A SARS-CoV protein, ORF-6, induces caspase-3 mediated, ER stress and JNK-dependent apoptosis.
Identifieur interne : 003279 ( Main/Merge ); précédent : 003278; suivant : 003280A SARS-CoV protein, ORF-6, induces caspase-3 mediated, ER stress and JNK-dependent apoptosis.
Auteurs : Zhongde Ye [République populaire de Chine] ; Chung Kai Wong ; Peng Li ; Yong XieSource :
- Biochimica et biophysica acta [ 0006-3002 ] ; 2008.
Descripteurs français
- KwdFr :
- Activation enzymatique, Animaux, Apoptose, Caspase-3 (physiologie), Chaperons moléculaires (biosynthèse), Humains, JNK Mitogen-Activated Protein Kinases (antagonistes et inhibiteurs), JNK Mitogen-Activated Protein Kinases (physiologie), Oligopeptides (pharmacologie), Protéines de la matrice virale (antagonistes et inhibiteurs), Protéines de la matrice virale (physiologie), Protéines du choc thermique HSP70 (biosynthèse), Protéines membranaires (biosynthèse), Protéines virales (antagonistes et inhibiteurs), Protéines virales (biosynthèse), Régulation positive, Réticulum endoplasmique (métabolisme).
- MESH :
- antagonistes et inhibiteurs : JNK Mitogen-Activated Protein Kinases, Protéines de la matrice virale, Protéines virales.
- biosynthèse : Chaperons moléculaires, Protéines du choc thermique HSP70, Protéines membranaires, Protéines virales.
- métabolisme : Réticulum endoplasmique.
- pharmacologie : Oligopeptides.
- physiologie : Caspase-3, JNK Mitogen-Activated Protein Kinases, Protéines de la matrice virale.
- Activation enzymatique, Animaux, Apoptose, Humains, Régulation positive.
English descriptors
- KwdEn :
- Animals, Apoptosis, Caspase 3 (physiology), Chlorocebus aethiops, Endoplasmic Reticulum (metabolism), Enzyme Activation, HSP70 Heat-Shock Proteins (biosynthesis), Humans, JNK Mitogen-Activated Protein Kinases (antagonists & inhibitors), JNK Mitogen-Activated Protein Kinases (physiology), Membrane Proteins (biosynthesis), Molecular Chaperones (biosynthesis), Oligopeptides (pharmacology), Up-Regulation, Viral Matrix Proteins (antagonists & inhibitors), Viral Matrix Proteins (physiology), Viral Proteins (antagonists & inhibitors), Viral Proteins (biosynthesis).
- MESH :
- chemical , antagonists & inhibitors : JNK Mitogen-Activated Protein Kinases, Viral Matrix Proteins, Viral Proteins.
- chemical , biosynthesis : HSP70 Heat-Shock Proteins, Membrane Proteins, Molecular Chaperones, Viral Proteins.
- chemical , pharmacology : Oligopeptides.
- chemical , physiology : Caspase 3, JNK Mitogen-Activated Protein Kinases, Viral Matrix Proteins.
- metabolism : Endoplasmic Reticulum.
- Animals, Apoptosis, Chlorocebus aethiops, Enzyme Activation, Humans, Up-Regulation.
Abstract
Severe acute respiratory syndrome (SARS) coronavirus (CoV) spread from China to more than 30 countries, causing severe outbreaks of atypical pneumonia and over 800 deaths worldwide. CoV primarily infects the upper respiratory and gastrointestinal tract; however, SARS-CoV has a unique pathogenesis because it infects both the upper and lower respiratory tracts and leads to human respiratory diseases. SARS-CoV genome has shown containing 14 open reading frames (ORFs) and 8 of them encode novel proteins. Previous reports show that overexpression of ORF-3a, ORF-3b and ORF-7a induce apoptosis. In this report, we demonstrate that overexpression of ORF-6 also induces apoptosis and that Caspase-3 inhibitor and JNK inhibitor block ORF-6 induced apoptosis. Importantly, the protein level of ER chaperon protein, GRP94, was up-regulated when ORF-6 was overexpressed. All these data suggest that ORF-6 induces apoptosis via Caspase-3 mediated, ER stress and JNK-dependent pathways.
DOI: 10.1016/j.bbagen.2008.07.009
PubMed: 18708124
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pubmed:18708124Le document en format XML
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<term>Endoplasmic Reticulum (metabolism)</term>
<term>Enzyme Activation</term>
<term>HSP70 Heat-Shock Proteins (biosynthesis)</term>
<term>Humans</term>
<term>JNK Mitogen-Activated Protein Kinases (antagonists & inhibitors)</term>
<term>JNK Mitogen-Activated Protein Kinases (physiology)</term>
<term>Membrane Proteins (biosynthesis)</term>
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<term>Viral Matrix Proteins (physiology)</term>
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<term>Viral Proteins (biosynthesis)</term>
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<term>Animaux</term>
<term>Apoptose</term>
<term>Caspase-3 (physiologie)</term>
<term>Chaperons moléculaires (biosynthèse)</term>
<term>Humains</term>
<term>JNK Mitogen-Activated Protein Kinases (antagonistes et inhibiteurs)</term>
<term>JNK Mitogen-Activated Protein Kinases (physiologie)</term>
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<term>Protéines de la matrice virale (physiologie)</term>
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<term>Protéines membranaires (biosynthèse)</term>
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<term>Protéines virales (biosynthèse)</term>
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<term>JNK Mitogen-Activated Protein Kinases</term>
<term>Viral Matrix Proteins</term>
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<term>Protéines virales</term>
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<front><div type="abstract" xml:lang="en">Severe acute respiratory syndrome (SARS) coronavirus (CoV) spread from China to more than 30 countries, causing severe outbreaks of atypical pneumonia and over 800 deaths worldwide. CoV primarily infects the upper respiratory and gastrointestinal tract; however, SARS-CoV has a unique pathogenesis because it infects both the upper and lower respiratory tracts and leads to human respiratory diseases. SARS-CoV genome has shown containing 14 open reading frames (ORFs) and 8 of them encode novel proteins. Previous reports show that overexpression of ORF-3a, ORF-3b and ORF-7a induce apoptosis. In this report, we demonstrate that overexpression of ORF-6 also induces apoptosis and that Caspase-3 inhibitor and JNK inhibitor block ORF-6 induced apoptosis. Importantly, the protein level of ER chaperon protein, GRP94, was up-regulated when ORF-6 was overexpressed. All these data suggest that ORF-6 induces apoptosis via Caspase-3 mediated, ER stress and JNK-dependent pathways.</div>
</front>
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