Kim Hwan-Hee, Park Jung-Hoon, Jeong Kyoung-Sin, Lee Suman
Functional Genomics Lab, Graduate School of Life Science and Biotechnology, CHA Research Institute, College of Medicine, Pochon CHA University, Bundang-Gu, Sungnam-Si, Kyunggi-Do, Republic of Korea.
Electrophoresis. 2007 Nov;28(21):3854-61. doi: 10.1002/elps.200600733.
A large portion of the genome represents repetitive elements. Identifier (ID) elements, the major elements of short interspersed repetitive elements, are widespread with about 150 000 copies in the rat genome. Each ID element contains six CpG dinucleotides, which might account for the global methylation status of rat. We validated the CpG methylation of the ID elements by various methods. The methylation of one CpG site (CpG-3) of the ID element was investigated by performing pyrosequencing. The methylation percentage of the CpG-3 site was 53.6% (SD = 2.2) on average from six rat tissues with blood, but 24.6% (SD = 1.0) in rat pheochromocytoma, PC-12, cell line. This CpG-3 methylation was further verified by whole genome amplification (WGA), 5-azacytidine treatment, and proportional mixing of rat WGA genomic DNA (gDNA) with liver gDNA. Methylation-sensitive restriction enzyme PCR method showed that three other CpG sites (CpG-1, CpG-4, and CpG-5) within the ID element were also methylated (about 60%) in rat gDNA, but not in WGA gDNA. The ID elements may be good candidates for routine analysis of the global DNA methylation changes of rat for pharmaceutical treatment and their use can make basic epigenetic research possible with high accuracy.
基因组的很大一部分由重复元件组成。标识符(ID)元件是短散在重复元件的主要组成部分,在大鼠基因组中广泛分布,约有150000个拷贝。每个ID元件包含六个CpG二核苷酸,这可能解释了大鼠的整体甲基化状态。我们通过多种方法验证了ID元件的CpG甲基化。通过焦磷酸测序研究了ID元件的一个CpG位点(CpG-3)的甲基化情况。来自六个含血大鼠组织的CpG-3位点的平均甲基化百分比为53.6%(标准差=2.2),但在大鼠嗜铬细胞瘤PC-12细胞系中为24.6%(标准差=1.0)。通过全基因组扩增(WGA)、5-氮杂胞苷处理以及大鼠WGA基因组DNA(gDNA)与肝脏gDNA的比例混合进一步验证了这种CpG-3甲基化。甲基化敏感限制性内切酶PCR方法显示,ID元件内的其他三个CpG位点(CpG-1、CpG-4和CpG-5)在大鼠gDNA中也被甲基化(约60%),但在WGA gDNA中未被甲基化。ID元件可能是用于药物治疗大鼠整体DNA甲基化变化常规分析的良好候选者,其应用可以使高精度的基础表观遗传学研究成为可能。