Lindsay S, Monk M, Holliday R, Huschtscha L, Davies K E, Riggs A D, Flavell R A
Ann Hum Genet. 1985 May;49(2):115-27. doi: 10.1111/j.1469-1809.1985.tb01683.x.
Methylation of CCGG sites was examined in four regions of the X chromosome with four X-chromosome clones, three obtained by cloning random segments and one encoding a structural gene. In DNA from human peripheral blood cells unmethylated sites correlating with the inactive X chromosome were detected in the vicinity of two of the random clones and also in the vicinity of a cloned sequence of the X-linked phosphoglycerate kinase gene (PGK). The third random clone covered a region whose methylation pattern was unchanged between the active and inactive X chromosomes. Differential methylation at the sites detected appears to have no functional role in the maintenance of the inactive X chromosome since both active and inactive X chromosomes were found to be undermethylated in DNA from human lymphoblastoid cells.
使用四个X染色体克隆对X染色体的四个区域中的CCGG位点甲基化情况进行了检测,其中三个克隆是通过克隆随机片段获得的,另一个克隆编码一个结构基因。在来自人类外周血细胞的DNA中,在两个随机克隆附近以及X连锁磷酸甘油酸激酶基因(PGK)的一个克隆序列附近检测到了与失活X染色体相关的未甲基化位点。第三个随机克隆覆盖的区域,其甲基化模式在活性和失活X染色体之间没有变化。由于在人类淋巴母细胞的DNA中发现活性和失活X染色体均发生低甲基化,因此所检测位点的差异甲基化似乎在维持失活X染色体方面没有功能作用。