Glover T W, Coyle-Morris J, Pearce-Birge L, Berger C, Gemmill R M
Am J Hum Genet. 1986 Mar;38(3):309-18.
Experiments were performed to determine the role of DNA demethylation in fragile X expression. Fragile X positive lymphoblastoid cells were treated with 5-azacytidine and harvested for analysis of fragile X expression both directly following treatment and after a recovery period in the absence of the drug. The effectiveness of 5-azacytidine treatment in inducing DNA demethylation was concurrently monitored by analysis of methylation changes at random autosomal loci in isolated DNA from treated cells. Under conditions where 5-azacytidine was found to inhibit fragile X expression, no DNA demethylation was observed. At the time when demethylation did occur, fragile X expression was not affected. These results strongly indicate that DNA demethylation is not involved in fragile X expression.
进行实验以确定DNA去甲基化在脆性X表达中的作用。用5-氮杂胞苷处理脆性X阳性淋巴母细胞,并在处理后直接以及在无药物的恢复期后收获细胞用于分析脆性X表达。通过分析来自处理细胞的分离DNA中随机常染色体位点的甲基化变化,同时监测5-氮杂胞苷处理诱导DNA去甲基化的有效性。在发现5-氮杂胞苷抑制脆性X表达的条件下,未观察到DNA去甲基化。当发生去甲基化时,脆性X表达未受影响。这些结果有力地表明DNA去甲基化不参与脆性X表达。