Evidence map›Paper›PMID 34965427›Full record

ArticleCell reports2021

Immune regulator LGP2 targets Ubc13/UBE2N to mediate widespread interference with K63 polyubiquitination and NF-κB activation.

Jessica J Lenoir, Jean-Patrick Parisien, Curt M Horvath

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  3. Review
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  5. Article
  6. Review
  7. Article
  8. Combined Genetic Association and Differed Expression Analysis ofKidney diseases (Basel, Switzerland) · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Emerging Roles of Non-proteolytic Ubiquitination in Tumorigenesis.Frontiers in cell and developmental biology · 2022
    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

3 authors at 1 institution in 2 countries.

Jessica J LenoirDepartment of Molecular Biosciences, Northwestern University, Evanston, IL, USA.
Jean-Patrick ParisienDepartment of Molecular Biosciences, Northwestern University, Evanston, IL, USA.
Curt M HorvathDepartment of Molecular Biosciences, Northwestern University, Evanston, IL, USA. Electronic address: horvath@northwestern.edu.
Northwestern University · US

Funding

CELLULAR &MOLECULAR BASIS OF DISEASE TRAINING PROGRAMT32GM008061 · NIGMS · NORTHWESTERN UNIVERSITY · PI CARTHEW, RICHARD W. · 1985 to 2022
$17.1M
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
Mechanisms and Modifiers of Zika Virus Innate Immune EvasionR21AI148949 · NIAID · NORTHWESTERN UNIVERSITY · PI HORVATH, CURT M · 2020 to 2021
$426k
NIAID NIH HHS R01 AI073919NIAID NIH HHS R21 AI148949NIGMS NIH HHS R01 GM111652NIGMS NIH HHS T32 GM008061
6 · The paper itself

Abstract

Lysine 63-linked polyubiquitin (K63-Ub) chains activate a range of cellular immune and inflammatory signaling pathways, including the mammalian antiviral response. Interferon and antiviral genes are triggered by TRAF family ubiquitin ligases that form K63-Ub chains. LGP2 is a feedback inhibitor of TRAF-mediated K63-Ub that can interfere with diverse immune signaling pathways. Our results demonstrate that LGP2 inhibits K63-Ub by association with and sequestration of the K63-Ub-conjugating enzyme, Ubc13/UBE2N. The LGP2 helicase subdomain, Hel2i, mediates protein interaction that engages and inhibits Ubc13/UBE2N, affecting control over a range of K63-Ub ligase proteins, including TRAF6, TRIM25, and RNF125, all of which are inactivated by LGP2. These findings establish a unifying mechanism for LGP2-mediated negative regulation that can modulate a variety of K63-Ub signaling pathways.

Indexed as

Gene Expression RegulationUbiquitinationCytokinesHumansInterferon Regulatory Factor-3Intracellular Signaling Peptides and ProteinsLysineNF-kappa BRNA HelicasesSignal TransductionTNF Receptor-Associated Factor 6UbiquitinUbiquitin-Conjugating EnzymesCytokinesDHX58 protein, humanInterferon Regulatory Factor-3Intracellular Signaling Peptides and ProteinsIRF3 protein, humanLysineNF-kappa BRNA HelicasesTifab protein, humanTNF Receptor-Associated Factor 6UBE2N protein, humanUbiquitinUbiquitin-Conjugating EnzymesDHX58IFNK63-UbLGP2RNF125TRAF6TRIM25Ubc13UBE2N

Identifiers

PMID34965427
PMCPMC8787715
OpenAlexW4200597106

What OpenQuestion holds

Textmetadata
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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.