Transcripts encoding K12, v-FLIP, v-cyclin, and the microRNA cluster of Kaposi's sarcoma-associated herpesvirus originate from a common promoter

M Pearce, S Matsumura, AC Wilson - Journal of virology, 2005 - Am Soc Microbiol
M Pearce, S Matsumura, AC Wilson
Journal of virology, 2005Am Soc Microbiol
Kaposi's sarcoma-associated herpesvirus (KSHV) is the causative agent of three
malignancies associated with AIDS and immunosuppression. Tumor cells harbor latent virus
and express kaposin (open reading frame [ORF] K12), v-FLIP (ORF 71), v-Cyclin (ORF 72),
and latency-associated nuclear antigen (LANA; ORF 73). ORFs 71 to 73 are transcribed as
multicistronic RNAs initiating from adjacent constitutive and inducible promoters upstream of
ORF 73. Here we characterize a third promoter embedded within the ORF 71-to-73 …
Abstract
Kaposi's sarcoma-associated herpesvirus (KSHV) is the causative agent of three malignancies associated with AIDS and immunosuppression. Tumor cells harbor latent virus and express kaposin (open reading frame [ORF] K12), v-FLIP (ORF 71), v-Cyclin (ORF 72), and latency-associated nuclear antigen (LANA; ORF 73). ORFs 71 to 73 are transcribed as multicistronic RNAs initiating from adjacent constitutive and inducible promoters upstream of ORF 73. Here we characterize a third promoter embedded within the ORF 71-to-73 transcription unit specifying transcripts that encode ORF 71/72 or K12. These transcripts may also be the source of 11 microRNAs arranged as a cluster between K12 and ORF 71. Our studies reveal a complex arrangement of interlaced transcription units, incorporating four important protein-encoding genes required for latency and pathogenesis and the entire KSHV microRNA repertoire.
American Society for Microbiology