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首页> 外文期刊>Nucleic acids research >DNA-methylase from regenerating rat liver: purification and characterisation
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DNA-methylase from regenerating rat liver: purification and characterisation

机译:从再生大鼠肝脏的DNA-甲基酶:纯化和表征

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摘要

DNA methylase has been purified 660-fold from nuclei from regenerating rat liver. The enzyme is able to methylate single stranded (ss) and double stranded (ds) DNA, the only reaction product being 5-methylcytosine. Previously unmethylated double stranded DNA from prokaryotes (M.luteus) as well as from euka- ryotes (Ascaris suis) can serve as substrates. The synthetic copolymers (dG-dC)n . (dC-dG)n and (dG,dC)n are also methylated. While SV40 DNA is almost not methylated, PM2 DNA is a good sub strate even in the supercoiled form. The enzyme methylates 1 in 17 bases in heterologous M.luteus DNA, but only 1 in 590 in homologous rat liver DNA. The high methylation level of M.hrteus DNA, an analysis of the methylated pyrimidine isostichs and a preliminary dinucleotide analysis suggest that all the CpGs in a DNA can be methylated.
机译:DNA甲基酶已从再生大鼠肝脏中纯化660倍。酶能够甲酸盐单链(SS)和双链(DS)DNA,唯一的反应产物为5-甲基胞嘧啶。以前未甲基化的双链DNA来自原核生物(M.luteus)以及来自Euka-ryotes(蛔虫Suis)可以用作底物。合成共聚物(DG-DC)n。 (DC-DG)N和(DG,DC)N也甲基化。虽然SV40 DNA几乎不甲基化,但PM2 DNA均匀亚脱晶均匀。酶在17个碱基中在异源M.Luteus DNA中甲酸盐1,但在同源大鼠肝脏DNA中仅为590中。 M.HRTEUS DNA的高甲基化水平,甲基化嘧啶isostichs的分析和初步的二核苷酸分析表明DNA中的所有CPG可以甲基化。

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