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中国仓鼠二氢叶酸还原酶基因起始区域由多个潜在的新生链起始位点组成。

The Chinese hamster dihydrofolate reductase origin consists of multiple potential nascent-strand start sites.

作者信息

Dijkwel P A, Hamlin J L

机构信息

Biochemistry Department, University of Virginia School of Medicine, Charlottesville 22908, USA.

出版信息

Mol Cell Biol. 1995 Jun;15(6):3023-31. doi: 10.1128/MCB.15.6.3023.

Abstract

Previous two-dimensional gel replicon-mapping studies on the amplified dihydrofolate reductase (DHFR) domain in CHOC 400 cells suggested that replication can initiate at any of a large number of sites scattered throughout a 55-kb region lying between two convergently transcribed genes. It could be argued that this unusual distributive initiation mode is unique to amplified chromosomal loci. In this paper, we report the first application of the two-dimensional gel techniques to the analysis of a single-copy locus in mammalian cells. Results obtained with both synchronized and exponentially growing CHO cells suggest that (i) initiation can also occur at any of a large number of sites distributed throughout the intergenic region in the nonamplified DHFR locus, (ii) initiation is confined to the first 2 to 2.5 h of the S period, and (iii) initiation occurs only in a fraction of the DHFR loci in each cell cycle.

摘要

先前对CHOC 400细胞中扩增的二氢叶酸还原酶(DHFR)结构域进行的二维凝胶复制子图谱研究表明,复制可以在散布于两个反向转录基因之间55 kb区域的大量位点中的任何一个位点起始。可以认为这种不寻常的分散起始模式是扩增染色体位点所特有的。在本文中,我们报告了二维凝胶技术首次应用于哺乳动物细胞中单拷贝位点的分析。对同步化和指数生长的CHO细胞获得的结果表明:(i)在未扩增的DHFR基因座的基因间区域中,起始也可以发生在散布于其中的大量位点中的任何一个位点;(ii)起始局限于S期的前2至2.5小时;(iii)在每个细胞周期中,只有一部分DHFR基因座发生起始。

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