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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...

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Autores principales: Hirosawa, Moe, Fujita, Yoshihiko, Parr, Callum J. C., Hayashi, Karin, Kashida, Shunnichi, Hotta, Akitsu, Woltjen, Knut, Saito, Hirohide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
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.
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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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