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阐明反馈控制在翻译终止中的作用的数学建模框架。

A mathematical modelling framework for elucidating the role of feedback control in translation termination.

机构信息

Department of Chemical Engineering and Chemical Technology, Centre for Process Systems Engineering, Institute for Systems and Synthetic Biology, Imperial College London, South Kensington Campus, London SW7 2AZ, UK.

出版信息

J Theor Biol. 2010 Jun 7;264(3):808-21. doi: 10.1016/j.jtbi.2010.01.015. Epub 2010 Feb 20.

Abstract

Translation is the final stage of gene expression where messenger RNA is used as a template for protein polymerization from appropriate amino acids. Release of the completed protein requires a release factor protein acting at the termination/stop codon to liberate it. In this paper we focus on a complex feedback control mechanism involved in the translation and synthesis of release factor proteins, which has been observed in different systems. These release factor proteins are involved in the termination stage of their own translation. Further, mutations in the release factor gene can result in a premature stop codon. In this case translation can result either in early termination and the production of a truncated protein or readthrough of the premature stop codon and production of the complete release factor protein. Thus during translation of the release factor mRNA containing a premature stop codon, the full length protein negatively regulates its production by its action on a premature stop codon, while positively regulating its production by its action on the regular stop codon. This paper develops a mathematical modelling framework to investigate this complex feedback control system involved in translation. A series of models is established to carefully investigate the role of individual mechanisms and how they work together. The steady state and dynamic behaviour of the resulting models are examined both analytically and numerically.

摘要

翻译是基因表达的最后阶段,其中信使 RNA 被用作从适当的氨基酸聚合蛋白质的模板。完成的蛋白质的释放需要释放因子蛋白在终止/停止密码子处作用以将其释放。在本文中,我们专注于在不同系统中观察到的涉及释放因子蛋白翻译和合成的复杂反馈控制机制。这些释放因子蛋白参与其自身翻译的终止阶段。此外,释放因子基因中的突变可导致过早的终止密码子。在这种情况下,翻译可能导致过早终止和产生截断的蛋白质,或者通读过早的终止密码子并产生完整的释放因子蛋白。因此,在含有过早终止密码子的释放因子 mRNA 的翻译过程中,全长蛋白通过其在过早终止密码子上的作用负调节其产生,同时通过其在常规终止密码子上的作用正调节其产生。本文开发了一个数学建模框架来研究这种涉及翻译的复杂反馈控制系统。建立了一系列模型来仔细研究各个机制的作用以及它们如何协同工作。通过分析和数值方法检查了所得模型的稳态和动态行为。

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