Nakabeppu Y, Miyata T, Kondo H, Iwanaga S, Sekiguchi M
J Biol Chem. 1984 Nov 25;259(22):13730-6.
Nucleotide sequence of a DNA fragment containing the alkA gene and its control region has been determined using a chemical method. Only one open reading frame responsible for 3-methyladenine DNA glycosylase II was found. The hypothetical polypeptide deduced from the DNA sequence, with a molecular weight of 31,400, has an amino-terminal sequence and total amino acid composition identical to that of purified 3-methyladenine DNA glycosylase II. We constructed hybrid plasmids carrying an alkA'-lacZ' fusion, with the proper control region for alkA expression. A hybrid polypeptide with beta-galactosidase activity was formed when lac mutant cells harboring such plasmids were incubated with low doses of N-methyl-N'-nitro-N-nitrosoguanidine or methylmethane sulfonate. Other DNA-damaging agents, such as ethylmethane sulfonate, nalidixic acid, and ultraviolet light did not induce the enzyme activity. The induction was controlled by the ada and adc, but not by the recA and lexA genes.
利用化学方法测定了包含alkA基因及其调控区的DNA片段的核苷酸序列。仅发现一个负责3-甲基腺嘌呤DNA糖基化酶II的开放阅读框。从DNA序列推导的假定多肽,分子量为31,400,其氨基末端序列和总氨基酸组成与纯化的3-甲基腺嘌呤DNA糖基化酶II相同。我们构建了携带alkA'-lacZ'融合体的杂交质粒,其具有用于alkA表达的适当调控区。当携带此类质粒的lac突变细胞与低剂量的N-甲基-N'-硝基-N-亚硝基胍或甲磺酸甲酯一起孵育时,形成了具有β-半乳糖苷酶活性的杂交多肽。其他DNA损伤剂,如乙磺酸甲酯、萘啶酸和紫外线,不会诱导该酶活性。这种诱导受ada和adc控制,但不受recA和lexA基因控制。