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基于合成前体微小RNA的短发夹RNA作为有效的RNA干扰触发因子。

Synthetic Pre-miRNA-Based shRNA as Potent RNAi Triggers.

作者信息

Terasawa Kazuya, Shimizu Kazuharu, Tsujimoto Gozoh

机构信息

Department of Pharmacogenomics, Graduate School of Pharmaceutical Sciences, Kyoto University, 46-29 Yoshida Shimoadachi-cho, Sakyo-ku, Kyoto 606-8501, Japan.

出版信息

J Nucleic Acids. 2011;2011:131579. doi: 10.4061/2011/131579. Epub 2011 Jul 12.

Abstract

RNA interference (RNAi) is a powerful tool for studying gene function owing to the ease with which it can selectively silence genes of interest, and it has also attracted attention because of its potential for therapeutic applications. Chemically synthesized small interfering RNAs (siRNAs) and DNA vector-based short hairpin RNAs (shRNAs) are now widely used as RNAi triggers. In contrast to expressed shRNAs, the use of synthetic shRNAs is limited. Here we designed shRNAs modeled on a precursor microRNA (pre-miRNA) and evaluated their biological activity. We demonstrated that chemically synthetic pre-miRNA-based shRNAs have more potent RNAi activity than their corresponding siRNAs and found that their antisense strands are more efficiently incorporated into the RNA-induced silencing complex. Although greater off-target effects and interferon responses were induced by shRNAs than by their corresponding siRNAs, these effects could be overcome by simply using a lower concentration or by optimizing and chemically modifying shRNAs similar to synthetic siRNAs. These are challenges for the future.

摘要

RNA干扰(RNAi)是研究基因功能的强大工具,因为它能够轻松地选择性沉默感兴趣的基因,并且因其在治疗应用方面的潜力也备受关注。化学合成的小干扰RNA(siRNA)和基于DNA载体的短发夹RNA(shRNA)现在被广泛用作RNAi触发物。与表达的shRNA相比,合成shRNA的使用受到限制。在这里,我们设计了基于前体微小RNA(pre-miRNA)的shRNA并评估了它们的生物学活性。我们证明,化学合成的基于pre-miRNA的shRNA比其相应的siRNA具有更强的RNAi活性,并且发现它们的反义链更有效地整合到RNA诱导沉默复合体中。尽管shRNA比其相应的siRNA诱导了更大的脱靶效应和干扰素反应,但通过简单地使用较低浓度或通过优化和化学修饰shRNA(类似于合成siRNA),这些效应是可以克服的。这些都是未来面临的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e331/3139136/33f91e6c1f4b/JNA2011-131579.001.jpg

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