Genentech Computational Sciences, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA; Roche Informatics, Hoffman-La Roche Canada, 7070 Mississauga Road, Mississauga, ON, Canada.
Genentech Computational Sciences, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA.
Cell Genom. 2024 Nov 13;4(11):100693. doi: 10.1016/j.xgen.2024.100693. Epub 2024 Nov 6.
The CRISPR interference (CRISPRi) system is a powerful tool for selectively and efficiently silencing genes in functional genomics research applications. However, its off-target activity has not been systematically investigated. Here, we utilized a genome-wide CRISPRi-Cas9 single-guide RNA (sgRNA) library to investigate the presence of off-target activity and its effects on gene expression. Our findings suggest that off-target effects in CRISPRi are quite pervasive and have direct and indirect impacts on gene expression. Most of the identified off-targets can be accounted for by complementarity of the protospacer adjacent motif (PAM)-proximal genomic sequence with the 3' half of the sgRNA spacer sequence, the seed sequence. We also report that while the stability of off-target binding is primarily driven by the PAM-proximal seed sequences, variations in the length of these seed sequences and the degree of mismatch tolerance at various positions can differ across different sgRNAs.
CRISPR 干扰 (CRISPRi) 系统是功能基因组学研究应用中选择性和高效沉默基因的有力工具。然而,其脱靶活性尚未得到系统研究。在这里,我们利用全基因组 CRISPRi-Cas9 单指导 RNA (sgRNA) 文库来研究脱靶活性的存在及其对基因表达的影响。我们的研究结果表明,CRISPRi 中的脱靶效应非常普遍,对基因表达有直接和间接的影响。大多数鉴定出的脱靶效应可以通过前导序列相邻基序 (PAM) 近端基因组序列与 sgRNA 间隔序列 3' 半部分的互补性来解释,即种子序列。我们还报告说,尽管脱靶结合的稳定性主要由 PAM 近端种子序列驱动,但不同 sgRNA 之间,这些种子序列的长度变化和在不同位置的错配容忍度的程度可能不同。