The Peptidyl Transferase Center: a Window to the Past.

IF 8 1区 生物学 Q1 MICROBIOLOGY Microbiology and Molecular Biology Reviews Pub Date : 2021-12-15 Epub Date: 2021-11-10 DOI:10.1128/MMBR.00104-21
Madhan R Tirumalai, Mario Rivas, Quyen Tran, George E Fox
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Abstract

In his 2001 article, "Translation: in retrospect and prospect," the late Carl Woese made a prescient observation that there was a need for the then-current view of translation to be "reformulated to become an all-embracing perspective about which 21st century Biology can develop" (RNA 7:1055-1067, 2001, https://doi.org/10.1017/s1355838201010615). The quest to decipher the origins of life and the road to the genetic code are both inextricably linked with the history of the ribosome. After over 60 years of research, significant progress in our understanding of how ribosomes work has been made. Particularly attractive is a model in which the ribosome may facilitate an ∼180° rotation of the CCA end of the tRNA from the A-site to the P-site while the acceptor stem of the tRNA would then undergo a translation from the A-site to the P-site. However, the central question of how the ribosome originated remains unresolved. Along the path from a primitive RNA world or an RNA-peptide world to a proto-ribosome world, the advent of the peptidyl transferase activity would have been a seminal event. This functionality is now housed within a local region of the large-subunit (LSU) rRNA, namely, the peptidyl transferase center (PTC). The PTC is responsible for peptide bond formation during protein synthesis and is usually considered to be the oldest part of the modern ribosome. What is frequently overlooked is that by examining the origins of the PTC itself, one is likely going back even further in time. In this regard, it has been proposed that the modern PTC originated from the association of two smaller RNAs that were once independent and now comprise a pseudosymmetric region in the modern PTC. Could such an association have survived? Recent studies have shown that the extant PTC is largely depleted of ribosomal protein interactions. It is other elements like metallic ion coordination and nonstandard base/base interactions that would have had to stabilize the association of RNAs. Here, we present a detailed review of the literature focused on the nature of the extant PTC and its proposed ancestor, the proto-ribosome.

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肽基转移酶中心:通往过去的一扇窗
已故的卡尔-沃斯(Carl Woese)在其 2001 年发表的文章《翻译:回顾与展望》中先知先觉地指出,当时的翻译观需要 "重新表述,使之成为 21 世纪生物学可以发展的一个包罗万象的视角"(RNA 7:1055-1067, 2001, https://doi.org/10.1017/s1355838201010615)。破译生命起源的探索和通往遗传密码的道路都与核糖体的历史密不可分。经过 60 多年的研究,我们对核糖体工作原理的认识取得了重大进展。尤其吸引人的是这样一个模型:核糖体可以促进 tRNA 的 CCA 端从 A 位点向 P 位点旋转 180°,而 tRNA 的受体茎则从 A 位点翻译到 P 位点。然而,核糖体如何起源这一核心问题仍然悬而未决。在从原始 RNA 世界或 RNA 肽世界到原核糖体世界的道路上,肽基转移酶活性的出现将是一个开创性事件。这种功能现在位于大亚基(LSU)rRNA 的局部区域,即肽基转移酶中心(PTC)。PTC 负责蛋白质合成过程中肽键的形成,通常被认为是现代核糖体最古老的部分。但经常被忽视的是,研究 PTC 本身的起源很可能会追溯到更久远的年代。在这方面,有人提出,现代 PTC 起源于两个较小的 RNA 的结合,这两个 RNA 曾经是独立的,现在构成了现代 PTC 中的一个假对称区域。这样的联合是否能够存活下来?最近的研究表明,现存的 PTC 在很大程度上失去了核糖体蛋白质的相互作用。其他元素,如金属离子配位和非标准碱基/碱基相互作用,才是稳定 RNA 关联的必要条件。在此,我们将详细回顾有关现存 PTC 及其祖先(原核糖体)性质的文献。
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来源期刊
CiteScore
18.80
自引率
0.80%
发文量
27
期刊介绍: Microbiology and Molecular Biology Reviews (MMBR), a journal that explores the significance and interrelationships of recent discoveries in various microbiology fields, publishes review articles that help both specialists and nonspecialists understand and apply the latest findings in their own research. MMBR covers a wide range of topics in microbiology, including microbial ecology, evolution, parasitology, biotechnology, and immunology. The journal caters to scientists with diverse interests in all areas of microbial science and encompasses viruses, bacteria, archaea, fungi, unicellular eukaryotes, and microbial parasites. MMBR primarily publishes authoritative and critical reviews that push the boundaries of knowledge, appealing to both specialists and generalists. The journal often includes descriptive figures and tables to enhance understanding. Indexed/Abstracted in various databases such as Agricola, BIOSIS Previews, CAB Abstracts, Cambridge Scientific Abstracts, Chemical Abstracts Service, Current Contents- Life Sciences, EMBASE, Food Science and Technology Abstracts, Illustrata, MEDLINE, Science Citation Index Expanded (Web of Science), Summon, and Scopus, among others.
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