Ishigaki Yasuhito, Nagao Akihiro, Matsunaga Tsukasa
Division of Core Facility, Medical Research Institute, Kanazawa Medical University, Kahoku-gun, Japan.
Methods Mol Biol. 2010;623:109-21. doi: 10.1007/978-1-60761-588-0_7.
Currently, RNA interference technology is one of the most powerful tools in molecular biology and has been widely used in genetic manipulation. In addition to chemically synthesized small interfering RNA (siRNA), vector-based methods have been developed for stable gene silencing by the expression of a single short-hairpin RNA (shRNA). The artificially expressed RNA molecules are processed to form a silencing complex that causes the specific degradation of its target mRNA. However, silencing vectors containing a single shRNA-expressing sequence sometimes induce only poor knockdown. In order to improve the knockdown efficiency using shRNA, the multiple shRNA-expressing sequences were introduced into a single plasmid vector. Compared with the conventional single shRNA-expression vector, the multiple shRNA-expression vectors confer higher yields of stable clones with efficient knockdown and better correlations between knockdown level and the expression level of second marker gene, enhanced green fluorescent protein, in the vector. These features are very helpful for establishing stable knockdown clones and the detailed procedure is described in this chapter.
目前,RNA干扰技术是分子生物学中最强大的工具之一,已广泛应用于基因操作。除了化学合成的小干扰RNA(siRNA)外,基于载体的方法也已被开发出来,通过表达单个短发夹RNA(shRNA)实现稳定的基因沉默。人工表达的RNA分子被加工形成一个沉默复合体,导致其靶mRNA的特异性降解。然而,含有单个shRNA表达序列的沉默载体有时只能诱导较差的基因敲低效果。为了提高使用shRNA的基因敲低效率,多个shRNA表达序列被引入到单个质粒载体中。与传统的单shRNA表达载体相比,多shRNA表达载体能产生更高产量的稳定克隆,具有高效的基因敲低效果,并且在基因敲低水平与载体中第二个标记基因增强绿色荧光蛋白的表达水平之间具有更好的相关性。这些特性对于建立稳定的基因敲低克隆非常有帮助,本章将描述详细的操作步骤。