Park June Hyun, Hong Sun Woo, Yun Soyeong, Lee Dong-Ki, Shin Chanseok
1 Department of Agricultural Biotechnology, Seoul National University , Seoul, Republic of Korea.
Nucleic Acid Ther. 2014 Oct;24(5):364-71. doi: 10.1089/nat.2014.0494.
Small interfering RNAs (siRNAs) guide RNA-induced silencing complexes (RISC) to target mRNAs for sequence-specific silencing. A fundamental aspect of this highly coordinated process is a guide strand-specific loading of the siRNA duplex into the RISC for the accurate target recognition, which is currently dictated by certain duplex parameters such as thermodynamics. Here, we show that minor changes in the overhang structure have profound effects on the extent to which the individual strands of the siRNA duplex participate in RNAi activity. We demonstrate that the two strands of the siRNA are similarly eligible for assembly into RISC for the siRNAs with symmetric overhangs, whereas those with asymmetric RNA/deoxythymidine dinucleotide (dTdT) overhangs exhibit a distinct preference in favor of a strand with an RNA overhang that drives a mature RISC affinity to the desired target. We believe that this additional determinant provides a plausible and simple approach for improving the strand selection, thereby considerably increasing a specificity of target silencing.
小干扰RNA(siRNA)引导RNA诱导沉默复合体(RISC)靶向mRNA以实现序列特异性沉默。这一高度协调过程的一个基本方面是将siRNA双链体以引导链特异性方式加载到RISC中,以便准确识别靶标,目前这由某些双链体参数(如热力学)决定。在此,我们表明突出端结构的微小变化对siRNA双链体各链参与RNA干扰活性的程度有深远影响。我们证明,对于具有对称突出端的siRNA,两条链同样有资格组装到RISC中,而具有不对称RNA/脱氧胸苷二核苷酸(dTdT)突出端的siRNA则表现出明显的偏好,倾向于带有RNA突出端的链,该链可驱动成熟的RISC对所需靶标的亲和力。我们认为,这一额外的决定因素为改进链的选择提供了一种合理且简单的方法,从而显著提高靶标沉默的特异性。