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Characterization of a BAC transgenic mouse expressing Krt19-driven iCre recombinase in its digestive organs
Cytokeratin 19 (KRT19) protein is highly expressed in the epithelium of the gastrointestinal (GI) tract, hepatobiliary tissues, and pancreas of humans and mice. In the present study, we used an improved Cre (iCre) gene to enhance the efficiency of Cre expression in mammalian cells. We established a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687107/ https://www.ncbi.nlm.nih.gov/pubmed/31393940 http://dx.doi.org/10.1371/journal.pone.0220818 |
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author | Kanayama, Tomohiro Tomita, Hiroyuki Binh, Nguyen Huy Hatano, Yuichiro Aoki, Hitomi Okada, Hideshi Hirata, Akihiro Fujihara, Yoshitaka Kunisada, Takahiro Hara, Akira |
author_facet | Kanayama, Tomohiro Tomita, Hiroyuki Binh, Nguyen Huy Hatano, Yuichiro Aoki, Hitomi Okada, Hideshi Hirata, Akihiro Fujihara, Yoshitaka Kunisada, Takahiro Hara, Akira |
author_sort | Kanayama, Tomohiro |
collection | PubMed |
description | Cytokeratin 19 (KRT19) protein is highly expressed in the epithelium of the gastrointestinal (GI) tract, hepatobiliary tissues, and pancreas of humans and mice. In the present study, we used an improved Cre (iCre) gene to enhance the efficiency of Cre expression in mammalian cells. We established a new transgenic Krt19-iCre bacterial artificial chromosome (BAC) mouse model using the BAC recombineering strategy. Site-specific iCre expression pattern was examined in embryos, adults, and elderly Krt19-iCre mice crossed with Tomato or LacZ reporter mice. Both iCre and reporter protein expressions in adult Krt19-iCre;Tomato(flox/+) (Krt19-iCre Tomato reporter) mice were observed mainly in the epithelial cells of the GI tract, hepatobiliary tissues, and pancreas. However, the expression in the intrahepatic and small pancreatic duct were lower than those in the common bile and large pancreatic duct. In the Krt19-iCre; LacZ reporter embryos, β-galactosidase for the LacZ reporter was expressed in the glandular epithelial cells of the GI tract in 9.5-day embryos, 12-day embryos, and newborn mice. The reporter protein expression in Krt19-iCre-Tomato reporter mice was consistent with the KRT19 expression in human GI tissues. In conclusion, Krt19-iCre BAC transgenic mice can be used to investigate developmental and pathological conditions using the iCre-loxP system. |
format | Online Article Text |
id | pubmed-6687107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-66871072019-08-15 Characterization of a BAC transgenic mouse expressing Krt19-driven iCre recombinase in its digestive organs Kanayama, Tomohiro Tomita, Hiroyuki Binh, Nguyen Huy Hatano, Yuichiro Aoki, Hitomi Okada, Hideshi Hirata, Akihiro Fujihara, Yoshitaka Kunisada, Takahiro Hara, Akira PLoS One Research Article Cytokeratin 19 (KRT19) protein is highly expressed in the epithelium of the gastrointestinal (GI) tract, hepatobiliary tissues, and pancreas of humans and mice. In the present study, we used an improved Cre (iCre) gene to enhance the efficiency of Cre expression in mammalian cells. We established a new transgenic Krt19-iCre bacterial artificial chromosome (BAC) mouse model using the BAC recombineering strategy. Site-specific iCre expression pattern was examined in embryos, adults, and elderly Krt19-iCre mice crossed with Tomato or LacZ reporter mice. Both iCre and reporter protein expressions in adult Krt19-iCre;Tomato(flox/+) (Krt19-iCre Tomato reporter) mice were observed mainly in the epithelial cells of the GI tract, hepatobiliary tissues, and pancreas. However, the expression in the intrahepatic and small pancreatic duct were lower than those in the common bile and large pancreatic duct. In the Krt19-iCre; LacZ reporter embryos, β-galactosidase for the LacZ reporter was expressed in the glandular epithelial cells of the GI tract in 9.5-day embryos, 12-day embryos, and newborn mice. The reporter protein expression in Krt19-iCre-Tomato reporter mice was consistent with the KRT19 expression in human GI tissues. In conclusion, Krt19-iCre BAC transgenic mice can be used to investigate developmental and pathological conditions using the iCre-loxP system. Public Library of Science 2019-08-08 /pmc/articles/PMC6687107/ /pubmed/31393940 http://dx.doi.org/10.1371/journal.pone.0220818 Text en © 2019 Kanayama et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Kanayama, Tomohiro Tomita, Hiroyuki Binh, Nguyen Huy Hatano, Yuichiro Aoki, Hitomi Okada, Hideshi Hirata, Akihiro Fujihara, Yoshitaka Kunisada, Takahiro Hara, Akira Characterization of a BAC transgenic mouse expressing Krt19-driven iCre recombinase in its digestive organs |
title | Characterization of a BAC transgenic mouse expressing Krt19-driven iCre recombinase in its digestive organs |
title_full | Characterization of a BAC transgenic mouse expressing Krt19-driven iCre recombinase in its digestive organs |
title_fullStr | Characterization of a BAC transgenic mouse expressing Krt19-driven iCre recombinase in its digestive organs |
title_full_unstemmed | Characterization of a BAC transgenic mouse expressing Krt19-driven iCre recombinase in its digestive organs |
title_short | Characterization of a BAC transgenic mouse expressing Krt19-driven iCre recombinase in its digestive organs |
title_sort | characterization of a bac transgenic mouse expressing krt19-driven icre recombinase in its digestive organs |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687107/ https://www.ncbi.nlm.nih.gov/pubmed/31393940 http://dx.doi.org/10.1371/journal.pone.0220818 |
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