Chen Yang-Chao, Song Chao, Luo Chao-Quan
Department of Biochemistry, Sun Yat-sen Medical College, Sun Yat-sen University, Guangzhou, Guangdong, PR China.
Ai Zheng. 2003 Jun;22(6):566-70.
BACKGROUND & OBJECTIVE: RNA interference (RNAi) is an evolutionarily conserved posttranscriptional gene silencing, in which the introduction of double-stranded RNA into a cell leads to specific suppression of gene expression. RNAi has become an important tool for gene function studies. The aim of this study was to induce RNAi in mammalian cells by short hairpin RNAs (shRNAs) generated from a DNA vector, therefore, to provide a new approach for gene function analysis.
Dual Luciferase System was used to assess the intracellular effect of the shRNAs generated from a DNA vector. The inhibitory effect of this DNA vector-driven shRNAs at different condition was measured.
shRNAs generated from the DNA vector induced RNAi in human cells, and suppressed gene expression in a sequence-specific manner. The inhibitory effect was highly related to the target sites.
shRNAs induced RNAi in human cells and suppressed gene expression in a sequence-specific manner. This approach may be used for gene function study.
RNA干扰(RNAi)是一种进化上保守的转录后基因沉默现象,其中将双链RNA导入细胞会导致基因表达的特异性抑制。RNAi已成为基因功能研究的重要工具。本研究的目的是通过由DNA载体产生的短发夹RNA(shRNA)在哺乳动物细胞中诱导RNA干扰,从而为基因功能分析提供一种新方法。
使用双荧光素酶系统评估由DNA载体产生的shRNA的细胞内效应。测定该DNA载体驱动的shRNA在不同条件下的抑制作用。
由DNA载体产生的shRNA在人细胞中诱导RNA干扰,并以序列特异性方式抑制基因表达。抑制作用与靶位点高度相关。
shRNA在人细胞中诱导RNA干扰并以序列特异性方式抑制基因表达。该方法可用于基因功能研究。