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A Screen for Epstein-Barr Virus Proteins That Inhibit the DNA Damage Response Reveals a Novel Histone Binding Protein
Author(s) -
TingHin Ho,
Justine Sitz,
Qingtang Shen,
Ariane Leblanc-Lacroix,
Eric I. Campos,
Ivan Borozan,
Edyta Marcon,
Jack Greenblatt,
Amélie FradetTurcotte,
DongYan Jin,
Lori Frappier
Publication year - 2018
Publication title -
journal of virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.617
H-Index - 292
eISSN - 1070-6321
pISSN - 0022-538X
DOI - 10.1128/jvi.00262-18
Subject(s) - lytic cycle , biology , histone , epstein–barr virus , ubiquitin ligase , chromatin , virus , dna damage , gammaherpesvirinae , non histone protein , ubiquitin , microbiology and biotechnology , virology , dna , cancer research , herpesviridae , genetics , gene , viral disease
Epstein-Barr virus (EBV) infects most people worldwide and is causatively associated with several types of cancer, including ∼10% of gastric carcinomas. EBV encodes ∼80 proteins, many of which are believed to manipulate cellular regulatory pathways but are poorly characterized. The DNA damage response (DDR) is one such pathway that is critical for maintaining genome integrity and preventing cancer-associated mutations. In this study, a screen for EBV proteins that inhibit the DDR identified BKRF4 as a DDR inhibitor that binds histones and blocks their ubiquitylation at the DNA damage sites. We also present evidence that BKRF4 is expressed in both latent and lytic forms of EBV infection, where it downregulates the DDR, as well as in EBV-positive gastric tumors. The results suggest that BKRF4 could contribute to the development of gastric carcinoma through its ability to inhibit the DDR.

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