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A BAC-Based Transgenic Mouse Specifically Expresses an Inducible Cre in the Urothelium
Author(s) -
Tian Shen,
Nataliya Gladoun,
Mireia Castillo-Martín,
Dennis M. Bonal,
Josep Domingo-Domènech,
Daniel Charytonowicz,
Carlos CordonCardo
Publication year - 2012
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0035243
Subject(s) - recombineering , bacterial artificial chromosome , biology , transgene , gene , cre recombinase , conditional gene knockout , genetically modified mouse , gene expression , gene targeting , gene knockin , regulation of gene expression , microbiology and biotechnology , cloning (programming) , reporter gene , human artificial chromosome , gene knockout , genetics , homologous recombination , chromosome , phenotype , genome , computer science , programming language
Cre-loxp mediated conditional knockout strategy has played critical roles for revealing functions of many genes essential for development, as well as the causal relationships between gene mutations and diseases in the postnatal adult mice. One key factor of this strategy is the availability of mice with tissue- or cell type-specific Cre expression. However, the success of the traditional molecular cloning approach to generate mice with tissue specific Cre expression often depends on luck. Here we provide a better alternative by using bacterial artificial chromosome (BAC)-based recombineering to insert iCreERT2 cDNA at the ATG start of the Upk2 gene. The BAC-based transgenic mice express the inducible Cre specifically in the urothelium as demonstrated by mRNA expression and staining for LacZ expression after crossing with a Rosa26 reporter mouse. Taking into consideration the size of the gene of interest and neighboring genes included in a BAC, this method should be widely applicable for generation of mice with tissue specific gene expression or deletions in a more specific manner than previously reported.

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