Hunsicker Anke, Steber Markus, Mayer Günter, Meitert Johannes, Klotzsche Marcus, Blind Michael, Hillen Wolfgang, Berens Christian, Suess Beatrix
Lehrstuhl für Mikrobiologie, Friedrich-Alexander-Universität Erlangen-Nürnberg, Staudtstr. 5, 91058 Erlangen, Germany.
Chem Biol. 2009 Feb 27;16(2):173-80. doi: 10.1016/j.chembiol.2008.12.008.
We identified an RNA aptamer that induces TetR-controlled gene expression in Escherichia coli when expressed in the cell. The aptamer was found by a combined approach of in vitro selection for TetR binding and in vivo screening for TetR induction. The smallest active aptamer folds into a stem-loop with an internal loop interrupting the stem. Mutational analysis in vivo and in-line probing in vitro reveal this loop to be the protein binding site. The TetR-inducing activity of the aptamer directly correlates with its stability and the best construct is as efficient as the natural inducer tetracycline. Because of its small size, high induction efficiency, and the stability of the TetR aptamer under in vivo conditions, it is well suited to be an alternative RNA-based inducer of TetR-controlled gene expression.
我们鉴定出一种RNA适配体,当在细胞中表达时,它能在大肠杆菌中诱导受TetR控制的基因表达。该适配体是通过体外筛选TetR结合以及体内筛选TetR诱导的联合方法发现的。最小的活性适配体折叠成一个茎环结构,其内部环中断了茎。体内突变分析和体外线性探针分析表明这个环是蛋白质结合位点。该适配体的TetR诱导活性与其稳定性直接相关,最佳构建体与天然诱导剂四环素一样有效。由于其尺寸小、诱导效率高以及TetR适配体在体内条件下的稳定性,它非常适合作为TetR控制基因表达的基于RNA的替代诱导剂。