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A versatile, high-efficiency platform for CRISPR-based gene activation

CRISPR-mediated transcriptional activation (CRISPRa) is a powerful technology for inducing gene expression from endogenous loci with exciting applications in high throughput gain-of-function genomic screens and the engineering of cell-based models. However, current strategies for generating potent,...

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Autores principales: Heidersbach, Amy J., Dorighi, Kristel M., Gomez, Javier A., Jacobi, Ashley M., Haley, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9938141/
https://www.ncbi.nlm.nih.gov/pubmed/36804928
http://dx.doi.org/10.1038/s41467-023-36452-w
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author Heidersbach, Amy J.
Dorighi, Kristel M.
Gomez, Javier A.
Jacobi, Ashley M.
Haley, Benjamin
author_facet Heidersbach, Amy J.
Dorighi, Kristel M.
Gomez, Javier A.
Jacobi, Ashley M.
Haley, Benjamin
author_sort Heidersbach, Amy J.
collection PubMed
description CRISPR-mediated transcriptional activation (CRISPRa) is a powerful technology for inducing gene expression from endogenous loci with exciting applications in high throughput gain-of-function genomic screens and the engineering of cell-based models. However, current strategies for generating potent, stable, CRISPRa-competent cell lines present limitations for the broad utility of this approach. Here, we provide a high-efficiency, self-selecting CRISPRa enrichment strategy, which combined with piggyBac transposon technology enables rapid production of CRISPRa-ready cell populations compatible with a variety of downstream assays. We complement this with an optimized guide RNA scaffold that significantly enhances CRISPRa functionality. Finally, we describe a synthetic guide RNA tool set that enables transient, population-wide gene activation when used with the self-selecting CRISPRa system. Taken together, this versatile platform greatly enhances the potential for CRISPRa across a wide variety of cellular contexts.
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spelling pubmed-99381412023-02-19 A versatile, high-efficiency platform for CRISPR-based gene activation Heidersbach, Amy J. Dorighi, Kristel M. Gomez, Javier A. Jacobi, Ashley M. Haley, Benjamin Nat Commun Article CRISPR-mediated transcriptional activation (CRISPRa) is a powerful technology for inducing gene expression from endogenous loci with exciting applications in high throughput gain-of-function genomic screens and the engineering of cell-based models. However, current strategies for generating potent, stable, CRISPRa-competent cell lines present limitations for the broad utility of this approach. Here, we provide a high-efficiency, self-selecting CRISPRa enrichment strategy, which combined with piggyBac transposon technology enables rapid production of CRISPRa-ready cell populations compatible with a variety of downstream assays. We complement this with an optimized guide RNA scaffold that significantly enhances CRISPRa functionality. Finally, we describe a synthetic guide RNA tool set that enables transient, population-wide gene activation when used with the self-selecting CRISPRa system. Taken together, this versatile platform greatly enhances the potential for CRISPRa across a wide variety of cellular contexts. Nature Publishing Group UK 2023-02-17 /pmc/articles/PMC9938141/ /pubmed/36804928 http://dx.doi.org/10.1038/s41467-023-36452-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Heidersbach, Amy J.
Dorighi, Kristel M.
Gomez, Javier A.
Jacobi, Ashley M.
Haley, Benjamin
A versatile, high-efficiency platform for CRISPR-based gene activation
title A versatile, high-efficiency platform for CRISPR-based gene activation
title_full A versatile, high-efficiency platform for CRISPR-based gene activation
title_fullStr A versatile, high-efficiency platform for CRISPR-based gene activation
title_full_unstemmed A versatile, high-efficiency platform for CRISPR-based gene activation
title_short A versatile, high-efficiency platform for CRISPR-based gene activation
title_sort versatile, high-efficiency platform for crispr-based gene activation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9938141/
https://www.ncbi.nlm.nih.gov/pubmed/36804928
http://dx.doi.org/10.1038/s41467-023-36452-w
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