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一种副黏病毒复制酶将宿主 HSP70 招募到膜上进行病毒 RNA 复制。

A furoviral replicase recruits host HSP70 to membranes for viral RNA replication.

机构信息

State Key Laboratory Breeding Base for Zhejiang Sustain Pest and Disease Control; MOA and Zhejiang Key Laboratory of Plant Protection and Biotechnology, Institute of Virology and Biotechnology, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, China.

College of Chemistry and Life Science, Zhejiang Normal University, Jinhua 321004, China.

出版信息

Sci Rep. 2017 Apr 3;7:45590. doi: 10.1038/srep45590.

Abstract

Many host factors have been identified to be involved in viral infection. However, although furoviruses cause important diseases of cereals worldwide, no host factors have yet been identified that interact with furoviral genes or participate in the viral infection cycle. In this study, both TaHSP70 and NbHSP70 were up-regulated in Chinese wheat mosaic furovirus (CWMV)-infected plants. Their overexpression and inhibition were correlated with the accumulation of viral genomic RNAs, suggesting that the HSP70 genes could be necessary for CWMV infection. The subcellular distributions of TaHSP70 and NbHSP70 were significantly affected by CWMV infection or by infiltration of RNA1 alone. Further assays showed that the viral replicase encoded by CWMV RNA1 interacts with both TaHSP70 and NbHSP70 in vivo and vitro and that its region aa167-333 was responsible for the interaction. Subcellular assays showed that the viral replicase could recruit both TaHSP70 and NbHSP70 from the cytoplasm or nucleus to the granular aggregations or inclusion-like structures on the intracellular membrane system, suggesting that both HSP70s may be recruited into the viral replication complex (VRC) to promote furoviral replication. This is the first host factor identified to be involved in furoviral infection, which extends the list and functional scope of HSP70 chaperones.

摘要

许多宿主因素已被确定参与病毒感染。然而,尽管呋孢病毒会导致全球重要的谷类疾病,但尚未发现与呋孢病毒基因相互作用或参与病毒感染周期的宿主因素。在这项研究中,中国小麦花叶病毒(CWMV)感染的植物中 TaHSP70 和 NbHSP70 均上调。它们的过表达和抑制与病毒基因组 RNA 的积累相关,表明 HSP70 基因可能是 CWMV 感染所必需的。CWMV 感染或单独浸润 RNA1 显著影响 TaHSP70 和 NbHSP70 的亚细胞分布。进一步的实验表明,CWMV RNA1 编码的病毒复制酶在体内和体外与 TaHSP70 和 NbHSP70 相互作用,其 aa167-333 区域负责相互作用。亚细胞实验表明,病毒复制酶可以从细胞质或细胞核将 TaHSP70 和 NbHSP70 招募到细胞内膜系统上的颗粒聚集或包涵体样结构中,表明这两种 HSP70 都可能被招募到病毒复制复合物(VRC)中以促进呋孢病毒复制。这是第一个被确定参与呋孢病毒感染的宿主因素,它扩展了 HSP70 伴侣的列表和功能范围。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8fd/5377427/49018d69b66c/srep45590-f1.jpg

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