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Replication of M13 single—stranded DNA bearing a sitespecific ethenocytosine lesion by Escherichia coil cell extracts

机译:大肠埃希氏菌卷曲细胞提取物复制带有定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,N4-Ethenocytosine (εC),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 (εC) 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 εC,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,N4-氨基胞嘧啶(εC)(一种非配对DNA病变)的诱变作用的调查揭示了在大肠杆菌中存在一种新型的,不依赖SOS的诱导诱变机制,称为UVM可以诱变UV。通过DNA复制的改变介导,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被大肠杆菌细胞中的可溶性蛋白提取物复制。通过琼脂糖凝胶电泳进行分析,并通过限制性核酸内切酶分析确定了病灶的合成频率。我们的数据表明εC强烈抑制了DNA复制,但是在14%的已复制的DNA分子中确实发生了病灶DNA的合成。与先前体内观察到的非常相似,这表明该实验系统可能适合评估U中DNA复制的变化VM诱导的细胞。

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