Getah virus Nsp3 binds G3BP to block formation of bona fide stress granules

应力颗粒 细胞生物学 生物 病毒复制 化学 病毒 信使核糖核酸 基因 生物化学 病毒学 翻译(生物学)
作者
Xiaoyi Qi,Ruihan Zhao,Xiaohui Yao,Q. Liu,Panrao Liu,Zhenbang Zhu,Changchun Tu,Wenjie Gong,Xiang‐dong Li
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:279: 135274-135274 被引量:5
标识
DOI:10.1016/j.ijbiomac.2024.135274
摘要

Stress granules (SGs) are cytoplasmic aggregates of proteins and mRNA that form in response to diverse environmental stressors, including viral infections. Several viruses possess the ability to block the formation of stress granules by targeting the SGs marker protein G3BP. However, the molecular functions and mechanisms underlying the regulation of SGs formation by Getah virus (GETV) remain unclear. In this study, we found that GETV infection triggered the formation of Nsp3-G3BP aggregates, which differed in composition from SGs. Further studies revealed that the presence of these aggregates was dependent on the activation of the PKR/eIF2α signaling pathway. Interestingly, we found that Nsp3 HVD domain blocked the formation of SGs by binding to G3BP NTF2 domain. Moreover, knockout of G3BP in NCI-H1299 cells had no effect on GETV replication, while overexpression of G3BP to form the genuine SGs significantly inhibited GETV replication. Overall, our study elucidates a novel role GETV Nsp3 to change the composition of SG as well as cellular stress response.
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