Evidence map›Paper›PMID 38001254›Full record

ArticleCell death and differentiation2024

LUBAC is required for RIG-I sensing of RNA viruses.

Helena C Teague, Charlotte Lefevre, Eva Rieser, Lina Wolfram, Diego de Miguel, Daniel Patricio de Oliveira, Marisa Oliveira, Daniel S Mansur, Nerea Irigoyen, Henning Walczak and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Cell death and differentiation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Deubiquitinase OTULIN dampens RIG-I-dependent antiviral signaling by removing linear ubiquitination from TRAF6.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Review
  5. Article
  6. Review
  7. Innate Immune and Inflammatory Responses to Dengue Virus Infection.Current topics in microbiology and immunology · 2026
    Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. HOIL1 mediates MDA5 activation through ubiquitination of LGP2.bioRxiv : the preprint server for biology · 2024
    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

11 authors at 3 institutions in 3 countries.

Helena C TeagueDepartment of Pathology, University of Cambridge, Tennis Court Road, Cambridge, UK.
Charlotte LefevreDepartment of Pathology, University of Cambridge, Tennis Court Road, Cambridge, UK.
Eva RieserCentre for Cell Death, Cancer and inflammation (CCCI), UCL Cancer Institute, University College London, 72 Huntley Street, London, UK.
Lina WolframDepartment of Pathology, University of Cambridge, Tennis Court Road, Cambridge, UK.
Diego de MiguelCentre for Cell Death, Cancer and inflammation (CCCI), UCL Cancer Institute, University College London, 72 Huntley Street, London, UK.
Daniel Patricio de OliveiraDepartamento de Microbiologia, Imunologia e Parasitologia, Centro de Ciências Biológicas, Universidade Federal de Santa Catarina (UFSC), Florianópolis, SC, Brazil.
Marisa OliveiraDepartment of Pathology, University of Cambridge, Tennis Court Road, Cambridge, UK.
Daniel S MansurDepartamento de Microbiologia, Imunologia e Parasitologia, Centro de Ciências Biológicas, Universidade Federal de Santa Catarina (UFSC), Florianópolis, SC, Brazil.
Nerea IrigoyenDepartment of Pathology, University of Cambridge, Tennis Court Road, Cambridge, UK.ORCID 0000-0001-6346-3369
Henning WalczakCentre for Cell Death, Cancer and inflammation (CCCI), UCL Cancer Institute, University College London, 72 Huntley Street, London, UK.
Brian J FergusonDepartment of Pathology, University of Cambridge, Tennis Court Road, Cambridge, UK. bf234@cam.ac.uk.ORCID 0000-0002-6873-1032
University of Cambridge · GBUniversity of Cologne · DEUniversidade Federal de Santa Catarina · BR

Funding

Medical Research Council MR/S00811X/1Wellcome Trust 214342
6 · The paper itself

Abstract

The ability of cells to mount an interferon response to virus infections depends on intracellular nucleic acid sensing pattern recognition receptors (PRRs). RIG-I is an intracellular PRR that binds short double-stranded viral RNAs to trigger MAVS-dependent signalling. The RIG-I/MAVS signalling complex requires the coordinated activity of multiple kinases and E3 ubiquitin ligases to activate the transcription factors that drive type I and type III interferon production from infected cells. The linear ubiquitin chain assembly complex (LUBAC) regulates the activity of multiple receptor signalling pathways in both ligase-dependent and -independent ways. Here, we show that the three proteins that constitute LUBAC have separate functions in regulating RIG-I signalling. Both HOIP, the E3 ligase capable of generating M1-ubiquitin chains, and LUBAC accessory protein HOIL-1 are required for viral RNA sensing by RIG-I. The third LUBAC component, SHARPIN, is not required for RIG-I signalling. These data cement the role of LUBAC as a positive regulator of RIG-I signalling and as an important component of antiviral innate immune responses.

Indexed as

RNA VirusesUbiquitin-Protein LigasesDEAD Box Protein 58Signal TransductionUbiquitinUbiquitinationDEAD Box Protein 58UbiquitinUbiquitin-Protein Ligases

Identifiers

PMID38001254
PMCPMC10781740
OpenAlexW4388976719

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.