RNA interference in mammals: behind the screen

被引:19
作者
Campeau, Eric [1 ,2 ]
Gobeil, Stephane
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Lab, Berkeley, CA 94720 USA
[2] Univ Massachusetts, Sch Med, Program Gene Funct & Express, Worcester, MA USA
基金
加拿大健康研究院;
关键词
shRNA; siRNA; esiRNA; RNAi screen; lentivirus; retrovirus; C VIRUS-REPLICATION; FUNCTIONAL GENOMIC SCREEN; STEM-CELL IDENTITY; TUMOR-SUPPRESSOR; IMAGE-ANALYSIS; CANCER-CELLS; GENETIC SCREENS; BREAST-CANCER; IDENTIFICATION; REGULATORS;
D O I
10.1093/bfgp/elr018
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The discovery of RNA interference (RNAi) and the development of technologies exploiting its biology have enabled scientists to rapidly examine the consequences of depleting a particular gene product in a cell or an animal. The availability of genome-wide RNAi libraries targeting the mouse and human genomes has made it possible to carry out large scale, phenotype-based screens, which have yielded seminal information on diverse cellular processes ranging from virology to cancer biology. Today, several strategies are available to perform RNAi screens, each with their own technical and monetary considerations. Special care and budgeting must be taken into account during the design of these screens in order to obtain reliable results. In this review, we discuss a number of critical aspects to consider when planning an effective RNAi screening strategy, including selecting the right biological system, designing an appropriate selection scheme, optimizing technical aspects of the screen, and validating and verifying the hits. Similar to an artistic production, what happens behind the screen has a direct impact on its success.
引用
收藏
页码:215 / 226
页数:12
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