Válóczi Anna, Hornyik Csaba, Varga Nóra, Burgyán József, Kauppinen Sakari, Havelda Zoltán
Agricultural Biotechnology Center, Szent-Györgyi Albert ut 4, Gödöll H-2100, Hungary.
Nucleic Acids Res. 2004 Dec 14;32(22):e175. doi: 10.1093/nar/gnh171.
We describe here a new method for highly efficient detection of microRNAs by northern blot analysis using LNA (locked nucleic acid)-modified oligonucleotides. In order to exploit the improved hybridization properties of LNA with their target RNA molecules, we designed several LNA-modified oligonucleotide probes for detection of different microRNAs in animals and plants. By modifying DNA oligonucleotides with LNAs using a design, in which every third nucleotide position was substituted by LNA, we could use the probes in northern blot analysis employing standard end-labelling techniques and hybridization conditions. The sensitivity in detecting mature microRNAs by northern blots was increased by at least 10-fold compared to DNA probes, while simultaneously being highly specific, as demonstrated by the use of different single and double mismatched LNA probes. Besides being highly efficient as northern probes, the same LNA-modified oligonucleotide probes would also be useful for miRNA in situ hybridization and miRNA expression profiling by LNA oligonucleotide microarrays.
我们在此描述了一种通过使用锁核酸(LNA)修饰的寡核苷酸进行Northern印迹分析来高效检测微小RNA的新方法。为了利用LNA与靶RNA分子改善的杂交特性,我们设计了几种LNA修饰的寡核苷酸探针,用于检测动植物中的不同微小RNA。通过使用一种设计用LNA修饰DNA寡核苷酸,其中每隔三个核苷酸位置被LNA取代,我们可以在采用标准末端标记技术和杂交条件的Northern印迹分析中使用这些探针。与DNA探针相比,通过Northern印迹检测成熟微小RNA的灵敏度提高了至少10倍,同时具有高度特异性,这通过使用不同的单错配和双错配LNA探针得以证明。除了作为高效的Northern探针外,相同的LNA修饰寡核苷酸探针还可用于miRNA原位杂交和通过LNA寡核苷酸微阵列进行miRNA表达谱分析。