The Key Laboratory of Advanced Control and Optimization for Chemical Processes, Ministry of Education, East China University of Science and Technology, Shanghai, China; School of Biological Sciences, the University of Edinburgh, Edinburgh, United Kingdom; Shanghai Institute of Intelligent Science and Technology, Tongji University, Shanghai, China.
School of Biological Sciences, the University of Edinburgh, Edinburgh, United Kingdom; School of Mathematics, the University of Edinburgh, Edinburgh, United Kingdom.
Biophys J. 2020 Sep 1;119(5):1002-1014. doi: 10.1016/j.bpj.2020.07.020. Epub 2020 Aug 3.
Transcriptional bursting is a major source of noise in gene expression. The telegraph model of gene expression, whereby transcription switches between on and off states, is the dominant model for bursting. Recently, it was shown that the telegraph model cannot explain a number of experimental observations from perturbation data. Here, we study an alternative model that is consistent with the data and which explicitly describes RNA polymerase recruitment and polymerase pause release, two steps necessary for messenger RNA (mRNA) production. We derive the exact steady-state distribution of mRNA numbers and an approximate steady-state distribution of protein numbers, which are given by generalized hypergeometric functions. The theory is used to calculate the relative sensitivity of the coefficient of variation of mRNA fluctuations for thousands of genes in mouse fibroblasts. This indicates that the size of fluctuations is mostly sensitive to the rate of burst initiation and the mRNA degradation rate. Furthermore, we show that 1) the time-dependent distribution of mRNA numbers is accurately approximated by a modified telegraph model with a Michaelis-Menten like dependence of the effective transcription rate on RNA polymerase abundance, and 2) the model predicts that if the polymerase recruitment rate is comparable or less than the pause release rate, then upon gene replication, the mean number of RNA per cell remains approximately constant. This gene dosage compensation property has been experimentally observed and cannot be explained by the telegraph model with constant rates.
转录爆发是基因表达噪声的主要来源。基因表达的电报模型,即转录在开和关状态之间切换,是爆发的主要模型。最近,有研究表明,该电报模型无法解释来自扰动数据的许多实验观察结果。在这里,我们研究了一种替代模型,该模型与数据一致,并明确描述了 RNA 聚合酶募集和聚合酶暂停释放这两个信使 RNA(mRNA)产生所必需的步骤。我们推导出了 mRNA 数量的精确稳态分布和蛋白质数量的近似稳态分布,它们由广义超几何函数给出。该理论用于计算在小鼠成纤维细胞中数千个基因的 mRNA 波动的变异系数的相对灵敏度。这表明,波动的大小主要取决于爆发起始的速率和 mRNA 降解速率。此外,我们还表明,1)mRNA 数量的时变分布可以通过具有类似于米氏常数的 RNA 聚合酶丰度对有效转录速率的依赖的修改后的电报模型来精确逼近,并且 2)该模型预测,如果聚合酶募集速率与暂停释放速率相当或更慢,则在基因复制后,每个细胞中的 RNA 数量均值将保持大致恒定。这种基因剂量补偿特性已经在实验中观察到,并且无法通过具有恒定速率的电报模型来解释。