Gene trap and gene inversion methods for conditional gene inactivation in the mouse
Author(s) -
HongBo Xin,
KeYu Deng,
Bo Shui,
Shimian Qu,
Qi Sun,
Jane Lee,
Kai Su Greene,
Jason Wilson,
Ying Yu,
Morris E. Feldman,
Michael I. Kotlikoff
Publication year - 2005
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gni016
Subject(s) - biology , recombinase , gene , homologous recombination , gene targeting , conditional gene knockout , cre recombinase , genetics , gene knockout , cre lox recombination , computational biology , site specific recombination , recombination , transgene , phenotype , genetically modified mouse
Conditional inactivation of individual genes in mice using site-specific recombinases is an extremely powerful method for determining the complex roles of mammalian genes in developmental and tissue-specific contexts, a major goal of post-genomic research. However, the process of generating mice with recombinase recognition sequences placed at specific locations within a gene, while maintaining a functional allele, is time consuming, expensive and technically challenging. We describe a system that combines gene trap and site-specific DNA inversion to generate mouse embryonic stem (ES) cell clones for the rapid production of conditional knockout mice, and the use of this system in an initial gene trap screen. Gene trapping should allow the selection of thousands of ES cell clones with defined insertions that can be used to generate conditional knockout mice, thereby providing extensive parallelism that eliminates the time-consuming steps of targeting vector construction and homologous recombination for each gene
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