Choosing the Right Tool for the Job: RNAi, TALEN, or CRISPR

被引:340
作者
Boettcher, Michael [1 ]
McManus, Michael T. [1 ]
机构
[1] Univ Calif San Francisco, Dept Microbiol & Immunol, Keck Ctr Noncoding RNA, UCSF Diabet Ctr, San Francisco, CA 94143 USA
关键词
ZINC-FINGER NUCLEASES; HUMAN-CELLS; GENOME-WIDE; GENE-EXPRESSION; MAMMALIAN-CELLS; TRANSCRIPTION FACTORS; ENGINEERED NUCLEASES; GUIDED ENDONUCLEASE; CAS NUCLEASES; SPECIFICITY;
D O I
10.1016/j.molcel.2015.04.028
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The most widely used approach for defining gene function is to reduce or completely disrupt its normal expression. For over a decade, RNAi has ruled the lab, offering a magic bullet to disrupt gene expression in many organisms. However, new biotechnological tools-specifically CRISPR-based technologies-have become available and are squeezing out RNAi dominance in mammalian cell studies. These seemingly competing technologies leave research investigators with the question: "Which technology should I use in my experiment?" This review offers a practical resource to compare and contrast these technologies, guiding the investigator when and where to use this fantastic array of powerful tools.
引用
收藏
页码:575 / 585
页数:11
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