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通过限制性内切酶切口平移检测人类异染色质的低甲基化。

Hypomethylation of human heterochromatin detected by restriction enzyme nick translation.

作者信息

Mitchell A R

机构信息

MRC Human Genetics Unit, Western General Hospital, Edinburgh, Scotland, United Kingdom.

出版信息

Exp Cell Res. 1992 Sep;202(1):203-6. doi: 10.1016/0014-4827(92)90421-4.

Abstract

Using the restriction enzymes MspI and HpaII in the nick translation procedure it has been shown that decondensation of the paracentric heterochromatin of chromosome 9 during human spermatogenesis is associated with hypomethylation of the DNA sequences in this domain. Somatic cells treated with 5'-azacytidine also showed decondensation of centromeric heterochromatin. In this instance, however, hypomethylation is detected both in the extended heterochromatin at the centromeres and in the euchromatin of the chromosome arms.

摘要

在缺口平移过程中使用限制性内切酶MspI和HpaII已表明,人类精子发生过程中9号染色体臂旁异染色质的解聚与该区域DNA序列的低甲基化有关。用5'-氮杂胞苷处理的体细胞也显示着丝粒异染色质的解聚。然而,在这种情况下,在着丝粒处扩展的异染色质以及染色体臂的常染色质中均检测到低甲基化。

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