Zinc-finger nucleases: new strategies to target the rat genome

被引:25
作者
Geurts, Aron M. [1 ,2 ]
Moreno, Carol [2 ]
机构
[1] Med Coll Wisconsin, Cardiovasc Res Ctr, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Dept Physiol, Human & Mol Genet Ctr, PhysGen Knockout Team, Milwaukee, WI 53226 USA
基金
美国国家卫生研究院;
关键词
disease; DNA repair; gene disruption; genome; stem cell; zinc-finger nuclease; EMBRYONIC STEM-CELLS; KNOCKOUT RATS; HOMOLOGOUS RECOMBINATION; LENTIVIRAL VECTOR; TRANSGENIC RATS; GENE KNOCKOUT; MUTAGENESIS; GENERATION; DNA; DROSOPHILA;
D O I
10.1042/CS20100201
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The importance of genetic laboratory models, such as mice and rats, becomes evident when there is a poor understanding of the nature of human disease. Many rat models for human disease, created over the years by phenotype-driven strategies, now provide a foundation for the identification of their genetic determinants. These models are especially valuable with the emerging need for validation of genes found in genome-wide association studies for complex diseases. The manipulation of the rat genome using engineered zinc-finger nucleases now introduces a key technology for manipulating the rat genome, which is broadly applicable. The ability to generate knockout rat models using zinc-finger nuclease technology will now enable its full emergence as an exceptional physiological and genetic research model.
引用
收藏
页码:303 / 311
页数:9
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