首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >In Z-DNA the sequence G-C-G-C is neither methylated by Hha I methyltransferase nor cleaved by Hha I restriction endonuclease.
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In Z-DNA the sequence G-C-G-C is neither methylated by Hha I methyltransferase nor cleaved by Hha I restriction endonuclease.

机译:在Z-DNA中序列G-C-G-C既不被Hha I甲基转移酶甲基化也不被Hha I限制性核酸内切酶切割。

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摘要

Plasmids carrying 24- or 32-base-pair inserts of alternating (dG-dC) residues were used to analyze the level of methylation of the G-C-G-C sites by Hha I DNA methyltransferase and their cleavage by Hha I endonuclease in the B-DNA or Z-DNA conformation. In supercoiled plasmids in which the inserts formed Z-DNA, the extent of methylation at the insert G-C-G-C sites was dramatically lower than the level of methylation at the G-C-G-C sites located outside the insert in the same plasmid. Similarly, cleavage by Hha I endonuclease was sharply lowered when the insert was in the Z-DNA form. In the relaxed plasmid, all its G-C-G-C sites were methylated to the same extent and the unmethylated sites were readily cleaved. After treatment with the methylase, the supercoiled plasmid was linearized and then digested with Hha I restriction endonuclease. This exposed unmethylated G-C-G-C sites from the insert that had been protected against cleavage in the Z conformation. A chemical reaction was used to study the distribution of the unmethylated cytosine residues. No accumulation of unmethylated cytosine residues was found anywhere along the entire 32-base-pair insert, which is consistent with a cooperative B-Z transition.
机译:使用带有24个或32个碱基对的交替(dG-dC)残基插入片段的质粒来分析Hha I DNA甲基转移酶对GCGC位点的甲基化水平以及B-DNA或Z中被Hha I核酸内切酶切割的程度-DNA构象。在插入物形成Z-DNA的超螺旋质粒中,插入物G-C-G-C位点处的甲基化程度明显低于同一质粒中位于插入物外的G-C-G-C位点处的甲基化水平。同样,当插入物为Z-DNA形式时,Hha I核酸内切酶的切割作用急剧降低。在松弛的质粒中,其所有的G-C-G-C位点都被甲基化到相同的程度,未甲基化的位点容易被切割。用甲基酶处理后,将超螺旋质粒线性化,然后用Hha I限制性核酸内切酶消化。这暴露了来自插入物的未甲基化的G-C-G-C位点,该位点已被保护免受Z构象的切割。使用化学反应来研究未甲基化的胞嘧啶残基的分布。在整个32个碱基对的插入片段中的任何位置都未发现未甲基化的胞嘧啶残基的积累,这与B-Z协同转变是一致的。

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