Fedorov N A, Kuz'michev V A, Kritskii G A, Vinogradova Iu E
Biokhimiia. 1977 Jun;42(6):1020-3.
Methylation of pyrimidine isoplythes of newly synthesized DNA from activated human blood lymphocytes was studied under normal conditions and in chronic lymphocytic leukemia. The analysis of distribution of labelled 5-methylcytosine in DNA pyrimidine oligonucleotides, differing in their lengths, showed a considerable increase in the methylation of pyrimidine oligonucleotide fragments of DNA from lymphocytic leukemia lymphocytes as compared to normal. The greatest differences were observed in methylation with respect to longer fragments, e.g. under chronic lymphocytic leukemia the level of methylation of the cytosine residues of DNA in isoplythes I and II, as well as in the fraction of isoplyth III and in longer fragments exceeded that of the normal DNA isoplythes, 3.7-, 2.1- and 8.3-fold respectively.
在正常条件下以及慢性淋巴细胞白血病患者中,对来自活化人血淋巴细胞的新合成DNA的嘧啶同聚物甲基化进行了研究。对不同长度的DNA嘧啶寡核苷酸中标记的5-甲基胞嘧啶分布分析表明,与正常情况相比,淋巴细胞白血病淋巴细胞的DNA嘧啶寡核苷酸片段甲基化显著增加。在较长片段的甲基化方面观察到最大差异,例如在慢性淋巴细胞白血病中,同聚物I和II中DNA胞嘧啶残基的甲基化水平,以及同聚物III部分和较长片段中的甲基化水平分别超过正常DNA同聚物的3.7倍、2.1倍和8.3倍。