Translating human genetics into mouse: The impact of ultra-rapid in vivo genome editing

被引:26
作者
Aida, Tomomi [1 ]
Imahashi, Risa [1 ]
Tanaka, Kohichi [1 ,2 ,3 ]
机构
[1] Tokyo Med & Dent Univ, Med Res Inst, Lab Mol Neurosci, Bunkyo Ku, Tokyo 1138510, Japan
[2] Tokyo Med & Dent Univ, Ctr Brain Integrat Res, Bunkyo Ku, Tokyo 1138510, Japan
[3] CREST, JST, Kawaguchi, Saitama 3320012, Japan
关键词
clustered; regularly interspaced; short palindromic repeats- associated endonuclease; genome editing; mouse; transcription activator-like effector nucleases; zinc-finger nucleases; GLUTAMATE TRANSPORTERS GLAST; ONE-STEP GENERATION; DE-NOVO MUTATIONS; EMBRYO MICROINJECTION; COMMON DISEASE; MICE LACKING; MECP2; AUTISM; PHOSPHORYLATION; ROLES;
D O I
10.1111/dgd.12101
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Gene-targeted mutant animals, such as knockout or knockin mice, have dramatically improved our understanding of the functions of genes in vivo and the genetic diversity that characterizes health and disease. However, the generation of targeted mice relies on gene targeting in embryonic stem (ES) cells, which is a time-consuming, laborious, and expensive process. The recent groundbreaking development of several genome editing technologies has enabled the targeted alteration of almost any sequence in any cell or organism. These technologies have now been applied to mouse zygotes (in vivo genome editing), thereby providing new avenues for simple, convenient, and ultra-rapid production of knockout or knockin mice without the need for ES cells. Here, we review recent achievements in the production of gene-targeted mice by in vivo genome editing.
引用
收藏
页码:34 / 45
页数:12
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