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Characterization of Nucleocytoplasmic Shuttling of Pseudorabies Virus Protein UL46

Pseudorabies virus (PRV) is the etiological agent of Aujeszky's disease, which has caused severe economic loss in China since its re-emergence in 2011. UL46, a late gene of herpesvirus, codes for the abundant but non-essential viral phosphoproteins 11 and 12 (VP11/12). In this study, VP11/12 wa...

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Detalles Bibliográficos
Autores principales: Xu, Jing-jing, Gao, Fei, Wu, Ji-qiang, Zheng, Hao, Tong, Wu, Cheng, Xue-fei, Liu, Yuting, Zhu, Haojie, Fu, Xinling, Jiang, Yifeng, Li, Liwei, Kong, Ning, Li, Guoxin, Tong, Guangzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7472561/
https://www.ncbi.nlm.nih.gov/pubmed/32974393
http://dx.doi.org/10.3389/fvets.2020.00484
Descripción
Sumario:Pseudorabies virus (PRV) is the etiological agent of Aujeszky's disease, which has caused severe economic loss in China since its re-emergence in 2011. UL46, a late gene of herpesvirus, codes for the abundant but non-essential viral phosphoproteins 11 and 12 (VP11/12). In this study, VP11/12 was found to localize inside both the nucleus and cytoplasm. The nuclear localization signal (NLS) of VP11/12 was identified as (3)RRARGTRRASWKDASR(18). Further research identified α5 and α7 to be the receptors for NLS and the chromosome region maintenance 1 (CRM1) to be the receptor for the nuclear export signal. Moreover, we found that PRV VP11/12 interacts with EP0 and the stimulator of interferon genes protein (STING), whereas the NLS of VP11/12 is the important part for VP11/12 to interact with UL48. To our knowledge, this is the first study to provide reliable evidence verifying the nuclear localization of VP11/12 and its role as an additional shuttling tegument protein for PRV. In addition, this is also the first study to elucidate the interactions between PRV VP11/12 and EP0 as well as between PRV VP11/12 and STING, while identifying the precise interaction sites of PRV VP11/12 and VP16.