Razin A, Urieli S, Pollack Y, Gruenbaum Y, Glaser G
Nucleic Acids Res. 1980 Apr 25;8(8):1783-92. doi: 10.1093/nar/8.8.1783.
Two pairs of restriction enzyme isoschizomers were used to study in vivo methylation of E. coli and extrachromosomal DNA. By use of the restriction enzymes MboI (which cleaves only the unmethylated GATC sequence) and its isoschizomer Sau3A (indifferent to methylated adenine at this sequence), we found that all the GATC sites in E. coli and in extrachromosomal DNAs are symmetrically methylated on both strands. The calculated number of GATC sites in E. coli DNA can account for all its m6Ade residues. Foreign DNA, like mouse mtDNA, which is not methylated at GATC sites became fully methylated at these sequences when introduced by transfection into E. coli cells. This experiment provides the first evidence for the operation of a de novo methylation mechanism for E. coli methylases not involved in restriction modification. When the two restriction enzyme isoschizomers, EcoRII and ApyI, were used to analyze the methylation pattern of CCTAGG sequences in E. coli C and phi X174 DNA, it was found that all these sites are methylated. The number of CCTAGG sites in E. coli C DNA does not account for all m5Cyt residues.
使用两对限制性内切酶同裂酶来研究大肠杆菌和染色体外DNA的体内甲基化情况。通过使用限制性内切酶MboI(其仅切割未甲基化的GATC序列)及其同裂酶Sau3A(对此序列处甲基化的腺嘌呤不敏感),我们发现大肠杆菌和染色体外DNA中的所有GATC位点在两条链上均对称甲基化。计算得出的大肠杆菌DNA中GATC位点的数量可解释其所有的6-甲基腺嘌呤残基。外来DNA,如小鼠线粒体DNA,其在GATC位点未甲基化,但通过转染导入大肠杆菌细胞后,这些序列处会完全甲基化。该实验为不参与限制修饰的大肠杆菌甲基化酶的从头甲基化机制的运作提供了首个证据。当使用两种限制性内切酶同裂酶EcoRII和ApyI分析大肠杆菌C和φX174 DNA中CCTAGG序列的甲基化模式时,发现所有这些位点均被甲基化。大肠杆菌C DNA中CCTAGG位点的数量不能解释所有的5-甲基胞嘧啶残基。