B cell terminal differentiation factor XBP-1 induces reactivation of Kaposi's sarcoma-associated herpesvirus

被引:55
|
作者
Yu, Fuqu
Feng, Jiaying
Harada, Josephine N.
Chanda, Sumit K.
Kenney, Shannon C.
Sun, Ren
机构
[1] Univ Calif Los Angeles, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
[2] Zhejiang Univ, Dept Bioengn, Hangzhou, Peoples R China
[3] Novartis Res Fdn, Genom Inst, San Diego, CA 92121 USA
[4] Univ Wisconsin, Sch Med & Publ Hlth, Dept Med, Madison, WI 53706 USA
关键词
KSHV; reactivation; XBP-1;
D O I
10.1016/j.febslet.2007.06.056
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The herpesvirus life cycle has two distinct phases: latency and lytic replication. The viral immediate early protein replication and transcription activator (RTA) plays a central role in mediating the balance between these two phases. Here, we demonstrate that a B cell terminal differentiation factor X-box binding protein 1 (XBP-1) can effectively initiates Kaposi's sarcoma-associated herpesvirus (KSHV) reactivation by activating the RTA promoter, which results in the induction of other viral lytic transcripts. We also showed splicing of the XBP-1 mRNA which specifically occurs during B cell differentiation is critical in triggering KSHV reactivation. This work demonstrates the integration of KSHV reactivation mechanisms with host cell differentiation. (c) 2007 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:3485 / 3488
页数:4
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