The bICP0 protein encoded by bovine herpesvirus 1 stimulates productive infection and viral gene expression but inhibits interferon (IFN)-dependent transcription. bICP0 inhibits beta IFN (IFN-beta) promoter activity and induces degradation of IFN regulatory factor 3 (IRF3). Although bICP0 inhibits the trans-activation activity of IRF7, IRF7 protein levels are not reduced. In this study, we demonstrate that bICP0 is associated with IRF7. Furthermore, bICP0 inhibits the ability of IRF7 to trans-activate the IFN-beta promoter in the absence of IRF3 expression. The interaction between bICP0 and IRF7 correlates with reduced trans-activation of the IFN-beta promoter by IRF7.
The infected cell protein 0 encoded by bovine herpesvirus 1 (bICP0) associates with interferon regulatory factor 7 and consequently inhibits beta interferon promoter activity.
牛疱疹病毒 1 型 (bICP0) 编码的感染细胞蛋白 0 与干扰素调节因子 7 结合,从而抑制 β 干扰素启动子活性
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作者:Saira Kazima, Zhou You, Jones Clinton
| 期刊: | Journal of Virology | 影响因子: | 3.800 |
| 时间: | 2009 | 起止号: | 2009 Apr;83(8):3977-81 |
| doi: | 10.1128/JVI.02400-08 | 种属: | Bovine |
| 研究方向: | 细胞生物学 | 疾病类型: | 疱疹 |
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