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CRISPR/Cas9 系统体外和体内敲低 microRNA。

CRISPR/Cas9 System to Knockdown MicroRNA In Vitro and In Vivo.

机构信息

Department of Genetics and Stanley S. Scott Cancer Center, Louisiana State University Health Sciences Center, New Orleans, LA, USA.

出版信息

Methods Mol Biol. 2021;2300:133-139. doi: 10.1007/978-1-0716-1386-3_13.

Abstract

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.

摘要

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。

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