| Literature DB >> 22832122 |
Takatoshi Nawa1, Hisashi Ishida, Tomohide Tatsumi, Wei Li, Satoshi Shimizu, Takahiro Kodama, Hayato Hikita, Atsushi Hosui, Takuya Miyagi, Tatsuya Kanto, Naoki Hiramatsu, Norio Hayashi, Tetsuo Takehara.
Abstract
HBV has two enhancer (En) regions each of which promotes its own transcription. En II regulates production of pregenomic RNA, a key product of HBV replication, more strongly than En I. Although IFN-α has been found to suppress En I activity, its effect on En II activity has not been examined. Here we used luciferase assay to demonstrate that IFN-α suppresses En II activity. Analysis with several deletion/mutation constructs identified two major segments, nt 1703-1727 and nt 1746-1770, within the En II sequence as being responsible for the suppressive effects of IFN-α. Pre-treatment with protein kinase C (PKC) inhibitors blocked this effect regardless of the expression levels of phospho-STAT1 and Mx upon IFN-α stimulation. These results indicate that IFN-α suppresses En II activity via the PKC pathway, which may be an alternative suppressive pathway for HBV replication. (136 words).Entities:
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Year: 2012 PMID: 22832122 DOI: 10.1016/j.virol.2012.07.002
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616