...
首页> 外文期刊>Journal of Theoretical Biology >A mathematical modelling framework for elucidating the role of feedback control in translation termination.
【24h】

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

机译:用于阐明反馈控制在翻译终止中的作用的数学建模框架。

获取原文
获取原文并翻译 | 示例
           

摘要

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.
机译:翻译是基因表达的最后阶段,其中将信使RNA用作从适当氨基酸进行蛋白质聚合的模板。释放完成的蛋白质需要作用于终止/终止密码子的释放因子蛋白质以释放它。在本文中,我们关注于涉及释放因子蛋白翻译和合成的复杂反馈控制机制,该机制已在不同系统中观察到。这些释放因子蛋白参与其自身翻译的终止阶段。此外,释放因子基因的突变会导致终止密码子过早。在这种情况下,翻译可导致早期终止和截短蛋白的产生,或导致过早终止密码子的通读和完整释放因子蛋白的产生。因此,在翻译包含过早终止密码子的释放因子mRNA的过程中,全长蛋白通过其对过早终止密码子的作用来负调节其产生,而通过其对规则终止密码子的作用来正向调节其产生。本文开发了一个数学建模框架来研究此复杂的翻译控制系统。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。解析模型和数值模型检查了所得模型的稳态和动态行为。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号