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人类和蚊子染色体中DNA甲基化位点的直接可视化。

Direct visualization of the sites of DNA methylation in human, and mosquito chromosomes.

作者信息

Bianchi N O, Vidal-Rioja L, Cleaver J E

出版信息

Chromosoma. 1986;94(5):362-6. doi: 10.1007/BF00328636.

Abstract

Human and mosquito fixed chromosomes were digested with restriction endonucleases that are inhibited by the presence of 5-methylcytosine in their restriction sites (Hha I, Hin PI, Hpa II), and with endonucleases for which cleavage is less dependent on the state of methylation (Taq I, Msp I). Methylation-dependent enzymes extracted low DNA amounts from human chromosomes, while methylation-independent enzymes extracted moderate to high amounts of DNA. After DNA demethylation with 5-azacytidine the isoschizomers Hpa II (methylation-dependent) and Msp I (methylation-independent) extracted 12-fold and 1.4-fold amounts of DNA from human chromosomes, respectively. These findings indicate that human DNA has a high concentration of Hpa II and Msp I restriction sites (CCGG), and that the internal C of this sequence is methylated in most cases, while the external cytosine is methylated less often. All the enzymes tested released moderate amounts of DNA from mosquito chromosomes whether or not the DNA was demethylated with 5-azacytidine. Hpa II induced banding in the centromere chromosome regions. After demethylation with 5-azacytidine this banding disappeared. Mosquito DNA has therefore, moderate to high frequencies of nonmethylated CpG duplets. The only exception is the centromeric DNA, in which the high levels of C methylation present produce cleavage by Hpa II and the appearance of banding. Centromere regions of human chromosomes 1 have a moderately low concentration of Hpa II-Msp I restriction sites.

摘要

用其识别位点中存在5-甲基胞嘧啶会受到抑制的限制性内切酶(Hha I、Hin PI、Hpa II)以及切割对甲基化状态依赖性较小的内切酶(Taq I、Msp I)消化人类和蚊子的固定染色体。依赖甲基化的酶从人类染色体中提取的DNA量较低,而不依赖甲基化的酶提取的DNA量为中等至高。用5-氮杂胞苷进行DNA去甲基化后,同裂酶Hpa II(依赖甲基化)和Msp I(不依赖甲基化)分别从人类染色体中提取的DNA量增加了12倍和1.4倍。这些发现表明,人类DNA中Hpa II和Msp I识别位点(CCGG)的浓度很高,并且在大多数情况下该序列内部的C是甲基化的,而外部的胞嘧啶甲基化的频率较低。无论DNA是否用5-氮杂胞苷去甲基化,所有测试的酶从蚊子染色体中释放的DNA量都适中。Hpa II在着丝粒染色体区域诱导条带形成。用5-氮杂胞苷去甲基化后,这种条带消失。因此,蚊子DNA中未甲基化的CpG二联体频率为中等至高。唯一的例外是着丝粒DNA,其中高水平的C甲基化导致Hpa II切割并出现条带。人类1号染色体的着丝粒区域中Hpa II - Msp I识别位点的浓度适中偏低。

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