Beyond reader proteins: RNA binding proteins and RNA modifications in conversation to regulate gene expression.

IF 6.4 2区 生物学 Q1 CELL BIOLOGY
Christian Fagre, Wendy Gilbert
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引用次数: 0

Abstract

Post-transcriptional mRNA modifications play diverse roles in gene expression and RNA function. In many cases, RNA modifications function by altering how cellular machinery such as RNA binding proteins (RBPs) interact with RNA substrates. For instance, N6-methyladenosine (m6A) is recognized by the well-characterized YTH domain-containing family of "reader" proteins. For other mRNA modifications, similar global readers of modification status have not been clearly defined. Rather, most interactions between RBPs and RNA modifications have a more complicated dependence on sequence context and binding modality. The current handful of studies that demonstrate modifications impacting protein binding likely represent only a fraction of the full landscape. In this review, we dissect the known instances of RNA modifications altering RBP binding, specifically m6A, N1-methyladenosine (m1A), 5-methylcytosine (m5C), pseudouridine (Ψ), and internal N7-methylguanosine. We then review the biochemical properties of these and other identified mRNA modifications including dihydrouridine (D), N4-acetylcytosine (ac4C), and 2'-O-Methylation (Nme). We focus on how these properties would be likely to impact RNA:RBP interactions, including by changes to hydrogen bond potential, base-stacking efficiency, and RNA conformational preferences. The effects of RNA modifications on secondary structure have been well-studied, and we briefly discuss how structural effects imparted by modifications can lead to protein binding changes. Finally, we discuss strategies for uncovering as-yet-to-be identified modification-sensitive RBP:RNA Interactions. Coordinating future efforts to intersect the epitranscriptome and the RNA-protein interactome will illuminate the rules governing RNA modification recognition and the mechanisms responsible for the biological consequences of mRNA modification. This article is categorized under: RNA Structure and Dynamics > RNA Structure, Dynamics and Chemistry RNA Interactions with Proteins and Other Molecules > Protein-RNA Recognition RNA Processing > RNA Editing and Modification.

超越读者蛋白:RNA 结合蛋白与 RNA 修饰对话调节基因表达。
转录后 mRNA 修饰在基因表达和 RNA 功能中发挥着不同的作用。在许多情况下,RNA修饰通过改变细胞机制(如 RNA 结合蛋白(RBPs))与 RNA 底物的相互作用而发挥作用。例如,N6-甲基腺苷(m6A)可被特征明确的含 YTH 结构域的 "阅读器 "蛋白家族识别。对于其他 mRNA 修饰,类似的修饰状态全局阅读器尚未明确定义。相反,大多数 RBPs 与 RNA 修饰之间的相互作用对序列上下文和结合方式的依赖更为复杂。目前证明修饰会影响蛋白质结合的少量研究可能只代表了全部研究的一小部分。在这篇综述中,我们剖析了已知的 RNA 修饰改变 RBP 结合的实例,特别是 m6A、N1-甲基腺苷(m1A)、5-甲基胞嘧啶(m5C)、假尿苷(Ψ)和内部 N7-甲基鸟苷。然后,我们回顾了这些修饰和其他已确定的 mRNA 修饰(包括二氢尿嘧啶(D)、N4-乙酰胞嘧啶(ac4C)和 2'-O- 甲基化(Nme))的生化特性。我们重点研究了这些特性可能会如何影响 RNA 与 RBP 的相互作用,包括氢键势能、碱基堆积效率和 RNA 构象偏好的变化。我们对 RNA 修饰对二级结构的影响进行了深入研究,并简要讨论了修饰对结构的影响如何导致蛋白质结合发生变化。最后,我们讨论了揭示尚未发现的对修饰敏感的 RBP:RNA 相互作用的策略。协调未来的努力,交叉表转录组和 RNA 蛋白相互作用组,将阐明 RNA 修饰识别的规则以及造成 mRNA 修饰生物学后果的机制。本文归类于RNA 结构和动力学 > RNA 结构、动力学和化学 RNA 与蛋白质和其他分子的相互作用 > 蛋白质-RNA 识别 RNA 处理 > RNA 编辑和修饰。
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
CiteScore
14.80
自引率
4.10%
发文量
67
审稿时长
6-12 weeks
期刊介绍: WIREs RNA aims to provide comprehensive, up-to-date, and coherent coverage of this interesting and growing field, providing a framework for both RNA experts and interdisciplinary researchers to not only gain perspective in areas of RNA biology, but to generate new insights and applications as well. Major topics to be covered are: RNA Structure and Dynamics; RNA Evolution and Genomics; RNA-Based Catalysis; RNA Interactions with Proteins and Other Molecules; Translation; RNA Processing; RNA Export/Localization; RNA Turnover and Surveillance; Regulatory RNAs/RNAi/Riboswitches; RNA in Disease and Development; and RNA Methods.
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