SARS coronavirus 8b reduces viral replication by down-regulating E via an ubiquitin-independent proteasome pathway
Identifieur interne : 002463 ( Main/Exploration ); précédent : 002462; suivant : 002464SARS coronavirus 8b reduces viral replication by down-regulating E via an ubiquitin-independent proteasome pathway
Auteurs : Choong-Tat Keng [Singapour] ; Sara Kerström [Suède] ; Cynthia Sau-Wai Leung [République populaire de Chine] ; Leo L. M. Poon [République populaire de Chine] ; J. S. Malik Peiris [République populaire de Chine] ; Ali Mirazimi [Suède] ; Yee-Joo Tan [Singapour]Source :
- Microbes and Infection [ 1286-4579 ] ; 2010.
Descripteurs français
- KwdFr :
- Animaux, Cellules Vero, Infections à coronavirus (métabolisme), Mutagenèse dirigée, Proteasome endopeptidase complex (métabolisme), Protéines de l'enveloppe virale (métabolisme), Protéines virales (métabolisme), Protéines à fluorescence verte (génétique), Protéines à fluorescence verte (métabolisme), Régulation de l'expression des gènes viraux, Régulation négative, Réplication virale (génétique), Stabilité protéique, Techniques de knock-out de gènes, Ubiquitine (métabolisme), Ubiquitinylation (génétique), Virus du SRAS (génétique), Virus du SRAS (métabolisme), Virus du SRAS (physiologie).
- MESH :
- génétique : Protéines à fluorescence verte, Réplication virale, Ubiquitinylation, Virus du SRAS.
- métabolisme : Infections à coronavirus, Proteasome endopeptidase complex, Protéines de l'enveloppe virale, Protéines virales, Protéines à fluorescence verte, Ubiquitine, Virus du SRAS.
- physiologie : Virus du SRAS.
- Animaux, Cellules Vero, Mutagenèse dirigée, Régulation de l'expression des gènes viraux, Régulation négative, Stabilité protéique, Techniques de knock-out de gènes.
English descriptors
- KwdEn :
- Animals, Chlorocebus aethiops, Coronavirus Infections (metabolism), Down-Regulation, Gene Expression Regulation, Viral, Gene Knockout Techniques, Green Fluorescent Proteins (genetics), Green Fluorescent Proteins (metabolism), Mutagenesis, Site-Directed, Proteasome Endopeptidase Complex (metabolism), Protein Stability, SARS Virus (genetics), SARS Virus (metabolism), SARS Virus (physiology), Ubiquitin (metabolism), Ubiquitination (genetics), Vero Cells, Viral Envelope Proteins (metabolism), Viral Proteins (metabolism), Virus Replication (genetics).
- MESH :
- chemical , genetics : Green Fluorescent Proteins.
- genetics : SARS Virus, Ubiquitination, Virus Replication.
- metabolism : Coronavirus Infections, Green Fluorescent Proteins, Proteasome Endopeptidase Complex, SARS Virus, Ubiquitin, Viral Envelope Proteins, Viral Proteins.
- physiology : SARS Virus.
- Animals, Chlorocebus aethiops, Down-Regulation, Gene Expression Regulation, Viral, Gene Knockout Techniques, Mutagenesis, Site-Directed, Protein Stability, Vero Cells.
Abstract
The severe acute respiratory syndrome coronavirus (SARS-CoV) 8b protein, which is not expressed by other known coronaviruses, can down-regulate the envelope (E) protein via a proteasome-dependent pathway. Here, we showed that the down-regulation of E is not dependent on the lysine residues on 8b and the reduction of polyubiquitination of E mutants is not correlated with their down-regulation by 8b, suggesting an ubiquitin-independent proteasome pathway is involved. A time-course study revealed that 8b was expressed at late-stages of SARS-CoV infection. By using Vero E6 cells stably expressing green fluorescence protein-tagged 8b, ectopic expression of 8b was shown to significantly reduce the production of progeny virus and down-regulate E expression. Taken together, these results suggest that 8b negatively modulates virus replication by down-regulating E via an ubiquitin-independent proteasome pathway.
Url:
- http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7110893
- https://hal-riip.archives-ouvertes.fr/pasteur-00588905
DOI: 10.1016/j.micinf.2010.10.017
PubMed: 21035562
PubMed Central: 7110893
Affiliations:
- République populaire de Chine, Singapour, Suède
- Svealand
- Stockholm
- Université nationale de Singapour
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Le document en format XML
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<front><div type="abstract" xml:lang="en"><p>The severe acute respiratory syndrome coronavirus (SARS-CoV) 8b protein, which is not expressed by other known coronaviruses, can down-regulate the envelope (E) protein via a proteasome-dependent pathway. Here, we showed that the down-regulation of E is not dependent on the lysine residues on 8b and the reduction of polyubiquitination of E mutants is not correlated with their down-regulation by 8b, suggesting an ubiquitin-independent proteasome pathway is involved. A time-course study revealed that 8b was expressed at late-stages of SARS-CoV infection. By using Vero E6 cells stably expressing green fluorescence protein-tagged 8b, ectopic expression of 8b was shown to significantly reduce the production of progeny virus and down-regulate E expression. Taken together, these results suggest that 8b negatively modulates virus replication by down-regulating E via an ubiquitin-independent proteasome pathway.</p>
</div>
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<back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Peiris, J S" uniqKey="Peiris J">J.S. Peiris</name>
</author>
<author><name sortKey="Lai, S T" uniqKey="Lai S">S.T. Lai</name>
</author>
<author><name sortKey="Poon, L L" uniqKey="Poon L">L.L. Poon</name>
</author>
<author><name sortKey="Guan, Y" uniqKey="Guan Y">Y. Guan</name>
</author>
<author><name sortKey="Yam, L Y" uniqKey="Yam L">L.Y. Yam</name>
</author>
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<li>Suède</li>
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</country>
</tree>
</affiliations>
</record>
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