Shinomiya T, Ina S
Mitsubishi Kasei Institute of Life Sciences, Tokyo, Japan.
Mol Cell Biol. 1994 Nov;14(11):7394-403. doi: 10.1128/mcb.14.11.7394-7403.1994.
We have mapped an initiation region of DNA replication at a single-copy chromosomal locus in exponentially proliferating Drosophila tissue culture cells, using two-dimensional (2D) gel replicon mapping methods and PCR-mediated analysis of nascent strands. The initiation region was first localized downstream of the DNA polymerase alpha gene by determining direction of replication forks with the neutral/alkaline 2D gel method. Distribution of replication origins in the initiation region was further analyzed by using two types of 2D gel methods (neutral/neutral and neutral/alkaline) and PCR-mediated nascent-strand analysis. Results obtained by three independent methods were essentially consistent with each other and indicated that multiple replication origins are distributed in a broad zone of approximately 10 kb. The nucleotide sequence of an approximately 20-kb region that encompasses the initiation region was determined and searched for sequence elements potentially related to function of replication origins.
我们利用二维(2D)凝胶复制子图谱分析方法和PCR介导的新生链分析,在指数增殖的果蝇组织培养细胞中的单拷贝染色体位点绘制了DNA复制起始区域。通过中性/碱性二维凝胶法确定复制叉的方向,首先将起始区域定位在DNA聚合酶α基因的下游。使用两种二维凝胶方法(中性/中性和中性/碱性)和PCR介导的新生链分析进一步分析起始区域中复制起点的分布。通过三种独立方法获得的结果基本一致,表明多个复制起点分布在大约10 kb的广泛区域。确定了包含起始区域的大约20 kb区域的核苷酸序列,并搜索了可能与复制起点功能相关的序列元件。