Department of Chemistry and Biochemistry, Biophysics Program, Institute for Physical Science and Technology, University of Maryland, College Park, MD, USA.
Biophys J. 2012 Dec 5;103(11):2320-30. doi: 10.1016/j.bpj.2012.10.026.
Riboswitches, structured elements in the untranslated regions of messenger RNAs, regulate gene expression by binding specific metabolites. We introduce a kinetic network model that describes the functions of riboswitches at the systems level. Using experimental data for flavin mononucleotide riboswitch as a guide, we show that efficient function, implying a large dynamic range without compromising the requirement to suppress transcription, is determined by a balance between the transcription speed, the folding and unfolding rates of the aptamer, and the binding rates of the metabolite. We also investigated the effect of negative feedback accounting for binding to metabolites, which are themselves the products of genes that are being regulated. For a range of transcription rates negative feedback suppresses gene expression by nearly 10-fold. Negative feedback speeds the gene expression response time, and suppresses the change of steady-state protein concentration by half relative to that without feedback, when there is a modest spike in DNA concentration. A dynamic phase diagram expressed in terms of transcription speed, folding rates, and metabolite binding rates predicts different scenarios in riboswitch-mediated transcription regulation.
核糖开关是信使 RNA 非翻译区的结构元件,通过结合特定代谢物来调节基因表达。我们引入了一个动力学网络模型,从系统层面描述了核糖开关的功能。我们以黄素单核苷酸核糖开关的实验数据为指导,表明高效的功能(意味着在不影响转录抑制的要求下具有较大的动态范围)取决于转录速度、适体的折叠和展开速率以及代谢物结合速率之间的平衡。我们还研究了负反馈对结合代谢物的影响,代谢物本身就是被调控基因的产物。对于一系列转录率,负反馈通过近 10 倍抑制基因表达。当 DNA 浓度适度增加时,负反馈会加快基因表达的响应时间,并将稳态蛋白质浓度的变化抑制一半,而无需反馈。用转录速度、折叠速率和代谢物结合速率表示的动态相图预测了核糖开关介导的转录调控中的不同情况。