van Bergen B G, van der Ley P A, van Driel W, van Mansfeld A D, van der Vliet P C
Nucleic Acids Res. 1983 Apr 11;11(7):1975-89. doi: 10.1093/nar/11.7.1975.
Nuclear extracts from adenovirus type 5 (Ad5) infected HeLa cells were used to study the template requirements for adenovirus DNA replication in vitro. When XbaI digested Ad5 DNA, containing the parental terminal protein (TP), was used as a template preferential synthesis of the terminal fragments was observed. The newly synthesized DNA was covalently bound to the 82 kD preterminal protein (pTP). Plasmid DNAs containing the Ad2 origin sequence or the Ad12 origin sequence with small deletions were analyzed for their capacity to support pTP-primed DNA replication. Circular plasmid DNAs were inactive. When plasmids were linearized to expose the adenovirus origin, both Ad2 and Ad12 TP-free fragments could support initiation and elongation similarly as Ad5 DNA-TP, although with lower efficiency. These observations indicate that the parental terminal protein is dispensable for initiation in vitro. The presence of 29 nucleotides ahead of the molecular end or a deletion of 14 base pairs extending into the conserved sequence (9-22) destroyed the template activity. DNA with a large deletion within the first 8 base pairs could still support replication while a small deletion could not. The results suggest that only G residues at a distance of 4-8 nucleotides from the start of the conserved sequence can be used as template during initiation of DNA replication.
利用来自5型腺病毒(Ad5)感染的HeLa细胞的核提取物,在体外研究腺病毒DNA复制的模板需求。当使用含有亲本末端蛋白(TP)的经XbaI消化的Ad5 DNA作为模板时,观察到末端片段的优先合成。新合成的DNA与82 kD前末端蛋白(pTP)共价结合。分析了含有Ad2起始序列或带有小缺失的Ad12起始序列的质粒DNA支持pTP引发的DNA复制的能力。环状质粒DNA无活性。当将质粒线性化以暴露腺病毒起始位点时,不含Ad2和Ad12 TP的片段都可以像Ad5 DNA-TP一样支持起始和延伸,尽管效率较低。这些观察结果表明,亲本末端蛋白在体外起始过程中是可有可无的。分子末端前29个核苷酸的存在或延伸到保守序列(9-22)中的14个碱基对的缺失破坏了模板活性。在前8个碱基对内有大缺失的DNA仍可支持复制,而小缺失则不能。结果表明,在DNA复制起始过程中,只有距保守序列起始处4-8个核苷酸距离的G残基可以用作模板。