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Efficient Generation of Genome-Modified Mice Using Campylobacter jejuni-Derived CRISPR/Cas

Mammalian zygote-mediated genome-engineering by Clustered Regularly Interspaced Short Palindromic Repeat (CRISPR)/Cas is currently used for the generation of genome-modified animals. Here, we report that a Campylobacter jejuni-derived orthologous CRISPR/Cas system recognizes a 5′-NNNVRYAC sequence a...

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Detalles Bibliográficos
Autores principales: Fujii, Wataru, Ikeda, Arisa, Sugiura, Koji, Naito, Kunihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5713256/
https://www.ncbi.nlm.nih.gov/pubmed/29088065
http://dx.doi.org/10.3390/ijms18112286
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author Fujii, Wataru
Ikeda, Arisa
Sugiura, Koji
Naito, Kunihiko
author_facet Fujii, Wataru
Ikeda, Arisa
Sugiura, Koji
Naito, Kunihiko
author_sort Fujii, Wataru
collection PubMed
description Mammalian zygote-mediated genome-engineering by Clustered Regularly Interspaced Short Palindromic Repeat (CRISPR)/Cas is currently used for the generation of genome-modified animals. Here, we report that a Campylobacter jejuni-derived orthologous CRISPR/Cas system recognizes a 5′-NNNVRYAC sequence as a protospacer-adjacent motif in mouse zygotes, and is applicable for efficient generation of knockout mice. Moreover, this novel CRISPR/Cas can be used for zygote-mediated knock-in at a unique locus, suggesting that this system could help to expand the feasibility of the zygote-mediated generation of genome-modified animals.
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spelling pubmed-57132562017-12-07 Efficient Generation of Genome-Modified Mice Using Campylobacter jejuni-Derived CRISPR/Cas Fujii, Wataru Ikeda, Arisa Sugiura, Koji Naito, Kunihiko Int J Mol Sci Article Mammalian zygote-mediated genome-engineering by Clustered Regularly Interspaced Short Palindromic Repeat (CRISPR)/Cas is currently used for the generation of genome-modified animals. Here, we report that a Campylobacter jejuni-derived orthologous CRISPR/Cas system recognizes a 5′-NNNVRYAC sequence as a protospacer-adjacent motif in mouse zygotes, and is applicable for efficient generation of knockout mice. Moreover, this novel CRISPR/Cas can be used for zygote-mediated knock-in at a unique locus, suggesting that this system could help to expand the feasibility of the zygote-mediated generation of genome-modified animals. MDPI 2017-10-31 /pmc/articles/PMC5713256/ /pubmed/29088065 http://dx.doi.org/10.3390/ijms18112286 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Fujii, Wataru
Ikeda, Arisa
Sugiura, Koji
Naito, Kunihiko
Efficient Generation of Genome-Modified Mice Using Campylobacter jejuni-Derived CRISPR/Cas
title Efficient Generation of Genome-Modified Mice Using Campylobacter jejuni-Derived CRISPR/Cas
title_full Efficient Generation of Genome-Modified Mice Using Campylobacter jejuni-Derived CRISPR/Cas
title_fullStr Efficient Generation of Genome-Modified Mice Using Campylobacter jejuni-Derived CRISPR/Cas
title_full_unstemmed Efficient Generation of Genome-Modified Mice Using Campylobacter jejuni-Derived CRISPR/Cas
title_short Efficient Generation of Genome-Modified Mice Using Campylobacter jejuni-Derived CRISPR/Cas
title_sort efficient generation of genome-modified mice using campylobacter jejuni-derived crispr/cas
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5713256/
https://www.ncbi.nlm.nih.gov/pubmed/29088065
http://dx.doi.org/10.3390/ijms18112286
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