Gou Deming, Weng Tingting, Wang Yang, Wang Zhixin, Zhang Honghao, Gao Li, Chen Zhongming, Wang Pengcheng, Liu Lin
Department of Physiological Sciences, Oklahoma State University, Stillwater, OK 74078, USA.
J Gene Med. 2007 Sep;9(9):751-63. doi: 10.1002/jgm.1080.
The application of RNA interference (RNAi) as a research and therapeutic tool depends on its ability to silence genes in a sequence-specific manner. Recent studies have reported that the effective knockdown of genes can be achieved by multiple short hairpin RNAs (shRNAs) in a single vector. Moreover, this approach can depress several genes simultaneously. However, current methods for the construction of multiple shRNA vectors often suffer from vector instability and are time-consuming. Here, we describe a simple, quick and low-cost approach to construct a single vector expressing four shRNA sequences driven by four different promoters. Using this vector, we were able to improve the gene silencing efficiency and make it possible to silence four different genes simultaneously, further expanding the application spectrum of RNAi, both in functional studies and therapeutic strategies.
RNA干扰(RNAi)作为一种研究和治疗工具的应用取决于其以序列特异性方式沉默基因的能力。最近的研究报道,通过单个载体中的多个短发夹RNA(shRNA)可以实现基因的有效敲低。此外,这种方法可以同时抑制多个基因。然而,目前构建多个shRNA载体的方法常常存在载体不稳定且耗时的问题。在此,我们描述了一种简单、快速且低成本的方法来构建一个由四个不同启动子驱动表达四个shRNA序列的单一载体。使用该载体,我们能够提高基因沉默效率,并使同时沉默四个不同基因成为可能,进一步扩大了RNAi在功能研究和治疗策略中的应用范围。