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抑制E2与Brd4的结合可增强牛乳头瘤病毒转化细胞的病毒基因组丢失和表型逆转。

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

作者信息

You Jianxin, Schweiger Michal-Ruth, Howley Peter M

机构信息

Department of Pathology, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, MA 02115, USA.

出版信息

J Virol. 2005 Dec;79(23):14956-61. doi: 10.1128/JVI.79.23.14956-14961.2005.

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.

摘要

牛乳头瘤病毒E2蛋白通过与Brd4的C端结构域(CTD)结合,将病毒基因组与分裂细胞中的有丝分裂染色体相连。Brd4-CTD的表达在细胞中竞争E2与内源性Brd4的结合。在此,我们扩展了之前将Brd4鉴定为E2有丝分裂染色体受体的研究,以表明Brd4-CTD的表达使BPV-1转化细胞中有丝分裂染色体上的病毒DNA释放出来。此外,Brd4-CTD的稳定表达提高了BPV-1转化的C127细胞形态逆转的频率,导致所得扁平回复株中的病毒DNA完全消除。

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