Hendriks R W, Hinds H, Chen Z Y, Craig I W
Department of Biochemistry, University of Oxford, United Kingdom.
Genomics. 1992 Nov;14(3):598-603. doi: 10.1016/s0888-7543(05)80157-0.
The DXS255 locus at Xp11.22 is highly polymorphic due to a 26-bp variable number of tandem repeats (VNTR) motif. In previous studies, one of the MspI sites flanking the VNTR manifested a correlation between methylation and X chromosome inactivation. Here we show, by DNA sequence analysis, that this MspI site is located within the CpG island at the 5' end of a LINE-1 element, which is 2.5 kb from the VNTR. The methylation status of the CpG island was assessed in Southern blotting experiments using the methylation-sensitive enzymes HpaII, HhaI, and BssHII. All these sites were completely methylated on active X chromosomes, consistent with previously reported findings of full methylation of LINE-1 elements throughout the genome. However, on inactive X chromosomes these sites were predominantly unmethylated, although patterns were found to be heterogeneous. The results suggest that LINE-1 elements on the inactive X chromosome are not suppressed by full methylation of their CpG islands. The differential methylation of the DXS255 CpG island provides the basis for a highly informative X inactivation analysis system.
位于Xp11.22的DXS255基因座由于存在一个26个碱基对的串联重复可变数目(VNTR)基序而具有高度多态性。在先前的研究中,VNTR侧翼的一个MspI位点显示出甲基化与X染色体失活之间的相关性。在此我们通过DNA序列分析表明,这个MspI位点位于一个LINE-1元件5'端的CpG岛内,该元件距离VNTR为2.5 kb。在Southern印迹实验中使用甲基化敏感酶HpaII、HhaI和BssHII评估了CpG岛的甲基化状态。在活跃的X染色体上,所有这些位点均完全甲基化,这与先前报道的全基因组LINE-1元件完全甲基化的结果一致。然而,在失活的X染色体上,这些位点主要未甲基化,尽管发现其模式存在异质性。结果表明,失活X染色体上的LINE-1元件不会因其CpG岛的完全甲基化而受到抑制。DXS255 CpG岛的差异甲基化为一个信息丰富的X失活分析系统提供了基础。