Evidence map›Paper›PMID 28273895›Full record

ArticleScientific reports2017

The dynamic interacting landscape of MAPL reveals essential functions for SUMOylation in innate immunity.

Karine Doiron, Vanessa Goyon, Etienne Coyaud, Sanjeeva Rajapakse, Brian Raught, Heidi M McBride

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Immune regulation by the SUMO family.Nature reviews. Immunology · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. The RING finger protein family in health and disease.Signal transduction and targeted therapy · 2022
    Review
  10. Regulation of Metabolism by Mitochondrial MUL1 E3 Ubiquitin Ligase.Frontiers in cell and developmental biology · 2022
    Article
  11. SUMO and SUMOylation Pathway at the Forefront of Host Immune Response.Frontiers in cell and developmental biology · 2021
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review
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 2 institutions in 1 country.

Karine DoironMontreal Neurological Institute, McGill University, 3801 University Ave, Montreal, Quebec, H3A 2B4, Canada.
Vanessa GoyonMontreal Neurological Institute, McGill University, 3801 University Ave, Montreal, Quebec, H3A 2B4, Canada.
Etienne CoyaudPrincess Margaret Cancer Centre, University Health Network, 101 College St., Toronto, ON M5G 1L7, Canada.
Sanjeeva RajapakseMontreal Neurological Institute, McGill University, 3801 University Ave, Montreal, Quebec, H3A 2B4, Canada.
Brian RaughtPrincess Margaret Cancer Centre, University Health Network, 101 College St., Toronto, ON M5G 1L7, Canada.
Heidi M McBrideMontreal Neurological Institute, McGill University, 3801 University Ave, Montreal, Quebec, H3A 2B4, Canada. Heidi.mcbride@mcgill.ca.ORCID 0000-0003-4666-2280
Montreal Neurological Institute and Hospital · CAUniversity Health Network · CA

Funding

CIHR
6 · The paper itself

Abstract

Activation of the innate immune response triggered by dsRNA viruses occurs through the assembly of the Mitochondrial Anti-Viral Signaling (MAVS) complex. Upon recognition of viral dsRNA, the cytosolic receptor RIG-I is activated and recruited to MAVS to activate the immune signaling response. We here demonstrate a strict requirement for a mitochondrial anchored protein ligase, MAPL (also called MUL1) in the signaling events that drive the transcriptional activation of antiviral genes downstream of Sendai virus infection, both in vivo and in vitro. A biotin environment scan of MAPL interacting polypeptides identified a series of proteins specific to Sendai virus infection; including RIG-I, IFIT1, IFIT2, HERC5 and others. Upon infection, RIG-I is SUMOylated in a MAPL-dependent manner, a conjugation step that is required for its activation. Consistent with this, MAPL was not required for signaling downstream of a constitutively activated form of RIG-I. These data highlight a critical role for MAPL and mitochondrial SUMOylation in the early steps of antiviral signaling.

Indexed as

Immunity, InnateAdaptor Proteins, Signal TransducingAnimalsApoptosis Regulatory ProteinsCarrier ProteinsCells, CulturedIntracellular Signaling Peptides and ProteinsMiceProtein Interaction MappingProteinsReceptors, Retinoic AcidRespirovirus InfectionsRNA-Binding ProteinsSendai virusSignal TransductionSumoylationAdaptor Proteins, Signal TransducingApoptosis Regulatory ProteinsCarrier ProteinsHERC5 protein, humanIFIT1 protein, humanIFIT2 protein, humanIntracellular Signaling Peptides and ProteinsMUL1 protein, humanPLAAT4 protein, humanProteinsReceptors, Retinoic AcidRNA-Binding ProteinsUbiquitin-Protein Ligases

Identifiers

PMID28273895
PMCPMC5427825
OpenAlexW2592412207

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.