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草鱼呼肠孤病毒II型编码蛋白的生化分析

Biochemical profiling of the protein encoded by grass carp reovirus genotype II.

作者信息

Liu Man, Xu Chen, Zhou Yong, Xue Mingyang, Jiang Nan, Li Yiqun, Huang Zhenyu, Meng Yan, Liu Wenzhi, Kong Xianghui, Fan Yuding

机构信息

Engineering Lab of Henan Province for Aquatic Animal Disease Control, College of Fisheries, Henan Normal University, Xinxiang 453000, China.

Yangtze River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Wuhan 430223, China.

出版信息

iScience. 2024 Jul 20;27(8):110502. doi: 10.1016/j.isci.2024.110502. eCollection 2024 Aug 16.

Abstract

In this study, we obtained the whole genome sequence of GCRV-DY197 and investigated the localization, post-translational modifications, and host interactions of the 11 viral proteins encoded by GCRV-DY197 in grass carp ovary (GCO) cells. The whole genome sequence is 24,704 kb and contains 11 segments (S1-S11). Subcellular localization showed that the VP1, VP2, VP3, VP5, VP56, and VP35 proteins were localized in both cytoplasm and nucleus, whereas the NS79, VP4, VP41, VP6, and NS38 proteins were localized in the cytoplasm. The NS79 and NS38 proteins were phosphorylated, and the ubiquitination modification sites were identified in VP41 and NS38. An interaction network containing 9 viral proteins and 140 host proteins was also constructed. These results offer a theoretical basis for an in-depth understanding of the biochemical characteristics and pathogenic mechanism of GCRV-II.

摘要

在本研究中,我们获得了草鱼呼肠孤病毒DY197(GCRV-DY197)的全基因组序列,并研究了GCRV-DY197编码的11种病毒蛋白在草鱼卵巢(GCO)细胞中的定位、翻译后修饰及与宿主的相互作用。全基因组序列为24,704 kb,包含11个片段(S1-S11)。亚细胞定位显示,VP1、VP2、VP3、VP5、VP56和VP35蛋白定位于细胞质和细胞核,而NS79、VP4、VP41、VP6和NS38蛋白定位于细胞质。NS79和NS38蛋白发生了磷酸化,并且在VP41和NS38中鉴定出了泛素化修饰位点。还构建了一个包含9种病毒蛋白和140种宿主蛋白的相互作用网络。这些结果为深入了解GCRV-II的生化特性和致病机制提供了理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a363/11363571/02ff6fe4f662/fx1.jpg

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