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+1核糖体移码的动力学

Dynamics of +1 ribosomal frameshifting.

作者信息

Xie Ping

机构信息

Key Laboratory of Soft Matter Physics and Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China.

出版信息

Math Biosci. 2014 Mar;249:44-51. doi: 10.1016/j.mbs.2014.01.008. Epub 2014 Feb 4.

DOI:10.1016/j.mbs.2014.01.008
PMID:24508018
Abstract

It has been well characterized that the amino acid starvation can induce +1 frameshifting. However, how the +1 frameshifting occurs has not been fully understood. Here, taking Escherichia coli RF2 programmed frameshifting as an example we present systematical analysis of the +1 frameshifting that could occur during every state-transition step in elongation phase of protein synthesis, showing that the +1 frameshifting can occur only during the period after deacylated tRNA dissociation from the posttranslocation state and before the recognition of the next "hungry" codon. The +1 frameshifting efficiency is theoretically studied, with the simple analytical solutions showing that the high efficiency is almost solely due to the occurrence of ribosome pausing which in turn results from the insufficient RF2. The analytical solutions also provide a consistent explanation of a lot of independent experimental data.

摘要

氨基酸饥饿可诱导 +1 移码,这一点已得到充分表征。然而,+1 移码是如何发生的尚未完全清楚。在此,以大肠杆菌 RF2 程序性移码为例,我们对蛋白质合成延伸阶段每个状态转换步骤中可能发生的 +1 移码进行了系统分析,结果表明 +1 移码仅发生在脱酰基 tRNA 从转位后状态解离之后以及识别下一个“饥饿”密码子之前的时间段。对 +1 移码效率进行了理论研究,简单的解析解表明,高效率几乎完全是由于核糖体暂停的发生,而核糖体暂停又是由 RF2 不足导致的。这些解析解还对许多独立的实验数据提供了一致的解释。

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Dynamics of +1 ribosomal frameshifting.+1核糖体移码的动力学
Math Biosci. 2014 Mar;249:44-51. doi: 10.1016/j.mbs.2014.01.008. Epub 2014 Feb 4.
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A dynamical model of programmed -1 ribosomal frameshifting.程序性-1核糖体移码的动力学模型。
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[tRNA-binding centers of Escherichia coli ribosomes and their structural organization].[大肠杆菌核糖体的tRNA结合中心及其结构组织]
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Twice exploration of tRNA +1 frameshifting in an elongation cycle of protein synthesis.在蛋白质合成的延伸循环中对 tRNA+1 移码的两次探索。
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Selective charging of tRNA isoacceptors explains patterns of codon usage.tRNA 同工受体的选择性充电解释了密码子使用模式。
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Ribosome recycling factor and release factor 3 action promotes TnaC-peptidyl-tRNA Dropoff and relieves ribosome stalling during tryptophan induction of tna operon expression in Escherichia coli.核糖体循环因子和释放因子3的作用促进TnaC-肽基-tRNA脱落,并在大肠杆菌色氨酸诱导tna操纵子表达过程中缓解核糖体停滞。
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Function of the ribosomal E-site: a mutagenesis study.核糖体E位点的功能:一项诱变研究。
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Maintaining the ribosomal reading frame: the influence of the E site during translational regulation of release factor 2.维持核糖体阅读框:E位点在释放因子2翻译调控过程中的影响
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