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Generation and characterization of CD19-iCre mice as a tool for efficient and specific conditional gene targeting in B cells

The Cre/loxP system is a powerful tool for generating conditional gene knockout (KO) mice and elucidate gene function in vivo. CD19-Cre and Mb1-iCre transgenic mice are commonly used for generating B cell-specific KO mice and investigate the development, as well as the physiological and pathophysiol...

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Autores principales: Yasuda, Tomoharu, Saito, Yuichi, Ono, Chisato, Kawata, Kazuhiko, Baba, Akemi, Baba, Yoshihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943778/
https://www.ncbi.nlm.nih.gov/pubmed/33750849
http://dx.doi.org/10.1038/s41598-021-84786-6
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author Yasuda, Tomoharu
Saito, Yuichi
Ono, Chisato
Kawata, Kazuhiko
Baba, Akemi
Baba, Yoshihiro
author_facet Yasuda, Tomoharu
Saito, Yuichi
Ono, Chisato
Kawata, Kazuhiko
Baba, Akemi
Baba, Yoshihiro
author_sort Yasuda, Tomoharu
collection PubMed
description The Cre/loxP system is a powerful tool for generating conditional gene knockout (KO) mice and elucidate gene function in vivo. CD19-Cre and Mb1-iCre transgenic mice are commonly used for generating B cell-specific KO mice and investigate the development, as well as the physiological and pathophysiological roles of B cells. However, the CD19-Cre line low efficiency and the Mb1-iCre line occasional ectopic recombination represent challenges for their use. Thus, we developed a CD19-codon-improved Cre (CD19-iCre) knock-in mouse with the T2A-iCre sequence inserted into the Cd19 locus, just before the stop codon. The CD19-iCre mice were compared with existing models, crossed with the Rosa26-EYFP reporter mice, and their recombination activity in B cells carrying different Cre alleles was assessed. CD19-iCre mice showed more effective Cre recombination in the early B cell developmental stages compared with the CD19-Cre mice. The efficiencies of the CD19-iCre and Mb1-iCre lines were similar; however, the B lineage-specific recombination was more stringent in the CD19-iCre line. Furthermore, the utility value of the CD19-iCre model was superior than that of the CD19-Cre mice regarding deletion efficiency in IL10-floxed mice. Thus, the CD19-iCre line is a valuable tool for highly efficient gene targeting specific to the B cell compartment.
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spelling pubmed-79437782021-03-10 Generation and characterization of CD19-iCre mice as a tool for efficient and specific conditional gene targeting in B cells Yasuda, Tomoharu Saito, Yuichi Ono, Chisato Kawata, Kazuhiko Baba, Akemi Baba, Yoshihiro Sci Rep Article The Cre/loxP system is a powerful tool for generating conditional gene knockout (KO) mice and elucidate gene function in vivo. CD19-Cre and Mb1-iCre transgenic mice are commonly used for generating B cell-specific KO mice and investigate the development, as well as the physiological and pathophysiological roles of B cells. However, the CD19-Cre line low efficiency and the Mb1-iCre line occasional ectopic recombination represent challenges for their use. Thus, we developed a CD19-codon-improved Cre (CD19-iCre) knock-in mouse with the T2A-iCre sequence inserted into the Cd19 locus, just before the stop codon. The CD19-iCre mice were compared with existing models, crossed with the Rosa26-EYFP reporter mice, and their recombination activity in B cells carrying different Cre alleles was assessed. CD19-iCre mice showed more effective Cre recombination in the early B cell developmental stages compared with the CD19-Cre mice. The efficiencies of the CD19-iCre and Mb1-iCre lines were similar; however, the B lineage-specific recombination was more stringent in the CD19-iCre line. Furthermore, the utility value of the CD19-iCre model was superior than that of the CD19-Cre mice regarding deletion efficiency in IL10-floxed mice. Thus, the CD19-iCre line is a valuable tool for highly efficient gene targeting specific to the B cell compartment. Nature Publishing Group UK 2021-03-09 /pmc/articles/PMC7943778/ /pubmed/33750849 http://dx.doi.org/10.1038/s41598-021-84786-6 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yasuda, Tomoharu
Saito, Yuichi
Ono, Chisato
Kawata, Kazuhiko
Baba, Akemi
Baba, Yoshihiro
Generation and characterization of CD19-iCre mice as a tool for efficient and specific conditional gene targeting in B cells
title Generation and characterization of CD19-iCre mice as a tool for efficient and specific conditional gene targeting in B cells
title_full Generation and characterization of CD19-iCre mice as a tool for efficient and specific conditional gene targeting in B cells
title_fullStr Generation and characterization of CD19-iCre mice as a tool for efficient and specific conditional gene targeting in B cells
title_full_unstemmed Generation and characterization of CD19-iCre mice as a tool for efficient and specific conditional gene targeting in B cells
title_short Generation and characterization of CD19-iCre mice as a tool for efficient and specific conditional gene targeting in B cells
title_sort generation and characterization of cd19-icre mice as a tool for efficient and specific conditional gene targeting in b cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943778/
https://www.ncbi.nlm.nih.gov/pubmed/33750849
http://dx.doi.org/10.1038/s41598-021-84786-6
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