揭示RNA聚合酶的空间相互作用对基因表达噪声的影响:新生和成熟RNA数量的分析分布

Juraj Szavits-Nossan, Ramon Grima
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引用次数: 0

摘要

电报模型是基因随机表达的标准模型,可以精确求解得到成熟RNA数目在每个细胞中的分布。对这个模型的修改也导致了新生RNA数量的分析分布。这些溶液通常用于分析单细胞数据,包括转录参数的推断。然而,这些模型忽略了转录延伸的重要机制特征,如RNA聚合酶的随机运动及其立体相互作用。在这里,我们构建了一个基因表达模型,描述启动子在无活性状态和活性状态之间的转换,RNA聚合酶在活性状态下的结合,它们的随机运动,包括沿基因的空间相互作用,以及它们的解结合导致成熟转录物随后衰变。在本构表达和慢启动子切换两种重要的极限情况下,我们得到了新生和成熟rnan数的稳态分布。我们表明,RNA波动受到RNA聚合酶之间的空间相互作用的抑制,这种抑制甚至可以导致亚泊松波动;这些效应对新生RNA最为明显,而对成熟RNA则不那么明显,因为成熟RNA不是转录的直接传感器。我们发现我们的微观机制模型的参数和标准模型的参数之间存在一种关系,这种关系确保了它们在参数空间的广大区域(包括缓慢、中间和快速启动子切换)上对第一和第二RNA数矩的预测具有出色的一致性,前提是RNA数分布是泊松的或超泊松的。此外,我们发现了成熟RNA数据的局限性,特别是表明它不能区分基因上高度不同的RNA聚合酶交通模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Uncovering the effect of RNA polymerase steric interactions on gene expression noise: analytical distributions of nascent and mature RNA numbers
The telegraph model is the standard model of stochastic gene expression, which can be solved exactly to obtain the distribution of mature RNA numbers per cell. A modification of this model also leads to an analytical distribution of the nascent RNA numbers. These solutions are routinely used for the analysis of single-cell data, including the inference of transcriptional parameters. However, these models neglect important mechanistic features of transcription elongation, such as the stochastic movement of RNA polymerases and their steric interactions. Here we construct a model of gene expression describing promoter switching between inactive and active states, binding of RNA polymerases in the active state, their stochastic movement including steric interactions along the gene, and their unbinding leading to a mature transcript that subsequently decays. We derive the steady-state distributions of the nascent and mature RNA numbers in two important limiting cases: constitutive expression and slow promoter switching. We show that RNA fluctuations are suppressed by steric interactions between RNA polymerases, and that this suppression can even lead to sub-Poissonian fluctuations; these effects are most pronounced for nascent RNA and less prominent for mature RNA, since the latter is not a direct sensor of transcription. We find a relationship between the parameters of our microscopic mechanistic model and those of the standard models that ensures excellent consistency in their prediction of the first and second RNA number moments over vast regions of parameter space, encompassing slow, intermediate, and rapid promoter switching, provided the RNA number distributions are Poissonian or super-Poissonian. Furthermore, we identify the limitations of inference from mature RNA data, specifically showing that it cannot differentiate between highly distinct RNA polymerase traffic patterns on a gene.
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