首页> 外文期刊>Nucleic Acids Research >NOVEL ACTIVITIES OF HUMAN URACIL DNA N-GLYCOSYLASE FOR CYTOSINE-DERIVED PRODUCTS OF OXIDATIVE DNA DAMAGE
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NOVEL ACTIVITIES OF HUMAN URACIL DNA N-GLYCOSYLASE FOR CYTOSINE-DERIVED PRODUCTS OF OXIDATIVE DNA DAMAGE

机译:人类尿嘧啶DNA N-糖基化酶对胞嘧啶衍生的氧化性DNA损伤产物的新活性

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摘要

Uracil DNA N-glycosylase is a repair enzyme that releases uracil from DNA, A major function of this enzyme is presumably to protect the genome from pre-mutagenic uracil resulting from deamination of cytosine in DNA, Here, we report that human uracil DNA N-glycosylase also recognizes three uracil derivatives that are generated as major products of cytosine in DNA by hydroxyl radical attack or other oxidative processes, DNA substrates were prepared by gamma-irradiation of DNA in aerated aqueous solution and incubated with human uracil DNA N-glycosylase, heat-inactivated enzyme or buffer. Ethanol-precipitated DNA and supernatant fractions were then separated, Supernatant fractions after derivatization, and pellets after hydrolysis and derivatization were analyzed by gas chromatography/isotope-dilution mass spectrometry, The results demonstrated that human uracil DNA N-glycosylase excised isodialuric acid, 5-hydroxyuracil and alloxan from DNA with apparent K-m values of similar to 530, 450 and 660 nM, respectively, The excision of these uracil analogues is consistent with the recently described mechanism for recognition of uracil by human uracil DNA N-glycosylase [Mol,C.D., Arval,A,S., Slupphaug,G., Kavil,B., Alseth,l., Krokan,H.E. and Tainer,J.A. (1995) Cell, 80, 869-878], Nine other pyrimidine and purine-derived products that were identified in DNA samples were not substrates for the enzyme, The results indicate that human uracil DNA N-glycosylase may have a function in the repair of oxidative DNA damage.
机译:尿嘧啶DNA N-糖基化酶是一种从DNA释放尿嘧啶的修复酶,该酶的主要功能可能是保护基因组免受DNA中胞嘧啶脱氨导致的致突变尿嘧啶的侵害。在此,我们报道了人类尿嘧啶DNA N-糖基化酶还识别三种尿嘧啶衍生物,它们是通过羟基自由基攻击或其他氧化过程在DNA中作为胞嘧啶的主要产物而生成的。DNA底物是通过在充气水溶液中对DNA进行γ辐照制备的,并与人尿嘧啶DNA N-糖基化酶一起孵育,加热-灭活的酶或缓冲液。然后分离乙醇沉淀的DNA和上清液馏分,衍生化后的上清液馏分,水解和衍生化后的沉淀通过气相色谱/同位素稀释质谱法进行分析,结果表明,人尿嘧啶DNA N-糖基化酶切除了异戊二酸5-表观Km值分别接近530、450和660 nM的DNA中的羟基尿嘧啶和四氧嘧啶。这些尿嘧啶类似物的切除与最近描述的人尿嘧啶DNA N-糖基化酶[Mol,CD, Arval,A.S。,Slupphaug,G。,Kavil,B。,Alseth,l。,Krokan,HE和泰纳(J.A.) (1995)Cell,80,869-878],DNA样品中鉴定出的其他9种嘧啶和嘌呤衍生产物不是该酶的底物,结果表明人尿嘧啶DNA N-糖基化酶可能在修复中起作用DNA的氧化损伤。

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