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首页> 外文期刊>Molecular and Cellular Biology >Mapping an origin of DNA replication at a single-copy locus in exponentially proliferating mammalian cells.
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Mapping an origin of DNA replication at a single-copy locus in exponentially proliferating mammalian cells.

机译:在成倍增殖的哺乳动物细胞中,在单拷贝基因座上绘制DNA复制起点。

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A general method for determining the physical location of an origin of bidirectional DNA replication has been developed recently and shown to be capable of correctly identifying the simian virus 40 origin of replication (L. Vassilev and E. M. Johnson, Nucleic Acids Res. 17:7693-7705, 1989). The advantage of this method over others previously reported is that it avoids the use of metabolic inhibitors, the requirement for cell synchronization, and the need for multiple copies of the origin sequence. Application of this method to exponentially growing Chinese hamster ovary cells containing the nonamplified, single-copy dihydrofolate reductase gene locus revealed that DNA replication begins bidirectionally in an initiation zone approximately 2.5 kilobases long centered about 17 kilobases downstream of the DHFR gene, coinciding with previously described early replicating sequences. These results demonstrate the utility of this mapping protocol for identifying cellular origins of replication and suggest that the same cellular origin is used in both the normal and the amplified DHFR locus.
机译:最近已经开发了一种用于确定双向DNA复制起点的物理位置的通用方法,并且该方法能够正确识别猿猴病毒40复制起点(L. Vassilev和EM Johnson,Nucleic Acids Res。17:7693-)。 7705,1989)。与以前报道的其他方法相比,此方法的优势在于它避免了使用代谢抑制剂,避免了细胞同步的需要以及避免了对原始序列的多个拷贝的需要。将该方法应用于含有非扩增的单拷贝二氢叶酸还原酶基因基因座的中国仓鼠卵巢细胞的指数增长显示,DNA复制在DHFR基因下游约2.5 kb长的起始区域(约17 kb碱基的中心)双向开始复制。早期复制序列。这些结果证明了该映射方案用于鉴定复制的细胞起源的实用性,并且表明在正常和扩增的DHFR基因座中都使用了相同的细胞起源。

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