Herpesvirus tegument protein activates NF-kappaB signaling through the TRAF6 adaptor protein.
Ontology highlight
ABSTRACT: Viruses remodel the host cell to optimize their replication both by delivery of virion proteins into the cell and by de novo expression of viral proteins. The HSV particle contains several proteins that function to prepare the host cell for viral replication, including the VP16 transcriptional activator protein and virion host shutoff protein. HSV infection activates NF-kappaB pathways through Toll-like receptor (TLR) 2 and non-TLR pathways, and NF-kappaB activity is required for efficient viral replication. In a screen of the HSV proteome, we observed that the HSV U(L)37 tegument protein activates NF-kappaB signaling in a TLR2-independent manner. Expression of U(L)37 in transfected cells leads to IkappaB degradation and activation of both reporter genes and the endogenous IL-8 gene. This
SUBMITTER: Liu X
PROVIDER: S-EPMC2516262 | biostudies-literature | 2008 Aug
REPOSITORIES: biostudies-literature
ACCESS DATA