Caplen N J, Parrish S, Imani F, Fire A, Morgan R A
Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Proc Natl Acad Sci U S A. 2001 Aug 14;98(17):9742-7. doi: 10.1073/pnas.171251798. Epub 2001 Jul 31.
Short interfering RNAs (siRNAs) are double-stranded RNAs of approximately 21-25 nucleotides that have been shown to function as key intermediaries in triggering sequence-specific RNA degradation during posttranscriptional gene silencing in plants and RNA interference in invertebrates. siRNAs have a characteristic structure, with 5'-phosphate/3'-hydroxyl ends and a 2-base 3' overhang on each strand of the duplex. In this study, we present data that synthetic siRNAs can induce gene-specific inhibition of expression in Caenorhabditis elegans and in cell lines from humans and mice. In each case, the interference by siRNAs was superior to the inhibition of gene expression mediated by single-stranded antisense oligonucleotides. The siRNAs seem to avoid the well documented nonspecific effects triggered by longer double-stranded RNAs in mammalian cells. These observations may open a path toward the use of siRNAs as a reverse genetic and therapeutic tool in mammalian cells.
小干扰RNA(siRNA)是约21 - 25个核苷酸的双链RNA,已被证明在植物转录后基因沉默和无脊椎动物RNA干扰过程中,作为触发序列特异性RNA降解的关键中介发挥作用。siRNA具有特征性结构,双链的每条链都有5'-磷酸/3'-羟基末端以及2个碱基的3'端悬垂。在本研究中,我们提供的数据表明,合成的siRNA可在秀丽隐杆线虫以及人和小鼠的细胞系中诱导基因特异性表达抑制。在每种情况下,siRNA的干扰作用均优于单链反义寡核苷酸介导的基因表达抑制。siRNA似乎避免了哺乳动物细胞中较长双链RNA引发的、已被充分证明的非特异性效应。这些观察结果可能为在哺乳动物细胞中使用siRNA作为反向遗传学和治疗工具开辟一条道路。