4.6 Article

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

Journal

JOURNAL OF VIROLOGY
Volume 79, Issue 22, Pages 14457-14464

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.79.22.14457-14464.2005

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Funding

  1. NIGMS NIH HHS [GM61139-04, R01 GM061139] Funding Source: Medline

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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.

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