Department of Genetics and Stanley S. Scott Cancer Center, Louisiana State University Health Sciences Center, New Orleans, LA, USA.
Methods Mol Biol. 2021;2300:133-139. doi: 10.1007/978-1-0716-1386-3_13.
MicroRNAs (miRNAs) are a class of small noncoding single-stranded RNA molecules containing 18-22 nucleotides that play an important role in the regulation of gene expression at the post-transcriptional and translational levels. Loss-of-function studies are the fundamental strategy to examine miRNA function and target genes in cellular and molecular biology. Traditional methods for miRNA loss-of-function studies include miRNA-specific antisense inhibitors, miRNA sponges, and genetic knockout. However, efficiency, specificity, and stability of these methods are not adequate. Our study suggests that CRISPR/Cas9 is an economic, convenient, and innovative strategy with high efficiency, specificity, and stability for the modulation of miRNA expression. Herein, we describe a detailed protocol for knocking out miRNA genes in vitro and in vivo with the CRISPR/Cas9 system.
微小 RNA(miRNA)是一类含有 18-22 个核苷酸的小非编码单链 RNA 分子,在转录后和翻译水平上调节基因表达中发挥重要作用。失活功能研究是在细胞和分子生物学中研究 miRNA 功能和靶基因的基本策略。传统的 miRNA 失活功能研究方法包括 miRNA 特异性反义抑制剂、miRNA 海绵和基因敲除。然而,这些方法的效率、特异性和稳定性并不充分。我们的研究表明,CRISPR/Cas9 是一种经济、方便和创新的策略,具有高效、特异性和稳定性,可用于调节 miRNA 的表达。本文描述了一种利用 CRISPR/Cas9 系统在体外和体内敲除 miRNA 基因的详细方案。