Bisulfite Sequencing of RNA for Transcriptome-Wide Detection of 5-Methylcytosine.


Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2019
Historique:
entrez: 13 12 2018
pubmed: 13 12 2018
medline: 31 5 2019
Statut: ppublish

Résumé

A powerful method to determine the methylation status of specific cytosine residues within RNA is bisulfite sequencing. In combination with high-throughput sequencing methods cytosine methylation can be determined at nucleotide resolution on a transcriptome-wide level. Nevertheless, several critical aspects need to be considered before starting such a project. Below we describe a detailed step-by-step protocol for planning and performing a transcriptome-wide bisulfite sequencing experiment and subsequent data analysis to determine methyl-cytosine in poly(A)RNA from cells and tissues.

Identifiants

pubmed: 30539543
doi: 10.1007/978-1-4939-8808-2_1
doi:

Substances chimiques

RNA, Messenger 0
RNA 63231-63-0
5-Methylcytosine 6R795CQT4H

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-21

Subventions

Organisme : Austrian Science Fund FWF
ID : P 27024
Pays : Austria

Auteurs

Lukas Trixl (L)

Division of Molecular Biology, Biocenter, Medical University of Innsbruck, Innsbruck, Austria.

Dietmar Rieder (D)

Division of Bioinformatics, Biocenter, Medical University of Innsbruck, Innsbruck, Austria.

Thomas Amort (T)

Division of Molecular Biology, Biocenter, Medical University of Innsbruck, Innsbruck, Austria.

Alexandra Lusser (A)

Division of Molecular Biology, Biocenter, Medical University of Innsbruck, Innsbruck, Austria. alexandra.lusser@i-med.ac.at.

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Classifications MeSH