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• W2100068174 startingPage "e78242" @default.
• W2100068174 abstract "The herpes simplex virus type 1 (HSV-1) immediate early protein, ICP4, participates in the regulation of viral gene expression by both activating and repressing RNA polII transcription. We used affinity purification of ICP4 expressed in infected cells followed by mass spectrometry and western blot analysis to determine the composition of cellular complexes associated with ICP4 throughout infection. ICP4 was associated with TFIID complexes containing a distinct set of TAFs. These complexes were most abundant early, but were detected throughout infection, whereas Mediator was found in ICP4 containing complexes later in infection, indicating a temporal pattern for the utilization of these complexes for the transcription of the viral genome. The form of Mediator copurifying with ICP4 was enriched for the kinase domain and also lacked the activator-specific component, Med26, suggesting that Mediator-ICP4 interactions may be involved in repression of viral transcription. The N-terminal 774 amino acids of ICP4, which retains partial function, were sufficient to form complexes with TFIID and Mediator, although these interactions were not as strong as with full-length ICP4. Additionally, components involved in transcription elongation, chromatin remodeling, and mRNA processing were isolated with ICP4. Together our data indicate that ICP4 plays a more integrated role in mediating HSV transcription, possibly affecting multiple steps in transcription and gene expression." @default.
• W2100068174 created "2016-06-24" @default.
• W2100068174 creator A5067907541 @default.
• W2100068174 creator A5082742080 @default.
• W2100068174 date "2013-10-11" @default.
• W2100068174 modified "2023-10-05" @default.
• W2100068174 title "Temporal Association of Herpes Simplex Virus ICP4 with Cellular Complexes Functioning at Multiple Steps in PolII Transcription" @default.
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• W2100068174 doi "https://doi.org/10.1371/journal.pone.0078242" @default.
• W2100068174 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3795685" @default.
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