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The Caulobacter crescentus DNA-(adenine-N6)-methyltransferase CcrM methylates DNA in a distributive manner

机译:新月形芽孢杆菌DNA-(腺嘌呤-N6)-甲基转移酶CcrM以分布方式甲基化DNA

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摘要

The specificity and processivity of DNA methyltransferases have important implications regarding their biological functions. We have investigated the sequence specificity of CcrM and show here that the enzyme has a high specificity for GANTC sites, with only minor preferences at the central position. It slightly prefers hemimethylated DNA, which represents the physiological substrate. In a previous work, CcrM was reported to be highly processive [Berdis et al. (1998) Proc. Natl Acad. Sci. USA95: 2874–2879]. However upon review of this work, we identified a technical error in the setup of a crucial experiment in this publication, which prohibits making any statement about the processivity of CcrM. In this study, we performed a series of in vitro experiments to study CcrM processivity. We show that it distributively methylates six target sites on the pUC19 plasmid as well as two target sites located on a 129-mer DNA fragment both in unmethylated and hemimethylated state. Reaction quenching experiments confirmed the lack of processivity. We conclude that the original statement that CcrM is processive is no longer valid.
机译:DNA甲基转移酶的特异性和可合成性对其生物学功能具有重要意义。我们研究了CcrM的序列特异性,并在此表明该酶对GANTC位点具有高特异性,而在中心位置只有极少的偏爱。它稍微偏爱代表生理底物的半甲基化DNA。在以前的工作中,据报道CcrM具有高度的合成能力[Berdis等。 (1998)美国国家科学院院刊。 Natl Acad。科学USA95:2874–2879]。但是,在回顾这项工作时,我们发现该出版物中关键实验的设置存在技术错误,该错误禁止发表有关CcrM合成能力的任何陈述。在这项研究中,我们进行了一系列体外实验来研究CcrM的合成能力。我们表明,它在未甲基化和半甲基化状态下对pUC19质粒上的六个靶位以及两个位于129-mer DNA片段上的靶位进行甲基化。反应淬灭实验证实了缺乏合成能力。我们得出结论,关于CcrM具有持续性的原始说法不再有效。

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