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Targeted Gene Silencing by Small Interfering RNA-Based Knock-Down Technology

机译:基于小干扰RNA的敲低技术的靶向基因沉默。

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摘要

RNA interference (RNAi) has emerged as a powerful tool for the silencing of gene expression in animals and plants. RNAi is mediated by approximately 21-nt small interfering RNAs (siRNAs), which are originally produced from larger double stranded RNAs (dsRNAs) in vivo through the action of Dicer. Recently, many groups have reported systems designed to express siRNAs in mammalian cells through transfection of either oligonucleotides or plasmids encoding siRNAs. Although the use of siRNAs to silence genes in vertebrate cells was only reported three years ago, the emerging literature indicates that most vertebrate genes can be studied with this technology. This review summarizes some approaches to generate siRNAs, the delivery and application of siRNAs to target cells and the utility of siRNAs as analytical and potential therapeutic tools.
机译:RNA干扰(RNAi)已成为沉默动植物基因表达的强大工具。 RNAi由大约21 nt的小干扰RNA(siRNA)介导,它们最初是通过Dicer的作用从体内较大的双链RNA(dsRNA)产生的。最近,许多研究小组报道了设计用于通过转染寡核苷酸或编码siRNA的质粒在哺乳动物细胞中表达siRNA的系统。尽管仅三年前才报道使用siRNA沉默脊椎动物细胞中的基因,但新兴文献表明,大多数脊椎动物基因都可以使用该技术进行研究。这篇综述总结了生成siRNA的一些方法,将siRNA传递和应用到靶细胞以及将siRNA用作分析和潜在治疗工具的用途。

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