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Nucleic Acids Res ; 52(9): 5016-5032, 2024 May 22.
Article in English | MEDLINE | ID: mdl-38471819

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.


Subject(s)
Epstein-Barr Virus Infections , Herpesvirus 4, Human , Transcription Initiation, Genetic , Virus Replication , Humans , Herpesvirus 4, Human/physiology , Host-Pathogen Interactions , Promoter Regions, Genetic , TATA Box , Transcription Factors/metabolism , Transcription Initiation Site , Transcription, Genetic , Viral Proteins/metabolism , Viral Proteins/genetics , Epstein-Barr Virus Infections/metabolism , Epstein-Barr Virus Infections/virology
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