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最近邻碱基影响烷基化剂诱导的G:C到A:T的转换。

Nearest neighbor affects G:C to A:T transitions induced by alkylating agents.

作者信息

Glickman B W, Horsfall M J, Gordon A J, Burns P A

机构信息

Biology Department, York University, Toronto, Ontario, Canada.

出版信息

Environ Health Perspect. 1987 Dec;76:29-32. doi: 10.1289/ehp.877629.

Abstract

The influence of local DNA sequence on the distribution of G:C to A:T transitions induced in the lacI gene of E. coli by a series of alkylating agents has been analyzed. In the case of nitrosoguanidine, two nitrosoureas and a nitrosamine, a strong preference for mutation at sites proceeded 5' by a purine base was noted. This preference was observed with both methyl and ethyl donors where the predicted common ultimate alkylating species is the alkyl diazonium ion. In contrast, this preference was not seen following treatment with ethylmethanesulfonate. The observed preference for 5'PuG-3' site over 5'-PyG-3' sites corresponds well with alterations observed in the Ha-ras oncogene recovered after treatment with NMU. This indicates that the mutations recovered in the oncogenes are likely the direct consequence of the alkylation treatment and that the local sequence effects seen in E. coli also appear to occur in mammalian cells.

摘要

分析了局部DNA序列对一系列烷化剂在大肠杆菌lacI基因中诱导的G:C到A:T转换分布的影响。在亚硝基胍、两种亚硝基脲和一种亚硝胺的情况下,发现嘌呤碱基在5'端的位点发生突变的强烈偏好。在用甲基和乙基供体处理时都观察到了这种偏好,其中预测的常见最终烷化物种是烷基重氮离子。相比之下,用甲磺酸乙酯处理后未观察到这种偏好。观察到的对5'PuG-3'位点而非5'-PyG-3'位点的偏好与用NMU处理后回收的Ha-ras癌基因中观察到的变化非常吻合。这表明在癌基因中回收的突变可能是烷化处理的直接结果,并且在大肠杆菌中看到的局部序列效应似乎也发生在哺乳动物细胞中。

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ON THE TOPOGRAPHY OF THE GENETIC FINE STRUCTURE.论遗传精细结构的拓扑学
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