Proceedings of the National Academy of Sciences · 2005 · 585 citations · 44 references
Life SciencesMicrobiologyMolecular BiologyImmunology Of Infectious DiseasesMolecular VirologyVirologyKaposi SarcomaMicrorna BiologyOncogenic VirusesViral InfectionsViral LatencyViral PersistenceLatency-associated MicrornasLatency-associated Transcripts
MicroRNAs are small endogenous RNAs that regulate gene expression, and their compact size makes them attractive tools for viruses to suppress host defense pathways. The authors propose that KSHV‑encoded miRNAs are essential for establishing or maintaining viral latency and driving oncogenesis. Computational target prediction revealed that these miRNAs potentially downregulate several host mRNAs already known to be suppressed during KSHV infection. KSHV expresses an array of 11 miRNAs from a single ~4‑kb noncoding locus, with individual miRNAs reaching up to 2,200 copies per cell in latently infected cells.
MicroRNAs (miRNAs) are an endogenously encoded class of small RNAs that have been proposed to function as key posttranscriptional regulators of gene expression in a range of eukaryotic species, including humans. The small size of miRNA precursors makes them potentially ideal for use by viruses as inhibitors of host cell defense pathways. Here, we demonstrate that the pathogenic human herpesvirus Kaposi's sarcoma-associated herpesvirus (KSHV) encodes an array of 11 distinct miRNAs, all of which are expressed at readily detectable levels in latently KSHV infected cells. Individual KSHV miRNAs were expressed at up to 2,200 copies per cell. The KSHV miRNAs are expressed from what appears to be a single genetic locus that largely coincides with an ≈4-kb noncoding sequence located between the KSHV v-cyclin and K12 / Kaposin genes, both of which are also expressed in latently infected cells. Computer analysis of potential mRNA targets for these viral miRNAs identified a number of interesting candidate genes, including several mRNAs previously shown to be down-regulated in KSHV-infected cells. We hypothesize that these viral miRNAs play a critical role in the establishment and/or maintenance of KSHV latent infection in vivo and, hence, in KSHV-induced oncogenesis.
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