Iyer Sukanya, Doktycz Mitchel J
Graduate Program in Genome Science and Technology, University of Tennessee , Knoxville, Tennessee 37996, United States.
ACS Synth Biol. 2014 Jun 20;3(6):340-6. doi: 10.1021/sb4000756. Epub 2013 Sep 26.
Realizing the potential of cell-free systems will require development of ligand-sensitive gene promoters that control gene expression in response to a ligand of interest. Here, we describe an approach to designing ligand-sensitive transcriptional control in cell-free systems that is based on the combination of a DNA aptamer that binds thrombin and the T7 bacteriophage promoter. Placement of the aptamer near the T7 promoter, and using a primarily single-stranded template, results in up to a 6-fold change in gene expression in a ligand concentration-dependent manner. We further demonstrate that the sensitivity to thrombin concentration and the fold change in expression can be tuned by altering the position of the aptamer. The results described here pave the way for the use of DNA aptamers to achieve modular regulation of transcription in response to a wide variety of ligands in cell-free systems.
要实现无细胞系统的潜力,需要开发能响应目标配体来控制基因表达的配体敏感型基因启动子。在此,我们描述了一种在无细胞系统中设计配体敏感型转录控制的方法,该方法基于结合凝血酶的DNA适配体与T7噬菌体启动子的组合。将适配体置于T7启动子附近,并使用主要为单链的模板,会使基因表达以配体浓度依赖的方式发生高达6倍的变化。我们进一步证明,通过改变适配体的位置,可以调节对凝血酶浓度的敏感性和表达的变化倍数。本文所述结果为利用DNA适配体在无细胞系统中实现对多种配体响应的转录模块化调控铺平了道路。