Analysis of RNA-DNA Triplex Structures In Vitro and In Vivo.

Biotinylated RNA Electrophoretic mobility shift assay Noncoding RNA Psoralen Pull-down RNA–DNA triplexes Triplex capture

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:
2020
Historique:
entrez: 19 7 2020
pubmed: 19 7 2020
medline: 13 3 2021
Statut: ppublish

Résumé

RNA can bind within the major groove of purine-rich DNA via Hoogsteen base pairing and form a triple helical RNA-DNA structure that anchors the RNA to specific DNA sequences, thereby targeting RNA-associated regulatory proteins to distinct genomic sites. Here we present methods to analyze the potential of a given RNA to form triplexes in vitro and to validate these structures in vivo.

Identifiants

pubmed: 32681516
doi: 10.1007/978-1-0716-0680-3_16
doi:

Substances chimiques

triplex DNA 0
RNA 63231-63-0
DNA 9007-49-2

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

229-246

Auteurs

Anna Postepska-Igielska (A)

Division of Molecular Biology of the Cell II, German Cancer Research Center, DKFZ-ZMBH Alliance, Heidelberg, Germany.

Alena Blank-Giwojna (A)

Division of Molecular Biology of the Cell II, German Cancer Research Center, DKFZ-ZMBH Alliance, Heidelberg, Germany.

Ingrid Grummt (I)

Division of Molecular Biology of the Cell II, German Cancer Research Center, DKFZ-ZMBH Alliance, Heidelberg, Germany. I.Grummt@dkfz.de.

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Classifications MeSH