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8-Hydroxyadenine (7,8-dihydro-8-oxoadenine) induces misincorporation in in vitro DNA synthesis and mutations in NIH 3T3 cells.

机译:8-Hydroxyadenine(7,8-dihydro-8-oxoadenine)在NIH 3T3细胞的体外DNA合成和突变中诱导错误掺入。

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摘要

An oligodeoxyribonucleotide containing 8-hydroxyadenine (OH8Ade) was chemically synthesized and single- and double-stranded c-Ha-ras gene fragments with OH8Ade at the second position of codon 61 were prepared. The single-stranded ras gene fragment was used as a template for in vitro DNA synthesis with the Klenow fragment of Escherichia coli DNA polymerase I, Taq DNA polymerase, rat DNA polymerase beta and mouse DNA polymerase alpha. The former two enzymes exclusively incorporated dTMP opposite OH8Ade. The DNA polymerases alpha and beta misinserted dGMP, and dAMP and dGMP, respectively. The c-Ha-ras gene was constructed using the double-stranded ras gene fragment containing OH8Ade and was transfected into NIH 3T3 cells. The gene with OH8Ade induced focus formation, indicating that OH8Ade elicited point mutations in cells. When c-Ha-ras genes present in transformed cells were analyzed, an A-->G transition and an A-->C transversion were detected. These results indicate that OH8Ade induced misincorporation in in vitro DNA synthesis and mutations in mammalian cells.
机译:化学合成包含8-羟基腺嘌呤(OH8Ade)的寡脱氧核糖核苷酸,并制备在密码子61第二位具有OH8Ade的单链和双链c-Ha-ras基因片段。使用单链ras基因片段作为模板,与大肠杆菌DNA聚合酶I,Taq DNA聚合酶,大鼠DNA聚合酶β和小鼠DNA聚合酶α的Klenow片段进行体外DNA合成。前两种酶专门掺入了与OH8Ade相反的dTMP。 DNA聚合酶分别错插了α和βdGMP,以及dAMP和dGMP。使用含有OH8Ade的双链ras基因片段构建了c-Ha-ras基因,并将其转染到NIH 3T3细胞中。具有OH8Ade的基因诱导了焦点形成,表明OH8Ade引起了细胞中的点突变。分析转化细胞中存在的c-Ha-ras基因时,检测到A→G过渡和A→C颠倒。这些结果表明,OH8Ade诱导了体外DNA合成中的错误掺入以及哺乳动物细胞中的突变。

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