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由7个核苷酸互补引发的小干扰RNA介导的脱靶基因沉默。

siRNA-mediated off-target gene silencing triggered by a 7 nt complementation.

作者信息

Lin Xiaoyu, Ruan Xiaoan, Anderson Mark G, McDowell Jeffrey A, Kroeger Paul E, Fesik Stephen W, Shen Yu

机构信息

Cancer Research, Global Pharmaceutical Research and Development, AP10, Abbott Laboratories 100 Abbott Park Road, Abbott Park, IL 60064, USA.

出版信息

Nucleic Acids Res. 2005 Aug 9;33(14):4527-35. doi: 10.1093/nar/gki762. Print 2005.

Abstract

A growing body of evidence suggests that siRNA could generate off-target effects through different mechanisms. However, the full impact of off-target gene regulation on phenotypic induction and accordingly on data interpretation in the context of large-scale siRNA library screen has not been reported. Here we report on off-target gene silencing effects observed in a large-scale knockdown experiment designed to identify novel regulators of the HIF-1 pathway. All of the three 'top hits' from our screen have been demonstrated to result from off-target gene silencing. Two of the three 'siRNA hits' were found to directly trigger down-regulation of hif-1alpha mRNA through a 7 nt motif, AGGCAGT, that is present in both the hif-1alpha mRNA and the siRNAs. Further analysis revealed that the generation of off-target gene silencing via this 7 nt motif depends on the characteristics of the target mRNA, including the sequence context surrounding the complementary region, the position of the complementary region in the mRNA and the copy number of the complementary region. Interestingly, the off-target siRNA against hif-1alpha was also shown to trigger mRNA degradation with high probability of other genes that possess multiple copies of the AGGCAGT motif in the 3'-untranslated region. Lessons learned from this study will be a valuable asset to aid in designing siRNAs with more stringent target selectivity and improving 'hits-follow-up' strategies for future large-scale knockdown experiments.

摘要

越来越多的证据表明,小干扰RNA(siRNA)可通过不同机制产生脱靶效应。然而,在大规模siRNA文库筛选的背景下,脱靶基因调控对表型诱导以及相应数据解读的全面影响尚未见报道。在此,我们报告在一项旨在鉴定缺氧诱导因子-1(HIF-1)信号通路新调控因子的大规模敲低实验中观察到的脱靶基因沉默效应。我们筛选出的所有三个“顶级命中”结果均已证明是由脱靶基因沉默导致的。在三个“siRNA命中”结果中,有两个被发现通过一个7核苷酸基序AGGCAGT直接触发hif-1α mRNA的下调,该基序同时存在于hif-1α mRNA和siRNA中。进一步分析表明,通过这个7核苷酸基序产生脱靶基因沉默取决于靶mRNA的特征,包括互补区域周围的序列背景、互补区域在mRNA中的位置以及互补区域的拷贝数。有趣的是,针对hif-1α的脱靶siRNA还显示出极有可能触发其他在3'-非翻译区拥有多个AGGCAGT基序拷贝的基因的mRNA降解。从这项研究中吸取的经验教训将成为一项宝贵资产,有助于设计具有更严格靶标选择性的siRNA,并改进未来大规模敲低实验的“命中跟进”策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8641/1184219/47dd7cf57afd/gki762f1.jpg

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