Viral reprogramming of host transcription initiation

Author:

Ungerleider Nathan A1,Roberts Claire1,O’Grady Tina M1ORCID,Nguyen Trang T1,Baddoo Melody1,Wang Jia1,Ishaq Eman1,Concha Monica1,Lam Meggie1,Bass Jordan1,Nguyen Truong D1,Van Otterloo Nick1,Wickramarachchige-Dona Nadeeshika1,Wyczechowska Dorota2,Morales Maria3,Ma Tianfang4ORCID,Dong Yan5ORCID,Flemington Erik K1ORCID

Affiliation:

1. Department of Pathology & Laboratory Medicine, Tulane University School of Medicine, Tulane Cancer Center , New Orleans , LA , USA

2. Stanley S. Scott Cancer Center, Louisiana State University Health Sciences Center , New Orleans , LA , USA

3. Tulane Cancer Center , New Orleans , LA , USA

4. Dana-Farber Cancer Institute , Boston , MA , USA

5. Department of Structural and Cellular Biology, Tulane University School of Medicine, Tulane Cancer Center , New Orleans , LA , USA

Abstract

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.

Funder

National Institutes of Health

Department of Defense

The Leukemia & Lymphoma Society

Publisher

Oxford University Press (OUP)

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