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选择性调节核糖体生物发生和蛋白质产生以提高病毒翻译效率。

Selective regulation in ribosome biogenesis and protein production for efficient viral translation.

机构信息

Key Laboratory of Animal Epidemiology of the Ministry of Agriculture, College of Veterinary Medicine, China Agricultural University, Beijing, 100193, China.

出版信息

Arch Microbiol. 2021 Apr;203(3):1021-1032. doi: 10.1007/s00203-020-02094-5. Epub 2020 Oct 29.

Abstract

As intracellular parasites, viruses depend heavily on host cell structures and their functions to complete their life cycle and produce new viral particles. Viruses utilize or modulate cellular translational machinery to achieve efficient replication; the role of ribosome biogenesis and protein synthesis in viral replication particularly highlights the importance of the ribosome quantity and/or quality in controlling viral protein synthesis. Recently reported studies have demonstrated that ribosome biogenesis factors (RBFs) and ribosomal proteins (RPs) act as multifaceted regulators in selective translation of viral transcripts. Here we summarize the recent literature on RBFs and RPs and their association with subcellular redistribution, post-translational modification, enzyme catalysis, and direct interaction with viral proteins. The advances described in this literature establish a rationale for targeting ribosome production and function in the design of the next generation of antiviral agents.

摘要

作为细胞内寄生虫,病毒严重依赖宿主细胞结构和功能来完成其生命周期并产生新的病毒颗粒。病毒利用或调节细胞翻译机制以实现高效复制;核糖体生物发生和蛋白质合成在病毒复制中的作用特别强调了核糖体数量和/或质量在控制病毒蛋白合成中的重要性。最近的研究报告表明,核糖体生物发生因子(RBFs)和核糖体蛋白(RPs)作为病毒转录物选择性翻译的多功能调节剂。在这里,我们总结了最近关于 RBFs 和 RPs 及其与亚细胞重新分布、翻译后修饰、酶催化以及与病毒蛋白直接相互作用的文献。该文献中描述的进展为靶向核糖体产生和功能以设计下一代抗病毒药物提供了依据。

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