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A universal method for generating knockout mice in multiple genetic backgrounds using zygote electroporation
Genetically engineered mouse models are essential tools for understanding mammalian gene functions and disease pathogenesis. Genome editing allows the generation of these models in multiple inbred strains of mice without backcrossing. Zygote electroporation dramatically removed the barrier for intro...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10497038/ https://www.ncbi.nlm.nih.gov/pubmed/37623822 http://dx.doi.org/10.1242/bio.059970 |
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author | Tamari, Tomohiro Ikeda, Yoshihisa Morimoto, Kento Kobayashi, Keiko Mizuno-Iijima, Saori Ayabe, Shinya Kuno, Akihiro Mizuno, Seiya Yoshiki, Atsushi |
author_facet | Tamari, Tomohiro Ikeda, Yoshihisa Morimoto, Kento Kobayashi, Keiko Mizuno-Iijima, Saori Ayabe, Shinya Kuno, Akihiro Mizuno, Seiya Yoshiki, Atsushi |
author_sort | Tamari, Tomohiro |
collection | PubMed |
description | Genetically engineered mouse models are essential tools for understanding mammalian gene functions and disease pathogenesis. Genome editing allows the generation of these models in multiple inbred strains of mice without backcrossing. Zygote electroporation dramatically removed the barrier for introducing the CRISPR-Cas9 complex in terms of cost and labour. Here, we demonstrate that the generalised zygote electroporation method is also effective for generating knockout mice in multiple inbred strains. By combining in vitro fertilisation and electroporation, we obtained founders for knockout alleles in eight common inbred strains. Long-read sequencing analysis detected not only intended mutant alleles but also differences in read frequency of intended and unintended alleles among strains. Successful germline transmission of knockout alleles demonstrated that our approach can establish mutant mice targeting the same locus in multiple inbred strains for phenotyping analysis, contributing to reverse genetics and human disease research. |
format | Online Article Text |
id | pubmed-10497038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-104970382023-09-13 A universal method for generating knockout mice in multiple genetic backgrounds using zygote electroporation Tamari, Tomohiro Ikeda, Yoshihisa Morimoto, Kento Kobayashi, Keiko Mizuno-Iijima, Saori Ayabe, Shinya Kuno, Akihiro Mizuno, Seiya Yoshiki, Atsushi Biol Open Methods & Techniques Genetically engineered mouse models are essential tools for understanding mammalian gene functions and disease pathogenesis. Genome editing allows the generation of these models in multiple inbred strains of mice without backcrossing. Zygote electroporation dramatically removed the barrier for introducing the CRISPR-Cas9 complex in terms of cost and labour. Here, we demonstrate that the generalised zygote electroporation method is also effective for generating knockout mice in multiple inbred strains. By combining in vitro fertilisation and electroporation, we obtained founders for knockout alleles in eight common inbred strains. Long-read sequencing analysis detected not only intended mutant alleles but also differences in read frequency of intended and unintended alleles among strains. Successful germline transmission of knockout alleles demonstrated that our approach can establish mutant mice targeting the same locus in multiple inbred strains for phenotyping analysis, contributing to reverse genetics and human disease research. The Company of Biologists Ltd 2023-09-06 /pmc/articles/PMC10497038/ /pubmed/37623822 http://dx.doi.org/10.1242/bio.059970 Text en © 2023. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Methods & Techniques Tamari, Tomohiro Ikeda, Yoshihisa Morimoto, Kento Kobayashi, Keiko Mizuno-Iijima, Saori Ayabe, Shinya Kuno, Akihiro Mizuno, Seiya Yoshiki, Atsushi A universal method for generating knockout mice in multiple genetic backgrounds using zygote electroporation |
title | A universal method for generating knockout mice in multiple genetic backgrounds using zygote electroporation |
title_full | A universal method for generating knockout mice in multiple genetic backgrounds using zygote electroporation |
title_fullStr | A universal method for generating knockout mice in multiple genetic backgrounds using zygote electroporation |
title_full_unstemmed | A universal method for generating knockout mice in multiple genetic backgrounds using zygote electroporation |
title_short | A universal method for generating knockout mice in multiple genetic backgrounds using zygote electroporation |
title_sort | universal method for generating knockout mice in multiple genetic backgrounds using zygote electroporation |
topic | Methods & Techniques |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10497038/ https://www.ncbi.nlm.nih.gov/pubmed/37623822 http://dx.doi.org/10.1242/bio.059970 |
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