Lu Xibin, Guo Yuhan, Gu Shu, Tan Deng, Cheng Baoyun, Li Zhoufang, Huang Wei
Core Research Facilities Southern University of Science and Technology Shenzhen P. R. China.
Forward Pharmaceuticals Limited Co Shenzhen P. R. China.
Eng Life Sci. 2020 Sep 7;20(12):585-593. doi: 10.1002/elsc.202000032. eCollection 2020 Dec.
Although the efficiency and versatility of CRISPR-Cas9 system has been greatly improved over conventional genome editing methods such as zinc finger or TALEN, it is still time-consuming and labor-intensive for screening knockout/knock-in cell clones due to differences of the targeted location or efficacies of guide RNAs (gRNAs). Here, we adapted a targeted knock-in strategy with CRISPR-Cas9 system and characterized the efficiency for generating single or double knockout cell lines. Specifically, a homology-arm based donor cassette consisting of genes encoding a fluorescence protein and antibiotic selection marker driven by a constitutive promoter was co-transfected with a gRNA expressing unit. Based on FACS sorting and antibiotic drug selection, positive cell clones were confirmed by genotyping and at the protein expression level. The results indicated that more than 70% of analyzed clones identified by cell sorting and selection were successfully targeted in both single and double knockout experiments. The procedure takes less than three weeks to obtain knockout cell lines. We believe that this methodology could be applicable and versatile in generating knockout cell clones with high efficiency in most cell lines.
尽管与锌指或TALEN等传统基因组编辑方法相比,CRISPR-Cas9系统的效率和通用性有了很大提高,但由于导向RNA(gRNA)靶向位置或效率的差异,筛选敲除/敲入细胞克隆仍然耗时且费力。在此,我们采用了一种基于CRISPR-Cas9系统的靶向敲入策略,并对生成单敲除或双敲除细胞系的效率进行了表征。具体而言,将一个由编码荧光蛋白的基因和由组成型启动子驱动的抗生素选择标记组成的基于同源臂的供体盒与一个gRNA表达单元共转染。基于荧光激活细胞分选(FACS)和抗生素药物筛选,通过基因分型和蛋白质表达水平确认阳性细胞克隆。结果表明,在单敲除和双敲除实验中,通过细胞分选和筛选鉴定的分析克隆中,超过70%被成功靶向。该方法获得敲除细胞系所需时间不到三周。我们相信,这种方法在大多数细胞系中高效生成敲除细胞克隆方面具有适用性和通用性。