Martinez Javier, Patkaniowska Agnieszka, Urlaub Henning, Lührmann Reinhard, Tuschl Thomas
Department of Cellular Biochemistry, Max-Planck-Institute for Biophysical Chemistry, Am Fassberg 11, D-37077, Göttingen, Germany.
Cell. 2002 Sep 6;110(5):563-74. doi: 10.1016/s0092-8674(02)00908-x.
Small interfering RNAs (siRNAs) are the mediators of mRNA degradation in the process of RNA interference (RNAi). Here, we describe a human biochemical system that recapitulates siRNA-mediated target RNA degradation. By using affinity-tagged siRNAs, we demonstrate that a single-stranded siRNA resides in the RNA-induced silencing complex (RISC) together with eIF2C1 and/or eIF2C2 (human GERp95) Argonaute proteins. RISC is rapidly formed in HeLa cell cytoplasmic extract supplemented with 21 nt siRNA duplexes, but also by adding single-stranded antisense RNAs, which range in size between 19 and 29 nucleotides. Single-stranded antisense siRNAs are also effectively silencing genes in HeLa cells, especially when 5'-phosphorylated, and expand the repertoire of RNA reagents suitable for gene targeting.
小干扰RNA(siRNA)是RNA干扰(RNAi)过程中mRNA降解的介导因子。在此,我们描述了一种重现siRNA介导的靶RNA降解的人类生化系统。通过使用亲和标记的siRNA,我们证明单链siRNA与eIF2C1和/或eIF2C2(人类GERp95)AGO蛋白一起存在于RNA诱导沉默复合体(RISC)中。在补充有21个核苷酸的siRNA双链体的HeLa细胞质提取物中,RISC能快速形成,添加大小在19至29个核苷酸之间的单链反义RNA也能形成RISC。单链反义siRNA在HeLa细胞中也能有效沉默基因,尤其是5'-磷酸化时,并且扩展了适用于基因靶向的RNA试剂种类。