Manavella Pablo Andrés, Rubio-Somoza Ignacio
Max Planck Institute for Developmental Biology, Tübingen, Germany.
Methods Mol Biol. 2011;732:121-30. doi: 10.1007/978-1-61779-083-6_9.
Small RNA (sRNA)-mediated gene silencing constitutes a powerful tool for the molecular characterization- of a given gene. The RNAi technology has been largely used for this purpose. This approach is based on the cloning of an inverted repeated fragment of the gene to be silenced. Even when this approach -produces a strong repression of the target gene it also involves the production of multiple small RNAs species that can easily lead to off targeting. Taking advantage of the latest insights into the new post-biogenesis layer of regulation in microRNA (miRNA) activity, it is possible to overcome the above-mentioned limitation. Artificial microRNAs (amiRNAs) are 21mer small RNAs, which can be genetically engineered and they function to specifically silence single or multiple genes of interest. Since generally just one miRNA molecule is generated from each precursor, the specificity of this technology is much higher than longer inverted repeats. Application of this technology results in highly specific mRNA downregulation by computationally designed sequences programmed to target one or a set of custom-selected transcripts.
小RNA(sRNA)介导的基因沉默是对特定基因进行分子表征的有力工具。RNA干扰技术已广泛用于此目的。该方法基于待沉默基因反向重复片段的克隆。即使这种方法能强烈抑制靶基因,它也会产生多种小RNA,容易导致脱靶。利用对微小RNA(miRNA)活性新的生物合成后调控层面的最新见解,有可能克服上述限制。人工微小RNA(amiRNA)是21个核苷酸的小RNA,可通过基因工程改造,其功能是特异性沉默单个或多个感兴趣的基因。由于通常每个前体仅产生一个miRNA分子,该技术的特异性远高于较长的反向重复序列。应用该技术可通过经计算设计以靶向一个或一组定制选择转录本的序列实现高度特异性的mRNA下调。