Evidence map›Paper›PMID 35858564›Full record

ArticleCell reports2022

Alphaherpesvirus US3 protein-mediated inhibition of the m6A mRNA methyltransferase complex.

Robert J J Jansens, Ruth Verhamme, Aashiq H Mirza, Anthony Olarerin-George, Cliff Van Waesberghe, Samie R Jaffrey, Herman W Favoreel

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
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  10. The role of NJournal of virology · 2025
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  11. Article
  12. Article
  13. Review
  14. Regulation of RNA methylation linked to drug resistance in gastric cancer.Frontiers in cell and developmental biology · 2025
    Review
  15. Review
  16. Article
  17. Article
  18. Ghost authors revealed: The structure and function of human NWiley interdisciplinary reviews. RNA · 2023
    Review
  19. Article
  20. 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

7 authors at 2 institutions in 2 countries.

Robert J J JansensDepartment of Translational Physiology, Infectiology and Public Health, Faculty of Veterinary Medicine, Ghent University, 9820 Merelbeke, Belgium; Department of Pharmacology, Weill Medical College, Cornell University, New York, NY 10065, USA.
Ruth VerhammeDepartment of Translational Physiology, Infectiology and Public Health, Faculty of Veterinary Medicine, Ghent University, 9820 Merelbeke, Belgium.
Aashiq H MirzaDepartment of Pharmacology, Weill Medical College, Cornell University, New York, NY 10065, USA.
Anthony Olarerin-GeorgeDepartment of Pharmacology, Weill Medical College, Cornell University, New York, NY 10065, USA.
Cliff Van WaesbergheDepartment of Translational Physiology, Infectiology and Public Health, Faculty of Veterinary Medicine, Ghent University, 9820 Merelbeke, Belgium.
Samie R JaffreyDepartment of Pharmacology, Weill Medical College, Cornell University, New York, NY 10065, USA.
Herman W FavoreelDepartment of Translational Physiology, Infectiology and Public Health, Faculty of Veterinary Medicine, Ghent University, 9820 Merelbeke, Belgium. Electronic address: herman.favoreel@ugent.be.
Cornell University · USGhent University · BE

Funding

CANCER PHARMACOLOGYT32CA062948 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI LORRAINE J GUDAS · 1994 to 2026
$12.1M
New mechanisms and technologies for understanding post-transcriptional gene regulation in neuronsR35NS111631 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI SAMIE R JAFFREY · 2019 to 2026
$8.6M
Engineering RNA-activated fluorescence switches for RNA imaging and analyte sensiR01NS064516 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI JAFFREY, SAMIE R · 2009 to 2018
$3.6M
Characterizing the transcriptome-wide location and function of 8oxoGF32GM120987 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI OLARERIN-GEORGE, ANTHONY · 2017 to 2017
$59k
NCI NIH HHS T32 CA062948NIGMS NIH HHS F32 GM120987NINDS NIH HHS R01 NS064516NINDS NIH HHS R35 NS111631
6 · The paper itself

Abstract

Chemical modifications of mRNA, the so-called epitranscriptome, represent an additional layer of post-transcriptional regulation of gene expression. The most common epitranscriptomic modification, N6-methyladenosine (m6A), is generated by a multi-subunit methyltransferase complex. We show that alphaherpesvirus kinases trigger phosphorylation of several components of the m6A methyltransferase complex, including METTL3, METTL14, and WTAP, which correlates with inhibition of the complex and a near complete loss of m6A levels in mRNA of virus-infected cells. Expression of the viral US3 protein is necessary and sufficient for phosphorylation and inhibition of the m6A methyltransferase complex. Although m6A methyltransferase complex inactivation is not essential for virus replication in cell culture, the consensus m6A methylation motif is under-represented in alphaherpesvirus genomes, suggesting evolutionary pressure against methylation of viral transcripts. Together, these findings reveal that phosphorylation can be associated with inactivation of the m6A methyltransferase complex, in this case mediated by the viral US3 protein.

Indexed as

AdenosineMethyltransferasesMethylationRNA, MessengerViral Proteins6-methyladenine mRNA methyltransferaseAdenosineMethyltransferasesRNA, MessengerViral ProteinsCP: MicrobiologyCP: Molecular biologyherpesm6APRVpseudorabiesUS3writer complex

Identifiers

PMID35858564
PMCPMC9347262
OpenAlexW4286250853

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.