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与异位表达的ciRS7衍生环状RNA相比,RNA聚合酶II转录的TuD发夹的增强型定制微小RNA海绵活性。

Enhanced Tailored MicroRNA Sponge Activity of RNA Pol II-Transcribed TuD Hairpins Relative to Ectopically Expressed ciRS7-Derived circRNAs.

作者信息

Hollensen Anne Kruse, Andersen Sofie, Hjorth Karina, Bak Rasmus O, Hansen Thomas B, Kjems Jørgen, Aagaard Lars, Damgaard Christian Kroun, Mikkelsen Jacob Giehm

机构信息

Department of Biomedicine, Health, Aarhus University, 8000 Aarhus C, Denmark; Department of Molecular Biology and Genetics, Science and Technology, Aarhus University, 8000 Aarhus C, Denmark.

Department of Biomedicine, Health, Aarhus University, 8000 Aarhus C, Denmark.

出版信息

Mol Ther Nucleic Acids. 2018 Dec 7;13:365-375. doi: 10.1016/j.omtn.2018.09.009. Epub 2018 Sep 21.

Abstract

As key regulators of gene expression, microRNAs (miRNAs) have emerged as targets in basic experimentation and therapy. Administration of DNA-encoded RNA molecules, targeting miRNAs through base pairing, is one viable strategy for inhibiting specific miRNAs. A naturally occurring circular RNA (circRNA), ciRS-7, serving as a miRNA-7 (miR-7) sponge was recently identified. This has sparked tremendous interest in adapting circRNAs for suppressing miRNA function. In parallel, we and others have demonstrated efficacy of expressed anti-miRNA Tough Decoy (TuD) hairpins. To compare properties of such inhibitors, we express ciRS-7 and TuD-containing miRNA suppressor transcripts from identical vector formats adapted from RNA polymerase II-directed expression plasmids previously used for production of ciRS-7. In general, markedly higher levels of miR-7 suppression with TuD transcripts relative to ciRS-7 are observed, leading to superior miRNA sponge effects using expressed TuD hairpins. Notably however, we find that individual ciRS-7 transcripts are more potent inhibitors of miR-7 activity than individual TuD7-containing transcripts, although each miR-7 seed match target site in ciRS-7 is, on average, less potent than the perfectly matched target sites in the TuD motif. All together, our studies call for improved means of designing and producing circRNAs for customized miRNA targeting to match TuD hairpins for tailored miRNA suppression.

摘要

作为基因表达的关键调节因子,微小RNA(miRNA)已成为基础实验和治疗的靶点。通过碱基配对靶向miRNA的DNA编码RNA分子给药是抑制特定miRNA的一种可行策略。最近发现了一种天然存在的环状RNA(circRNA),即ciRS-7,它可作为miRNA-7(miR-7)的海绵。这引发了人们对利用circRNA抑制miRNA功能的极大兴趣。与此同时,我们和其他人已经证明了表达的抗miRNA Tough Decoy(TuD)发夹的有效性。为了比较这些抑制剂的特性,我们从先前用于生产ciRS-7的RNA聚合酶II指导的表达质粒改编的相同载体形式中表达ciRS-7和含TuD的miRNA抑制转录本。一般来说,相对于ciRS-7,TuD转录本对miR-7的抑制水平明显更高,使用表达的TuD发夹可产生更好的miRNA海绵效应。然而,值得注意的是,我们发现单个ciRS-7转录本比单个含TuD7的转录本对miR-7活性的抑制作用更强,尽管ciRS-7中每个miR-7种子匹配靶位点平均而言比TuD基序中完全匹配的靶位点效力更低。总之,我们的研究呼吁改进设计和生产circRNA的方法,以实现定制的miRNA靶向,使其与TuD发夹相匹配,以实现定制的miRNA抑制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00e2/6198105/fbf362060ef7/fx1.jpg

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