RNAi screening comes of age: improved techniques and complementary approaches

被引:240
作者
Mohr, Stephanie E. [1 ,2 ]
Smith, Jennifer A. [3 ]
Shamu, Caroline E. [3 ]
Neumueller, Ralph A. [2 ]
Perrimon, Norbert [1 ,2 ,4 ]
机构
[1] Harvard Univ, Sch Med, Drosophila RNAi Screening Ctr, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, ICCB Longwood Screening Facil, Boston, MA 02115 USA
[4] Howard Hughes Med Inst, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
SYNTHETIC LETHAL INTERACTIONS; CANCER-CELL LINES; GENETIC SCREENS; DROSOPHILA-MELANOGASTER; CAENORHABDITIS-ELEGANS; SHRNA LIBRARIES; OVARIAN-CANCER; CULTURE CELLS; HOST FACTORS; REGULATORS;
D O I
10.1038/nrm3860
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Gene silencing through sequence-specific targeting of mRNAs by RNAi has enabled genome-wide functional screens in cultured cells and in vivo in model organisms. These screens have resulted in the identification of new cellular pathways and potential drug targets. Considerable progress has been made to improve the quality of RNAi screen data through the development of new experimental and bioinformatics approaches. The recent availability of genome-editing strategies, such as the CRISPR (clustered regularly interspaced short palindromic repeats)-Cas9 system, when combined with RNAi, could lead to further improvements in screen data quality and follow-up experiments, thus promoting our understanding of gene function and gene regulatory networks.
引用
收藏
页码:591 / 600
页数:10
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