Nieminuszczy Jadwiga, Grzesiuk Elzbieta
Department of Molecular Biology, Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warszawa, Poland.
Acta Biochim Pol. 2007;54(3):459-68. Epub 2007 Sep 6.
Environmental and endogenous alkylating agents generate cytotoxic and mutagenic lesions in DNA. Exposure of prokaryotic cells to sublethal doses of DNA alkylating agents induces so called adaptive response (Ada response) involving the expression of a set of genes which allows the cells to tolerate the toxic and mutagenic action of such agents. The Ada response includes the expression of four genes: ada, alkA, alkB, and aidB. The product of ada gene, Ada protein, is an activator of transcription of all four genes. DNA bases damaged by alkylation are removed by distinct strategies. The most toxic lesion 3meA is removed by specific DNA glycosylase initiating base excising repair. The toxic and mutagenic O6meG is repaired directly by methyltransferases. 1meA and 3meC are corrected by AlkB DNA dioxygenase. The mechanisms of action of E. coli AlkB dioxygenase and its human homologs ABH2 and ABH3 are described in more details.
环境和内源性烷化剂会在DNA中产生细胞毒性和诱变损伤。将原核细胞暴露于亚致死剂量的DNA烷化剂会诱导所谓的适应性反应(Ada反应),这涉及一组基因的表达,使细胞能够耐受此类试剂的毒性和诱变作用。Ada反应包括四个基因的表达:ada、alkA、alkB和aidB。ada基因的产物Ada蛋白是所有四个基因转录的激活剂。烷基化损伤的DNA碱基通过不同的策略去除。毒性最大的损伤3meA通过启动碱基切除修复的特定DNA糖基化酶去除。毒性和诱变性的O6meG由甲基转移酶直接修复。1meA和3meC由AlkB DNA双加氧酶校正。大肠杆菌AlkB双加氧酶及其人类同源物ABH2和ABH3的作用机制将更详细地描述。