Effect of asymmetric terminal structures of short RNA duplexes on the RNA interference activity and strand selection

被引:83
作者
Sano, Masayuki [1 ]
Sierant, Malgorzata [2 ]
Miyagishi, Makoto [3 ]
Nakanishi, Mahito [1 ]
Takagi, Yasuomi [4 ]
Sutou, Shizuyo [5 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Biotherapeut Res Lab, Tsukuba, Ibaraki 3058562, Japan
[2] Polish Acad Sci, Dept Bioorgan Chem, Ctr Mol & Macromol Studies, PL-90363 Lodz, Poland
[3] Int Med Ctr Japan, Res Inst, Dept Gene Diagnost & Therapeut, Tokyo, Japan
[4] IGENE Therapeut Inc, Nihonbashi, Tokyo 1038355, Japan
[5] Shujitsu Univ, Sch Pharm, Okayama 7038516, Japan
基金
日本学术振兴会;
关键词
D O I
10.1093/nar/gkn584
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Short interfering RNAs (siRNAs) are valuable reagents for sequence-specific inhibition of gene expression via the RNA interference (RNAi) pathway. Although it has been proposed that the relative thermodynamic stability at the 5'-ends of siRNAs plays a crucial role in siRNA strand selection, we demonstrate here that a character of the 2-nt 3'-overhang of siRNAs is the predominant determinant of which strand participates in the RNAi pathway. We show that siRNAs with a unilateral 2-nt 3'-overhang on the antisense strand are more effective than siRNAs with 3'-overhangs at both ends, due to preferential loading of the antisense strand into the RNA-induced silencing complex (RISC). Regardless of the relative thermodynamic stabilities at the ends of siRNAs, overhang-containing strands are predominantly selected as the guide strand; whereas, relative stability markedly influences opposite strand selection. Moreover, we show that sense strand modifications, such as deletions or DNA substitutions, of siRNAs with unilateral overhang on the antisense strand have no negative effect on the antisense strand selection, but may improve RNAi potency. Our findings provide useful guidelines for the design of potent siRNAs and contribute to understanding the crucial factors in determining strand selection in mammalian cells.
引用
收藏
页码:5812 / 5821
页数:10
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