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The coronavirus nucleocapsid protein is ADP-ribosylated
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 ~55 kDa ADP-ribosylated protein in mouse hepatitis virus (MHV)-infected c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5871557/ https://www.ncbi.nlm.nih.gov/pubmed/29199039 http://dx.doi.org/10.1016/j.virol.2017.11.020 |
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author | Grunewald, Matthew E. Fehr, Anthony R. Athmer, Jeremiah Perlman, Stanley |
author_facet | Grunewald, Matthew E. Fehr, Anthony R. Athmer, Jeremiah Perlman, Stanley |
author_sort | Grunewald, Matthew E. |
collection | PubMed |
description | 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 ~55 kDa 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. |
format | Online Article Text |
id | pubmed-5871557 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58715572019-04-01 The coronavirus nucleocapsid protein is ADP-ribosylated Grunewald, Matthew E. Fehr, Anthony R. Athmer, Jeremiah Perlman, Stanley Virology Article 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 ~55 kDa 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. Elsevier Inc. 2018-04 2017-12-01 /pmc/articles/PMC5871557/ /pubmed/29199039 http://dx.doi.org/10.1016/j.virol.2017.11.020 Text en © 2017 Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Grunewald, Matthew E. Fehr, Anthony R. Athmer, Jeremiah Perlman, Stanley The coronavirus nucleocapsid protein is ADP-ribosylated |
title | The coronavirus nucleocapsid protein is ADP-ribosylated |
title_full | The coronavirus nucleocapsid protein is ADP-ribosylated |
title_fullStr | The coronavirus nucleocapsid protein is ADP-ribosylated |
title_full_unstemmed | The coronavirus nucleocapsid protein is ADP-ribosylated |
title_short | The coronavirus nucleocapsid protein is ADP-ribosylated |
title_sort | coronavirus nucleocapsid protein is adp-ribosylated |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5871557/ https://www.ncbi.nlm.nih.gov/pubmed/29199039 http://dx.doi.org/10.1016/j.virol.2017.11.020 |
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