2 Structure of the Bacterial Ribosome and Some Implications for Translational Regulation

H. Noller
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引用次数: 12

Abstract

Translational regulation is based on modulation of translational function, most often involving the initiation phase. Not surprisingly, regulation of protein synthesis differs markedly between bacteria and eukarya, reflecting the many differences between their respective mechanisms of initiation. Although the structures of all ribosomes share commonly conserved cores, which are responsible for the main processes of translational elongation, many of the molecular components involved in translational initiation are specific to the different phylogenetic domains. These include the initiation factors, the Shine-Dalgarno sequence, formylation of the methionyl initiator tRNA, the ability to reinitiate on polycistronic mRNAs, and so on. Thus, it is not at all clear how far our knowledge of 70S (prokaryotic) ribosome structure will go toward providing insight into the mechanisms of eukaryotic translational regulation. Nevertheless, this information will help to understand prokaryotic initiation, and at least provide a starting point for interpreting the emerging structures of eukaryotic ribosomes. Most of the steps of protein synthesis appear to be based on RNA, including the many interactions between mRNA, tRNA, and rRNA that occur during the elongation phase. The roles of the proteins, such as the elongation factors and ribosomal proteins, may be to refine underlying RNA-based mechanisms, optimizing the speed and accuracy of translation. Translational initiation, at least in part, is therefore likely to involve modulation of RNA-based processes by proteins such as the initiation factors. We are beginning to understand how some of these processes work, from several decades of biochemical and genetic studies combined with the more recent...
细菌核糖体的结构及其对翻译调控的影响
翻译调节是基于翻译功能的调节,通常涉及起始阶段。不足为奇的是,蛋白质合成的调控在细菌和真核生物之间明显不同,反映了它们各自的起始机制之间的许多差异。尽管所有核糖体的结构都有共同保守的核心,这些核心负责翻译延伸的主要过程,但许多参与翻译起始的分子成分是特定于不同系统发育结构域的。这些包括起始因子、Shine-Dalgarno序列、甲硫基启动器tRNA的甲酰化、在多顺反电子mrna上重新启动的能力等等。因此,目前尚不清楚我们对70S(原核)核糖体结构的了解将在多大程度上有助于深入了解真核生物翻译调节的机制。尽管如此,这些信息将有助于理解原核起始,并至少为解释真核核糖体的新结构提供一个起点。蛋白质合成的大多数步骤似乎都是基于RNA的,包括在延伸期发生的mRNA, tRNA和rRNA之间的许多相互作用。延伸因子和核糖体蛋白等蛋白质的作用可能是完善基于rna的潜在机制,优化翻译的速度和准确性。因此,至少部分地,翻译起始可能涉及诸如起始因子之类的蛋白质对基于rna的过程的调节。从几十年的生化和基因研究,再加上最近的……
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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