Dittmer D, Lagunoff M, Renne R, Staskus K, Haase A, Ganem D
Department of Microbiology and Immunology, University of California San Francisco, San Francisco, California 94143-0414, USA.
J Virol. 1998 Oct;72(10):8309-15. doi: 10.1128/JVI.72.10.8309-8315.1998.
Infection with Kaposi's sarcoma-associated herpesvirus (KSHV) is closely associated with Kaposi's sarcoma (KS) and primary effusion lymphoma, with viral genomes present in a latent state in the majority of tumor cells. Here we describe a cluster of latently expressed viral genes whose mRNAs are generated from a common promoter. Two mRNAs in this region encode the latency-associated nuclear antigen, the product of open reading frame 73 (ORF73). The larger RNA, of 5.8 kb, is an unspliced transcript that includes ORF72 and -71 at its 3' end; it initiates at nucleotides (nt) 127880 to 127886 from a promoter lacking recognizable TATA elements. A less abundant mRNA, of 5.4 kb, is a variant of this transcript, in which 336 nt of 5' noncoding information has been removed by RNA splicing. A third, more abundant RNA is generated from the same promoter region via splicing from the common splice donor at nt 127813 to an acceptor 5' to ORF72; this transcript is the presumed mRNA for ORF72, which encodes the viral cyclin D homolog. All three RNAs are 3' coterminal. In situ hybridization analysis with probes that can detect all three transcripts shows that the RNAs are detectable in a large fraction of BCBL-1 cells prior to lytic induction and in >70% of KS spindle cells in primary KS tumors. This confirms that these transcripts are indeed latent RNAs and suggests a role for their products in viral persistence and/or KSHV-associated proliferation.
卡波西肉瘤相关疱疹病毒(KSHV)感染与卡波西肉瘤(KS)和原发性渗出性淋巴瘤密切相关,病毒基因组在大多数肿瘤细胞中呈潜伏状态存在。在此,我们描述了一组潜伏表达的病毒基因,其mRNA由一个共同的启动子产生。该区域的两个mRNA编码潜伏相关核抗原,即开放阅读框73(ORF73)的产物。较大的RNA为5.8 kb,是一种未剪接的转录本,其3'端包含ORF72和-71;它从一个缺乏可识别TATA元件的启动子的核苷酸(nt)127880至127886处起始。一种含量较少的mRNA为5.4 kb,是该转录本的一个变体,其中5'非编码信息的336 nt已通过RNA剪接去除。第三种含量较多的RNA通过从nt 127813处的共同剪接受体剪接到ORF72的5'端受体,从同一启动子区域产生;该转录本被认为是ORF72的mRNA,ORF72编码病毒细胞周期蛋白D同源物。所有三种RNA的3'端是共末端的。用能检测所有三种转录本的探针进行原位杂交分析表明,在裂解诱导前,大部分BCBL-1细胞中可检测到这些RNA,在原发性KS肿瘤的>70%的KS梭形细胞中也可检测到。这证实了这些转录本确实是潜伏RNA,并提示它们的产物在病毒持续存在和/或KSHV相关增殖中起作用。