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Executing cell-specific cross-linking immunoprecipitation and sequencing (seCLIP) in C. elegans

The single-end enhanced cross-linking immunoprecipitation (seCLIP) method is well suited for efficient and unbiased transcriptome-wide interrogation of RNA-binding protein (RBP) interaction sites. Here, we provide a protocol for executing cell-specific seCLIP for any desired RBP in Caenorhabditis el...

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Detalles Bibliográficos
Autores principales: Blazie, Stephen M., Jin, Yishi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9803825/
https://www.ncbi.nlm.nih.gov/pubmed/36566382
http://dx.doi.org/10.1016/j.xpro.2022.101959
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author Blazie, Stephen M.
Jin, Yishi
author_facet Blazie, Stephen M.
Jin, Yishi
author_sort Blazie, Stephen M.
collection PubMed
description The single-end enhanced cross-linking immunoprecipitation (seCLIP) method is well suited for efficient and unbiased transcriptome-wide interrogation of RNA-binding protein (RBP) interaction sites. Here, we provide a protocol for executing cell-specific seCLIP for any desired RBP in Caenorhabditis elegans. We begin with steps and recommendations for transgene construction and Cas9-mediated chromosomal integration. We provide detailed procedures for isolation of RBP-associated RNA fragments, subsequent library preparation, and sequencing. We further discuss best practices for data analysis, interpretation of results, and troubleshooting. For complete details on the use and execution of this protocol, please refer to Blazie et al. (2021).(1)
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spelling pubmed-98038252023-01-01 Executing cell-specific cross-linking immunoprecipitation and sequencing (seCLIP) in C. elegans Blazie, Stephen M. Jin, Yishi STAR Protoc Protocol The single-end enhanced cross-linking immunoprecipitation (seCLIP) method is well suited for efficient and unbiased transcriptome-wide interrogation of RNA-binding protein (RBP) interaction sites. Here, we provide a protocol for executing cell-specific seCLIP for any desired RBP in Caenorhabditis elegans. We begin with steps and recommendations for transgene construction and Cas9-mediated chromosomal integration. We provide detailed procedures for isolation of RBP-associated RNA fragments, subsequent library preparation, and sequencing. We further discuss best practices for data analysis, interpretation of results, and troubleshooting. For complete details on the use and execution of this protocol, please refer to Blazie et al. (2021).(1) Elsevier 2022-12-24 /pmc/articles/PMC9803825/ /pubmed/36566382 http://dx.doi.org/10.1016/j.xpro.2022.101959 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Blazie, Stephen M.
Jin, Yishi
Executing cell-specific cross-linking immunoprecipitation and sequencing (seCLIP) in C. elegans
title Executing cell-specific cross-linking immunoprecipitation and sequencing (seCLIP) in C. elegans
title_full Executing cell-specific cross-linking immunoprecipitation and sequencing (seCLIP) in C. elegans
title_fullStr Executing cell-specific cross-linking immunoprecipitation and sequencing (seCLIP) in C. elegans
title_full_unstemmed Executing cell-specific cross-linking immunoprecipitation and sequencing (seCLIP) in C. elegans
title_short Executing cell-specific cross-linking immunoprecipitation and sequencing (seCLIP) in C. elegans
title_sort executing cell-specific cross-linking immunoprecipitation and sequencing (seclip) in c. elegans
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9803825/
https://www.ncbi.nlm.nih.gov/pubmed/36566382
http://dx.doi.org/10.1016/j.xpro.2022.101959
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