Immunoprecipitation and Sequencing of Acetylated RNA.

Epitranscriptome N4-acetylcytidine ac4C acRIP-seq mRNA modifications

Journal

Bio-protocol
ISSN: 2331-8325
Titre abrégé: Bio Protoc
Pays: United States
ID NLM: 101635102

Informations de publication

Date de publication:
20 Jun 2019
Historique:
received: 29 03 2019
revised: 22 05 2019
accepted: 23 05 2019
entrez: 3 3 2021
pubmed: 20 6 2019
medline: 20 6 2019
Statut: epublish

Résumé

Generation of the epitranscriptome through chemical modifications of protein-coding messenger RNAs (mRNAs) has emerged as a new mechanism of post-transcriptional gene regulation. While most mRNA modifications are methylation events, a single acetylated ribonucleoside has been described in eukaryotes, occurring at the N4-position of cytidine (N4-acetylcytidine or ac4C). Using a combination of antibody-based enrichment of acetylated regions and deep sequencing, we recently reported ac4C as a novel mRNA modification that is catalyzed by the N-acetyltransferase enzyme NAT10. In this protocol, we describe in detail the procedures to identify acetylated mRNA regions transcriptome-wide using acetylated RNA immunoprecipitation and sequencing (acRIP-seq).

Identifiants

pubmed: 33654795
doi: 10.21769/BioProtoc.3278
pii: e3278
pmc: PMC7854089
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e3278

Informations de copyright

Copyright © 2019 The Authors; exclusive licensee Bio-protocol LLC.

Déclaration de conflit d'intérêts

Competing interestsThe authors declare no competing interests.

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Auteurs

Daniel Arango (D)

Laboratory of Receptor Biology and Gene Expression, National Cancer Institute, NIH, Bethesda, MD 20892, USA.

David Sturgill (D)

Laboratory of Receptor Biology and Gene Expression, National Cancer Institute, NIH, Bethesda, MD 20892, USA.

Shalini Oberdoerffer (S)

Laboratory of Receptor Biology and Gene Expression, National Cancer Institute, NIH, Bethesda, MD 20892, USA.

Classifications MeSH