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信使核糖核酸波动和调控核糖核酸塑造负反馈回路的动态变化。

Messenger RNA fluctuations and regulatory RNAs shape the dynamics of a negative feedback loop.

作者信息

Rodríguez Martínez María, Soriano Jordi, Tlusty Tsvi, Pilpel Yitzhak, Furman Itay

机构信息

Department of Physics of Complex Systems, Weizmann Institute of Science, Rehovot, Israel.

出版信息

Phys Rev E Stat Nonlin Soft Matter Phys. 2010 Mar;81(3 Pt 1):031924. doi: 10.1103/PhysRevE.81.031924. Epub 2010 Mar 30.

Abstract

Single-cell experiments of simple regulatory networks can markedly differ from cell population experiments. Such differences arise from stochastic events in individual cells that are averaged out in cell populations. For instance, while individual cells may show sustained oscillations in the concentrations of some proteins, such oscillations may appear damped in the population average. In this paper we investigate the role of RNA stochastic fluctuations as a leading force to produce a sustained excitatory behavior at the single-cell level. As opposed to some previous models, we build a fully stochastic model of a negative feedback loop that explicitly takes into account the RNA stochastic dynamics. We find that messenger RNA random fluctuations can be amplified during translation and produce sustained pulses of protein expression. Motivated by the recent appreciation of the importance of noncoding regulatory RNAs in post-transcription regulation, we also consider the possibility that a regulatory RNA transcript could bind to the messenger RNA and repress translation. Our findings show that the regulatory transcript helps reducing gene expression variability both at the single-cell level and at the cell population level.

摘要

简单调控网络的单细胞实验可能与细胞群体实验有显著差异。这种差异源于单个细胞中的随机事件,这些事件在细胞群体中会被平均化。例如,虽然单个细胞可能在某些蛋白质浓度上表现出持续振荡,但在群体平均值中这种振荡可能会显得有阻尼。在本文中,我们研究了RNA随机波动作为在单细胞水平产生持续兴奋行为的主导力量的作用。与一些先前的模型不同,我们构建了一个负反馈环的完全随机模型,该模型明确考虑了RNA随机动力学。我们发现信使RNA随机波动在翻译过程中可以被放大,并产生蛋白质表达的持续脉冲。受近期对非编码调控RNA在转录后调控中重要性的认识的启发,我们还考虑了调控RNA转录本可能与信使RNA结合并抑制翻译的可能性。我们的研究结果表明,调控转录本有助于在单细胞水平和细胞群体水平上降低基因表达的变异性。

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