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对由质粒载体表达的小干扰RNA或短发夹RNA诱导的肿瘤细胞基因沉默进行定量和时间分析。

Quantitative and temporal analysis of gene silencing in tumor cells induced by small interfering RNA or short hairpin RNA expressed from plasmid vectors.

作者信息

Takahashi Yuki, Yamaoka Kiyoshi, Nishikawa Makiya, Takakura Yoshinobu

机构信息

Department of Biopharmaceutics and Drug Metabolism, Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto, Japan.

出版信息

J Pharm Sci. 2009 Jan;98(1):74-80. doi: 10.1002/jps.21398.

Abstract

Vector-based RNA interference (RNAi) has attracted great interest, because of its more prolonged gene silencing effect compared with small interfering RNA (siRNA). However, the intensity and duration of vector-based RNAi effect has received little attention. In this study, the gene silencing kinetics of short hairpin RNA (shRNA)-expressing plasmid DNA (pDNA) driven by U6, H1 or tRNA promoter (pU6-shLuc, pH1-shLuc, and ptRNA-shLuc) was studied in melanoma cells expressing firefly luciferase. A bootstrap method-based moment analysis was performed to statistically and quantitatively evaluate the profile of gene silencing. The analysis showed that pU6-shLuc induced a significantly greater and longer gene silencing than that produced by other promoter-driven shRNA expression vectors. In addition, it was found that pU6-shLuc was at least 100-fold more potent in gene silencing than siRNA targeting the same gene on a numerical basis. These statistical considerations demonstrated that U6 promoter-driven shRNA expressing pDNA is the most effective in inducing gene silencing effect as far as the intensity and duration of RNAi effect is concerned.

摘要

基于载体的RNA干扰(RNAi)因其与小干扰RNA(siRNA)相比具有更长时间的基因沉默效应而备受关注。然而,基于载体的RNAi效应的强度和持续时间却很少受到关注。在本研究中,我们在表达萤火虫荧光素酶的黑色素瘤细胞中研究了由U6、H1或tRNA启动子驱动的短发夹RNA(shRNA)表达质粒DNA(pDNA)(pU6-shLuc、pH1-shLuc和ptRNA-shLuc)的基因沉默动力学。采用基于自抽样法的矩分析对基因沉默情况进行统计和定量评估。分析表明,与其他启动子驱动的shRNA表达载体相比,pU6-shLuc诱导的基因沉默作用更强且持续时间更长。此外,我们发现,从数值上看,pU6-shLuc在基因沉默方面的效力至少是靶向同一基因的siRNA的100倍。这些统计学考量表明,就RNAi效应的强度和持续时间而言,U6启动子驱动的shRNA表达pDNA在诱导基因沉默效应方面最为有效。

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