Pronk R, Stuiver M H, van der Vliet P C
Laboratory for Physiological Chemistry, Utrecht University, The Netherlands.
Chromosoma. 1992;102(1 Suppl):S39-45. doi: 10.1007/BF02451784.
Initiation of Adenovirus DNA replication in vitro requires the presence of three viral proteins (pTP, pol, DBP) and two cellular transcription factors, NFI and Oct-1, that stimulate replication more than 100-fold. NFI assists in binding and positioning of the DNA polymerase in the origin whereas Oct-1 changes the structure of origin DNA. Optimal templates contain, in addition to origin sequences, the covalently bound viral terminal protein (TP). This terminal protein stimulates the template activity over 20 fold compared to protein-free templates. To study the way in which TP exerts its function in vitro we devised a novel method to isolate and label a short origin containing fragment in which the TP was bound in a functional form. This fragment replicated very efficiently and could be used for studying the binding of other replication proteins. Employing alpha-chymotrypsin digestion we show that for enhancement of replication in vitro only a small part of TP is required.
腺病毒DNA在体外的复制起始需要三种病毒蛋白(pTP、pol、DBP)和两种细胞转录因子NFI和Oct-1的存在,它们可将复制刺激100倍以上。NFI协助DNA聚合酶在起始位点的结合和定位,而Oct-1改变起始位点DNA的结构。最佳模板除了起始序列外,还包含共价结合的病毒末端蛋白(TP)。与无蛋白模板相比,这种末端蛋白可将模板活性提高20倍以上。为了研究TP在体外发挥功能的方式,我们设计了一种新方法来分离和标记一个含有短起始片段的片段,其中TP以功能形式结合。该片段复制效率非常高,可用于研究其他复制蛋白的结合。通过α-胰凝乳蛋白酶消化,我们表明在体外增强复制仅需要一小部分TP。