Kaput J, Sneider T W
Nucleic Acids Res. 1979 Dec 20;7(8):2303-22. doi: 10.1093/nar/7.8.2303.
Bacterial restriction endonucleases containing the dinucleotide CpG in their cleavage sequences were used to compare the methylation patterns of primarily repeated DNA sequences in (1) bovine somatic cell native DNAs vs bovine sperm cell native DNA and (2) native vs renatured bovine liver and sperm cell DNAs. The restriction patterns of sperm native DNA differ markedly from those of somatic cell native DNAs when using Hpa II, Hha I, and Ava I but not when using the enzymes Eco RI and Msp I. Digestion patterns of germ cell renatured DNA differed significantly from those of germ cell native DNA when using Hpa II but not when using Msp I or Eco RI. The results may not be due to artifacts of renaturation of the DNAs. The results are consistent with the concept that germ cell DNA may be strand asymmetrically hemimethylated. The data also suggest that methylation of the 5'-cytosine in the sequence CCGG renders this site insensitive to cleavage by Msp I.
使用切割序列中含有二核苷酸 CpG 的细菌限制性内切核酸酶,比较了以下几种情况下主要重复 DNA 序列的甲基化模式:(1)牛体细胞天然 DNA 与牛精子细胞天然 DNA;(2)天然牛肝和精子细胞 DNA 与复性后的牛肝和精子细胞 DNA。使用 Hpa II、Hha I 和 Ava I 时,精子天然 DNA 的限制性图谱与体细胞天然 DNA 的限制性图谱明显不同,但使用 Eco RI 和 Msp I 酶时则不然。使用 Hpa II 时,生殖细胞复性 DNA 的消化图谱与生殖细胞天然 DNA 的消化图谱有显著差异,但使用 Msp I 或 Eco RI 时则没有。结果可能并非由于 DNA 复性的假象。这些结果与生殖细胞 DNA 可能是链不对称半甲基化的概念一致。数据还表明,序列 CCGG 中 5'-胞嘧啶的甲基化使该位点对 Msp I 的切割不敏感。