Department of Medical Cell Biology and Genetics, Guangdong Key Laboratory of Genomic Stability and Disease Prevention, Shenzhen Key Laboratory of Anti-aging and Regenerative Medicine, and Shenzhen Engineering Laboratory of Regenerative Technologies for Orthopaedic Diseases, Health Science Center, Shenzhen University, Shenzhen, China.
Lungene Technologies Co., Ltd, Shenzhen, China.
Methods Mol Biol. 2022;2549:233-257. doi: 10.1007/7651_2021_455.
High-throughput CRISPR guide RNA (gRNA) library screen, that is, CRISPR/Cas9 screen, enables the unbiased identification of gene functions in a variety of biological processes. Typical pooled CRISPR/Cas9 screen couples a gRNA library and a guided Cas9 or dCas9 endonuclease to target specific gene loci, and then systematically uncover the causal link between candidate genes and observed cellular phenotypes via gRNA depletion or enrichment in screens. Here, we describe a detailed method of puromycin (PURO) concentration titration and lentiviral CRISPR gRNA library titration in Cas9 expressing monoclonal human iPSC line (Cas9+MNhiPSC) prior to performing the screens, conducting pooled CRISPR gRNA library screens in Cas9+MNhiPSC, genomic DNA extraction from the selected cell subpopulation and sequencing library preparation as well as next generation sequencing (NGS) to generate gRNA read counts. In CRISPR/Cas9 screen, we aim for 30% transduction efficiency (i.e., multiplicity of infection = 0.3) to ensure most of infected cells receive only one gRNA. The principles in this method can be applied to CRISPR perturbation (knockout, activation, repression or base editing) screens with other CRISPR gRNA libraries across many other cell models and other species.
高通量 CRISPR 向导 RNA(gRNA)文库筛选,即 CRISPR/Cas9 筛选,可用于在各种生物学过程中 unbiased 地鉴定基因功能。典型的 pooled CRISPR/Cas9 筛选将 gRNA 文库与靶向特定基因座的向导 Cas9 或 dCas9 内切酶偶联,然后通过筛选中 gRNA 的耗竭或富集,系统地揭示候选基因与观察到的细胞表型之间的因果关系。在这里,我们描述了在进行 pooled CRISPR gRNA 文库筛选之前,在表达 Cas9 的单克隆人诱导多能干细胞系(Cas9+MNhiPSC)中进行嘌呤霉素(PURO)浓度滴定和慢病毒 CRISPR gRNA 文库滴定的详细方法,包括在 Cas9+MNhiPSC 中进行 pooled CRISPR gRNA 文库筛选、从选定的细胞亚群中提取基因组 DNA 并制备测序文库以及下一代测序(NGS)以生成 gRNA 读数。在 CRISPR/Cas9 筛选中,我们的目标是 30%的转导效率(即感染复数=0.3),以确保大多数感染的细胞只接收一个 gRNA。该方法的原理可以应用于其他 CRISPR gRNA 文库的 CRISPR 扰动(敲除、激活、抑制或碱基编辑)筛选,适用于许多其他细胞模型和其他物种。