首页> 外文期刊>Molecular and Cellular Biology >Mapping an initiation region of DNA replication at a single-copy chromosomal locus in Drosophila melanogaster cells by two-dimensional gel methods and PCR-mediated nascent-strand analysis: multiple replication origins in a broad zone.
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Mapping an initiation region of DNA replication at a single-copy chromosomal locus in Drosophila melanogaster cells by two-dimensional gel methods and PCR-mediated nascent-strand analysis: multiple replication origins in a broad zone.

机译:通过二维凝胶法和PCR介导的新生链分析,在果蝇黑腹果蝇细胞的单拷贝染色体基因座上绘制DNA复制的起始区域:在广泛区域中存在多个复制起点。

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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 (neutraleutral 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.
机译:我们已使用二维(2D)凝胶复制子作图方法和PCR介导的新生链,在指数繁殖的果蝇组织培养细胞中绘制了单拷贝染色体基因座上DNA复制的起始区域。首先通过用中性/碱性2D凝胶法确定复制叉的方向,将起始区域定位在DNA聚合酶α基因的下游。通过使用两种类型的2D凝胶方法(中性/中性和中性/碱性)和PCR介导的新生链分析,进一步分析了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上彼此一致,表明多个复制起点分布在大约10 kb的宽广区域中。确定了围绕起始区域的约20kb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。

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