%0 Journal Article %A Johns, Helen L. %A Doceul, Virginie %A Everett, Helen %A Crooke, Helen %A Charleston, Bryan %A Seago, Julian %T The classical swine fever virus N-terminal protease Npro binds to cellular HAX-1 %D 2010 %J Journal of General Virology, %V 91 %N 11 %P 2677-2686 %@ 1465-2099 %R https://doi.org/10.1099/vir.0.022897-0 %I Microbiology Society, %X The positive-stranded RNA genome of classical swine fever virus (CSFV) encodes 12 known proteins. The first protein to be translated is the N-terminal protease (Npro). Npro helps evade the innate interferon response by targeting interferon regulatory factor-3 for proteasomal degradation and also participates in the evasion of dsRNA-induced apoptosis. To elucidate the mechanisms by which Npro functions, we performed a yeast two-hybrid screen in which the anti-apoptotic protein HAX-1 was identified. The Npro–HAX-1 interaction was confirmed using co-precipitation assays. A dramatic redistribution of both Npro and HAX-1 was observed in co-transfected cells, as well as in transfected cells infected with wild-type CSFV, but not in cells infected with an Npro-deleted CSFV strain. %U https://www.microbiologyresearch.org/content/journal/jgv/10.1099/vir.0.022897-0