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Protocol to study sufficiency of cis-regulatory elements in mouse embryonic stem cells using a CRISPR-mediated knockin approach

cis-regulatory elements (CREs) orchestrate the spatiotemporal control of gene expression. The regulatory activity of CREs is typically assessed by reporter assays, in which CREs are studied outside their endogenous context. To circumvent this problem, we developed a CRISPR-Cas9 knockin approach to s...

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Detalles Bibliográficos
Autores principales: Pachano, Tomas, Rada-Iglesias, Alvaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234469/
https://www.ncbi.nlm.nih.gov/pubmed/35769926
http://dx.doi.org/10.1016/j.xpro.2022.101492
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author Pachano, Tomas
Rada-Iglesias, Alvaro
author_facet Pachano, Tomas
Rada-Iglesias, Alvaro
author_sort Pachano, Tomas
collection PubMed
description cis-regulatory elements (CREs) orchestrate the spatiotemporal control of gene expression. The regulatory activity of CREs is typically assessed by reporter assays, in which CREs are studied outside their endogenous context. To circumvent this problem, we developed a CRISPR-Cas9 knockin approach to study CREs in a scar-free genomic context. Here, we describe the design, transfection, and screening protocol to insert CREs in mouse embryonic stem cells. Our strategy can provide important insights into the sufficiency of CREs for gene expression control. For complete details on the use and execution of this protocol, please refer to Pachano et al. (2021).
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spelling pubmed-92344692022-06-28 Protocol to study sufficiency of cis-regulatory elements in mouse embryonic stem cells using a CRISPR-mediated knockin approach Pachano, Tomas Rada-Iglesias, Alvaro STAR Protoc Protocol cis-regulatory elements (CREs) orchestrate the spatiotemporal control of gene expression. The regulatory activity of CREs is typically assessed by reporter assays, in which CREs are studied outside their endogenous context. To circumvent this problem, we developed a CRISPR-Cas9 knockin approach to study CREs in a scar-free genomic context. Here, we describe the design, transfection, and screening protocol to insert CREs in mouse embryonic stem cells. Our strategy can provide important insights into the sufficiency of CREs for gene expression control. For complete details on the use and execution of this protocol, please refer to Pachano et al. (2021). Elsevier 2022-06-21 /pmc/articles/PMC9234469/ /pubmed/35769926 http://dx.doi.org/10.1016/j.xpro.2022.101492 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
Pachano, Tomas
Rada-Iglesias, Alvaro
Protocol to study sufficiency of cis-regulatory elements in mouse embryonic stem cells using a CRISPR-mediated knockin approach
title Protocol to study sufficiency of cis-regulatory elements in mouse embryonic stem cells using a CRISPR-mediated knockin approach
title_full Protocol to study sufficiency of cis-regulatory elements in mouse embryonic stem cells using a CRISPR-mediated knockin approach
title_fullStr Protocol to study sufficiency of cis-regulatory elements in mouse embryonic stem cells using a CRISPR-mediated knockin approach
title_full_unstemmed Protocol to study sufficiency of cis-regulatory elements in mouse embryonic stem cells using a CRISPR-mediated knockin approach
title_short Protocol to study sufficiency of cis-regulatory elements in mouse embryonic stem cells using a CRISPR-mediated knockin approach
title_sort protocol to study sufficiency of cis-regulatory elements in mouse embryonic stem cells using a crispr-mediated knockin approach
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234469/
https://www.ncbi.nlm.nih.gov/pubmed/35769926
http://dx.doi.org/10.1016/j.xpro.2022.101492
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