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Autoregulatory systems controlling translation factor expression: Thermostat-like control of translational accuracy

机译:自动调节系统控制翻译因子的表达:类似恒温器的翻译精度控制

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摘要

In both prokaryotes and eukaryotes, the expression of a large number of genes is controlled by negative feedback, in some cases operating at the level of translation of the mRNA transcript. Of particular interest are those cases where the proteins concerned have cell-wide function in recognizing a particular codon or RNA sequence. Examples include the bacterial translation termination release factor RF2, initiation factor IF3, and eukaryote poly(A) binding protein. The regulatory loops that control their synthesis establish a negative feedback control mechanism based upon that protein's RNA sequence recognition function in translation (for example, stop codon recognition) without compromising the accurate recognition of that codon, or sequence during general, cell-wide translation. Here, the bacterial release factor RF2 and initiation factor IF3 negative feedback loops are reviewed and compared with similar negative feedback loops that regulate the levels of the eukaryote release factor, eRF1, established artificially by mutation. The control properties of such negative feedback loops are discussed as well as their evolution. The role of negative feedback to control translation factor expression is considered in the context of a growing body of evidence that both IF3 and RF2 can play a role in stimulating stalled ribosomes to abandon translation in response to amino acid starvation. Here, we make the case that negative feedback control serves primarily to limit the overexpression of these translation factors, preventing the loss of fitness resulting from an unregulated increase in the frequency of ribosome drop-off.
机译:在原核生物和真核生物中,大量基因的表达都受到负反馈的控制,在某些情况下,其在mRNA转录物的翻译水平上起作用。特别令人感兴趣的是那些相关蛋白质在识别特定密码子或RNA序列中具有全细胞功能的情况。实例包括细菌翻译终止释放因子RF2,起始因子IF3和真核生物poly(A)结合蛋白。控制其合成的调节环基于翻译中该蛋白质的RNA序列识别功能(例如,终止密码子识别)建立了一个负反馈控制机制,而不会损害该密码子或一般细胞范围内翻译过程中序列的准确识别。在此,对细菌释放因子RF2和起始因子IF3负反馈环进行了回顾,并与类似的负反馈环进行了比较,该负反馈环调节了通过突变人工建立的真核生物释放因子eRF1的水平。讨论了这种负反馈回路的控制特性及其演变。越来越多的证据表明,IF3和RF2均可在刺激失速的核糖体以响应氨基酸饥饿而放弃翻译中发挥作用,越来越多的证据考虑了负反馈控制翻译因子表达的作用。在这里,我们假设负反馈控制主要是为了限制这些翻译因子的过表达,从而防止由于核糖体脱落频率的不规则增加而导致的适应性丧失。

著录项

  • 来源
    《RNA》 |2010年第4期|655-663|共9页
  • 作者单位

    School of Medical Sciences, Institute of Medical Sciences, University of Aberdeen, Aberdeen, AB25 2ZD, United Kingdom;

    Centre for Process Systems Engineering, Department of Chemical Engineering and Chemical Technology, Faculty of Engineering, Imperial College London, London SW7 2AZ, United Kingdom;

    Centre for Process Systems Engineering, Department of Chemical Engineering and Chemical Technology, Faculty of Engineering, Imperial College London, London SW7 2AZ, United Kingdom;

    School of Medical Sciences, Institute of Medical Sciences, University of Aberdeen, Aberdeen, AB25 2ZD, United Kingdom;

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  • 原文格式 PDF
  • 正文语种 eng
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  • 关键词

    release factor RF2; initiation factor IF3; negative feedback; eukaryote release factor eRF1; ribosomal frameshifting;

    机译:释放因子RF2;起始因子IF3;负反馈;真核生物释放因子eRF1;核糖体移码;

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