Bai Zhiqiang, Huang Yufei, Li Wan, Zhu Ying, Jung Jae U, Lu Chun, Gao Shou-Jiang
Department of Immunology and Microbiology, Nanjing Medical University, Nanjing, China.
J Virol. 2014 Jan;88(1):377-92. doi: 10.1128/JVI.02689-13. Epub 2013 Oct 23.
Kaposi's sarcoma-associated herpesvirus (KSHV) encodes over 90 genes and 25 microRNAs (miRNAs). The KSHV life cycle is tightly regulated to ensure persistent infection in the host. In particular, miRNAs, which primarily exert their effects by binding to the 3' untranslated regions (3'UTRs) of target transcripts, have recently emerged as key regulators of KSHV life cycle. Although studies with RNA cross-linking immunoprecipitation approach have identified numerous targets of KSHV miRNAs, few of these targets are of viral origin because most KSHV 3'UTRs have not been characterized. Thus, the extents of viral genes targeted by KSHV miRNAs remain elusive. Here, we report the mapping of the 3'UTRs of 74 KSHV genes and the effects of KSHV miRNAs on the control of these 3'UTR-mediated gene expressions. This analysis reveals new bicistronic and polycistronic transcripts of KSHV genes. Due to the 5'-distal open reading frames (ORFs), KSHV bicistronic or polycistronic transcripts have significantly longer 3'UTRs than do KSHV monocistronic transcripts. Furthermore, screening of the 3'UTR reporters has identified 28 potential new targets of KSHV miRNAs, of which 11 (39%) are bicistronic or polycistronic transcripts. Reporter mutagenesis demonstrates that miR-K3 specifically targets ORF31-33 transcripts at the lytic locus via two binding sites in the ORF33 coding region, whereas miR-K10a-3p and miR-K10b-3p and their variants target ORF71-73 transcripts at the latent locus through distinct binding sites in both 5'-distal ORFs and intergenic regions. Our results indicate that KSHV miRNAs frequently target the 5'-distal coding regions of bicistronic or polycistronic transcripts and highlight the unique features of KSHV miRNAs in regulating gene expression and life cycle.
卡波西肉瘤相关疱疹病毒(KSHV)编码90多个基因和25个微小RNA(miRNA)。KSHV的生命周期受到严格调控,以确保在宿主体内持续感染。特别是,miRNA主要通过与靶转录本的3'非翻译区(3'UTR)结合发挥作用,最近已成为KSHV生命周期的关键调节因子。尽管采用RNA交联免疫沉淀方法的研究已经确定了KSHV miRNA的众多靶标,但这些靶标中很少有病毒来源的,因为大多数KSHV 3'UTR尚未得到表征。因此,KSHV miRNA靶向的病毒基因范围仍然不清楚。在这里,我们报告了74个KSHV基因的3'UTR图谱以及KSHV miRNA对这些3'UTR介导的基因表达控制的影响。该分析揭示了KSHV基因新的双顺反子和多顺反子转录本。由于5'端远端开放阅读框(ORF),KSHV双顺反子或多顺反子转录本的3'UTR比KSHV单顺反子转录本长得多。此外,对3'UTR报告基因的筛选确定了28个KSHV miRNA潜在的新靶标,其中11个(39%)是双顺反子或多顺反子转录本。报告基因诱变表明,miR-K3通过ORF33编码区的两个结合位点特异性靶向裂解位点的ORF31-33转录本,而miR-K10a-3p和miR-K10b-3p及其变体通过5'端远端ORF和基因间区域中不同的结合位点靶向潜伏位点的ORF71-73转录本。我们的结果表明,KSHV miRNA经常靶向双顺反子或多顺反子转录本的5'端远端编码区,并突出了KSHV miRNA在调节基因表达和生命周期方面的独特特征。