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Cell-type-specific genome editing with a microRNA-responsive CRISPR–Cas9 switch
The CRISPR–Cas9 system is a powerful genome-editing tool useful in a variety of biotechnology and biomedical applications. Here we developed a synthetic RNA-based, microRNA (miRNA)-responsive CRISPR–Cas9 system (miR-Cas9 switch) in which the genome editing activity of Cas9 can be modulated through e...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570128/ https://www.ncbi.nlm.nih.gov/pubmed/28525578 http://dx.doi.org/10.1093/nar/gkx309 |
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author | Hirosawa, Moe Fujita, Yoshihiko Parr, Callum J. C. Hayashi, Karin Kashida, Shunnichi Hotta, Akitsu Woltjen, Knut Saito, Hirohide |
author_facet | Hirosawa, Moe Fujita, Yoshihiko Parr, Callum J. C. Hayashi, Karin Kashida, Shunnichi Hotta, Akitsu Woltjen, Knut Saito, Hirohide |
author_sort | Hirosawa, Moe |
collection | PubMed |
description | The CRISPR–Cas9 system is a powerful genome-editing tool useful in a variety of biotechnology and biomedical applications. Here we developed a synthetic RNA-based, microRNA (miRNA)-responsive CRISPR–Cas9 system (miR-Cas9 switch) in which the genome editing activity of Cas9 can be modulated through endogenous miRNA signatures in mammalian cells. We created miR-Cas9 switches by using a miRNA-complementary sequence in the 5΄-UTR of mRNA encoding Streptococcus pyogenes Cas9. The miR-21-Cas9 or miR-302-Cas9 switches selectively and efficiently responded to miR-21-5p in HeLa cells or miR-302a-5p in human induced pluripotent stem cells, and post-transcriptionally attenuated the Cas9 activity only in the target cells. Moreover, the miR-Cas9 switches could differentially control the genome editing by sensing endogenous miRNA activities within a heterogeneous cell population. Our miR-Cas9 switch system provides a promising framework for cell-type selective genome editing and cell engineering based on intracellular miRNA information. |
format | Online Article Text |
id | pubmed-5570128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55701282017-08-29 Cell-type-specific genome editing with a microRNA-responsive CRISPR–Cas9 switch Hirosawa, Moe Fujita, Yoshihiko Parr, Callum J. C. Hayashi, Karin Kashida, Shunnichi Hotta, Akitsu Woltjen, Knut Saito, Hirohide Nucleic Acids Res Methods Online The CRISPR–Cas9 system is a powerful genome-editing tool useful in a variety of biotechnology and biomedical applications. Here we developed a synthetic RNA-based, microRNA (miRNA)-responsive CRISPR–Cas9 system (miR-Cas9 switch) in which the genome editing activity of Cas9 can be modulated through endogenous miRNA signatures in mammalian cells. We created miR-Cas9 switches by using a miRNA-complementary sequence in the 5΄-UTR of mRNA encoding Streptococcus pyogenes Cas9. The miR-21-Cas9 or miR-302-Cas9 switches selectively and efficiently responded to miR-21-5p in HeLa cells or miR-302a-5p in human induced pluripotent stem cells, and post-transcriptionally attenuated the Cas9 activity only in the target cells. Moreover, the miR-Cas9 switches could differentially control the genome editing by sensing endogenous miRNA activities within a heterogeneous cell population. Our miR-Cas9 switch system provides a promising framework for cell-type selective genome editing and cell engineering based on intracellular miRNA information. Oxford University Press 2017-07-27 2017-05-19 /pmc/articles/PMC5570128/ /pubmed/28525578 http://dx.doi.org/10.1093/nar/gkx309 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Methods Online Hirosawa, Moe Fujita, Yoshihiko Parr, Callum J. C. Hayashi, Karin Kashida, Shunnichi Hotta, Akitsu Woltjen, Knut Saito, Hirohide Cell-type-specific genome editing with a microRNA-responsive CRISPR–Cas9 switch |
title | Cell-type-specific genome editing with a microRNA-responsive CRISPR–Cas9 switch |
title_full | Cell-type-specific genome editing with a microRNA-responsive CRISPR–Cas9 switch |
title_fullStr | Cell-type-specific genome editing with a microRNA-responsive CRISPR–Cas9 switch |
title_full_unstemmed | Cell-type-specific genome editing with a microRNA-responsive CRISPR–Cas9 switch |
title_short | Cell-type-specific genome editing with a microRNA-responsive CRISPR–Cas9 switch |
title_sort | cell-type-specific genome editing with a microrna-responsive crispr–cas9 switch |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570128/ https://www.ncbi.nlm.nih.gov/pubmed/28525578 http://dx.doi.org/10.1093/nar/gkx309 |
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