首页> 美国卫生研究院文献>The EMBO Journal >Nonenzymatic methylation of DNA by the intracellular methyl group donor S-adenosyl-L-methionine is a potentially mutagenic reaction.
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Nonenzymatic methylation of DNA by the intracellular methyl group donor S-adenosyl-L-methionine is a potentially mutagenic reaction.

机译:细胞内甲基供体S-腺苷-L-甲硫氨酸对DNA的非酶甲基化作用是潜在的诱变反应。

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摘要

Incubation of DNA with S-adenosyl-L-methionine (SAM) in neutral aqueous solution leads to base modification, with formation of small amounts of 7-methylguanine and 3-methyladenine. The products have been identified by high performance liquid chromatography of DNA hydrolysates and by the selective release of free 3-methyladenine from SAM-treated DNA by a specific DNA glycosylase. We conclude that SAM acts as a weak DNA-alkylating agent. Several control experiments including extensive purification of [3H-methyl]SAM preparations and elimination of the alkylating activity by pretreatment of SAM with a phage T3-induced SAM cleaving enzyme, have been performed to determine that the activity observed was due to SAM itself and not to a contaminating substance. We estimate that SAM, at an intracellular concentration of 4 X 10(-5) M, causes DNA alkylation at a level similar to that expected from continuous exposure of cells to 2 X 10(-8) M methyl methane-sulphonate. This ability of SAM to act as a methyl donor in a nonenzymatic reaction could result in a background of mutagenesis and carcinogenesis. The data provide an explanation for the apparently universal occurrence of multiple DNA repair enzymes specific for methylation damage.
机译:将DNA与S-腺苷-L-蛋氨酸(SAM)在中性水溶液中孵育会导致碱基修饰,并形成少量的7-甲基鸟嘌呤和3-甲基腺嘌呤。通过DNA水解产物的高效液相色谱法和通过特定DNA糖基化酶从SAM处理的DNA中选择性释放游离的3-甲基腺嘌呤来鉴定产品。我们得出结论,SAM充当弱DNA烷基化剂。已经进行了一些控制实验,包括大量纯化[3H-甲基] SAM制剂和通过用噬菌体T3诱导的SAM裂解酶预处理SAM消除烷基化活性,以确定观察到的活性是由于SAM本身而不是由于SAM污染物质。我们估计,SAM在细胞内浓度为4 X 10(-5)M时,会导致DNA烷基化,其水平与将细胞连续暴露于2 X 10(-8)M甲磺酸甲酯所预期的水平相似。 SAM在非酶促反应中充当甲基供体的这种能力可能导致诱变和致癌的背景。数据为甲基化损伤特异的多种DNA修复酶的普遍存在提供了解释。

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