Efficient method to generate single-copy transgenic mice by site-specific integration in embryonic stem cells

被引:370
作者
Beard, C
Hochedlinger, K
Plath, K
Wutz, A
Jaenisch, R
机构
[1] Whitehead Inst, Cambridge, MA 02142 USA
[2] Inst Mol Pathol, Vienna, Austria
[3] MIT, Dept Biol, Cambridge, MA USA
关键词
transgenic; embryonic stem cells; inducible gene expression; tetracycline; site specific recombination; FLPe recombinase;
D O I
10.1002/gene.20180
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Transgenic and gene-targeted mutant mice provide powerful tools for analysis of the cellular processes involved in early development and in the pathogenesis of many diseases. Here we describe a transgene integration strategy mediated by site-specific recombination that allows establishment of multiple embryonic stem (ES) cell lines carrying tetracycline-inducible genes targeted to a specific locus to assure predictable temporal and spatial expression in ES cells and mice. Using homologous recombination we inserted an frt homing site into which tetracycline-inducible transgenes can be integrated efficiently in the presence of FLPe recombinase. This strategy and the vectors described here are generally applicable to any locus in ES cells and should allow for the rapid production of mice with transgenes efficiently targeted to a defined site. genesis 44:23-28, 2006. (c) 2006 Wiley-Liss, Inc.
引用
收藏
页码:23 / 28
页数:6
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