Knotty is nice: metabolite binding and RNA-mediated gene regulation by the preQ1 riboswitch family.

IF 4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Daniil Kiliushik, Coleman Goenner, Matthew Law, Griffin M Schroeder, Yoshita Srivastava, Jermaine L Jenkins, Joseph E Wedekind
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引用次数: 0

Abstract

Riboswitches sense specific cellular metabolites, leading to messenger RNA conformational changes that regulate downstream genes. Here we review the three known prequeosine1 (preQ1) riboswitch classes, which encompass five gene-regulatory motifs derived from distinct consensus models of folded RNA pseudoknots. Structural and functional analyses reveal multiple gene-regulation strategies ranging from partial occlusion of the ribosome-binding Shine-Dalgarno sequence (SDS), SDS sequestration driven by kinetic or thermodynamic folding pathways, direct preQ1 recognition by the SDS, and complete SDS burial in the riboswitch architecture. Family members can also induce elemental transcriptional pausing, which depends on ligand-mediated pseudoknot formation. Accordingly, preQ1 family members provide insight into a wide range of gene-regulatory tactics as well as a diverse repertoire of chemical approaches used to recognize the preQ1 metabolite. From a broader perspective, future challenges for the field will include the identification of new riboswitches in messenger RNAs that do not possess an SDS or those that induce ligand-dependent transcriptional pausing. When choosing an antibacterial target, the field must also consider how well a riboswitch accommodates mutations. Investigation of riboswitches in their natural context will also be critical to elucidate how RNA-mediated gene regulation influences organism fitness, thus providing a firm foundation for antibiotic development.

结实就是好:前 Q1 核糖开关家族的代谢物结合和 RNA 介导的基因调控。
核糖开关能感知特定的细胞代谢物,导致信使 RNA 构象发生变化,从而调控下游基因。在这里,我们回顾了已知的三种 prequeosine1(preQ1)核糖开关类别,其中包括从折叠 RNA 伪核苷酸的不同共识模型中衍生出的五个基因调控图案。结构和功能分析揭示了多种基因调控策略,包括部分封闭核糖体结合的 Shine-Dalgarno 序列(SDS)、由动力学或热力学折叠途径驱动的 SDS 封存、SDS 直接识别 preQ1 以及 SDS 完全埋藏在核糖开关结构中。家族成员还能诱导元素转录暂停,这取决于配体介导的假结的形成。因此,preQ1 家族成员提供了对各种基因调控策略以及用于识别 preQ1 代谢物的各种化学方法的深入了解。从更广泛的角度来看,该领域未来面临的挑战将包括鉴定信使 RNA 中不具有 SDS 的新核糖开关或那些诱导配体依赖性转录暂停的核糖开关。在选择抗菌靶点时,该领域还必须考虑核糖开关对突变的适应性。在自然环境中研究核糖开关对于阐明 RNA 介导的基因调控如何影响生物体的适应性也至关重要,从而为抗生素开发奠定坚实的基础。
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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来源期刊
Journal of Biological Chemistry
Journal of Biological Chemistry Biochemistry, Genetics and Molecular Biology-Biochemistry
自引率
4.20%
发文量
1233
期刊介绍: The Journal of Biological Chemistry welcomes high-quality science that seeks to elucidate the molecular and cellular basis of biological processes. Papers published in JBC can therefore fall under the umbrellas of not only biological chemistry, chemical biology, or biochemistry, but also allied disciplines such as biophysics, systems biology, RNA biology, immunology, microbiology, neurobiology, epigenetics, computational biology, ’omics, and many more. The outcome of our focus on papers that contribute novel and important mechanistic insights, rather than on a particular topic area, is that JBC is truly a melting pot for scientists across disciplines. In addition, JBC welcomes papers that describe methods that will help scientists push their biochemical inquiries forward and resources that will be of use to the research community.
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