Theoretical Biology, Department of Biology, Utrecht University, Utrecht, The Netherlands.
PLoS Comput Biol. 2018 Oct 5;14(10):e1006386. doi: 10.1371/journal.pcbi.1006386. eCollection 2018 Oct.
In bacterial cells, gene expression, metabolism, and growth are highly interdependent and tightly coordinated. As a result, stochastic fluctuations in expression levels and instantaneous growth rate show intricate cross-correlations. These correlations are shaped by feedback loops, trade-offs and constraints acting at the cellular level; therefore a quantitative understanding requires an integrated approach. To that end, we here present a mathematical model describing a cell that contains multiple proteins that are each expressed stochastically and jointly limit the growth rate. Conversely, metabolism and growth affect protein synthesis and dilution. Thus, expression noise originating in one gene propagates to metabolism, growth, and the expression of all other genes. Nevertheless, under a small-noise approximation many statistical quantities can be calculated analytically. We identify several routes of noise propagation, illustrate their origins and scaling, and establish important connections between noise propagation and the field of metabolic control analysis. We then present a many-protein model containing >1000 proteins parameterized by previously measured abundance data and demonstrate that the predicted cross-correlations between gene expression and growth rate are in broad agreement with published measurements.
在细菌细胞中,基因表达、代谢和生长高度相互依存且紧密协调。因此,表达水平和瞬时生长率的随机波动表现出复杂的交叉相关性。这些相关性由细胞水平上的反馈回路、权衡和约束形成;因此,定量理解需要综合方法。为此,我们在这里提出了一个数学模型,描述了一个包含多个蛋白质的细胞,这些蛋白质的表达都是随机的,并且共同限制了生长率。相反,代谢和生长会影响蛋白质的合成和稀释。因此,源于一个基因的表达噪声会传播到代谢、生长和所有其他基因的表达。然而,在小噪声近似下,许多统计量可以进行解析计算。我们确定了几种噪声传播途径,说明了它们的起源和规模,并在噪声传播和代谢控制分析领域之间建立了重要的联系。然后,我们提出了一个包含 >1000 个蛋白质的多蛋白模型,这些蛋白质由之前测量的丰度数据进行参数化,并证明了基因表达和生长速率之间的预测相关性与已发表的测量结果基本一致。