首页> 外文期刊>Journal of Molecular Biology >The activity of the murine DNA methyltransferase Dnmt1 is controlled by interaction of the catalytic domain with the N-terminal part of the enzyme leading to an allosteric activation of the enzyme after binding to methylated DNA
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The activity of the murine DNA methyltransferase Dnmt1 is controlled by interaction of the catalytic domain with the N-terminal part of the enzyme leading to an allosteric activation of the enzyme after binding to methylated DNA

机译:鼠DNA甲基转移酶Dnmt1的活性受催化域与酶N末端部分的相互作用的控制,导致与甲基化DNA结合后酶的变构活化

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摘要

The mammalian DNA methyltransferase Dnmt1 is responsible for the maintenance of the pattern of DNA methylation in vivo. It is a large multidomain enzyme comprising 1620 amino acid residues. We have purified and characterized individual domains of Dnmt1 (NLS-containing domain, NlsD, amino acid residues: 1-343; replication foci-directing domain, 350-609; Zn-binding domain (ZnD), 613-748; polybromo domain, 746-1110; and the catalytic domain (CatD), 1124-1620). CatD, ZnD and NlsD bind to DNA, demonstrating the existence of three independent DNA-binding sites in Dnmt1. CatD shows a preference for binding to hemimethylated CpG-sites; ZnD prefers methylated CpGs; and NlsD specifically binds to CpG-sites, but does not discriminate between unmethylated and methylated DNA. These results are not compatible with the suggestion that the target recognition domain of Dnmt1 resides in the N terminus of the enzyme. We show by protein-protein interaction assays that ZnD and CatD interact with each other. The isolated catalytic domain does not methylate DNA, neither alone nor in combination with other domains. Full-length Dnmt1 was purified from baculovirus-infected insect cells. Under the experimental conditions, Dnmt1 has a strong (50-fold) preference for hemimethylated DNA. Dnmt1 is stimulated to methylate unmodified CpG sites by the addition of fully methylated DNA. This effect is dependent on Zn, suggesting that binding of methylated DNA to ZnD triggers the allosteric activation of the catalytic center of Dnmt1. The allosteric activation model can explain kinetic data obtained by others. It suggests that Dnmt1 might be responsible for spreading of methylation, a process that is observed during aging and carcenogenesis but may be important for de novo methylation of DNA. (C) 2001 Academic Press. [References: 52]
机译:哺乳动物DNA甲基转移酶Dnmt1负责体内DNA甲基化模式的维持。它是一种大型多域酶,包含1620个氨基酸残基。我们已经纯化并鉴定了Dnmt1的单个结构域(含NLS的结构域,NlsD,氨基酸残基:1-343;复制焦点导向结构域,350-609; Zn结合结构域(ZnD),613-748;多溴结构域, 746-1110;和催化结构域(CatD),1124-1620)。 CatD,ZnD和NlsD与DNA结合,表明Dnmt1中存在三个独立的DNA结合位点。 CatD显示出优先结合半甲基化CpG位点; ZnD更喜欢甲基化的CpGs。 NlsD与CpG位点特异性结合,但不能区分未甲基化和甲基化的DNA。这些结果与Dnmt1的目标识别域位于酶的N末端的建议不符。我们通过蛋白质-蛋白质相互作用测定法显示ZnD和CatD彼此相互作用。分离的催化结构域既不单独也不与其他结构域结合,也不使DNA甲基化。从杆状病毒感染的昆虫细胞中纯化全长Dnmt1。在实验条件下,Dnmt1对半甲基化DNA具有强烈的偏好(50倍)。通过添加完全甲基化的DNA,刺激Dnmt1甲基化未修饰的CpG位点。这种作用取决于锌,表明甲基化DNA与ZnD的结合会触发Dnmt1催化中心的变构活化。变构激活模型可以解释其他人获得的动力学数据。这表明Dnmt1可能是导致甲基化扩散的原因,这一过程在衰老和致癌过程中观察到,但对DNA的从头甲基化可能很重要。 (C)2001学术出版社。 [参考:52]

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