Swindle C S, Engler J A
Department of Biochemistry and Molecular Genetics, Schools of Medicine and Dentistry, University of Alabama at Birmingham, 35294-0005, USA.
J Virol. 1998 Mar;72(3):1994-2001. doi: 10.1128/JVI.72.3.1994-2001.1998.
The E1 and E2 proteins are the only virus-encoded factors required for human papillomavirus (HPV) DNA replication. The E1 protein is a DNA helicase responsible for initiation of DNA replication at the viral origin. Its recruitment to the origin is facilitated by binding to E2, for which specific recognition elements are located at the origin. The remaining replication functions for the virus, provided by the host cell's replication machinery, may be mediated by further interactions with E1 and E2. Histone H1 was identified as an HPV type 11 (HPV-11) E1-binding protein by far-Western blotting and by microsequence analyses of a 34-kDa protein purified by E1 affinity chromatography. E1 also bound in vitro to H1 isolated under native conditions in association with intact nucleosomes. In addition, E1 and H1 were coimmunoprecipitated by an E1 antiserum from a nuclear extract prepared from cells expressing recombinant E1. Bound H1 was displaced from HPV-11 DNA by the addition of E1, suggesting that E1 can promote replication initiation and elongation by alteration of viral chromatin structure and disruption of nucleosomes at the replication fork. Furthermore, a region of the HPV-11 genome containing the origin of replication was identified which had weaker affinity for H1 than that of the remaining genome. This result suggests that the presence of a DNA structure at or near the HPV origin facilitates initiation of DNA replication by exclusion of H1. These results are similar to those of studies of simian virus 40 DNA replication, in which a large T antigen-H1 interaction and an H1-resistant region at the origin of DNA replication have also been demonstrated.
E1和E2蛋白是人类乳头瘤病毒(HPV)DNA复制所需的仅有的病毒编码因子。E1蛋白是一种DNA解旋酶,负责在病毒起源处启动DNA复制。它通过与E2结合而被招募到起源处,在起源处有特定的识别元件与E2结合。病毒的其余复制功能由宿主细胞的复制机制提供,可能通过与E1和E2的进一步相互作用来介导。通过远缘Western印迹法以及对经E1亲和层析纯化的34 kDa蛋白进行微序列分析,组蛋白H1被鉴定为HPV 11型(HPV-11)E1结合蛋白。E1在体外也能与在天然条件下分离的、与完整核小体结合的H1结合。此外,在表达重组E1的细胞制备的核提取物中,E1和H1能被E1抗血清共免疫沉淀。加入E1后,结合的H1从HPV-11 DNA上被置换下来,这表明E1可通过改变病毒染色质结构和破坏复制叉处的核小体来促进复制起始和延伸。此外,还鉴定出HPV-11基因组中一个包含复制起点的区域,该区域对H1的亲和力比基因组其余部分弱。这一结果表明,HPV起源处或其附近的DNA结构的存在通过排除H1促进了DNA复制的起始。这些结果与猿猴病毒40 DNA复制的研究结果相似,在该研究中也证明了大T抗原与H1的相互作用以及DNA复制起点处的H1抗性区域。