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Article Dans Une Revue Molecular Systems Biology Année : 2008

Hepatitis C virus infection protein network.

P. O. Vidalain

Résumé

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 TGFbeta 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.
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Dates et versions

pasteur-00456466 , version 1 (15-02-2010)

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Paternité

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B. de Chassey, V. Navratil, L. Tafforeau, M. S. Hiet, A. Aublin-Gex, et al.. Hepatitis C virus infection protein network.. Molecular Systems Biology, 2008, 4 (230), pp.230. ⟨10.1038/msb.2008.66⟩. ⟨pasteur-00456466⟩
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