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

Selective regulation in ribosome biogenesis and protein production for efficient viral translation.
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核糖体生物发生和蛋白质生产的选择性调控以实现有效的病毒翻译

DOI:
10.1007/s00203-020-02094-5
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发表时间:
2021-04
影响因子:
2.8
通讯作者:
Wang XJ
Wang XJ
中科院分区:
生物学4区
文献类型:
--
作者:
Dong HJ;Zhang R;Kuang Y;Wang XJ

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作为细胞内寄生物,病毒严重依赖宿主细胞的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有效复制;核糖体生物发生和蛋白质合成在病毒复制中的作用特别突出了核糖体数量和/或质量在控制病毒蛋白质合成中的重要性。最近的研究表明,核糖体生物合成因子(RBFs)和核糖体蛋白(RPs)在病毒转录本的选择性翻译中起着多方面的调节作用。在这里,我们总结了最近的文献RBFs和RP及其关联的亚细胞再分布,翻译后修饰,酶催化,并直接与病毒蛋白的相互作用。本文献中描述的进展为在下一代抗病毒剂的设计中靶向核糖体的产生和功能建立了理论基础。
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.
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