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N-乙基-N-亚硝基脲在SOS诱导的大肠杆菌中诱导A:T到C:G的颠换突变以及转换突变。

N-ethyl-N-nitrosourea induces A:T to C:G transversion mutations as well as transition mutations in SOS-induced Escherichia coli.

作者信息

Eckert K A, Ingle C A, Drinkwater N R

机构信息

McArdle Laboratory for Cancer Research, University of Wisconsin, Madison 53706.

出版信息

Carcinogenesis. 1989 Dec;10(12):2261-7. doi: 10.1093/carcin/10.12.2261.

Abstract

The fixation of DNA lesions induced in Escherichia coli by N-ethyl-N-nitrosourea (ENU) occurs by both SOS-dependent and SOS-independent pathways. To determine whether these pathways result in differential processing of ENU-induced lesions, we have analyzed the DNA sequence changes of mutations induced at a plasmid-encoded herpes simplex virus type 1 thymidine kinase gene by ENU treatment of plasmid-bearing RecA- and RecA+ bacteria, and by transformation of RecA-, RecA+ and SOS-induced RecA+ bacteria with ENU-modified plasmid DNA. Transition mutations were the predominant types of base substitution mutations observed for wild-type and RecA- E. coli, consistent with the SOS-independent mispairing of O6-ethylguanine and O4-ethylthymine adducts during DNA replication. Under conditions of SOS processing of ENU lesions, however, we observed the frequent induction of A:T----C:G transversion mutations. The proportion of A:T----C:G transversion mutations (42%) observed after transformation of SOS-induced bacteria with ENU modified DNA was approximately equal to that of the G:C----A:T transitions (46%). The frequencies of these mutations were increased 20- and 5-fold respectively over that observed for non-induced RecA+ cells. We suggest that ethylated DNA lesions which normally block DNA replication can be processed to yield A:T----C:G transversion mutations in SOS-induced E. coli.

摘要

N-乙基-N-亚硝基脲(ENU)在大肠杆菌中诱导产生的DNA损伤修复通过SOS依赖和SOS非依赖两种途径进行。为了确定这些途径是否导致ENU诱导损伤的不同处理方式,我们分析了通过ENU处理携带质粒的RecA-和RecA+细菌,以及用ENU修饰的质粒DNA转化RecA-、RecA+和SOS诱导的RecA+细菌,在质粒编码的单纯疱疹病毒1型胸苷激酶基因上诱导产生的突变的DNA序列变化。转换突变是野生型和RecA-大肠杆菌中观察到的碱基替换突变的主要类型,这与DNA复制过程中O6-乙基鸟嘌呤和O4-乙基胸腺嘧啶加合物的SOS非依赖错配一致。然而,在ENU损伤的SOS处理条件下,我们观察到频繁诱导A:T----C:G颠换突变。用ENU修饰的DNA转化SOS诱导细菌后观察到的A:T----C:G颠换突变比例(42%)与G:C----A:T转换比例(46%)大致相等。这些突变的频率分别比未诱导的RecA+细胞中观察到的频率增加了20倍和5倍。我们认为,通常会阻断DNA复制的乙基化DNA损伤在SOS诱导的大肠杆菌中可以被处理产生A:T----C:G颠换突变。

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