Kanginakudru Sriramana, DeSmet Marsha, Thomas Yanique, Morgan Iain M, Androphy Elliot J
Department of Dermatology, Indiana University School of Medicine, Indianapolis, IN, USA.
Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN, USA.
Virology. 2015 Apr;478:129-35. doi: 10.1016/j.virol.2015.01.011. Epub 2015 Feb 7.
The evolutionarily conserved DNA topoisomerase II beta-binding protein 1 (TopBP1) functions in DNA replication, DNA damage response, and cell survival. We analyzed the role of TopBP1 in human and bovine papillomavirus genome replication. Consistent with prior reports, TopBP1 co-localized in discrete nuclear foci and was in complex with papillomavirus E2 protein. Similar to E2, TopBP1 is recruited to the region of the viral origin of replication during G1/S and early S phase. TopBP1 knockdown increased, while over-expression decreased transient virus replication, without affecting cell cycle. Similarly, using cell lines harboring HPV-16 or HPV-31 genome, TopBP1 knockdown increased while over-expression reduced viral copy number relative to genomic DNA. We propose a model in which TopBP1 serves dual roles in viral replication: it is essential for initiation of replication yet it restricts viral copy number.
进化上保守的DNA拓扑异构酶IIβ结合蛋白1(TopBP1)在DNA复制、DNA损伤反应和细胞存活中发挥作用。我们分析了TopBP1在人乳头瘤病毒和牛乳头瘤病毒基因组复制中的作用。与先前的报道一致,TopBP1共定位于离散的核灶,并与乳头瘤病毒E2蛋白形成复合物。与E2相似,TopBP1在G1/S期和S期早期被招募到病毒复制起点区域。敲低TopBP1会增加瞬时病毒复制,而过表达则会减少瞬时病毒复制,且不影响细胞周期。同样,使用携带HPV-16或HPV-31基因组的细胞系,相对于基因组DNA,敲低TopBP1会增加病毒拷贝数,而过表达则会减少病毒拷贝数。我们提出了一个模型,其中TopBP1在病毒复制中发挥双重作用:它对于复制起始至关重要,但它会限制病毒拷贝数。