Miniou P, Bourc'his D, Molina Gomes D, Jeanpierre M, Viegas-Péquignot E
U383 INSERM, Hôpital Necker-Enfants Malades, Paris, France.
Cytogenet Cell Genet. 1997;77(3-4):308-13. doi: 10.1159/000134605.
The methylation status of young Alu sequences was investigated in four ICF patients. In fibroblast and leukocyte DNAs, Alu repeats were either undermethylated (HhaI and HpaII digestion) or demethylated (BstUI digestion), in contrast with the methylated status of Alus in control subjects. The methylation profile exhibited in ICF patients reproduces the normal profile of placental or sperm DNA. High-sensitivity immunocytochemical detection of HhaI and HpaII restriction sites on metaphase chromosomes provided further evidence of this undermethylation. The DNA methylation defect in ICF patients, first detected in satellite DNAs (constitutive heterochromatin) and CpG islands of genes on the inactive X chromosome (facultative heterochromatin), thus includes Alu sequences that are widely distributed throughout the human genome.
在四名ICF患者中研究了年轻Alu序列的甲基化状态。在成纤维细胞和白细胞DNA中,Alu重复序列要么甲基化不足(经HhaI和HpaII消化),要么去甲基化(经BstUI消化),这与对照受试者中Alu的甲基化状态形成对比。ICF患者中表现出的甲基化谱再现了胎盘或精子DNA的正常谱。对中期染色体上HhaI和HpaII限制性位点的高灵敏度免疫细胞化学检测为这种甲基化不足提供了进一步证据。ICF患者中的DNA甲基化缺陷最初在卫星DNA(组成型异染色质)和失活X染色体上基因的CpG岛(兼性异染色质)中检测到,因此包括广泛分布于整个人类基因组中的Alu序列。