Baker Charles, Jia Tao, Kulkarni Rahul V
Department of Physics, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061, USA.
Phys Rev E Stat Nonlin Soft Matter Phys. 2012 Jun;85(6 Pt 1):061915. doi: 10.1103/PhysRevE.85.061915. Epub 2012 Jun 20.
A wealth of new research has highlighted the critical roles of small noncoding RNAs (sRNAs) in diverse processes, such as quorum sensing and cellular responses to stress. The pathways controlling these processes often have a central motif composed of a master regulator protein whose expression is controlled by multiple sRNAs. However, the stochastic gene expression of a single target gene regulated by multiple sRNAs is currently not well understood. To address this issue, we analyze a stochastic model of regulation of gene expression by multiple sRNAs. For this model, we derive exact analytic results for the regulated protein distribution, including compact expressions for its mean and variance. The derived results provide insights into the roles of multiple sRNAs in fine-tuning the noise in gene expression. In particular, we show that, in contrast to regulation by a single sRNA, multiple sRNAs provide a mechanism for independently controlling the mean and variance of the regulated protein distribution.
大量新研究突出了小非编码RNA(sRNA)在多种过程中的关键作用,如群体感应和细胞对压力的反应。控制这些过程的途径通常有一个核心基序,由一个主调节蛋白组成,其表达由多个sRNA控制。然而,目前对于由多个sRNA调控的单个靶基因的随机基因表达还了解不足。为了解决这个问题,我们分析了一个由多个sRNA调控基因表达的随机模型。对于这个模型,我们推导出了受调控蛋白质分布的精确解析结果,包括其均值和方差的简洁表达式。推导结果为多个sRNA在微调基因表达噪声中的作用提供了见解。特别是,我们表明,与单个sRNA的调控不同,多个sRNA提供了一种独立控制受调控蛋白质分布的均值和方差的机制。