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Replication of M13 single-stranded DNA bearing a site-specific ethenocytosine lesion by Escherichia coil cell extracts

机译:大肠杆菌细胞提取物复制带有特定位点乙脑胞嘧啶损伤的M13单链DNA

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摘要

Previous investigation on the mutagenic effects of 3, N~4-Ethenocytosine (epsilon C), a nonpairing DNA lesion, revealed the existence of a novel SOS-independent inducible mutagenic mechanism in E. coli termed UVM for UV modulation of mutagenesis. To investigate whether UVM is mediated by an alteration of DNA replication, we have set up an in vitro replication system in which phage M13 viral single-stranded DNA bearing a single site-specific (epsilon C) residue is replicated by soluble protein extracts from E. coli cells. Replication products were analyzed by agarose gel electrophoresis and the frequency of translesion synthesis was determined by restriction endonuclease analyses. Our data indicate that DNA replication is strongly inhibited by eC, but that translesion DNA synthesis does occur in about 14% of the replicated DNA molecules. These results are very similar to those observed previously in vivo, and suggest that this experimental system may be suitable for evaluating alterations in DNA replication in UVM-induced cells.
机译:先前对3,N〜4-Ethenocytosine(epsilon C)(一种非配对DNA病变)的诱变作用的调查显示,在大肠杆菌中存在一种新型的,独立于SOS的可诱导诱变机制,称为UVM,可用于诱变的UV调节。为了研究UVM是否是由DNA复制的改变介导的,我们建立了一个体外复制系统,其中带有单个位点特异性(εC)残基的噬菌体M13病毒单链DNA被E的可溶性蛋白提取物复制。大肠杆菌细胞。通过琼脂糖凝胶电泳分析复制产物,并通过限制性核酸内切酶分析确定转基因合成的频率。我们的数据表明,DNA复制受到eC的强烈抑制,但是跨病变的DNA合成确实发生在大约14%的复制的DNA分子中。这些结果与先前在体内观察到的结果非常相似,表明该实验系统可能适用于评估UVM诱导的细胞中DNA复制的变化。

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