CMOL, Niels Bohr Institute, Copenhagen, DK-2100, Denmark, Department of Genetics, Eotvos Lorand University, H-1117, Budapest, Hungary.
Nucleic Acids Res. 2011 Sep 1;39(16):6879-85. doi: 10.1093/nar/gkr390. Epub 2011 May 23.
Optimal response to environmental stimuli often requires activation of certain genes and repression of others. Dual function regulatory proteins play a key role in the differential regulation of gene expression. While repression can be achieved by any DNA binding protein through steric occlusion of RNA polymerase in the promoter region, activation often requires a surface on the regulatory protein to contact RNAP and thus facilitate transcription initiation. RNAP itself is also a DNA binding protein, therefore it can function as a transcriptional repressor. Searching the Escherichia coli promoter database we found that ∼14% of the identified 'forward' promoters overlap with a promoter oriented in the opposite direction. In this article we combine a mathematical model with experimental analysis of synthetic regulatory regions to investigate interference of overlapping promoters. We find that promoter interference depends on the characteristics of overlapping promoters. The model predicts that promoter strength and interference can be regulated separately, which provides unique opportunities for regulation. Our experimental data suggest that in principle any DNA binding protein can be used for both activation and repression of promoter transcription, depending on the context. These findings can be exploited in the construction of synthetic networks.
最优的环境刺激反应通常需要激活某些基因并抑制其他基因。双功能调控蛋白在基因表达的差异调控中起着关键作用。虽然通过在启动子区域中空间位阻 RNA 聚合酶可以实现抑制,但激活通常需要调控蛋白上的一个表面与 RNAP 接触,从而促进转录起始。RNAP 本身也是一种 DNA 结合蛋白,因此它可以作为转录抑制剂。在搜索大肠杆菌启动子数据库时,我们发现约 14%的鉴定出的“正向”启动子与一个相反方向的启动子重叠。在本文中,我们将数学模型与合成调控区域的实验分析相结合,研究重叠启动子的干扰。我们发现启动子干扰取决于重叠启动子的特征。该模型预测启动子强度和干扰可以分别调节,这为调节提供了独特的机会。我们的实验数据表明,原则上任何 DNA 结合蛋白都可以用于激活和抑制启动子转录,具体取决于具体情况。这些发现可用于构建合成网络。