Abstract
Brd4 protein has been proposed to act as a cellular receptor for the bovine papillomavirus type 1 (BPV1) E2 protein in the E2-mediated chromosome attachment and mitotic segregation of viral genomes. Here, we provide data that show the involvement of Brd4 in multiple early functions of the BPV1 life cycle, suggest a Brd4-dependent mechanism for E2-dependent transcription activation, and indicate the role of Brd4 in papillomavirus and polyomavirus replication as well as cell-specific utilization of Brd4-linked features in BPV1 DNA replication. Our data also show the potential therapeutic value of the disruption of the E2-Brd4 interaction for the development of antiviral drugs.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Bovine papillomavirus 1 / classification
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Bovine papillomavirus 1 / physiology*
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CHO Cells
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Cattle
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Cell Cycle Proteins
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Cell Line
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Cricetinae
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DNA Replication
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DNA, Viral / genetics
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Electroporation
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Fibroblasts / metabolism
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Fibroblasts / virology
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Genetic Vectors
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Nuclear Proteins
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Oncogene Proteins, Fusion / chemistry
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Oncogene Proteins, Fusion / genetics*
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Oncogene Proteins, Fusion / metabolism*
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Plasmids
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Protein Structure, Tertiary
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Transcription Factors
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Transcriptional Activation
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Virus Replication
Substances
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BRD4 protein, human
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Cell Cycle Proteins
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DNA, Viral
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Nuclear Proteins
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Oncogene Proteins, Fusion
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Transcription Factors