Novel methods for the generation of genetically engineered animal models

被引:2
|
作者
Cassidy, Annelise [1 ]
Onal, Melda [2 ]
Pelletier, Stephane [1 ,3 ]
机构
[1] Indiana Univ Purdue Univ Indianapolis, Indiana Univ Sch Med, Dept Med & Mol Genet, Indianapolis, IN 46202 USA
[2] Univ Arkansas Med Sci, Dept Physiol & Cell Biol, Little Rock, AR 72205 USA
[3] Indiana Univ Purdue Univ Indianapolis, Genome Editing Ctr, Dept Med & Mol Genet, Indianapolis, IN 46202 USA
关键词
Genetic engineering; Genome editing; Musculoskeletal system; CRISPR; ONE-STEP GENERATION; GENE-EXPRESSION; GENOMIC DNA; DUAL-RNA; MICE; CRISPR-CAS9; CAS9; ELECTROPORATION; RECOMBINATION; EFFICIENCY;
D O I
10.1016/j.bone.2022.116612
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Genetically modified mouse models have shaped our understanding of biological systems in both physiological and pathological conditions. For decades, mouse genome engineering has relied on transgenesis and spontaneous gene replacement in embryonic stem (ES) cells. While these technologies provided a wealth of knowledge, they remain imprecise and expensive to use. Recent advances in genome editing technologies such as the development of targetable nucleases, the improvement of delivery systems, and the simplification of targeting strategies now allow for the rapid, precise manipulation of the mouse genome. In this review article, we discuss novel methods and targeting strategies for the generation of mouse models for the study of bone and skeletal muscle biology.
引用
收藏
页数:16
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