Challberg M D, Rawlins D R
Proc Natl Acad Sci U S A. 1984 Jan;81(1):100-4. doi: 10.1073/pnas.81.1.100.
The first step in the replication of the adenovirus genome is the covalent attachment of the 5'-terminal nucleotide, dCMP, to the virus-encoded terminal protein precursor (pTP). This reaction can be observed in vitro and has been previously shown to be dependent upon either viral DNA or linearized plasmid DNA containing viral terminal sequences. Plasmids containing deletions or point mutations within the viral terminal sequence were constructed by site-directed mutagenesis. In the case of linear double-stranded templates, pTP-dCMP formation required sequences located within the first 18 base pairs of the viral genome. This sequence contains a segment of 10 base pairs that is conserved in all human adenovirus serotypes. Point mutations within the conserved segment greatly reduced the efficiency of initiation, while a point mutation at a nonconserved position within the first 18 base pairs had little effect. Single-stranded DNAs can also support pTP-dCMP formation in vitro. In contrast to the results obtained with duplex templates, experiments with a variety of single-stranded templates, including phage M13-adenovirus recombinants, denatured plasmids, and synthetic oligodeoxynucleotides, failed to reveal any requirements for specific nucleotide sequences. With single-stranded templates containing no dG residues, the specific deoxynucleoside triphosphate requirements of the initiation reaction were altered.
腺病毒基因组复制的第一步是将5'-末端核苷酸dCMP共价连接到病毒编码的末端蛋白前体(pTP)上。该反应可在体外观察到,并且先前已证明其依赖于病毒DNA或含有病毒末端序列的线性化质粒DNA。通过定点诱变构建了病毒末端序列内含有缺失或点突变的质粒。对于线性双链模板,pTP-dCMP的形成需要位于病毒基因组前18个碱基对内的序列。该序列包含一段10个碱基对的片段,在所有人类腺病毒血清型中都是保守的。保守片段内的点突变大大降低了起始效率,而前18个碱基对内非保守位置的点突变影响很小。单链DNA在体外也能支持pTP-dCMP的形成。与双链模板的结果相反,使用多种单链模板(包括噬菌体M13-腺病毒重组体、变性质粒和合成寡脱氧核苷酸)进行的实验未能揭示对特定核苷酸序列的任何要求。对于不含dG残基的单链模板,起始反应对特定脱氧核苷三磷酸的要求发生了改变。