Yamaguchi M, Hendrickson E A, DePamphilis M L
Mol Cell Biol. 1985 May;5(5):1170-83. doi: 10.1128/mcb.5.5.1170-1183.1985.
Unique single-stranded regions of simian virus 40 DNA, phage M13 virion DNA, and several homopolymers were used as templates for the synthesis of (p)ppRNA-DNA chains by CV-1 cell DNA primase-DNA polymerase alpha. Intact RNA primers, specifically labeled with an RNA capping enzyme, were typically 6 to 8 ribonucleotides long, although their lengths ranged from 1 to 9 bases. The fraction of intact RNA primers 1 to 4 ribonucleotides long was 14 to 73%, depending on the template used. RNA primer length varied among primers initiated at the same nucleotide, as well as with primers initiated at different sites. Thus, the size of an RNA primer depended on template sequence. Initiation sites were identified by mapping 5' ends of nascent RNA-DNA chains on the template sequence, identifying the 5'-terminal ribonucleotide, and partially sequencing one RNA primer. A total of 56 initiation events were identified on simian virus 40 DNA, an average of 1 every 16 bases. Some sites were preferred over others. A consensus sequence for initiation sites consisted of either 3'-dCTTT or 3'-dCCC centered within 7 to 25 pyrimidine-rich residues; the 5' ends of RNA primers were complementary to the dT or dC. High ATP/GTP ratios promoted initiation of RNA primer synthesis at 3'-dCTTT sites, whereas low ATP/GTP ratios promoted initiation at 3'-dCCC sites. Similarly, polydeoxythymidylic acid and polydeoxycytidylic acid were the only effective homopolymer templates. Thus, both template sequence and ribonucleoside triphosphate concentrations determine which initiation sites are used by DNA primase-DNA polymerase alpha. Remarkably, initiation sites selected in vitro were strikingly different from initiation sites selected during simian virus 40 DNA replication in vivo.
猿猴病毒40 DNA、噬菌体M13病毒粒子DNA以及几种同聚物的独特单链区域被用作模板,由CV-1细胞DNA引发酶-DNA聚合酶α合成(p)ppRNA-DNA链。用RNA加帽酶特异性标记的完整RNA引物通常长6至8个核糖核苷酸,不过其长度范围为1至9个碱基。长度为1至4个核糖核苷酸的完整RNA引物的比例为14%至73%,这取决于所使用的模板。在相同核苷酸起始的引物之间以及在不同位点起始的引物之间,RNA引物长度有所不同。因此,RNA引物的大小取决于模板序列。通过在模板序列上绘制新生RNA-DNA链的5'末端、鉴定5'-末端核糖核苷酸以及对一个RNA引物进行部分测序来确定起始位点。在猿猴病毒40 DNA上总共鉴定出56个起始事件,平均每16个碱基有1个。有些位点比其他位点更受青睐。起始位点的共有序列由位于7至25个富含嘧啶的残基内的3'-dCTTT或3'-dCCC组成;RNA引物的5'末端与dT或dC互补。高ATP/GTP比率促进在3'-dCTTT位点起始RNA引物合成,而低ATP/GTP比率促进在3'-dCCC位点起始。同样,聚脱氧胸苷酸和聚脱氧胞苷酸是仅有的有效的同聚物模板。因此,模板序列和核糖核苷三磷酸浓度都决定了DNA引发酶-DNA聚合酶α使用哪些起始位点。值得注意的是,体外选择的起始位点与猿猴病毒40 DNA在体内复制期间选择的起始位点显著不同。