Schwarz Dianne S, Hutvágner György, Du Tingting, Xu Zuoshang, Aronin Neil, Zamore Phillip D
Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Lazare Research Building, 364 Plantation Street, Worcester, MA 01605, USA.
Cell. 2003 Oct 17;115(2):199-208. doi: 10.1016/s0092-8674(03)00759-1.
A key step in RNA interference (RNAi) is assembly of the RISC, the protein-siRNA complex that mediates target RNA cleavage. Here, we show that the two strands of an siRNA duplex are not equally eligible for assembly into RISC. Rather, both the absolute and relative stabilities of the base pairs at the 5' ends of the two siRNA strands determine the degree to which each strand participates in the RNAi pathway. siRNA duplexes can be functionally asymmetric, with only one of the two strands able to trigger RNAi. Asymmetry is the hallmark of a related class of small, single-stranded, noncoding RNAs, microRNAs (miRNAs). We suggest that single-stranded miRNAs are initially generated as siRNA-like duplexes whose structures predestine one strand to enter the RISC and the other strand to be destroyed. Thus, the common step of RISC assembly is an unexpected source of asymmetry for both siRNA function and miRNA biogenesis.
RNA干扰(RNAi)中的关键步骤是RNA诱导沉默复合体(RISC)的组装,RISC是介导靶RNA切割的蛋白质-siRNA复合物。在此,我们表明,siRNA双链体的两条链并非同等适合组装到RISC中。相反,两条siRNA链5'端碱基对的绝对稳定性和相对稳定性都决定了每条链参与RNAi途径的程度。siRNA双链体在功能上可能是不对称的,两条链中只有一条能够触发RNAi。不对称性是一类相关的小单链非编码RNA——微小RNA(miRNA)的标志。我们认为,单链miRNA最初是以类似siRNA的双链体形式产生的,其结构注定一条链进入RISC,另一条链被降解。因此,RISC组装这一共同步骤是siRNA功能和miRNA生物合成中不对称性的一个意外来源。