Challenges to mapping and defining m6A function in viral RNA.


Journal

RNA (New York, N.Y.)
ISSN: 1469-9001
Titre abrégé: RNA
Pays: United States
ID NLM: 9509184

Informations de publication

Date de publication:
26 Mar 2024
Historique:
received: 22 01 2024
accepted: 09 02 2024
medline: 27 3 2024
pubmed: 27 3 2024
entrez: 26 3 2024
Statut: aheadofprint

Résumé

Viral RNA molecules contain multiple layers of regulatory information. This includes features beyond the primary sequence, such as RNA structures and RNA modifications, including N6-methyladenosine (m6A). Many recent studies have identified the presence and location of m6A in viral RNA and have found diverse regulatory roles for this modification during viral infection. However, to date, viral m6A mapping strategies have limitations that prevent a complete understanding of the function of m6A on individual viral RNA molecules. While m6A sites have been profiled on bulk RNA from many viruses, the resulting m6A maps of viral RNAs described to date present a composite picture of m6A across viral RNA molecules in the infected cell. Thus, for most viruses, it is unknown if unique viral m6A profiles exist throughout infection, nor if they regulate specific viral lifecycle stages. Here, we describe several challenges to defining the function of m6A in viral RNA molecules and provide a framework for future studies to understand how m6A regulates viral infection.

Identifiants

pubmed: 38531643
pii: rna.079959.124
doi: 10.1261/rna.079959.124
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Published by Cold Spring Harbor Laboratory Press for the RNA Society.

Auteurs

Stacy M Horner (SM)

Duke University, School of Medicine stacy.horner@duke.edu.

Matthew G Thompson (MG)

Duke University, School of Medicine.

Classifications MeSH