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ORF45-Mediated Prolonged c-Fos Accumulation Accelerates Viral Transcription during the Late Stage of Lytic Replication of Kaposi's Sarcoma-Associated Herpesvirus.

Xiaojuan LiShumin DuDenis AveyYuqing LiFanxiu ZhuErsheng Kuang
Published in: Journal of virology (2015)
During KSHV lytic replication, transient activation and sustained activation of ERK-RSK induce viral immediate early (IE) transcription and late transcription, respectively. Studies have revealed that ERK-RSK activates several transcription factors involved in IE gene expression, including Ets, AP-1, CREB, and C/EBP, which lead to the transient ERK-RSK activation-dependent IE transcription. Whereas c-Fos acts as a sensor of sustained ERK-RSK activation, ORF45-ERK-RSK signaling mediates c-Fos phosphorylation and accumulation during late KSHV lytic replication, consequently promoting viral transcription through the direct binding of c-Fos to multiple KSHV promoters. This finding indicates that c-Fos mediates distinct viral transcriptional progression following sustained ERK-RSK signaling during the KSHV lytic life cycle.
Keyphrases
  • transcription factor
  • signaling pathway
  • pi k akt
  • cell proliferation
  • gene expression
  • sars cov
  • dna binding
  • dna methylation
  • life cycle
  • oxidative stress
  • genome wide identification
  • cerebral ischemia
  • single cell