Mutant Cellular AP-1 Proteins Promote Expression of a Subset of Epstein-Barr Virus Late Genes in the Absence of Lytic Viral DNA Replication
Author(s) -
Danielle E. Lyons,
Kuan-Ping Yu,
Jason A. Vander Heiden,
Lee Heston,
Dirk P. Dittmer,
Ayman ElGuindy,
George Miller
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.01062-18
Subject(s) - lytic cycle , biology , dna replication factor cdt1 , viral replication , gene , viral structural protein , dna replication , transcription (linguistics) , mutant , viral entry , gene expression , control of chromosome duplication , microbiology and biotechnology , virology , genetics , virus , linguistics , philosophy
Mutant c-Jun and c-Fos proteins selectively activate expression of EBV lytic genes, including a subgroup of viral late genes, in the absence of viral DNA replication. These findings indicate that newly synthesized viral DNA is not invariably required for viral late gene expression. While viral DNA replication may be obligatory for late gene expression driven by viral transcription factors, it does not limit the ability of cellular transcription factors to activate expression of some viral late genes. Our results show that expression of all late genes may not be strictly dependent on viral lytic DNA replication. The c-Fos A151S mutation has been identified in a human cancer. c-Fos A151S in combination with wild-type c-Jun activates the EBV lytic cycle. Our data provide proof of principle that mutant cellular transcription factors could cause aberrant regulation of viral lytic cycle gene expression and play important roles in EBV-associated diseases.
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