Wakiyama Motoaki, Matsumoto Tomoko, Yokoyama Shigeyuki
RIKEN Genomic Sciences Center, 1-7-22 Suehiro-cho, Tsurumi, Yokohama 230-0045, Japan.
Biochem Biophys Res Commun. 2005 Jun 17;331(4):1163-70. doi: 10.1016/j.bbrc.2005.03.240.
The effect of RNA interference (RNAi) is generally more potent in Drosophila Schneider 2 (S2) cells than in mammalian cells. In mammalian cells, PolIII promoter-based DNA vectors can be used to express small interfering RNA (siRNA) or short hairpin RNA (shRNA); however, this has not been demonstrated in cultured Drosophila cells. Here we show that shRNAs transcribed from the Drosophila U6 promoter can efficiently trigger gene silencing in S2 cells. By targeting firefly luciferase mRNA, we assessed the efficacy of the shRNAs and examined the structural requirements for highly effective shRNAs. The silencing effect was dependent on the length of the stem region and the sequence of the loop region. Furthermore, we demonstrate that the expression of the endogenous cyclin E protein can be repressed by the U6 promoter-driven shRNAs. Drosophila U6 promoter-based shRNA expression systems may permit stable gene silencing in S2 cells.
RNA干扰(RNAi)在果蝇Schneider 2(S2)细胞中的作用通常比在哺乳动物细胞中更强。在哺乳动物细胞中,基于PolIII启动子的DNA载体可用于表达小干扰RNA(siRNA)或短发夹RNA(shRNA);然而,这在培养的果蝇细胞中尚未得到证实。在这里,我们表明从果蝇U6启动子转录的shRNA可以有效地在S2细胞中触发基因沉默。通过靶向萤火虫荧光素酶mRNA,我们评估了shRNA的功效,并研究了高效shRNA的结构要求。沉默效果取决于茎区的长度和环区的序列。此外,我们证明内源性细胞周期蛋白E蛋白的表达可以被U6启动子驱动的shRNA抑制。基于果蝇U6启动子的shRNA表达系统可能允许在S2细胞中实现稳定的基因沉默。