Donaldson Mary M, Boner Winifred, Morgan Iain M
Institute of Comparative Medicine, Division of Pathological Sciences, University of Glasgow Faculty of Veterinary Medicine, Bearsden Road, Glasgow, G61 1QH Scotland.
J Virol. 2007 Apr;81(8):4338-42. doi: 10.1128/JVI.02353-06. Epub 2007 Feb 7.
Human papillomavirus type 16 (HPV16) E2 regulates transcription from and replication of the viral genome, in association with viral and cellular factors. HPV16 E2 interacts functionally with TopBP1, a cellular protein essential for the initiation of cellular, and potentially viral, DNA replication. This report demonstrates that the absence of TopBP1 results in the redistribution of HPV16 E2 into an alternative cellular protein complex, resulting in enhanced affinity for chromatin. This redistribution does not significantly alter the ability of HPV16 E2 to either activate or repress transcription. We also show colocalization of both proteins on chromatin at late stages of mitosis, suggesting that TopBP1 could be the mitotic chromatin receptor for HPV16 E2. The possible significance of the results for the regulation of the viral life cycle is discussed.
16型人乳头瘤病毒(HPV16)E2蛋白与病毒及细胞因子共同作用,调节病毒基因组的转录和复制。HPV16 E2蛋白与TopBP1在功能上相互作用,TopBP1是一种对细胞DNA复制起始至关重要的细胞蛋白,对病毒DNA复制可能也很关键。本报告表明,缺乏TopBP1会导致HPV16 E2重新分布到另一种细胞蛋白复合物中,从而增强其对染色质的亲和力。这种重新分布不会显著改变HPV16 E2激活或抑制转录的能力。我们还显示,在有丝分裂后期,这两种蛋白在染色质上共定位,提示TopBP1可能是HPV16 E2的有丝分裂染色质受体。本文讨论了这些结果对病毒生命周期调节的潜在意义。