and CAPRIN1, inhibited their activity and lead to profound inhibition of ISG mRNA translation. This work describes a new and unexpected level of regulation for interferon stimulated gene expression and presents the first mechanism of action for an sfRNA as a molecular sponge of anti-viral effectors in human cells.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsBase SequenceCarrier ProteinsCell Cycle ProteinsCricetinaeDengue VirusDNA HelicaseseIF-2 KinaseHumansMembrane ProteinsMolecular Sequence DataPoly-ADP-Ribose Binding ProteinsProtein BiosynthesisRNA-Binding ProteinsRNA HelicasesAdaptor Proteins, Signal TransducingCAPRIN1 protein, humanCarrier ProteinsCell Cycle ProteinsDNA HelicaseseIF-2 KinaseG3BP1 protein, humanG3BP2 protein, humanIFITM2 protein, humanMembrane ProteinsPoly-ADP-Ribose Binding ProteinsRNA-Binding ProteinsRNA HelicasesRNA, MessengerRNA Recognition Motif ProteinsRNA, UntranslatedRNA, Viral

Identifiers

PMID24992036
PMCPMC4081823
OpenAlexW1999501439

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.