Evidence map›Paper›PMID 35007297›Full record

ArticlePLoS pathogens2022

Epstein-Barr Virus BGLF2 commandeers RISC to interfere with cellular miRNA function.

Ashley M Campbell, Carlos F De La Cruz-Herrera, Edyta Marcon, Jack Greenblatt, Lori Frappier

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Biochemistry and biophysics reports · 2025
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. GJournal of virology · 2022
    Article
  9. Review
  10. Regulation of Pyroptosis by ncRNA: A Novel Research Direction.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

5 authors at 1 institution in 1 country.

Ashley M CampbellDepartment of Molecular Genetics, University of Toronto, Toronto, Canada.ORCID 0000-0001-8795-1447
Carlos F De La Cruz-HerreraDepartment of Molecular Genetics, University of Toronto, Toronto, Canada.ORCID 0000-0002-7493-5154
Edyta MarconDonnelly Centre, University of Toronto, Toronto, Canada.
Jack GreenblattDepartment of Molecular Genetics, University of Toronto, Toronto, Canada.
Lori FrappierDepartment of Molecular Genetics, University of Toronto, Toronto, Canada.ORCID 0000-0003-0110-5472
University of Toronto · CA

Funding

CIHR FDN-154338
6 · The paper itself

Abstract

The Epstein-Barr virus (EBV) BGLF2 protein is a tegument protein with multiple effects on the cellular environment, including induction of SUMOylation of cellular proteins. Using affinity-purification coupled to mass-spectrometry, we identified the miRNA-Induced Silencing Complex (RISC), essential for miRNA function, as a top interactor of BGLF2. We confirmed BGLF2 interaction with the Ago2 and TNRC6 components of RISC in multiple cell lines and their co-localization in cytoplasmic bodies that also contain the stress granule marker G3BP1. In addition, BGLF2 expression led to the loss of processing bodies in multiple cell types, suggesting disruption of RISC function in mRNA regulation. Consistent with this observation, BGLF2 disrupted Ago2 association with multiple miRNAs. Using let-7 miRNAs as a model, we tested the hypothesis that BGLF2 interfered with the function of RISC in miRNA-mediated mRNA silencing. Using multiple reporter constructs with 3'UTRs containing let-7a regulated sites, we showed that BGLF2 inhibited let-7a miRNA activity dependent on these 3'UTRs, including those from SUMO transcripts which are known to be regulated by let-7 miRNAs. In keeping with these results, we showed that BGLF2 increased the cellular level of unconjugated SUMO proteins without affecting the level of SUMO transcripts. Such an increase in free SUMO is known to drive SUMOylation and would account for the effect of BGLF2 in inducing SUMOylation. We further showed that BGLF2 expression inhibited the loading of let-7 miRNAs into Ago2 proteins, and conversely, that lytic infection with EBV lacking BGLF2 resulted in increased interaction of let-7a and SUMO transcripts with Ago2, relative to WT EBV infection. Therefore, we have identified a novel role for BGLF2 as a miRNA regulator and shown that one outcome of this activity is the dysregulation of SUMO transcripts that leads to increased levels of free SUMO proteins and SUMOylation.

Indexed as

CarboxypeptidasesCell LineEpstein-Barr Virus InfectionsHerpesvirus 4, HumanHost-Parasite InteractionsHumansMicroRNAsSumoylationViral Fusion ProteinsBGLF2 protein, Epstein-barr virusCarboxypeptidasesMicroRNAsSCPEP1 protein, humanViral Fusion Proteins

Identifiers

PMID35007297
PMCPMC8782528
OpenAlexW4206109298

What Socratic 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 Socratic graph.