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单一位点特异性芳胺-DNA加合物介导的诱变作用。多个位点的突变诱导。

Mutagenesis by single site-specific arylamine-DNA adducts. Induction of mutations at multiple sites.

作者信息

Gupta P K, Johnson D L, Reid T M, Lee M S, Romano L J, King C M

机构信息

Department of Chemical Carcinogenesis, Michigan Cancer Foundation, Detroit, Michigan 48201.

出版信息

J Biol Chem. 1989 Nov 25;264(33):20120-30.

PMID:2684969
Abstract

Two related carcinogen adducts, N-(deoxyguanosin-8-yl)-2-aminofluorene (AF) or N-(deoxyguanosin-8-yl)-N-acetyl-2-aminofluorene (AAF), were introduced into the lacZ' gene at base position 6253 of the minus strand of M13mp9 viral DNA. The construction of this site-specifically modified DNA was accomplished by first preparing a gapped heteroduplex missing 7 nucleotides at position 6251-6257 followed by ligation with an unmodified heptamer or with a heptamer containing either an AF or AAF adduct. These site-specifically modified templates were transfected into competent wild-type Escherichia coli cells (JM103) and a uvrA strain (SMH12). The mutation spectrum was determined by phenotypic selection of colorless plaques indicating a defective beta-galactosidase marker enzyme and by an in situ hybridization procedure to detect single base pair mismatches in the adduct region. DNA sequencing was used to characterize 179 of the mutants obtained. We found that both adducts were capable of inducing base substitution mutations at the adduct site and in the local region of the adduct. A specific frameshift (+1G) was also observed at a displaced site. All of the frameshift mutations occurred at the ligation site of the modified oligonucleotide. Control experiments with an unmodified oligonucleotide did not show an enhancement of mutations at this site, indicating that the adducts may have been responsible for these frameshifts. The mutations spectra induced by these adducts suggest that mutagenesis depends not only on adduct structure but also the sequence in which the adduct is located and the host cell type used for mutation expression.

摘要

两种相关的致癌物加合物,即N-(脱氧鸟苷-8-基)-2-氨基芴(AF)或N-(脱氧鸟苷-8-基)-N-乙酰-2-氨基芴(AAF),被引入到M13mp9病毒DNA负链6253位碱基处的lacZ'基因中。这种位点特异性修饰DNA的构建首先是通过制备在6251 - 6257位缺失7个核苷酸的缺口异源双链体,然后与未修饰的七聚体或含有AF或AAF加合物的七聚体连接来完成的。这些位点特异性修饰的模板被转染到感受态野生型大肠杆菌细胞(JM103)和uvrA菌株(SMH12)中。通过对无色噬菌斑进行表型选择来确定突变谱,无色噬菌斑表明β-半乳糖苷酶标记酶有缺陷,并且通过原位杂交程序来检测加合物区域的单碱基对错配。DNA测序用于对获得的179个突变体进行表征。我们发现这两种加合物都能够在加合物位点及其局部区域诱导碱基置换突变。在一个移位位点还观察到了一个特定的移码突变(+1G)。所有的移码突变都发生在修饰寡核苷酸的连接位点。用未修饰寡核苷酸进行的对照实验在该位点未显示出突变增强,这表明加合物可能是这些移码突变的原因。这些加合物诱导的突变谱表明,诱变不仅取决于加合物的结构,还取决于加合物所在的序列以及用于突变表达的宿主细胞类型。

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