Paijmans Joris, ten Wolde Pieter Rein
FOM Institute AMOLF, Science Park 104, 1098 XG Amsterdam, The Netherlands.
Phys Rev E Stat Nonlin Soft Matter Phys. 2014 Sep;90(3):032708. doi: 10.1103/PhysRevE.90.032708. Epub 2014 Sep 25.
The diffusive arrival of transcription factors at the promoter sites on DNA sets a lower bound on how accurately a cell can regulate its protein levels. Using results from the literature on diffusion-influenced reactions, we derive an analytical expression for the lower bound on the precision of transcriptional regulation. In our theory, transcription factors can perform multiple rounds of one-dimensional (1D) diffusion along the DNA and 3D diffusion in the cytoplasm before binding to the promoter. Comparing our expression for the lower bound on the precision against results from Green's function reaction dynamics simulations shows that the theory is highly accurate under biologically relevant conditions. Our results demonstrate that, to an excellent approximation, the promoter switches between the transcription-factor bound and unbound state in a Markovian fashion. This remains true even in the presence of sliding, i.e., with 1D diffusion along the DNA. This has two important implications: (1) Minimizing the noise in the promoter state is equivalent to minimizing the search time of transcription factors for their promoters; (2) the complicated dynamics of 3D diffusion in the cytoplasm and 1D diffusion along the DNA can be captured in a well-stirred model by renormalizing the promoter association and dissociation rates, making it possible to efficiently simulate the promoter dynamics using Gillespie simulations. Based on the recent experimental observation that sliding can speed up the promoter search by a factor of 4, our theory predicts that sliding can enhance the precision of transcriptional regulation by a factor of 2.
转录因子通过扩散到达DNA上的启动子位点,为细胞调控蛋白质水平的精确程度设定了下限。利用文献中关于扩散影响反应的结果,我们推导出了转录调控精度下限的解析表达式。在我们的理论中,转录因子在与启动子结合之前,可以在DNA上进行多轮一维(1D)扩散,并在细胞质中进行三维扩散。将我们关于精度下限的表达式与格林函数反应动力学模拟的结果进行比较,结果表明该理论在生物学相关条件下具有很高的准确性。我们的结果表明,在很好的近似程度上,启动子以马尔可夫方式在转录因子结合和未结合状态之间切换。即使存在滑动,即沿着DNA进行一维扩散时,情况依然如此。这有两个重要意义:(1)最小化启动子状态的噪声等同于最小化转录因子寻找其启动子的时间;(2)通过对启动子的结合和解离速率进行重整化,可以在一个充分搅拌的模型中捕捉细胞质中三维扩散和沿着DNA的一维扩散的复杂动力学,从而有可能使用 Gillespie 模拟有效地模拟启动子动力学。基于最近的实验观察结果,即滑动可以将启动子搜索速度提高4倍,我们的理论预测滑动可以将转录调控的精度提高2倍。