A most formidable arsenal: genetic technologies for building a better mouse

被引:20
作者
Clark, James F. [1 ]
Dinsmore, Colin J. [1 ]
Soriano, Philippe [1 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Cell Dev & Regenerat Biol, New York, NY 10029 USA
关键词
gene targeting; CRISPR; mice; genetics; transgenesis; EMBRYONIC STEM-CELLS; RNA-GUIDED ENDONUCLEASE; DOUBLE-STRAND BREAKS; BETA-GLOBIN GENE; SITE-SPECIFIC RECOMBINATION; GERM-LINE TRANSMISSION; COPY TRANSGENIC MICE; OFF-TARGET SITES; HOMOLOGOUS RECOMBINATION; CRE-RECOMBINASE;
D O I
10.1101/gad.342089.120
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The mouse is one of the most widely used model organisms for genetic study. The tools available to alter the mouse genome have developed over the preceding decades from forward screens to gene targeting in stem cells to the recent influx of CRISPR approaches. In this review, we first consider the history of mice in genetic study, the development of classic approaches to genome modification, and how such approaches have been used and improved in recent years. We then turn to the recent surge of nuclease-mediated techniques and how they are changing the field of mouse genetics. Finally, we survey common classes of alleles used in mice and discuss how they might be engineered using different methods.
引用
收藏
页码:1256 / 1286
页数:31
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