Yoshinari Koichi, Miyagishi Makoto, Taira Kazunari
Gene Function Research Center, National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Higashi, Tsukuba Science City 305-8562, Japan.
Nucleic Acids Res. 2004 Feb 3;32(2):691-9. doi: 10.1093/nar/gkh221. Print 2004.
RNA interference (RNAi) is a gene-silencing phenomenon that involves the double-stranded RNA-mediated cleavage of mRNA, and small interfering RNAs (siRNAs) can cause RNAi in mammalian cells. There have been many attempts to clarify the mechanism of RNAi, but information about the relationship between the sequence and structure, in particular, a tight structure, of the target RNA and the activities of siRNAs are limited. In the present study, we examined this relationship by introducing the TAR element, which adopts a very stable secondary structure, at different positions within target RNAs. Our results suggested that the activities of siRNAs were affected by the tight stem-loop structure of TAR. In contrast, the position of the target within the mRNA, the binding of the Tat protein to the TAR, and the location of the target within a translated or a noncoding region had only marginal effects on RNAi. When the target sequence was placed in two different orientations, only one orientation had a significant effect on the activities of siRNA, demonstrating that the presence of certain nucleotides at some specific positions was favorable for RNAi. Systematic analysis of 47 different sites within 47 plasmids under identical conditions indicated that it is the target sequence itself, rather than its location, that is the major determinant of siRNA activity.
RNA干扰(RNAi)是一种基因沉默现象,涉及双链RNA介导的mRNA切割,小干扰RNA(siRNA)可在哺乳动物细胞中引发RNAi。人们进行了许多尝试来阐明RNAi的机制,但关于靶RNA的序列与结构,特别是紧密结构,与siRNA活性之间关系的信息有限。在本研究中,我们通过在靶RNA的不同位置引入具有非常稳定二级结构的TAR元件来研究这种关系。我们的结果表明,siRNA的活性受TAR紧密茎环结构的影响。相比之下,靶标在mRNA内的位置、Tat蛋白与TAR的结合以及靶标在翻译区或非编码区内的位置对RNAi的影响很小。当靶序列以两种不同方向放置时,只有一种方向对siRNA的活性有显著影响,这表明某些特定位置上某些核苷酸的存在有利于RNAi。在相同条件下对47个质粒中的47个不同位点进行系统分析表明,是靶序列本身而非其位置是siRNA活性的主要决定因素。