Department of Biomedical Sciences, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea.
Arch Pharm Res. 2018 Sep;41(9):875-884. doi: 10.1007/s12272-018-1029-z. Epub 2018 Apr 10.
The CRISPR-Cas9 system is a powerful tool for genome engineering, and its programmability and simplicity have enabled various types of gene manipulation such as gene disruption and transcriptional and epigenetic perturbation. Particularly, CRISPR-based pooled libraries facilitate high-throughput screening for functional regulatory elements in the human genome. In this review, we describe recent advances in CRISPR-Cas9 technology and its use in high-throughput genetic screening. We also discuss its potential for drug target discovery and current challenges of this technique in biomedical research.
CRISPR-Cas9 系统是一种强大的基因组工程工具,其可编程性和简单性使其能够实现各种类型的基因操作,如基因敲除和转录及表观遗传调控。特别是,基于 CRISPR 的池库有助于高通量筛选人类基因组中的功能调控元件。在这篇综述中,我们描述了 CRISPR-Cas9 技术的最新进展及其在高通量遗传筛选中的应用。我们还讨论了它在药物靶点发现中的潜力和该技术在生物医学研究中的当前挑战。