Development of nuclease-mediated site-specific genome modification

被引:19
|
作者
Wirt, Stacey E. [1 ]
Porteus, Matthew H. [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Pediat, Stanford, CA 94305 USA
关键词
ZINC-FINGER NUCLEASES; EMBRYONIC STEM-CELLS; DOUBLE-STRAND BREAKS; INTRACHROMOSOMAL HOMOLOGOUS RECOMBINATION; SEVERE COMBINED IMMUNODEFICIENCY; CHRONIC GRANULOMATOUS-DISEASE; TAL EFFECTOR NUCLEASES; GENE-THERAPY; KNOCKOUT RATS; RESTRICTION ENZYMES;
D O I
10.1016/j.coi.2012.08.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Genome engineering is an emerging strategy to treat monogenic diseases that relies on the use of engineered nucleases to correct mutations at the nucleotide level. Zinc finger nucleases can be designed to stimulate homologous recombination-mediated gene targeting at a variety of loci, including genes known to cause the primary immunodeficiencies (PIDs). Recently, these nucleases have been used to correct disease-causing mutations in human cells, as well as to create new animal models for human disease. Although a number of hurdles remain before they can be used clinically, engineered nucleases hold increasing promise as a therapeutic tool, particularly for the PIDs.
引用
收藏
页码:609 / 616
页数:8
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