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新的 tRNA 接触促进 T 盒核糖体开关中配体的结合。

New tRNA contacts facilitate ligand binding in a T box riboswitch.

机构信息

Molecular, Cellular, and Developmental Biology Graduate Program, The Ohio State University, Columbus, OH 43210.

Center for RNA Biology, The Ohio State University, Columbus, OH 43210.

出版信息

Proc Natl Acad Sci U S A. 2018 Apr 10;115(15):3894-3899. doi: 10.1073/pnas.1721254115. Epub 2018 Mar 26.

DOI:10.1073/pnas.1721254115
PMID:29581302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5899468/
Abstract

T box riboswitches are RNA regulatory elements widely used by organisms in the phyla Firmicutes and Actinobacteria to regulate expression of amino acid-related genes. Expression of T box family genes is down-regulated by transcription attenuation or inhibition of translation initiation in response to increased charging of the cognate tRNA. Three direct contacts with tRNA have been described; however, one of these contacts is absent in a subclass of T box RNAs and the roles of several structural domains conserved in most T box RNAs are unknown. In this study, structural elements of a T box riboswitch variant with an Ultrashort (US) Stem I were sequentially deleted, which resulted in a progressive decrease in binding affinity for the tRNA ligand. Selective 2'-hydroxyl acylation analyzed by primer extension (SHAPE) revealed structural changes in conserved riboswitch domains upon interaction with the tRNA ligand. Cross-linking and mutational analyses identified two interaction sites, one between the S-turn element in Stem II and the T arm of tRNA and the other between the Stem IIA/B pseudoknot and the D loop of tRNA These newly identified RNA contacts add information about tRNA recognition by the T box riboswitch and demonstrate a role for the S-turn and pseudoknot elements, which resemble structural elements that are common in many cellular RNAs.

摘要

T 盒核糖体开关是 RNA 调节元件,在厚壁菌门和放线菌门的生物中广泛用于调节与氨基酸相关的基因表达。T 盒家族基因的表达受到转录衰减或翻译起始抑制的调节,以响应同功 tRNA 的增加充电。已经描述了三个与 tRNA 的直接接触;然而,这些接触中有一个在 T 盒 RNA 的一个亚类中缺失,并且大多数 T 盒 RNA 中保守的几个结构域的作用是未知的。在这项研究中,具有 Ultrashort (US) Stem I 的 T 盒核糖体开关变体的结构元件被依次删除,这导致与 tRNA 配体的结合亲和力逐渐降低。选择性 2'-羟基酰化分析通过引物延伸 (SHAPE) 揭示了与 tRNA 配体相互作用时保守的核糖体开关结构域的结构变化。交联和突变分析确定了两个相互作用位点,一个在茎 II 的 S-turn 元件和 tRNA 的 T 臂之间,另一个在茎 IIA/B 假结和 tRNA 的 D 环之间。这些新鉴定的 RNA 接触增加了关于 T 盒核糖体开关识别 tRNA 的信息,并证明了 S-turn 和假结元件的作用,它们类似于许多细胞 RNA 中常见的结构元件。

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本文引用的文献

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Capture and Release of tRNA by the T-Loop Receptor in the Function of the T-Box Riboswitch.T 盒核糖开关功能中 T 环受体对 tRNA 的捕获与释放
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