A cluster of latently expressed genes in Kaposi's sarcoma-associated herpesvirus

D Dittmer, M Lagunoff, R Renne, K Staskus… - Journal of …, 1998 - Am Soc Microbiol
D Dittmer, M Lagunoff, R Renne, K Staskus, A Haase, D Ganem
Journal of virology, 1998Am Soc Microbiol
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 …
Abstract
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.
American Society for Microbiology