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A Tool to Design Bridging Oligos Used to Detect Pseudouridylation Sites on RNA after CMC Treatment.
Bogard, Baptiste; Tellier, Gilles; Francastel, Claire; Hubé, Florent.
Afiliação
  • Bogard B; UMR7216 Épigénétique et Destin Cellulaire, CNRS, Université Paris Cité, F-75013 Paris, France.
  • Tellier G; UMR7216 Épigénétique et Destin Cellulaire, CNRS, Université Paris Cité, F-75013 Paris, France.
  • Francastel C; UMR7216 Épigénétique et Destin Cellulaire, CNRS, Université Paris Cité, F-75013 Paris, France.
  • Hubé F; UMR7216 Épigénétique et Destin Cellulaire, CNRS, Université Paris Cité, F-75013 Paris, France.
Noncoding RNA ; 8(5)2022 Sep 23.
Article em En | MEDLINE | ID: mdl-36287115
ABSTRACT
Pseudouridylation is one of the most abundant modifications found in RNAs. To identify the Pseudouridylation sites (Psi) in RNAs, several techniques have been developed, but the most common and robust is the CMC (N-cyclohexyl-N'-(2-morpholinoethyl)carbodiimide) treatment, which consists in the addition of an adduct on Psi that inhibits the reverse transcription. Here, we describe a turnkey method and a tool to design the bridging oligo (DBO), which is somewhat difficult to design. Finally, we propose a trouble-shooting guide to help users.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Noncoding RNA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Noncoding RNA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França