Beuvink Iwan, Kolb Fabrice A, Budach Wolfgang, Garnier Arlette, Lange Joerg, Natt Francois, Dengler Uwe, Hall Jonathan, Filipowicz Witold, Weiler Jan
Novartis Institutes for BioMedical Research, Genome and Proteome Sciences, Basel, Switzerland.
Nucleic Acids Res. 2007;35(7):e52. doi: 10.1093/nar/gkl1118. Epub 2007 Mar 13.
Microarrays to examine the global expression levels of microRNAs (miRNAs) in a systematic in-parallel manner have become important tools to help unravel the functions of miRNAs and to understand their roles in RNA-based regulation and their implications in human diseases. We have established a novel miRNA-specific microarray platform that enables the simultaneous expression analysis of both known and predicted miRNAs obtained from human or mouse origin. Chemically modified 2'-O-(2-methoxyethyl)-(MOE) oligoribonucleotide probes were arrayed onto Evanescent Resonance (ER) microchips by robotic spotting. Supplementing the complementary probes against miRNAs with carefully designed mismatch controls allowed for accurate sequence-specific determination of miRNA expression profiles obtained from a panel of mouse tissues. This revealed new expression signatures of known miRNAs as well as of novel miRNAs previously predicted using bioinformatic methods. Systematic confirmation of the array data with northern blotting and, in particular, real-time PCR suggests that the described microarray platform is a powerful tool to analyze miRNA expression patterns with rapid throughput and high fidelity.
以系统并行方式检测微小RNA(miRNA)整体表达水平的微阵列,已成为帮助揭示miRNA功能、理解其在基于RNA的调控中的作用以及在人类疾病中的意义的重要工具。我们建立了一种新型的miRNA特异性微阵列平台,该平台能够同时对源自人类或小鼠的已知和预测miRNA进行表达分析。通过机器人点样将化学修饰的2'-O-(2-甲氧基乙基)-(MOE)寡核糖核苷酸探针阵列到倏逝共振(ER)微芯片上。用精心设计的错配对照补充针对miRNA的互补探针,能够准确地进行序列特异性测定,以确定从小鼠组织组中获得的miRNA表达谱。这揭示了已知miRNA以及先前使用生物信息学方法预测的新型miRNA的新表达特征。用Northern印迹法,特别是实时PCR对阵列数据进行系统确认,表明所描述的微阵列平台是一种能够以高通量和高保真度分析miRNA表达模式的强大工具。