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小核糖核酸病毒 3C-蛋白酶:确保病毒复制和颠覆宿主反应的关键酶。

Picornavirus 3C - a protease ensuring virus replication and subverting host responses.

机构信息

State Key Laboratory of Veterinary Etiological Biology and OIE/National Foot and Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, Gansu 730046, China.

State Key Laboratory of Veterinary Etiological Biology and OIE/National Foot and Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, Gansu 730046, China

出版信息

J Cell Sci. 2021 Mar 10;134(5):jcs253237. doi: 10.1242/jcs.253237.

Abstract

The protease 3C is encoded by all known picornaviruses, and the structural features related to its protease and RNA-binding activities are conserved; these contribute to the cleavage of viral polyproteins and the assembly of the viral RNA replication complex during virus replication. Furthermore, 3C performs functions in the host cell through its interaction with host proteins. For instance, 3C has been shown to selectively 'hijack' host factors involved in gene expression, promoting picornavirus replication, and to inactivate key factors in innate immunity signaling pathways, inhibiting the production of interferon and inflammatory cytokines. Importantly, 3C maintains virus infection by subtly subverting host cell death and modifying critical molecules in host organelles. This Review focuses on the molecular mechanisms through which 3C mediates physiological processes involved in virus-host interaction, thus highlighting the picornavirus-mediated pathogenesis caused by 3C.

摘要

蛋白酶 3C 由所有已知的小核糖核酸病毒编码,其与蛋白酶和 RNA 结合活性相关的结构特征是保守的;这些特征有助于病毒复制过程中病毒多蛋白的切割和病毒 RNA 复制复合物的组装。此外,3C 通过与宿主蛋白的相互作用在宿主细胞中发挥功能。例如,已经表明 3C 可以选择性地“劫持”参与基因表达的宿主因子,促进小核糖核酸病毒的复制,并使先天免疫信号通路中的关键因子失活,抑制干扰素和炎性细胞因子的产生。重要的是,3C 通过微妙地下调宿主细胞死亡和修饰宿主细胞器中的关键分子来维持病毒感染。这篇综述重点介绍了 3C 介导病毒-宿主相互作用中涉及的生理过程的分子机制,从而突出了 3C 介导的小核糖核酸病毒发病机制。

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