4.6 Article

Inhibition of interferon signaling by the Kaposi's sarcoma-associated herpesvirus full-length viral interferon regulatory factor 2 protein

期刊

JOURNAL OF VIROLOGY
卷 80, 期 6, 页码 3092-3097

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.80.6.3092-3097.2006

关键词

-

类别

资金

  1. MRC [MC_U130184136] Funding Source: UKRI
  2. Medical Research Council [MC_U130184136] Funding Source: researchfish
  3. Medical Research Council [MC_UU_12014/3, MC_U130184136] Funding Source: Medline
  4. Wellcome Trust [059008/Z/99/Z] Funding Source: Medline

向作者/读者索取更多资源

Interferon (IFN) signal transduction involves interferon regulatory factors (IRF). Kaposi's sarcoma-associated herpesvirus (KSHV) encodes four IRF homologues: viral IRF 1 (vIRF-1) to vIRF-4. Previous functional studies revealed that the first exon of vIRF-2 inhibited alpha/beta interferon (IFN-alpha/beta) signaling. We now show that full-length vIRF-2 protein, translated from two spliced exons, inhibited both IFN-alpha- and IFN-lambda-driven transactivation of a reporter promoter containing the interferon stimulated response element (ISRE). Transactivation of the ISRE promoter by IRF-1 was negatively regulated by vIRF-2 protein as well. Transactivation of a full-length IFN-beta reporter promoter by either IRF-3 or IRF-1, but not IRF-7, was also inhibited by vIRF-2 protein. Thus, vIRF-2 protein is an interferon induction antagonist that acts pleiotropically, presumably facilitating KSHV infection and dissemination in vivo.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据