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首页> 外文期刊>Nucleic Acids Research >DEMETHYLATION OF DNA BY PURIFIED CHICK EMBRYO 5-METHYLCYTOSINE-DNA GLYCOSYLASE REQUIRES BOTH PROTEIN AND RNA
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DEMETHYLATION OF DNA BY PURIFIED CHICK EMBRYO 5-METHYLCYTOSINE-DNA GLYCOSYLASE REQUIRES BOTH PROTEIN AND RNA

机译:纯化的雏鸡5-甲基胞嘧啶-DNA糖基化酶将DNA脱甲基化需要蛋白质和RNA

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摘要

We have previously purified and characterized a 5-methylcytosine (5-MeC)-DNA glycosylase from 12 day old chick embryos [Jost,J.P. at al. (1995) J. Biol. Chem. 270, 9734-9739]. The activity of the purified enzyme is abolished upon treatment with proteinase K and ribonuclease A. RNA copurifies with 5-MeC-DNA glycosylase activity throughout all chromatographic steps and preparative gel electrophoresis. RNA with a length of similar to 300-500 nucleotides was isolated from the gel purified enzyme. Upon extensive treatment with proteinase K, the gel eluted and labeled RNA did not show any significant change in molecular mass. The purified RNA incubated alone or in the presence of Mg2+ and deoxyribonucleotide phosphates had no 5-MeC-DNA glycosylase or demethylating activities. However, activity of 5-MeC-DNA glycosylase could be restored when the purified RNA was incubated with the inactive protein, free of RNA.
机译:我们之前已经从12天大的雏鸡胚胎中纯化并鉴定了5-甲基胞嘧啶(5-MeC)-DNA糖基化酶[Jost,J.P。在(1995)生物化学杂志。化学270,9734-9739]。经蛋白酶K和核糖核酸酶A处理后,纯化的酶的活性消失。在所有色谱步骤和制备型凝胶电泳中,RNA用5-MeC-DNA糖基化酶活性共纯化。从凝胶纯化的酶中分离出具有类似于300-500个核苷酸的长度的RNA。经蛋白酶K广泛处理后,凝胶洗脱和标记的RNA在分子量上没有显示任何显着变化。单独孵育或在Mg2 +和脱氧核糖核苷酸磷酸存在下孵育的纯化RNA没有5-MeC-DNA糖基化酶或脱甲基活性。但是,将纯化的RNA与无RNA的无活性蛋白孵育后,5-MeC-DNA糖基化酶的活性可以恢复。

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