Evidence map›Paper›PMID 29661858›Full record

ArticleEMBO reports2018

RNA sensor LGP2 inhibits TRAF ubiquitin ligase to negatively regulate innate immune signaling.

Jean-Patrick Parisien, Jessica J Lenoir, Roli Mandhana, Kenny R Rodriguez, Kenin Qian, Annie M Bruns, Curt M Horvath

Open access · bronzeAbstract read
In one paragraph

Article in EMBO reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

37 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
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  4. Review
  5. Article
  6. mViruses · 2024
    Review
  7. Activation of host nucleic acid sensors byCritical reviews in microbiology · 2024
    Review
  8. Article
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  11. Review
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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

7 authors at 2 institutions in 1 country.

Jean-Patrick ParisienDepartment of Molecular Biosciences, Northwestern University, Evanston, IL, USA.
Jessica J LenoirDepartment of Molecular Biosciences, Northwestern University, Evanston, IL, USA.
Roli MandhanaDepartment of Molecular Biosciences, Northwestern University, Evanston, IL, USA.
Kenny R RodriguezDepartment of Molecular Biosciences, Northwestern University, Evanston, IL, USA.
Kenin QianDepartment of Molecular Biosciences, Northwestern University, Evanston, IL, USA.
Annie M BrunsATLAS Institute, University of Colorado, Boulder, CO, USA.
Curt M HorvathDepartment of Molecular Biosciences, Northwestern University, Evanston, IL, USA horvath@northwestern.edu.ORCID 0000-0003-2449-225X
Northwestern University · USUniversity of Colorado Boulder · US

Funding

CELLULAR &MOLECULAR BASIS OF DISEASE TRAINING PROGRAMT32GM008061 · NIGMS · NORTHWESTERN UNIVERSITY · PI CARTHEW, RICHARD W. · 1985 to 2022
$17.1M
Mentoring For Success: Developing Fundamental Skills For Biomedical ResearchR25GM079300 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MCGEE, RICHARD · 2007 to 2020
$6.6M
Molecular Basis-Paramyxovirus-induced STAT DegradationR01AI050707 · NIAID · NORTHWESTERN UNIVERSITY · PI HORVATH, CURT M · 2002 to 2012
$3.3M
Helicase Regulation of dsRNA Signaling and Innate Antiviral Immune ResponsesR01AI073919 · NIAID · NORTHWESTERN UNIVERSITY · PI HORVATH, CURT M · 2008 to 2012
$1.8M
Analysis of Novel Virus-Induced RNAsR01GM111652 · NIGMS · NORTHWESTERN UNIVERSITY · PI HORVATH, CURT M · 2015 to 2018
$1.2M
NIAID NIH HHS R01 AI050707NIAID NIH HHS R01 AI073919NIGMS NIH HHS R01 GM111652NIGMS NIH HHS R25 GM079300NIGMS NIH HHS T32 GM008061
6 · The paper itself

Abstract

The production of type I interferon (IFN) is essential for cellular barrier functions and innate and adaptive antiviral immunity. In response to virus infections, RNA receptors RIG-I and MDA5 stimulate a mitochondria-localized signaling apparatus that uses TRAF family ubiquitin ligase proteins to activate master transcription regulators IRF3 and NFκB, driving IFN and antiviral target gene expression. Data indicate that a third RNA receptor, LGP2, acts as a negative regulator of antiviral signaling by interfering with TRAF family proteins. Disruption of LGP2 expression in cells results in earlier and overactive transcriptional responses to virus or dsRNA LGP2 associates with the C-terminus of TRAF2, TRAF3, TRAF5, and TRAF6 and interferes with TRAF ubiquitin ligase activity. TRAF interference is independent of LGP2 ATP hydrolysis, RNA binding, or its C-terminal domain, and LGP2 can regulate TRAF-mediated signaling pathways in

Indexed as

AnimalsFibroblastsGene Expression RegulationHEK293 CellsHumansImmunity, InnateInterferon Type IRNA, Double-StrandedRNA HelicasesRNA, ViralSignal TransductionTumor Necrosis Factor Receptor-Associated Peptides and ProteinsVirus DiseasesDHX58 protein, humanDhx58 protein, mouseInterferon Type IRNA, Double-StrandedRNA HelicasesRNA, ViralTumor Necrosis Factor Receptor-Associated Peptides and Proteinsinnate immunityinterferonLGP2RIG‐I‐like receptorsTRAF

Identifiers

PMID29661858
PMCPMC5989757
OpenAlexW2797986890

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.