Department of Microbiology, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA, USA.
J Virol. 2013 Mar;87(6):3461-70. doi: 10.1128/JVI.02746-12. Epub 2013 Jan 9.
In both mammalian and viral genomes, a large proportion of sequences are transcribed and annotated as noncoding RNAs. A polyadenylated RNA of 3.0 kb (T3.0) is transcribed from the opposite strand of the open reading frame 50 (ORF50) DNA template in the genome of Kaposi's sarcoma-associated herpesvirus (KSHV) and has been annotated previously as a noncoding RNA. ORF50 encodes the replication and transcription activator (RTA), which controls the switch of the virus between the latent and lytic phases of the life cycle. Here we show that T3.0 encodes a small peptide of 48 amino acids (designated viral small peptide 1 [vSP-1]). vSP-1 interacts with RTA at the protein abundance regulatory signal (PARS) motifs, and the association prevents RTA from being subjected to degradation through the ubiquitin-proteasome pathway. As a consequence, vSP-1 facilitates KSHV gene expression and lytic replication. This finding reveals a novel mechanism of gene regulation in the viral life cycle.
在哺乳动物和病毒基因组中,很大一部分序列被转录并注释为非编码 RNA。从卡波济肉瘤相关疱疹病毒 (KSHV) 基因组中开放阅读框 50 (ORF50) DNA 模板的反义链转录出一个 3.0 kb 的多聚腺苷酸化 RNA (T3.0),先前已将其注释为非编码 RNA。ORF50 编码复制和转录激活剂 (RTA),它控制病毒在生命周期潜伏和裂解阶段之间的转换。在这里,我们表明 T3.0 编码一个 48 个氨基酸的小肽 (命名为病毒小肽 1 [vSP-1])。vSP-1 在蛋白丰度调节信号 (PARS) 基序上与 RTA 相互作用,这种结合阻止 RTA 通过泛素-蛋白酶体途径降解。因此,vSP-1 促进了 KSHV 的基因表达和裂解复制。这一发现揭示了病毒生命周期中基因调控的一种新机制。