AI Article Synopsis

  • * EBV initiates transcription at nearly 29,674 new genomic sites within the cell, aided by a unique viral pre-initiation complex that requires few additional transcription factors.
  • * The study highlights how EBV uses its own transcription factors to drive new promoters and interact with existing cell promoters, affecting host gene expression and providing insights into fundamental eukaryotic gene regulation.

Article Abstract

Viruses are master remodelers of the host cell environment in support of infection and virus production. For example, viruses typically regulate cell gene expression through modulating canonical cell promoter activity. Here, we show that Epstein Barr virus (EBV) replication causes 'de novo' transcription initiation at 29674 new transcription start sites throughout the cell genome. De novo transcription initiation is facilitated in part by the unique properties of the viral pre-initiation complex (vPIC) that binds a TATT[T/A]AA, TATA box-like sequence and activates transcription with minimal support by additional transcription factors. Other de novo promoters are driven by the viral transcription factors, Zta and Rta and are influenced by directional proximity to existing canonical cell promoters, a configuration that fosters transcription through existing promoters and transcriptional interference. These studies reveal a new way that viruses interact with the host transcriptome to inhibit host gene expression and they shed light on primal features driving eukaryotic promoter function.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11109974PMC
http://dx.doi.org/10.1093/nar/gkae175DOI Listing

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