The coronavirus nucleocapsid protein is ADP-ribosylated.
Identifieur interne : 000739 ( PubMed/Checkpoint ); précédent : 000738; suivant : 000740The coronavirus nucleocapsid protein is ADP-ribosylated.
Auteurs : Matthew E. Grunewald [États-Unis] ; Anthony R. Fehr [États-Unis] ; Jeremiah Athmer [États-Unis] ; Stanley Perlman [États-Unis]Source :
- Virology [ 1096-0341 ] ; 2018.
Descripteurs français
- KwdFr :
- Animaux, Coronavirus (génétique), Coronavirus (métabolisme), Domaines protéiques, Humains, Lignée cellulaire, Protéines nucléocapside (génétique), Protéines nucléocapside (métabolisme), Protéines virales non structurales (génétique), Protéines virales non structurales (métabolisme), Régulation de l'expression des gènes viraux (physiologie).
- MESH :
- génétique : Coronavirus, Protéines nucléocapside, Protéines virales non structurales.
- métabolisme : Coronavirus, Protéines nucléocapside, Protéines virales non structurales.
- physiologie : Régulation de l'expression des gènes viraux.
- Animaux, Domaines protéiques, Humains, Lignée cellulaire.
English descriptors
- KwdEn :
- ADP-Ribosylation (physiology), Animals, Cell Line, Coronavirus (genetics), Coronavirus (metabolism), Gene Expression Regulation, Viral (physiology), Humans, Nucleocapsid Proteins (genetics), Nucleocapsid Proteins (metabolism), Protein Domains, Viral Nonstructural Proteins (genetics), Viral Nonstructural Proteins (metabolism).
- MESH :
- chemical , genetics : Nucleocapsid Proteins, Viral Nonstructural Proteins.
- genetics : Coronavirus.
- metabolism : Coronavirus, Nucleocapsid Proteins, Viral Nonstructural Proteins.
- physiology : ADP-Ribosylation, Gene Expression Regulation, Viral.
- Animals, Cell Line, Humans, Protein Domains.
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.
DOI: 10.1016/j.virol.2017.11.020
PubMed: 29199039
Affiliations:
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pubmed:29199039Le document en format XML
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<front><div type="abstract" xml:lang="en">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.</div>
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<Abstract><AbstractText>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.</AbstractText>
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