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Sensitive and specific detection of microRNAs by northern blot analysis using LNA-modified oligonucleotide probes

机译:使用LNA修饰的寡核苷酸探针通过Northern印迹分析灵敏而特异性地检测microRNA

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摘要

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.
机译:我们在这里描述了一种新的方法,可通过使用LNA(锁定核酸)修饰的寡核苷酸进行Northern印迹分析来高效检测microRNA。为了利用LNA与其靶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microRNA。通过使用设计(其中每个核苷酸的第三个核苷酸位置都被LNA取代)修饰LNA的DNA寡核苷酸,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microRNA的灵敏度提高了至少10倍,同时具有很高的特异性,这通过使用不同的单双错配LNA探针证明。除了可以作为Northern探针高效使用外,相同的LNA修饰寡核苷酸探针还可用于通过LNA寡核苷酸微阵列进行miRNA原位杂交和miRNA表达谱分析。

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