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The Epstein-Barr Virus BMRF1 Protein Activates Transcription and Inhibits the DNA Damage Response by Binding NuRD
Author(s) -
Samuel Gerald Salamun,
Justine Sitz,
Carlos F. de la Cruz-Herrera,
Jaime Yockteng-Melgar,
Edyta Marcon,
Jack Greenblatt,
Amélie FradetTurcotte,
Lori Frappier
Publication year - 2019
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.01070-19
Subject(s) - biology , transcription (linguistics) , dna binding protein , dna , microbiology and biotechnology , dna damage , virus , transcription factor , virology , genetics , gene , philosophy , linguistics
The Epstein-Barr virus (EBV) BMRF1 protein is critical for EBV infection, playing key roles in viral genome replication, activation of EBV genes, and inhibition of host DNA damage responses (DDRs). Here we show that BMRF1 targets the cellular nucleosome remodeling and deacetylation (NuRD) complex, using a motif in the BMRF1 transcriptional activation sequence. Mutation of this motif disrupts the ability of BMRF1 to activate transcription and interfere with DDRs, showing the importance of the NuRD interaction for BMRF1 functions. BMRF1 was shown to act at the same step in the DDR as NuRD, suggesting that it interferes with NuRD function.

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