Ørom Ulf Andersson, Kauppinen Sakari, Lund Anders H
Biotech Research and Innovation Centre, University of Copenhagen, Copenhagen, Denmark.
Gene. 2006 May 10;372:137-41. doi: 10.1016/j.gene.2005.12.031. Epub 2006 Feb 24.
microRNAs are short, endogenous non-coding RNAs that act as post-transcriptional modulators of gene expression. Important functions for microRNAs have been found in the regulation of development, cellular proliferation and differentiation, while perturbed miRNA expression patterns have been observed in many human cancers. Here we present a method for specific inhibition of miRNA function through interaction with LNA-modified antisense oligonucleotides and report the specificity of this application. We show that LNA-modified oligonucleotides can inhibit exogenously introduced miRNAs with high specificity using a heterologous reporter assay, and furthermore demonstrate their ability to inhibit an endogenous miRNA in Drosophila melanogaster cells, leading to up-regulation of the cognate target protein. The method shows stoichiometric and reliable inhibition of the targeted miRNA and can thus be applied to studies of miRNA functions and validation of putative target genes.
微小RNA是短的内源性非编码RNA,作为基因表达的转录后调节因子发挥作用。在发育、细胞增殖和分化的调控中已发现微小RNA具有重要功能,而在许多人类癌症中也观察到了微小RNA表达模式的紊乱。在此,我们提出一种通过与锁核酸(LNA)修饰的反义寡核苷酸相互作用来特异性抑制微小RNA功能的方法,并报告该应用的特异性。我们表明,使用异源报告基因检测,LNA修饰的寡核苷酸可以高特异性地抑制外源性引入的微小RNA,此外还证明了它们在黑腹果蝇细胞中抑制内源性微小RNA的能力,从而导致同源靶蛋白的上调。该方法显示出对靶向微小RNA的化学计量和可靠抑制,因此可应用于微小RNA功能的研究和推定靶基因的验证。