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Epitranscriptomic mapping of RNA modifications at single-nucleotide resolution using rhodamine sequencing (Rho-seq)

The recent development of epitranscriptomics revealed a new fundamental layer of gene expression, but the mapping of most RNA modifications remains technically challenging. Here, we describe our protocol for Rho-Seq, which enables the mapping of dihydrouridine RNA modification at single-nucleotide r...

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Detalles Bibliográficos
Autores principales: Finet, Olivier, Yague-Sanz, Carlo, Hermand, Damien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092995/
https://www.ncbi.nlm.nih.gov/pubmed/35573476
http://dx.doi.org/10.1016/j.xpro.2022.101369
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author Finet, Olivier
Yague-Sanz, Carlo
Hermand, Damien
author_facet Finet, Olivier
Yague-Sanz, Carlo
Hermand, Damien
author_sort Finet, Olivier
collection PubMed
description The recent development of epitranscriptomics revealed a new fundamental layer of gene expression, but the mapping of most RNA modifications remains technically challenging. Here, we describe our protocol for Rho-Seq, which enables the mapping of dihydrouridine RNA modification at single-nucleotide resolution. Rho-Seq relies on specific rhodamine-labeling of a subset of modified nucleotides that hinders reverse transcription. Although Rho-Seq was initially applied to the detection of dihydrouridine, we show here that it is applicable to other modifications including 7-methylguanosine or 4-thiouridine. For complete details on the use and execution of this protocol, please refer to Finet et al. (2022).
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spelling pubmed-90929952022-05-12 Epitranscriptomic mapping of RNA modifications at single-nucleotide resolution using rhodamine sequencing (Rho-seq) Finet, Olivier Yague-Sanz, Carlo Hermand, Damien STAR Protoc Protocol The recent development of epitranscriptomics revealed a new fundamental layer of gene expression, but the mapping of most RNA modifications remains technically challenging. Here, we describe our protocol for Rho-Seq, which enables the mapping of dihydrouridine RNA modification at single-nucleotide resolution. Rho-Seq relies on specific rhodamine-labeling of a subset of modified nucleotides that hinders reverse transcription. Although Rho-Seq was initially applied to the detection of dihydrouridine, we show here that it is applicable to other modifications including 7-methylguanosine or 4-thiouridine. For complete details on the use and execution of this protocol, please refer to Finet et al. (2022). Elsevier 2022-05-05 /pmc/articles/PMC9092995/ /pubmed/35573476 http://dx.doi.org/10.1016/j.xpro.2022.101369 Text en © 2022 The Authors 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
Finet, Olivier
Yague-Sanz, Carlo
Hermand, Damien
Epitranscriptomic mapping of RNA modifications at single-nucleotide resolution using rhodamine sequencing (Rho-seq)
title Epitranscriptomic mapping of RNA modifications at single-nucleotide resolution using rhodamine sequencing (Rho-seq)
title_full Epitranscriptomic mapping of RNA modifications at single-nucleotide resolution using rhodamine sequencing (Rho-seq)
title_fullStr Epitranscriptomic mapping of RNA modifications at single-nucleotide resolution using rhodamine sequencing (Rho-seq)
title_full_unstemmed Epitranscriptomic mapping of RNA modifications at single-nucleotide resolution using rhodamine sequencing (Rho-seq)
title_short Epitranscriptomic mapping of RNA modifications at single-nucleotide resolution using rhodamine sequencing (Rho-seq)
title_sort epitranscriptomic mapping of rna modifications at single-nucleotide resolution using rhodamine sequencing (rho-seq)
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092995/
https://www.ncbi.nlm.nih.gov/pubmed/35573476
http://dx.doi.org/10.1016/j.xpro.2022.101369
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