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PMID: 16282494 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Inhibition of E2 binding to Brd4 enhances viral genome loss and phenotypic reversion of bovine papillomavirus-transformed cells.

Journal of virology ·Vol. 79 ·No. 23 ·2005-12-00 ·Pages 14956-61

You J, Schweiger MR, Howley PM

Abstract

The bovine papillomavirus E2 protein tethers the viral genomes to mitotic chromosomes in dividing cells through binding to the C-terminal domain (CTD) of Brd4. Expression of the Brd4-CTD competes the binding of E2 to endogenous Brd4 in cells. Here we extend our previous study that identified Brd4 as the E2 mitotic chromosome receptor to show that Brd4-CTD expression released the viral DNA from mitotic chromosomes in BPV-1 transformed cells. Furthermore, stable expression of Brd4-CTD enhanced the frequency of morphological reversion of BPV-1 transformed C127 cells resulting in the complete elimination of the viral DNA in the resulting flat revertants.

MeSH Terms
Animals Binding Sites Bovine papillomavirus 1/chemistry Cell Cycle Proteins Cell Transformation, Viral/physiology Genome, Viral/physiology Nuclear Proteins Oncogene Proteins, Fusion/metabolism Phenotype Transcription Factors
Chemicals
BRD4 protein, human Cell Cycle Proteins Nuclear Proteins Oncogene Proteins, Fusion Transcription Factors
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
You Jianxin
Department of Pathology, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, MA 02115, USA.
Schweiger Michal-Ruth
Howley Peter M
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Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
2005-12-00
Pages
14956-61
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC1287565
Subset
IM
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