Hepatitis C Virus Infection Protein Network
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| dc.contributor.author |
de Chassey, B |
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| dc.contributor.author |
Navratil, V |
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| dc.contributor.author |
Tafforeau, L |
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| dc.contributor.author |
Hiet, M S |
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| dc.contributor.author |
Aublin-Gex, A |
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| dc.contributor.author |
Agaugué, S |
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| dc.contributor.author |
Meiffren, G |
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| dc.contributor.author |
Pradezynski, F |
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| dc.contributor.author |
Faria, B F |
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| dc.contributor.author |
Chantier, T |
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| dc.contributor.author |
Le Breton, M |
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| dc.contributor.author |
Pellet, J |
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| dc.contributor.author |
Davoust, N |
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| dc.contributor.author |
Mangeot, P E |
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| dc.contributor.author |
Chaboud, A |
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| dc.contributor.author |
Penin, F |
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| dc.contributor.author |
Jacob, Y |
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| dc.contributor.author |
Vidalain, P O |
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| dc.contributor.author |
Vidal, Marc
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| dc.contributor.author |
André, P |
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| dc.contributor.author |
Rabourdin-Combe, C |
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| dc.contributor.author |
Lotteau, V |
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| dc.date.accessioned |
2010-12-21T16:01:12Z |
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| dc.date.issued |
2008 |
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| dc.identifier.citation |
de Chassey, B., V. Navratil, L. Tafforeau, M. S. Hiet, A. Aublin-Gex, S. Agaugué, G. Meiffren, et al. 2008. Hepatitis C virus infection protein network. Molecular Systems Biology 4: 230. |
en_US |
| dc.identifier.issn |
1744-4292 |
en_US |
| dc.identifier.uri |
http://nrs.harvard.edu/urn-3:HUL.InstRepos:4632528 |
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| dc.description.abstract |
A proteome-wide mapping of interactions between hepatitis C virus (HCV) and human proteins was performed to provide a comprehensive view of the cellular infection. A total of 314 protein–protein interactions between HCV and human proteins was identified by yeast two-hybrid and 170 by literature mining. Integration of this data set into a reconstructed human interactome showed that cellular proteins interacting with HCV are enriched in highly central and interconnected proteins. A global analysis on the basis of functional annotation highlighted the enrichment of cellular pathways targeted by HCV. A network of proteins associated with frequent clinical disorders of chronically infected patients was constructed by connecting the insulin, Jak/STAT and TGFβ pathways with cellular proteins targeted by HCV. CORE protein appeared as a major perturbator of this network. Focal adhesion was identified as a new function affected by HCV, mainly by NS3 and NS5A proteins. |
en_US |
| dc.language.iso |
en_US |
en_US |
| dc.publisher |
Nature Publishing Group |
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| dc.relation.isversionof |
doi:10.1038/msb.2008.66 |
en_US |
| dc.relation.hasversion |
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2600670/pdf/ |
en_US |
| dash.license |
LAA |
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| dc.subject |
functional analysis |
en_US |
| dc.subject |
hepatitis C |
en_US |
| dc.subject |
interactome |
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| dc.subject |
virus–host cell |
en_US |
| dc.title |
Hepatitis C Virus Infection Protein Network |
en_US |
| dc.type |
Journal Article |
en_US |
| dc.description.version |
Version of Record |
en_US |
| dc.relation.journal |
Molecular Systems Biology |
en_US |
| dash.depositing.author |
Vidal, Marc
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| dc.date.available |
2010-12-21T16:01:12Z |
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| dash.affiliation.other |
HMS^Genetics |
en_US |
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