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体内组织特异性和细胞类型特异性RNA干扰

Tissue-specific and cell type-specific RNA interference in vivo.

作者信息

Rao Manjeet K, Wilkinson Miles F

机构信息

Department of Biochemistry and Molecular Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA.

出版信息

Nat Protoc. 2006;1(3):1494-501. doi: 10.1038/nprot.2006.260.

Abstract

RNA interference (RNAi) is an efficient method for silencing genes in cultured cells. Here we describe a simple RNAi approach for silencing genes in a cell type-specific and tissue-specific way in vivo. The approach, which mimics the means by which naturally occurring 'microRNA's are generated, uses a tissue-specific polymerase II promoter to drive the expression of a short hairpin RNA (shRNA) directed against the gene target. The shRNA is cleaved by ubiquitously expressed endonucleases to form an active small interfering RNA of about 22 nt. As a proof of principle, it has been shown that expression of a shRNA directed against the transcription factor Wilms tumor 1 in transgenic mice reduces that protein specifically in nurse cells in the testis. Our transgenic RNAi approach offers a cost-effective means of rapidly (within months) addressing the function(s) of genes of interest in a wide variety of specific cell types and tissues in mice in vivo.

摘要

RNA干扰(RNAi)是在培养细胞中使基因沉默的有效方法。在此,我们描述一种简单的RNAi方法,可在体内以细胞类型特异性和组织特异性方式使基因沉默。该方法模仿天然“微小RNA”的产生方式,利用组织特异性聚合酶II启动子驱动针对基因靶标的短发夹RNA(shRNA)的表达。shRNA被普遍表达的核酸内切酶切割,形成约22个核苷酸的活性小干扰RNA。作为原理验证,已表明在转基因小鼠中针对转录因子威尔姆斯瘤1表达的shRNA可特异性降低睾丸中滋养细胞中的该蛋白。我们的转基因RNAi方法提供了一种经济有效的手段,可在数月内快速研究小鼠体内多种特定细胞类型和组织中感兴趣基因的功能。

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