MicroRNAs encoded by Kaposi's sarcoma-associated herpesvirus regulate viral life cycle

被引:77
|
作者
Lu, Chih-Chung [1 ]
Li, Zhonghan [1 ]
Chu, Chia-Ying [1 ]
Feng, Jiaying [2 ]
Feng, Jun [2 ]
Sun, Ren [2 ]
Rana, Tariq M. [1 ]
机构
[1] Sanford Burnham Med Res Inst, Program RNA Biol, La Jolla, CA 92037 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
KSHV; miRNA; viral life cycle; RISC; REPLICATION-ASSOCIATED PROTEIN; DNA-REPLICATION; CELL-CYCLE; LYTIC REPLICATION; GENE; TRANSCRIPTION; EXPRESSION; BINDING; IDENTIFICATION; ACTIVATION;
D O I
10.1038/embor.2010.132
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
Kaposi's sarcoma-associated herpesvirus (KSHV) is linked with Kaposi's sarcoma and lymphomas. The pathogenesis of KSHV depends on the balance between two phases of the viral cycle: latency and lytic replication. In this study, we report that KSHV-encoded microRNAs (miRNAs) function as regulators by maintaining viral latency and inhibiting viral lytic replication. MiRNAs are short, noncoding, small RNAs that post-transcriptionally regulate the expression of messenger RNAs. Of the 12 viral miRNAs expressed in latent KSHV-infected cells, we observed that expression of miR-K3 can suppress both viral lytic replication and gene expression. Further experiments indicate that miR-K3 can regulate viral latency by targeting nuclear factor I/B. Nuclear factor I/B can activate the promoter of the viral immediate-early transactivator replication and transcription activator (RTA), and depletion of nuclear factor I/B by short hairpin RNAs had similar effects on the viral life cycle to those of miR-K3. Our results suggest a role for KSHV miRNAs in regulating the viral life cycle.
引用
收藏
页码:784 / 790
页数:7
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