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i-GONAD: a robust method for in situ germline genome engineering using CRISPR nucleases
We present a robust method called improved-Genome editing via Oviductal Nucleic Acids Delivery (i-GONAD) that delivers CRISPR ribonucleoproteins to E0.7 embryos via in situ electroporation. The method generates mouse models containing single-base changes, kilobase-sized deletions, and knock-ins. The...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828090/ https://www.ncbi.nlm.nih.gov/pubmed/29482575 http://dx.doi.org/10.1186/s13059-018-1400-x |
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author | Ohtsuka, Masato Sato, Masahiro Miura, Hiromi Takabayashi, Shuji Matsuyama, Makoto Koyano, Takayuki Arifin, Naomi Nakamura, Shingo Wada, Kenta Gurumurthy, Channabasavaiah B. |
author_facet | Ohtsuka, Masato Sato, Masahiro Miura, Hiromi Takabayashi, Shuji Matsuyama, Makoto Koyano, Takayuki Arifin, Naomi Nakamura, Shingo Wada, Kenta Gurumurthy, Channabasavaiah B. |
author_sort | Ohtsuka, Masato |
collection | PubMed |
description | We present a robust method called improved-Genome editing via Oviductal Nucleic Acids Delivery (i-GONAD) that delivers CRISPR ribonucleoproteins to E0.7 embryos via in situ electroporation. The method generates mouse models containing single-base changes, kilobase-sized deletions, and knock-ins. The efficiency of i-GONAD is comparable to that of traditional microinjection methods, which rely on ex vivo handling of zygotes and require recipient animals for embryo transfer. In contrast, i-GONAD avoids these technically difficult steps, and it can be performed at any laboratory with simple equipment and technical expertise. Further, i-GONAD-treated females retain reproductive function, suggesting future use of the method for germline gene therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-018-1400-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5828090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58280902018-02-28 i-GONAD: a robust method for in situ germline genome engineering using CRISPR nucleases Ohtsuka, Masato Sato, Masahiro Miura, Hiromi Takabayashi, Shuji Matsuyama, Makoto Koyano, Takayuki Arifin, Naomi Nakamura, Shingo Wada, Kenta Gurumurthy, Channabasavaiah B. Genome Biol Method We present a robust method called improved-Genome editing via Oviductal Nucleic Acids Delivery (i-GONAD) that delivers CRISPR ribonucleoproteins to E0.7 embryos via in situ electroporation. The method generates mouse models containing single-base changes, kilobase-sized deletions, and knock-ins. The efficiency of i-GONAD is comparable to that of traditional microinjection methods, which rely on ex vivo handling of zygotes and require recipient animals for embryo transfer. In contrast, i-GONAD avoids these technically difficult steps, and it can be performed at any laboratory with simple equipment and technical expertise. Further, i-GONAD-treated females retain reproductive function, suggesting future use of the method for germline gene therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-018-1400-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-26 /pmc/articles/PMC5828090/ /pubmed/29482575 http://dx.doi.org/10.1186/s13059-018-1400-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Method Ohtsuka, Masato Sato, Masahiro Miura, Hiromi Takabayashi, Shuji Matsuyama, Makoto Koyano, Takayuki Arifin, Naomi Nakamura, Shingo Wada, Kenta Gurumurthy, Channabasavaiah B. i-GONAD: a robust method for in situ germline genome engineering using CRISPR nucleases |
title | i-GONAD: a robust method for in situ germline genome engineering using CRISPR nucleases |
title_full | i-GONAD: a robust method for in situ germline genome engineering using CRISPR nucleases |
title_fullStr | i-GONAD: a robust method for in situ germline genome engineering using CRISPR nucleases |
title_full_unstemmed | i-GONAD: a robust method for in situ germline genome engineering using CRISPR nucleases |
title_short | i-GONAD: a robust method for in situ germline genome engineering using CRISPR nucleases |
title_sort | i-gonad: a robust method for in situ germline genome engineering using crispr nucleases |
topic | Method |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828090/ https://www.ncbi.nlm.nih.gov/pubmed/29482575 http://dx.doi.org/10.1186/s13059-018-1400-x |
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