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冠状病毒核衣壳蛋白被ADP核糖基化。

The coronavirus nucleocapsid protein is ADP-ribosylated.

作者信息

Grunewald Matthew E, Fehr Anthony R, Athmer Jeremiah, Perlman Stanley

机构信息

Department of Microbiology and Immunology, Carver College of Medicine, University of Iowa, 51 Newton Road, Iowa City, IA 52242, United States.

Department of Microbiology and Immunology, Carver College of Medicine, University of Iowa, 51 Newton Road, Iowa City, IA 52242, United States.

出版信息

Virology. 2018 Apr;517:62-68. doi: 10.1016/j.virol.2017.11.020. Epub 2017 Dec 1.

DOI:10.1016/j.virol.2017.11.020
PMID:29199039
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5871557/
Abstract

ADP-ribosylation is a common post-translational modification, although how it modulates RNA virus infection is not well understood. While screening for ADP-ribosylated proteins during coronavirus (CoV) infection, we detected a ~55kDa ADP-ribosylated protein in mouse hepatitis virus (MHV)-infected cells and in virions, which we identified as the viral nucleocapsid (N) protein. The N proteins of porcine epidemic diarrhea virus (PEDV), severe acute respiratory syndrome (SARS)-CoV and Middle East respiratory syndrome (MERS)-CoV were also ADP-ribosylated. ADP-ribosylation of N protein was also observed in cells exogenously expressing N protein by transduction using Venezuelan equine encephalitis virus replicon particles (VRPs). However, plasmid-derived N protein was not ADP-ribosylated following transient transfection but was ADP-ribosylated after MHV infection, indicating that this modification requires virus infection. In conclusion, we have identified a novel post-translation modification of the CoV N protein that may play a regulatory role for this important structural protein.

摘要

ADP核糖基化是一种常见的翻译后修饰,尽管其如何调节RNA病毒感染尚不清楚。在筛选冠状病毒(CoV)感染期间的ADP核糖基化蛋白时,我们在感染小鼠肝炎病毒(MHV)的细胞和病毒粒子中检测到一种约55kDa的ADP核糖基化蛋白,我们将其鉴定为病毒核衣壳(N)蛋白。猪流行性腹泻病毒(PEDV)、严重急性呼吸综合征(SARS)-CoV和中东呼吸综合征(MERS)-CoV的N蛋白也被ADP核糖基化。通过使用委内瑞拉马脑炎病毒复制子颗粒(VRP)转导在外源表达N蛋白的细胞中也观察到N蛋白的ADP核糖基化。然而,质粒来源的N蛋白在瞬时转染后未被ADP核糖基化,但在MHV感染后被ADP核糖基化,这表明这种修饰需要病毒感染。总之,我们鉴定出了CoV N蛋白一种新的翻译后修饰,其可能对这种重要的结构蛋白发挥调节作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/113c/7112041/0c86dc552e98/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/113c/7112041/dbc62f6c603b/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/113c/7112041/29f3797fedd1/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/113c/7112041/7bedfa4631ed/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/113c/7112041/a7f88e29c2b6/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/113c/7112041/0c86dc552e98/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/113c/7112041/dbc62f6c603b/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/113c/7112041/29f3797fedd1/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/113c/7112041/7bedfa4631ed/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/113c/7112041/a7f88e29c2b6/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/113c/7112041/0c86dc552e98/gr5_lrg.jpg

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