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T 盒核酶开关的非盒式打开——多价和多模式 RNA-RNA 相互作用的一瞥。

Unboxing the T-box riboswitches-A glimpse into multivalent and multimodal RNA-RNA interactions.

机构信息

Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland, USA.

出版信息

Wiley Interdiscip Rev RNA. 2020 Nov;11(6):e1600. doi: 10.1002/wrna.1600. Epub 2020 Jul 6.

Abstract

The T-box riboswitches are widespread bacterial noncoding RNAs that directly bind specific tRNAs, sense aminoacylation on bound tRNAs, and switch conformations to control amino-acid metabolism and to maintain nutritional homeostasis. The core mechanisms of tRNA recognition, amino acid sensing, and conformational switching by the T-boxes have been recently elucidated, providing a wealth of new insights into multivalent and multimodal RNA-RNA interactions. This review dissects the structures and tRNA-recognition mechanisms by the Stem I, Stem II, and Discriminator domains, which collectively compose the T-box riboswitches. It further compares and contrasts the two classes of T-boxes that regulate transcription and translation, respectively, and integrates recent findings to derive general themes, trends, and insights into complex RNA-RNA interactions. Specifically, the T-box paradigm reveals that noncoding RNAs can interact with each other through multiple coordinated contacts, concatenation of stacked helices, and mutually induced fit. Numerous tertiary contacts, especially those emanating from strings of single-stranded purines, act in concert to reinforce long-range base-pairing and stacking interactions. These coordinated, mixed-mode contacts allow the T-box RNA to sterically sense aminoacylation on the tRNA using a bipartite steric sieve, and to couple this readout to a conformational switch mediated by tRNA-T-box stacking. Together, the insights gleaned from the T-box riboswitches inform investigations into other complex RNA structures and assemblies, development of T-box-targeted antimicrobials, and may inspire design and engineering of novel RNA sensors, regulators, and interfaces. This article is categorized under: RNA Structure and Dynamics > RNA Structure, Dynamics and Chemistry Regulatory RNAs/RNAi/Riboswitches > Regulatory RNAs Regulatory RNAs/RNAi/Riboswitches > Riboswitches.

摘要

T 盒型核糖开关是广泛存在于细菌中的非编码 RNA,能够直接结合特定的 tRNA,感知结合 tRNA 的氨酰化状态,并通过构象改变来控制氨基酸代谢和维持营养稳态。最近,T 盒型核糖开关的 tRNA 识别、氨基酸感应和构象转变的核心机制已经被阐明,为多价和多模态 RNA-RNA 相互作用提供了丰富的新见解。本文剖析了由 Stem I、Stem II 和 Discriminator 结构域组成的 T 盒型核糖开关的结构和 tRNA 识别机制,并比较和对比了分别调控转录和翻译的两类 T 盒型核糖开关,整合了最近的研究结果,得出了关于复杂 RNA-RNA 相互作用的一般主题、趋势和见解。具体而言,T 盒型核糖开关的范例揭示了非编码 RNA 可以通过多个协调的相互作用、堆叠螺旋的串联和相互诱导的适配来相互作用。许多三级接触,尤其是来自单链嘌呤串的接触,协同作用,加强远程碱基配对和堆叠相互作用。这些协调的混合模式接触使 T 盒 RNA 能够使用二部分空间筛来立体感知 tRNA 上的氨酰化,并将这种读出与由 tRNA-T 盒堆叠介导的构象转变相耦合。从 T 盒型核糖开关中获得的见解为其他复杂 RNA 结构和组装的研究、针对 T 盒型核糖开关的抗菌药物的开发提供了信息,并可能启发新型 RNA 传感器、调节剂和界面的设计和工程。本文属于以下分类:RNA 结构和动态 > RNA 结构、动态和化学 调控 RNA/RNAi/核糖开关 > 调控 RNA 调控 RNA/RNAi/核糖开关 > 核糖开关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9fb/7583486/10a09de58c7c/WRNA-11-e1600-g001.jpg

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