Schäfer Alexandra, Cai Xuezhong, Bilello John P, Desrosiers Ronald C, Cullen Bryan R
Department of Molecular Genetics and Microbiology and Center for Virology, Duke University Medical Center, Durham, NC 27710, USA.
Virology. 2007 Jul 20;364(1):21-7. doi: 10.1016/j.virol.2007.03.029. Epub 2007 Apr 23.
Several pathogenic human herpesviruses have recently been shown to express virally encoded microRNAs in infected cells. Although the function of these microRNAs is largely unknown, they are hypothesized to play a role in mediating viral replication by downregulating cellular mRNAs encoding antiviral factors. Here, we report the cloning and analysis of microRNAs encoded by Rhesus Monkey Rhadinovirus (RRV), an animal virus model for the pathogenic human gamma-herpesvirus Kaposi's Sarcoma-Associated Herpesvirus (KSHV). RRV expresses several microRNAs that are encoded in the same genomic location as the previously reported KSHV microRNAs, yet these microRNAs are unrelated in primary sequence. These data set the stage for the mutational ablation and phenotypic analysis of RRV mutants lacking one or more viral microRNAs.
最近有研究表明,几种致病性人类疱疹病毒可在受感染细胞中表达病毒编码的微小RNA。尽管这些微小RNA的功能大多未知,但据推测它们通过下调编码抗病毒因子的细胞信使核糖核酸(mRNA)来介导病毒复制。在此,我们报告了恒河猴嗜淋巴病毒(RRV)编码的微小RNA的克隆与分析,RRV是致病性人类γ-疱疹病毒卡波西肉瘤相关疱疹病毒(KSHV)的动物病毒模型。RRV表达的几种微小RNA与先前报道的KSHV微小RNA位于相同的基因组位置,但这些微小RNA的一级序列并无关联。这些数据为缺乏一种或多种病毒微小RNA的RRV突变体的突变消除和表型分析奠定了基础。