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7-甲基苯并[a]蒽的反式-3,4-二氢二醇-1,2-环氧化物在G.C碱基对处的优先诱变作用。

Preferential mutagenesis at G.C base pairs by the anti 3,4-dihydrodiol 1,2-epoxide of 7-methylbenz[a]anthracene.

作者信息

Bigger C A, Flickinger D J, St John J, Harvey R G, Dipple A

机构信息

Chemistry of Carcinogenesis Laboratory, ABL-Basic Research Program, National Cancer Institute-Frederick Cancer Research and Development Center, Maryland 21701.

出版信息

Mol Carcinog. 1991;4(3):176-9. doi: 10.1002/mc.2940040303.

Abstract

The racemic anti-dihydrodiol epoxide of 7-methylbenz[a]anthracene preferentially induced mutations at G.C base pairs in the pS189 shuttle vector. Mutations were not randomly distributed throughout the supF target gene, but were concentrated at five hotspots. The hotspots for this agent did not correspond exactly to those produced by any other dihydrodiol epoxide examined to date, indicating that dihydrodiol epoxide structure and reactivity play a major role in determining mutagenic hotspots.

摘要

7-甲基苯并[a]蒽的外消旋反式二氢二醇环氧化物优先在pS189穿梭载体中的G.C碱基对处诱发突变。突变并非随机分布于整个supF靶基因,而是集中在五个热点区域。该诱变剂的热点区域与迄今为止所检测的任何其他二氢二醇环氧化物产生的热点区域并不完全对应,这表明二氢二醇环氧化物的结构和反应活性在决定诱变热点方面起主要作用。

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