Frappier L, Zannis-Hadjopoulos M
McGill Cancer Centre, Department of Medicine, McGill University, Montreal, Quebec, Canada.
Proc Natl Acad Sci U S A. 1987 Oct;84(19):6668-72. doi: 10.1073/pnas.84.19.6668.
Twelve clones of origin-enriched sequences (ORS) isolated from early replicating monkey (CV-1) DNA were examined for transient episomal replication in transfected CV-1, COS-7, and HeLa cells. Plasmid DNA was isolated at time intervals after transfection and screened by the Dpn I resistance assay or by the bromodeoxyuridine substitution assay to differentiate between input and replicated DNA. We have identified four monkey ORS (ORS3, -8, -9, and -12) that can support plasmid replication in mammalian cells. This replication is carried out in a controlled and semiconservative manner characteristic of mammalian replicons. ORS replication was most efficient in HeLa cells. Electron microscopy showed ORS8 and ORS12 plasmids of the correct size with replication bubbles. Using a unique restriction site in ORS12, we have mapped the replication bubble within the monkey DNA sequence.
从早期复制的猴(CV - 1)DNA中分离出12个富含起始序列(ORS)的克隆,检测它们在转染的CV - 1、COS - 7和HeLa细胞中的瞬时附加型复制情况。转染后的不同时间间隔提取质粒DNA,通过Dpn I抗性检测或溴脱氧尿苷替代检测进行筛选,以区分输入的DNA和复制的DNA。我们鉴定出四个猴ORS(ORS3、- 8、- 9和- 12),它们能够支持质粒在哺乳动物细胞中的复制。这种复制以哺乳动物复制子特有的可控和半保留方式进行。ORS复制在HeLa细胞中效率最高。电子显微镜显示,具有复制泡的ORS8和ORS12质粒大小正确。利用ORS12中的一个独特限制性位点,我们在猴DNA序列中定位了复制泡。