Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2050049 | FEBS Letters | 2008 | 5 Pages |
Abstract
Kaposi’s sarcoma-associated herpesvirus ‘replication transcriptional activator’ (Rta) plays a critical role in the switch from latency to lytic replication. Rta upregulates several lytic KSHV genes, including its own, through multiple mechanisms. We demonstrate that cellular HMGB1 binds and synergistically upregulates the ORF50 promoter in conjunction with Rta. No direct interaction between Rta and HMGB1 was observed, however a ternary complex is formed in the presence of Oct1. Furthermore, deletion of an Oct-1 binding site within the ORF50 promoter ablates the HMGB1-mediated synergistic response. These results suggest Rta autostimulation may be mediated by a transient complex involving Oct1 and HMGB1.
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Authors
Sally M. Harrison, Adrian Whitehouse,