Program for RNA Biology, Sanford-Burnham Medical Research Institute, 10901 North Torrey Pines Road, La Jolla, California 92037, USA.
EMBO Rep. 2010 Oct;11(10):784-90. doi: 10.1038/embor.2010.132. Epub 2010 Sep 17.
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.
卡波氏肉瘤相关疱疹病毒(KSHV)与卡波氏肉瘤和淋巴瘤有关。KSHV 的发病机制取决于病毒周期的两个阶段之间的平衡:潜伏期和裂解复制。在这项研究中,我们报告 KSHV 编码的 microRNAs(miRNAs)通过维持病毒潜伏期和抑制病毒裂解复制来发挥调节作用。miRNAs 是短的、非编码的、小的 RNA,通过转录后调节信使 RNA 的表达。在潜伏的 KSHV 感染细胞中表达的 12 种病毒 miRNA 中,我们观察到 miR-K3 的表达可以抑制病毒的裂解复制和基因表达。进一步的实验表明,miR-K3 可以通过靶向核因子 I/B 来调节病毒潜伏期。核因子 I/B 可以激活病毒即刻早期转录激活剂复制和转录激活剂(RTA)的启动子,而短发夹 RNA 对核因子 I/B 的耗竭对病毒生命周期的影响与 miR-K3 相似。我们的结果表明 KSHV miRNAs 在调节病毒生命周期中发挥作用。