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Native RNA G quadruplex immunoprecipitation (rG4IP) from mammalian cells

G quadruplex structures play an important role in regulating DNA replication and transcription and mRNA translation. Although there are several techniques that can determine its formation in vitro, the study of RNA G quadruplexes in vivo is not simple. In the current protocol, we describe an optimiz...

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Detalles Bibliográficos
Autores principales: Surani, Arif A., Montiel-Duarte, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127691/
https://www.ncbi.nlm.nih.gov/pubmed/35620077
http://dx.doi.org/10.1016/j.xpro.2022.101372
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author Surani, Arif A.
Montiel-Duarte, Cristina
author_facet Surani, Arif A.
Montiel-Duarte, Cristina
author_sort Surani, Arif A.
collection PubMed
description G quadruplex structures play an important role in regulating DNA replication and transcription and mRNA translation. Although there are several techniques that can determine its formation in vitro, the study of RNA G quadruplexes in vivo is not simple. In the current protocol, we describe an optimized technique (RNA G quadruplex immunoprecipitation [rG4IP]) to selectively pull down native cytoplasmic RNAs containing G quadruplex structures in mammalian cells. We also use a bicistronic plasmid to confirm and pinpoint the structure location. For complete details on the use and execution of this protocol, please refer to Surani et al. (2022).
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spelling pubmed-91276912022-05-25 Native RNA G quadruplex immunoprecipitation (rG4IP) from mammalian cells Surani, Arif A. Montiel-Duarte, Cristina STAR Protoc Protocol G quadruplex structures play an important role in regulating DNA replication and transcription and mRNA translation. Although there are several techniques that can determine its formation in vitro, the study of RNA G quadruplexes in vivo is not simple. In the current protocol, we describe an optimized technique (RNA G quadruplex immunoprecipitation [rG4IP]) to selectively pull down native cytoplasmic RNAs containing G quadruplex structures in mammalian cells. We also use a bicistronic plasmid to confirm and pinpoint the structure location. For complete details on the use and execution of this protocol, please refer to Surani et al. (2022). Elsevier 2022-05-20 /pmc/articles/PMC9127691/ /pubmed/35620077 http://dx.doi.org/10.1016/j.xpro.2022.101372 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Surani, Arif A.
Montiel-Duarte, Cristina
Native RNA G quadruplex immunoprecipitation (rG4IP) from mammalian cells
title Native RNA G quadruplex immunoprecipitation (rG4IP) from mammalian cells
title_full Native RNA G quadruplex immunoprecipitation (rG4IP) from mammalian cells
title_fullStr Native RNA G quadruplex immunoprecipitation (rG4IP) from mammalian cells
title_full_unstemmed Native RNA G quadruplex immunoprecipitation (rG4IP) from mammalian cells
title_short Native RNA G quadruplex immunoprecipitation (rG4IP) from mammalian cells
title_sort native rna g quadruplex immunoprecipitation (rg4ip) from mammalian cells
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127691/
https://www.ncbi.nlm.nih.gov/pubmed/35620077
http://dx.doi.org/10.1016/j.xpro.2022.101372
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