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Substitution and deletion mutations induced by 2-hydroxyadenine in Escherichia coli: effects of sequence contexts in leading and lagging strands.

机译:2-羟基腺嘌呤在大肠杆菌中诱导的取代和缺失突变:前导链和滞后链中序列背景的影响。

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摘要

To evaluate the mutation frequency and the mutation spectrum of 2-hydroxyadenine (2-OH-Ade), an oxidative DNA lesion, the modified base was site-specifically incorporated into a unique restriction enzyme site (SalI, GTCGA*C or AflII, CTTA*AG where A* represents 2-OH-Ade) in single- and double-stranded vectors. The 2-OH-Ade residues were introduced into (+)- and (-)-strands of the double-stranded vectors and into the (+)-strand of single-stranded vectors. When the vectors were transfected intoEscherichia coli, the modified base showed little to no cytotoxicity. The mutation frequencies of 2-OH-Ade in the SalI and AflII sites were approximately 0.8 and 0.07%, respectively, with double-stranded (+)-vectors. An increase in the mutation frequencies was not observed with single-stranded vectors. When incorporated into the (-)-strand, the mutation frequencies of 2-OH-Ade in the SalI and AflII sites were approximately 0.3 and 0.1%, respectively. The mutations observed most frequently were -1 deletions at both positions, in the case of the (+)-strand. On the other hand, we observed that 2-OH-Ade in the (-)-strand induced A-->G and A-->T substitutions. These results indicate that 2-OH-Ade residues in DNA induce substitution and deletion mutations without blocking replication inE.coli.
机译:为了评估氧化性DNA损伤2-羟基腺嘌呤(2-OH-Ade)的突变频率和突变谱,将修饰的碱基位点特异性掺入独特的限制性酶切位点(SalI,GTCGA * C或AflII,CTTA) * AG,其中A *表示单链和双链载体。将2-OH-Ade残基引入双链载体的(+)-和(-)链以及单链载体的(+)链。当将载体转染到大肠杆菌中时,修饰的碱基几乎没有或没有细胞毒性。使用双链(+)载体时,SalI和AflII位点中2-OH-Ade的突变频率分别约为0.8和0.07%。用单链载体未观察到突变频率的增加。当掺入(-)链中时,SalI和AflII位点中2-OH-Ade的突变频率分别约为0.3%和0.1%。对于(+)链,最常观察到的突变是两个位置的-1缺失。另一方面,我们观察到(-)链中的2-OH-Ade诱导了A-> G和A-> T取代。这些结果表明,DNA中的2-OH-Ade残基可诱导取代和缺失突变,而不会阻止大肠杆菌中的复制。

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