Chemical and Enzymatic Probing of Viral RNAs: From Infancy to Maturity and Beyond.

RNA SHAPE capillary electrophoresis chemical probe enzymatic probe high-throughput sequencing mutational profiling structure

Journal

Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722

Informations de publication

Date de publication:
22 09 2021
Historique:
received: 27 08 2021
revised: 13 09 2021
accepted: 16 09 2021
entrez: 26 10 2021
pubmed: 27 10 2021
medline: 10 2 2022
Statut: epublish

Résumé

RNA molecules are key players in a variety of biological events, and this is particularly true for viral RNAs. To better understand the replication of those pathogens and try to block them, special attention has been paid to the structure of their RNAs. Methods to probe RNA structures have been developed since the 1960s; even if they have evolved over the years, they are still in use today and provide useful information on the folding of RNA molecules, including viral RNAs. The aim of this review is to offer a historical perspective on the structural probing methods used to decipher RNA structures before the development of the selective 2'-hydroxyl acylation analyzed by primer extension (SHAPE) methodology and to show how they have influenced the current probing techniques. Actually, these technological breakthroughs, which involved advanced detection methods, were made possible thanks to the development of next-generation sequencing (NGS) but also to the previous works accumulated in the field of structural RNA biology. Finally, we will also discuss how high-throughput SHAPE (hSHAPE) paved the way for the development of sophisticated RNA structural techniques.

Identifiants

pubmed: 34696322
pii: v13101894
doi: 10.3390/v13101894
pmc: PMC8537439
pii:
doi:

Substances chimiques

RNA, Viral 0
RNA 63231-63-0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Orian Gilmer (O)

Université de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, UPR9002, F-67000 Strasbourg, France.

Erwan Quignon (E)

Université de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, UPR9002, F-67000 Strasbourg, France.

Anne-Caroline Jousset (AC)

Université de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, UPR9002, F-67000 Strasbourg, France.

Jean-Christophe Paillart (JC)

Université de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, UPR9002, F-67000 Strasbourg, France.

Roland Marquet (R)

Université de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, UPR9002, F-67000 Strasbourg, France.

Valérie Vivet-Boudou (V)

Université de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, UPR9002, F-67000 Strasbourg, France.

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Classifications MeSH