首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Both purified human 1N6-ethenoadenine-binding protein and purified human 3-methyladenine-DNA glycosylase act on 1N6-ethenoadenine and 3-methyladenine.
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Both purified human 1N6-ethenoadenine-binding protein and purified human 3-methyladenine-DNA glycosylase act on 1N6-ethenoadenine and 3-methyladenine.

机译:纯化的人1N6-乙腺嘌呤结合蛋白和纯化的人3-甲基腺嘌呤-DNA糖基化酶均作用于1N6-乙腺嘌呤和3-甲基腺嘌呤。

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摘要

We previously described a protein, isolated from human tissues and cells, that bound to a defined double-stranded oligonucleotide containing a single site-specifically placed 1,N6-ethenoadenine. It was further demonstrated that this protein was a glycosylase and released 1,N6-ethenoadenine. We now find that this enzyme also releases 3-methyladenine from methylated DNA and that 3-methyladenine-DNA glycosylase behaves in the same manner, binding to the ethenoadenine-containing oligonucleotide and cleaving both ethenoadenine and 3-methyladenine from DNA containing these adducts. The rate and extent of glycosylase activities toward the two adducts are similar.
机译:我们先前描述了一种从人体组织和细胞中分离的蛋白质,该蛋白质与定义的双链寡核苷酸结合,该双链寡核苷酸包含一个特定位点的1,N6-乙炔腺嘌呤。进一步证明该蛋白是糖基化酶并释放出1,N6-乙炔腺嘌呤。现在我们发现,该酶还从甲基化的DNA中释放出3-甲基腺嘌呤,并且3-甲基腺嘌呤-DNA糖基化酶的行为相同,与含乙炔腺嘌呤的寡核苷酸结合,并从包含这些加合物的DNA中裂解出乙腺嘌呤和3-甲基腺嘌呤。糖基化酶对两个加合物的活性的速率和程度是相似的。

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