Evidence map›Paper›PMID 23388725›Full record

ArticleJournal of virology2013

Methyltransferase PRMT1 is a binding partner of HBx and a negative regulator of hepatitis B virus transcription.

Shirine Benhenda, Aurélie Ducroux, Lise Rivière, Bijan Sobhian, Michael D Ward, Sarah Dion, Olivier Hantz, Ulrike Protzer, Marie-Louise Michel, Monsef Benkirane and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

62 citing papers in PubMed, 116 citations in OpenAlex.

  1. Review
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  14. Histone methylation in pre-cancerous liver diseases and hepatocellular carcinoma: recent overview.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
  15. Protein arginine methylation in viral infection and antiviral immunity.International journal of biological sciences · 2023
    Review
  16. Review
  17. Article
  18. Review
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  20. Article

2 more citing papers are in PubMed but not listed here.

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

13 authors at 6 institutions in 3 countries.

Shirine BenhendaUnité d'Oncogenèse et Virologie Moléculaire, Institut Pasteur, Paris, France.
Aurélie Ducroux
Lise Rivière
Bijan Sobhian
Michael D Ward
Sarah Dion
Olivier Hantz
Ulrike Protzer
Marie-Louise Michel
Monsef Benkirane
Oliver J Semmes
Marie-Annick Buendia
Christine Neuveut
Inserm · FRCentre National de la Recherche Scientifique · FREastern Virginia Medical School · USInstitut Pasteur · FRHelmholtz Zentrum München · DEInstitut de Génétique Moléculaire de Montpellier · FR

Funding

HTLV-I TAX MEDIATED DEREGULATION OF CELL STATER01CA076595 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI SEMMES, OLIVER JOHN · 1999 to 2016
$2.9M
NCI NIH HHS R01 CA076595
6 · The paper itself

Abstract

The hepatitis B virus X protein (HBx) is essential for virus replication and has been implicated in the development of liver cancer. HBx is recruited to viral and cellular promoters and activates transcription by interacting with transcription factors and coactivators. Here, we purified HBx-associated factors in nuclear extracts from HepG2 hepatoma cells and identified protein arginine methyltransferase 1 (PRMT1) as a novel HBx-interacting protein. We showed that PRMT1 overexpression reduced the transcription of hepatitis B virus (HBV), and this inhibition was dependent on the methyltransferase function of PRMT1. Conversely, depletion of PRMT1 correlated with increased HBV transcription. Using a quantitative chromatin immunoprecipitation assay, we found that PRMT1 is recruited to HBV DNA, suggesting a direct effect of PRMT1 on the regulation of HBV transcription. Finally, we showed that HBx expression inhibited PRMT1-mediated protein methylation. Downregulation of PRMT1 activity was further observed in HBV-replicating cells in an in vivo animal model. Altogether, our results support the notion that the binding of HBx to PRMT1 might benefit viral replication by relieving the inhibitory activity of PRMT1 on HBV transcription.

Indexed as

Host-Pathogen InteractionsTranscription, GeneticVirus ReplicationCell LineChromatin ImmunoprecipitationHepatitis B virusHepatocytesHumansImmune EvasionProtein-Arginine N-MethyltransferasesProtein BindingRepressor ProteinsTrans-ActivatorsViral Regulatory and Accessory Proteinshepatitis B virus X proteinPRMT1 protein, humanProtein-Arginine N-MethyltransferasesRepressor ProteinsTrans-ActivatorsViral Regulatory and Accessory Proteins

Identifiers

PMID23388725
PMCPMC3624337
OpenAlexW2044715640

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.