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用于RNA干扰的载体

Vectors for RNA interference.

作者信息

Wadhwa Renu, Kaul Sunil C, Miyagishi Makoto, Taira Kazunari

机构信息

National Institute of Advanced Industrial Science and Technology, Gene Function Research Center, 1-1-1 Higashi, Tsukuba, Ibaraki 305-8562, Japan.

出版信息

Curr Opin Mol Ther. 2004 Aug;6(4):367-72.

Abstract

Introduction of double-stranded RNA into cells causes gene silencing in a sequence-specific manner, involving the coordinated activity of enzymes such as Dicer and RNA-induced silencing complex. Several groups have recently demonstrated that this phenomenon of RNA interference (RNAi) occurs in mammalian cells when small interfering (si)RNAs are used, and have developed vector-based siRNA expression systems that can induce RNAi in living cells. These vector systems use polymerase III promoters, such as U6 or H1, and are classified into two groups based on the form of expressed RNA, tandem or hairpin. This review describes the basis for, and methodology of siRNA expression vectors for mammalian cells.

摘要

将双链RNA导入细胞会以序列特异性方式导致基因沉默,这涉及Dicer和RNA诱导沉默复合体等酶的协同作用。最近有几个研究小组证明,当使用小干扰(si)RNA时,这种RNA干扰(RNAi)现象会在哺乳动物细胞中发生,并且已经开发出基于载体的siRNA表达系统,该系统可以在活细胞中诱导RNAi。这些载体系统使用聚合酶III启动子,如U6或H1,并根据表达RNA的形式分为两组,串联或发夹结构。这篇综述描述了哺乳动物细胞siRNA表达载体的基础和方法。

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