Du Cheng, Ge Baosheng, Feng Xiaoyan, Chan Wing C, McKeithan Timothy W
Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Biochem Biophys Res Commun. 2006 Jun 23;345(1):99-105. doi: 10.1016/j.bbrc.2006.04.061. Epub 2006 Apr 25.
Small interfering RNA (siRNA) expression vectors using a Pol III promoter fall into two categories, vectors with a single Pol III promoter that express small hairpin RNA (shRNA) and vectors with two head-to-head (convergent) Pol III promoters that express siRNA. There are technical difficulties in preparing convergent siRNA vectors from cDNA. Here, we report construction of a novel convergent siRNA expression vector, pTHUB. Two XcmI sites were inserted between opposing Pol III promoters. After linearization with XcmI, pTHUB has a single 3' A overhang at each end that allows direct cloning of partially DNase I digested cDNA fragments (20-30 bp) tailed with ddT. A derivative method for generating 19 bp siRNA in pTHUB is also described. The suppression efficiency of the pTHUB vector is comparable to those of conventional shRNA vectors. We have made a siRNA library from a single cDNA. The same approach can be used to construct whole-genome siRNA libraries from cellular cDNA.
使用RNA聚合酶III(Pol III)启动子的小干扰RNA(siRNA)表达载体可分为两类,一类是带有单个Pol III启动子的载体,可表达小发夹RNA(shRNA);另一类是带有两个头对头(反向)Pol III启动子的载体,可表达siRNA。从cDNA制备反向siRNA载体存在技术难题。在此,我们报告了一种新型反向siRNA表达载体pTHUB的构建。在反向的Pol III启动子之间插入了两个XcmI位点。用XcmI线性化后,pTHUB的两端各有一个单一的3' A突出端,这使得可以直接克隆用ddT加尾的部分经DNA酶I消化的cDNA片段(20 - 30 bp)。本文还描述了在pTHUB中生成19 bp siRNA的衍生方法。pTHUB载体的抑制效率与传统shRNA载体相当。我们从单个cDNA构建了一个siRNA文库。同样的方法可用于从细胞cDNA构建全基因组siRNA文库。