清脆的
小发夹RNA
Cas9
CRISPR干扰
生物
基因
计算生物学
RNA干扰
基因组编辑
遗传学
引导RNA
核糖核酸
基因沉默
基因组工程
细胞生物学
基因敲除
作者
Bastiaan Evers,Katarzyna Jastrzebski,Jeroen P M Heijmans,Wipawadee Grernrum,Roderick L. Beijersbergen,René Bernards
摘要
High-throughput genetic screens have become essential tools for studying a wide variety of biological processes. Here we experimentally compare systems based on clustered regularly interspaced short palindromic repeat (CRISPR)/CRISPR-associated protein 9 (Cas9) or its transcriptionally repressive variant, CRISPR-interference (CRISPRi), with a traditional short hairpin RNA (shRNA)-based system for performing lethality screens. We find that the CRISPR technology performed best, with low noise, minimal off-target effects and consistent activity across reagents.
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