Nsp1 proteins of group I and SARS coronaviruses share structural and functional similarities.
Identifieur interne : 001670 ( PubMed/Curation ); précédent : 001669; suivant : 001671Nsp1 proteins of group I and SARS coronaviruses share structural and functional similarities.
Auteurs : Yongjin Wang [République populaire de Chine] ; Huiling Shi ; Pascal Rigolet ; Nannan Wu ; Lichen Zhu ; Xu-Guang Xi ; Astrid Vabret ; Xiaoming Wang ; Tianhou WangSource :
- Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases [ 1567-7257 ] ; 2010.
Descripteurs français
- KwdFr :
- Coronavirus (), Coronavirus (enzymologie), Coronavirus (génétique), Données de séquences moléculaires, Humains, Immunité innée, Lignée cellulaire, Modèles moléculaires, Prolifération cellulaire, RNA replicase (génétique), RNA replicase (métabolisme), Régulation de l'expression des gènes codant pour des enzymes, Régulation de l'expression des gènes viraux (physiologie), Séquence d'acides aminés.
- MESH :
- enzymologie : Coronavirus.
- génétique : Coronavirus, RNA replicase.
- métabolisme : RNA replicase.
- physiologie : Régulation de l'expression des gènes viraux.
- Coronavirus, Données de séquences moléculaires, Humains, Immunité innée, Lignée cellulaire, Modèles moléculaires, Prolifération cellulaire, Régulation de l'expression des gènes codant pour des enzymes, Séquence d'acides aminés.
English descriptors
- KwdEn :
- Amino Acid Sequence, Cell Line, Cell Proliferation, Coronavirus (classification), Coronavirus (enzymology), Coronavirus (genetics), Gene Expression Regulation, Enzymologic, Gene Expression Regulation, Viral (physiology), Humans, Immunity, Innate, Models, Molecular, Molecular Sequence Data, RNA Replicase (genetics), RNA Replicase (metabolism).
- MESH :
- chemical , genetics : RNA Replicase.
- classification : Coronavirus.
- enzymology : Coronavirus.
- genetics : Coronavirus.
- chemical , metabolism : RNA Replicase.
- physiology : Gene Expression Regulation, Viral.
- Amino Acid Sequence, Cell Line, Cell Proliferation, Gene Expression Regulation, Enzymologic, Humans, Immunity, Innate, Models, Molecular, Molecular Sequence Data.
Abstract
The nsp1 protein of the highly pathogenic SARS coronavirus suppresses host protein synthesis, including genes involved in the innate immune system. A bioinformatic analysis revealed that the nsp1 proteins of group I and SARS coronaviruses have similar structures. Nsp1 proteins of group I coronaviruses interacted with host ribosomal 40S subunit and did not inhibit IRF-3 activation. However, synthesis of host immune and non-immune proteins was inhibited by nsp1 proteins at both transcriptional and translational levels, similar to SARS coronavirus nsp1. These results indicate that different coronaviruses might employ the same nsp1 mechanism to antagonize host innate immunity and cell proliferation. However, nsp1 may not be the key determinant of viral pathogenicity, or the factor used by the SARS coronavirus to evade host innate immunity.
DOI: 10.1016/j.meegid.2010.05.014
PubMed: 20609418
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A bioinformatic analysis revealed that the nsp1 proteins of group I and SARS coronaviruses have similar structures. Nsp1 proteins of group I coronaviruses interacted with host ribosomal 40S subunit and did not inhibit IRF-3 activation. However, synthesis of host immune and non-immune proteins was inhibited by nsp1 proteins at both transcriptional and translational levels, similar to SARS coronavirus nsp1. These results indicate that different coronaviruses might employ the same nsp1 mechanism to antagonize host innate immunity and cell proliferation. 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These results indicate that different coronaviruses might employ the same nsp1 mechanism to antagonize host innate immunity and cell proliferation. However, nsp1 may not be the key determinant of viral pathogenicity, or the factor used by the SARS coronavirus to evade host innate immunity.</AbstractText><CopyrightInformation>Copyright 2010 Elsevier B.V. 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