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慢病毒介导的RNA干扰

Lentiviral-mediated RNA interference.

作者信息

Abbas-Terki Toufik, Blanco-Bose William, Déglon Nicole, Pralong William, Aebischer Patrick

机构信息

Institute of Neurosciences, Swiss Federal Institute of Technology, EPFL, Lausanne 1015, Switzerland.

出版信息

Hum Gene Ther. 2002 Dec 10;13(18):2197-201. doi: 10.1089/104303402320987888.

Abstract

RNA interference (RNAi) is a form of posttranscriptional gene silencing mediated by short double-stranded RNA, known as small interfering RNA (siRNA). These siRNAs are capable of binding to a specific mRNA sequence and causing its degradation. The recent demonstration of a plasmid vector that directs siRNA synthesis in mammalian cells prompted us to examine the ability of lentiviral vectors to encode siRNA as a means of providing long-term gene silencing in mammalian cells. The RNA-polymerase III dependent promoter (H1-RNA promoter) was inserted in the lentiviral genome to drive the expression of a small hairpin RNA (shRNA) against enhanced green fluorescent protein (EGFP). This construct successfully silenced EGFP expression in two stable cell lines expressing this protein, as analyzed by fluorescence microscopy, flow cytometry, and Western blotting. The silencing, which is dose dependent, occurs as early as 72 hr postinfection and persists for at least 25 days postinfection. The ability of lentiviruses encoding siRNA to silence genes specifically makes it possible to take full advantage of the possibilities offered by the lentiviral vector and provides a powerful tool for gene therapy and gene function studies.

摘要

RNA干扰(RNAi)是一种由短双链RNA介导的转录后基因沉默形式,这种短双链RNA被称为小干扰RNA(siRNA)。这些siRNA能够与特定的mRNA序列结合并导致其降解。最近一种能在哺乳动物细胞中指导siRNA合成的质粒载体的出现促使我们研究慢病毒载体编码siRNA作为在哺乳动物细胞中实现长期基因沉默的一种手段的能力。将RNA聚合酶III依赖性启动子(H1-RNA启动子)插入慢病毒基因组中,以驱动针对增强型绿色荧光蛋白(EGFP)的小发夹RNA(shRNA)的表达。通过荧光显微镜、流式细胞术和蛋白质印迹分析,该构建体成功地使两种表达这种蛋白的稳定细胞系中的EGFP表达沉默。这种沉默具有剂量依赖性,最早在感染后72小时出现,并在感染后持续至少25天。编码siRNA的慢病毒特异性沉默基因的能力使得充分利用慢病毒载体提供的可能性成为可能,并为基因治疗和基因功能研究提供了一个强大的工具。

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