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RNA 与蛋白质相互作用组是研究 RNA 病毒的宝贵资源:来自 SARS-CoV-2 研究的启示。

RNA-protein interactomes as invaluable resources to study RNA viruses: Insights from SARS CoV-2 studies.

机构信息

Department of Non-Coding RNAs, Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, Poland.

出版信息

Wiley Interdiscip Rev RNA. 2022 Nov;13(6):e1727. doi: 10.1002/wrna.1727. Epub 2022 Mar 27.

Abstract

Understanding the molecular mechanisms of severe respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is essential for the successful development of therapeutic strategies against the COVID-19 pandemic. Numerous studies have focused on the identification of host factors and cellular pathways involved in the viral replication cycle. The speed and magnitude of hijacking the translation machinery of host mRNA, and shutting down host transcription are still not well understood. Since SARS-CoV-2 relies on host RNA-binding proteins for the infection progression, several efforts have been made to define the SARS-CoV-2 RNA-bound proteomes (RNA-protein interactomes). Methodologies that enable the systemic capture of protein interactors of given RNA in vivo have been adapted for the identification of the SARS-CoV-2 RNA interactome. The obtained proteomic data aided by genome-wide and targeted CRISPR perturbation screens, revealed host factors with either pro- or anti-viral activity and highlighted cellular processes and factors involved in host response. We focus here on the recent studies on SARS-CoV-2 RNA-protein interactomes, with regard to both the technological aspects of RNA interactome capture methods and the obtained results. We also summarize several related studies, which were used in the interpretation of the SARS-CoV-2 RNA-protein interactomes. These studies provided the selection of host factors that are potentially suitable candidates for antiviral therapy. Finally, we underscore the importance of RNA-protein interactome studies in regard to the effective development of antiviral strategies against current and future threats. This article is categorized under: RNA Interactions with Proteins and Other Molecules > Protein-RNA Interactions: Functional Implications RNA in Disease and Development > RNA in Disease RNA Methods > RNA Analyses in Cells.

摘要

了解严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染的分子机制对于成功开发针对 COVID-19 大流行的治疗策略至关重要。许多研究都集中在鉴定参与病毒复制周期的宿主因素和细胞途径上。宿主 mRNA 翻译机制被病毒劫持的速度和程度,以及宿主转录被关闭的机制,仍然没有得到很好的理解。由于 SARS-CoV-2 依赖宿主 RNA 结合蛋白来进行感染,因此已经做出了几种努力来定义 SARS-CoV-2 的 RNA 结合蛋白组(RNA-蛋白质相互作用组)。已经适应了使体内给定 RNA 的蛋白质相互作用体系统捕获的方法,用于鉴定 SARS-CoV-2 的 RNA 相互作用组。获得的蛋白质组学数据通过全基因组和靶向 CRISPR 扰动筛选得到了补充,揭示了具有促病毒或抗病毒活性的宿主因子,并强调了参与宿主反应的细胞过程和因子。我们在这里重点介绍关于 SARS-CoV-2 RNA-蛋白质相互作用组的最新研究,包括 RNA 相互作用组捕获方法的技术方面和获得的结果。我们还总结了几项相关研究,这些研究用于解释 SARS-CoV-2 RNA-蛋白质相互作用组。这些研究为选择可能适合抗病毒治疗的宿主因子提供了依据。最后,我们强调了 RNA-蛋白质相互作用组研究在针对当前和未来威胁开发有效抗病毒策略方面的重要性。本文属于以下分类:RNA 与蛋白质和其他分子的相互作用 > 蛋白质-RNA 相互作用:功能意义 RNA 在疾病与发育中的作用 > RNA 在疾病中 RNA 方法学 > RNA 在细胞中的分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c330/9111084/13609348fea6/WRNA-9999-0-g003.jpg

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