Singer J, Roberts-Ems J, Luthardt F W, Riggs A D
Nucleic Acids Res. 1979 Dec 20;7(8):2369-85. doi: 10.1093/nar/7.8.2369.
The distribution and amount of 5-methylcytosine (5-MeCyt) in DNA was measured for early embryos of mouse strain CF1 (2 to 4 cell stage to blastocyst) and mouse teratocarcinoma cells. In each case, the pattern of methylation was examined by use of the restriction enzymes Hha I and HPA II HPA II, which cut DNA at the sites 5'GCGC and 5'CCGG respectively, when the cytosines at these sites are not methylated. Mouse embryo DNA was found to have the same level of methylation as adult mouse tissues, and no changes in methylation were seen during differentiation of the teratocarcinoma cells. The ratio of 5-MeCyt/Cyt in DNA was measured by high performance liquid chromatography for the differentiating teratocarcinoma cells and for several adult mouse and rabbit tissues. The variation between tissues or between teratocarcinoma cells at different stages of differentiation was less than 10 percent. These results are discussed in view of proposals that 5-MeCyt plays a role in differentiation.
对CF1品系小鼠(2至4细胞期至囊胚)的早期胚胎以及小鼠畸胎瘤细胞的DNA中5-甲基胞嘧啶(5-MeCyt)的分布和含量进行了测定。在每种情况下,通过使用限制性内切酶Hha I和HPA II来检测甲基化模式,当这些位点的胞嘧啶未甲基化时,Hha I和HPA II分别在5'GCGC和5'CCGG位点切割DNA。发现小鼠胚胎DNA的甲基化水平与成年小鼠组织相同,并且在畸胎瘤细胞分化过程中未观察到甲基化变化。通过高效液相色谱法测定了分化中的畸胎瘤细胞以及几种成年小鼠和兔组织DNA中5-MeCyt/Cyt的比率。不同组织之间或不同分化阶段的畸胎瘤细胞之间的差异小于10%。鉴于5-MeCyt在分化中起作用的提议,对这些结果进行了讨论。