Harris M P, Hay R T
MRC Virology Unit, Glasgow, Scotland.
J Mol Biol. 1988 May 5;201(1):57-67. doi: 10.1016/0022-2836(88)90438-x.
In-vivo studies have demonstrated that adenovirus type 2 and adenovirus type 4 have different DNA sequence requirements for the initiation of DNA replication. To investigate the basis of these differences an in-vitro system has been developed which will faithfully initiate adenovirus type 4 DNA replication. A plasmid containing 140 base-pairs of the right terminus of adenovirus type 4 supported initiation of DNA replication in vitro, provided that the plasmid was linearized in such a way as to locate the viral terminal sequences at the molecular ends of the DNA. Initiation by adenovirus type 4-infected cell extracts was also supported by a plasmid containing the complete adenovirus type 2 inverted terminal repeat (ITR). Deletion analysis of both adenovirus types 2 and 4 ITRs revealed that only the terminal 18 base-pairs of the genomes (perfectly conserved between the 2 viruses) were required for initiation in vitro. Thus, initiation was not enhanced by the presence of either the NFI site, the NFIII site or both sites together. Fractionation of a HeLa cell nuclear extract, by ion-exchange chromatography, identified a nuclear factor that stimulated the initiation reaction four- to fivefold. The stimulatory factor did not correspond to either of the cellular proteins NFI or NFIII which stimulate adenovirus type 2 DNA replication in vitro. Initiation in vitro was also supported by single-stranded DNA templates, albeit at a lower efficiency. Studies with synthetic oligonucleotides indicated a surprising specificity for initiation: whereas the strand used as template during initiation in vivo was active as a template for initiation in vitro, the complementary strand was inactive.
体内研究表明,2型腺病毒和4型腺病毒在DNA复制起始方面具有不同的DNA序列要求。为了研究这些差异的基础,已开发出一种体外系统,该系统能如实地起始4型腺病毒的DNA复制。一个含有4型腺病毒右末端140个碱基对的质粒支持体外DNA复制的起始,前提是该质粒以这样一种方式线性化,即把病毒末端序列定位在DNA的分子末端。一个含有完整的2型腺病毒反向末端重复序列(ITR)的质粒也支持由4型腺病毒感染的细胞提取物起始复制。对2型和4型腺病毒ITR的缺失分析表明,体外起始仅需要基因组末端的18个碱基对(这在两种病毒之间是完全保守的)。因此,NFI位点、NFIII位点或这两个位点同时存在并不会增强起始作用。通过离子交换色谱对HeLa细胞核提取物进行分级分离,鉴定出一种能将起始反应刺激4至5倍的核因子。该刺激因子与在体外刺激2型腺病毒DNA复制的细胞蛋白NFI或NFIII均不对应。单链DNA模板也支持体外起始,尽管效率较低。对合成寡核苷酸的研究表明起始具有惊人的特异性:体内起始过程中用作模板的链在体外作为起始模板是有活性的,而互补链则无活性。