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Tolerated wobble mutations in siRNAs decrease specificity but can enhance activity in vivo

机译:siRNA中容许的摆动突变降低了特异性但可以增强体内活性

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摘要

RNA interference (RNAi) has become an invaluable tool for functional genomics. A critical use of this tool depends on an understanding of the factors that determine the specificity and activity of the active agent, small interfering RNA (siRNA). Several studies have concluded that tolerance of mutations can be considerable and hence lead to off-target effects. In this study, we have investigated in vivo the toleration of wobble (G:U) mutations in high activity siRNAs against Flap Endonuclease 1 (Fen1) and Aquaporin-4 (Aqp4). Mutations in the central part of the antisense strand caused a pronounced decrease in activity, while mutations in the 5′ and 3′ends were tolerated very well. Furthermore, based on analysis of nine different mutated siRNAs with widely differing intrinsic activities, we conclude that siRNA activity can be significantly enhanced by wobble mutations (relative to mRNA), in the 5′ terminal of the antisense strand. These findings should facilitate design of active siRNAs where the target mRNA offers limited choice of siRNA positions.
机译:RNA干扰(RNAi)已成为功能基因组学的宝贵工具。该工具的关键用途取决于对决定活性剂小干扰RNA(siRNA)的特异性和活性的因素的理解。多项研究得出结论,突变的耐受性可能很高,因此会导致脱靶效应。在这项研究中,我们研究了体内对Flap内切核酸酶1(Fen1)和Aquaporin-4(Aqp4)的高活性siRNA中摆动(G:U)突变的耐受性。反义链中央部分的突变导致活性显着下降,而5'和3'端的突变被很好地耐受。此外,基于对具有广泛不同的内在活性的9种不同突变siRNA的分析,我们得出结论,通过在反义链5'端进行摆动突变(相对于mRNA),可以显着增强siRNA的活性。这些发现将有助于设计活性siRNA,其中靶mRNA提供的siRNA位置选择有限。

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