Nakamoto Kosuke, Akao Yukihiro, Ueno Yoshihito
United Graduate School of Agricultural Science, Gifu University, 1-1 Yanagido, Gifu 501-1193, Japan.
United Graduate School of Drug Discovery and Medical Information Sciences, Gifu University, 1-1 Yanagido, Gifu 501-1193, Japan.
Bioorg Med Chem Lett. 2018 Sep 15;28(17):2906-2909. doi: 10.1016/j.bmcl.2018.07.020. Epub 2018 Jul 11.
We designed and synthesized a photo-reactive and tag-free RNA probe for the identification of microRNA (miRNA) targets. To synthesize the RNA probe, we designed a novel nucleoside analog 1-O-[3-ethynyl-5-(3-trifluoromethyl-3H-diazirine-3-yl)]benzyl-β-d-ribofuranose containing aryl trifluoromethyl diazirine and ethynyl moieties. The RNA probe containing this analog was observed to form crosslinks with complementary RNA by UV irradiation and was rapidly tagged by Cu-catalyzed azide alkyne cycloaddition (CuAAC). In addition, the tag-free and photo-reactive miRNA-145 probe showed comparable gene silencing activity to that of unmodified miRNA-145. Therefore, miRNA probes containing the nucleoside analog are promising candidates for the identification of target mRNAs of miRNAs.
我们设计并合成了一种用于鉴定微小RNA(miRNA)靶标的光反应性且无标签的RNA探针。为了合成该RNA探针,我们设计了一种新型核苷类似物1-O-[3-乙炔基-5-(3-三氟甲基-3H-二氮杂环丙烯-3-基)]苄基-β-D-呋喃核糖,其含有芳基三氟甲基二氮杂环丙烯和乙炔基部分。观察到含有该类似物的RNA探针通过紫外线照射与互补RNA形成交联,并通过铜催化的叠氮化物炔烃环加成反应(CuAAC)快速标记。此外,无标签且具有光反应性的miRNA-145探针显示出与未修饰的miRNA-145相当的基因沉默活性。因此,含有该核苷类似物的miRNA探针有望成为鉴定miRNA靶标mRNA的候选物。