Takahashi Yuki, Yamaoka Kiyoshi, Nishikawa Makiya, Takakura Yoshinobu
Department of Biopharmaceutics and Drug Metabolism, Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto, Japan.
J Pharm Sci. 2009 Jan;98(1):74-80. doi: 10.1002/jps.21398.
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.
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。