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Publication : Generation of transgenic mouse line with prostate-specific expression of codon-improved Cre recombinase.

First Author  Kanayama M Year  2018
Journal  Prostate Int Volume  6
Issue  3 Pages  99-103
PubMed ID  30140659 Mgi Jnum  J:304912
Mgi Id  MGI:6511430 Doi  10.1016/j.prnil.2018.04.003
Citation  Kanayama M, et al. (2018) Generation of transgenic mouse line with prostate-specific expression of codon-improved Cre recombinase. Prostate Int 6(3):99-103
abstractText  Background: Genetically engineered mouse models are useful tools to decipher molecular mechanisms of diseases. As for prostates, a rat probasin promoter has been widely used to drive prostate-specific gene expression. To optimize its codon usage to that of mammals, we used codon-improved Cre recombinase (iCre) for prostate-specific Cre-loxP recombination. Materials and methods: We generated transgenic mice that express iCre driven by conventional probasin promoter in a prostate-specific manner (PB-iCre). Linearized PB-iCre transgene deoxyribonucleic acids (DNAs) were microinjected into pronuclei of fertilized mouse embryos. The integration of the transgene was confirmed by Southern blot analysis. A line of transgenic mice expressing a sufficient amount of iCre mRNA in its prostate was selected. To test recombinase activity of PB-iCre in vivo, its offspring was crossbred with Pten(flox/flox) mice in which murine prostate adenocarcinoma is reported to occur upon excision of loxP-flanked regions. Results: Eight founder animals were obtained, all of which showed germ line integration of PB-iCre transgene by Southern blot analysis. Among them, the prostate from only one line (line 58) expressed a sufficient amount of iCre mRNA. This line was crossbred with Pten(flox/flox) mice to generate PB-iCre58/Pten(flox/flox). As a result, 12-week-old PB-iCre58/Pten(flox/flox) mice presented with prostate adenocarcinoma that was histologically similar to human cribriform prostate cancer of Gleason grade 4. Conclusions: We have successfully established a transgenic mouse line that expresses iCre in a prostate-specific manner.
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