@article{mbs:/content/journal/jgv/10.1099/vir.0.007971-0, author = "Wang, Linding and Pietrek, Marcel and Brinkmann, Melanie M. and Hävemeier, Anika and Fischer, Irina and Hillenbrand, Bernd and Dittrich-Breiholz, Oliver and Kracht, Michael and Chanas, Simon and Blackbourn, David J. and Schulz, Thomas F.", title = "Identification and functional characterization of a spliced rhesus rhadinovirus gene with homology to the K15 gene of Kaposi's sarcoma-associated herpesvirus", journal= "Journal of General Virology", year = "2009", volume = "90", number = "5", pages = "1190-1201", doi = "https://doi.org/10.1099/vir.0.007971-0", url = "https://www.microbiologyresearch.org/content/journal/jgv/10.1099/vir.0.007971-0", publisher = "Microbiology Society", issn = "1465-2099", type = "Journal Article", abstract = "Rhesus monkey rhadinovirus (RRV) is a gamma-2 herpesvirus related to the human Kaposi's sarcoma-associated herpesvirus (KSHV or human herpesvirus 8). This study identified an alternatively spliced gene at the right side of the RRV genome (strain 17577) between open reading frame 75 and the terminal repeat region. Of its eight exons, the first seven encoded up to 12 transmembrane domains, whilst the eighth exon encoded a predicted C-terminal cytoplasmic domain. Structurally and positionally, this RRV gene therefore resembles the K15 gene of KSHV; it was provisionally named RK15 to avoid confusion with other RRV17577 genes. In ectopic expression studies, the 55 kDa RK15 protein isoform activated the JNK and NF-κB pathways, like the 45 kDa KSHV K15-encoded protein isoform. In contrast to K15, which activates angiogenic and inflammatory cytokines such as interleukin (IL)-8, IL-6 and CCL20, the range of cellular transcripts activated by the RRV K15 homologue was much more restricted, but included IL-6, IL-8 and FGF21. These data suggest functional differences between terminal membrane proteins at the right end of the genomes of Old World primate gamma-2 herpesviruses.", }