Huang Kun, Doyle Francis, Wurz Zachary E, Tenenbaum Scott A, Hammond Reza K, Caplan Jeffrey L, Meyers Blake C
Bio-Imaging Center, Delaware Biotechnology Institute, University of Delaware, Newark, DE 19711, USA.
Department of Plant and Soil Sciences, University of Delaware, Newark, DE 19716, USA.
Nucleic Acids Res. 2017 Aug 21;45(14):e130. doi: 10.1093/nar/gkx504.
Small RNAs, including microRNAs (miRNAs) and small interfering RNAs (siRNAs), play a variety of important regulatory roles in many eukaryotes. Their small size has made it challenging to study them directly in live cells. Here we describe an RNA-based fluorescent sensor for small RNA detection both in vitro and in vivo, adaptable for any small RNA. It utilizes an sxRNA switch for detection of miRNA-mRNA interactions combined with a fluorophore-binding sequence 'Spinach', a GFP-like RNA aptamer for which the RNA-fluorophore complex exhibits strong and consistent fluorescence under an excitation wavelength. Two example sensors, FASTmiR171 and FASTmiR122, can rapidly detect and quantify the levels of miR171 and miR122 in vitro. The sensors can determine relative levels of miRNAs in total RNA extracts with sensitivity similar to small RNA sequencing and northern blots. FASTmiR sensors were also used to estimate the copy number range of miRNAs in total RNA extracts. To localize and analyze the spatial distribution of small RNAs in live, single cells, tandem copies of FASTmiR122 were expressed in different cell lines. FASTmiR122 was able to quantitatively detect the differences in miR122 levels in Huh7 and HEK293T cells demonstrating its potential for tracking miRNA expression and localization in vivo.
包括微小RNA(miRNA)和小干扰RNA(siRNA)在内的小RNA在许多真核生物中发挥着多种重要的调控作用。它们的小尺寸使得直接在活细胞中研究它们具有挑战性。在这里,我们描述了一种基于RNA的荧光传感器,用于在体外和体内检测小RNA,适用于任何小RNA。它利用一个sxRNA开关来检测miRNA与mRNA的相互作用,并结合一个荧光团结合序列“菠菜”,这是一种类似绿色荧光蛋白的RNA适体,其RNA-荧光团复合物在激发波长下表现出强烈且一致的荧光。两个示例传感器FASTmiR171和FASTmiR122能够在体外快速检测和定量miR171和miR122的水平。这些传感器可以测定总RNA提取物中miRNA的相对水平,其灵敏度与小RNA测序和Northern印迹法相似。FASTmiR传感器还用于估计总RNA提取物中miRNA的拷贝数范围。为了在活的单细胞中定位和分析小RNA的空间分布,在不同细胞系中表达了FASTmiR122的串联拷贝。FASTmiR122能够定量检测Huh7和HEK293T细胞中miR122水平的差异,证明了其在体内追踪miRNA表达和定位的潜力。