Department of Biotechnology, Indian Institute of Technology Madras, Chennai, India.
Biophys J. 2011 Sep 21;101(6):1297-306. doi: 10.1016/j.bpj.2011.08.005. Epub 2011 Sep 20.
The temporal dynamics of the concentrations of several proteins are tightly regulated, particularly for critical nodes in biological networks such as transcription factors. An important mechanism to control transcription factor levels is through autoregulatory feedback loops where the protein can bind its own promoter. Here we use theoretical tools and computational simulations to further our understanding of transcription-factor autoregulatory loops. We show that the stochastic dynamics of feedback and mRNA synthesis can significantly influence the speed of response of autoregulatory genetic networks toward external stimuli. The fluctuations in the response-times associated with the accumulation of the transcription factor in the presence of negative or positive autoregulation can be minimized by confining the ratio of mRNA/protein lifetimes within 1:10. This predicted range of mRNA/protein lifetime agrees with ranges observed empirically in prokaryotes and eukaryotes. The theory can quantitatively and systematically account for the influence of regulatory element binding and unbinding dynamics on the transcription-factor concentration rise-times. The simulation results are robust against changes in several system parameters of the gene expression machinery.
几种蛋白质浓度的时间动态受到严格调控,特别是对于生物网络中的关键节点,如转录因子。控制转录因子水平的一个重要机制是通过自身反馈调节环,其中蛋白质可以结合其自身的启动子。在这里,我们使用理论工具和计算模拟来进一步了解转录因子自身调节环。我们表明,反馈和 mRNA 合成的随机动力学可以显著影响自身调节遗传网络对外界刺激的响应速度。通过将 mRNA/蛋白质寿命比限制在 1:10 内,可以最小化在负或正自身调节存在下转录因子积累时与响应时间相关的波动。这种预测的 mRNA/蛋白质寿命范围与在原核生物和真核生物中观察到的范围一致。该理论可以定量和系统地解释调节元件结合和解离动力学对转录因子浓度上升时间的影响。模拟结果对基因表达机制的几个系统参数的变化具有鲁棒性。