Probing RNA structure in vivo.
Journal
Current opinion in structural biology
ISSN: 1879-033X
Titre abrégé: Curr Opin Struct Biol
Pays: England
ID NLM: 9107784
Informations de publication
Date de publication:
12 2019
12 2019
Historique:
received:
05
04
2019
revised:
26
07
2019
accepted:
30
07
2019
pubmed:
16
9
2019
medline:
4
8
2020
entrez:
16
9
2019
Statut:
ppublish
Résumé
RNA structure underpins many essential functions in biology. New chemical reagents and techniques for probing RNA structure in living cells have emerged in recent years. High-throughput, genome-wide techniques such as Structure-seq2 and DMS-MaPseq exploit nucleobase modification by dimethylsulfate (DMS) to obtain complete structuromes, and are applicable to multiple domains of life and conditions. New reagents such as 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC), glyoxal, and nicotinoyl azide (NAz) greatly expand the capabilities of nucleobase probing in cells. Additionally, ribose-targeting reagents in selective 2'-hydroxyl acylation and primer extension (SHAPE) detect RNA flexibility in vivo. These techniques, coupled with crosslinking nucleobases in psoralen analysis of RNA interactions and structures (PARIS), provide new and diverse ways to elucidate RNA secondary and tertiary structure in vivo and genome-wide.
Identifiants
pubmed: 31521910
pii: S0959-440X(18)30217-3
doi: 10.1016/j.sbi.2019.07.008
pmc: PMC6888943
mid: NIHMS1536643
pii:
doi:
Substances chimiques
Sulfuric Acid Esters
0
RNA
63231-63-0
dimethyl sulfate
JW5CW40Z50
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, U.S. Gov't, Non-P.H.S.
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
151-158Subventions
Organisme : NIGMS NIH HHS
ID : R35 GM127064
Pays : United States
Informations de copyright
Copyright © 2019 Elsevier Ltd. All rights reserved.
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