Kang Moo-Il, Rhyu Mun-Gan, Kim Young-Ho, Jung Yu-Chae, Hong Seung-Jin, Cho Chul-Soo, Kim Hye-Soo
Department of Internal Medicine, The Catholic University of Korea, 505 Banpo-dong, Socho-gu, Seoul 137-701, Korea.
Genomics. 2006 May;87(5):580-90. doi: 10.1016/j.ygeno.2006.01.002. Epub 2006 Feb 20.
Alu and L1 retroelements have been suggested to initiate the spread of CpG methylation. In this study, the spread of CpG methylation was estimated based on the distance between the CpG islands and the nearest retroelements. All human genes (23,116) were examined and the correlations between the length of the CpG islands and the distance and density of the confronting retroelements were examined using nonoverlapping 5-kb windows. There was a linear relationship between the length of the CpG islands and the density of the Alu elements and an inverse relationship between the CpG islands and the L1 elements located more distantly, suggesting a suppressive effect of the Alu's on the spread of L1 methylation. Methylation analysis of the transitional CpG sites between the CpG islands and the nearest retroelements upstream of 16 genes was then carried out using DNA preparations from 11 different human tissues. Methylation-variable transitional CpGs were observed for the selected genes and the different tissues.
有人提出Alu和L1逆转录元件会引发CpG甲基化的传播。在本研究中,基于CpG岛与最近的逆转录元件之间的距离来估计CpG甲基化的传播情况。研究了所有人类基因(23,116个),并使用不重叠的5 kb窗口检查了CpG岛长度与相对的逆转录元件的距离和密度之间的相关性。CpG岛长度与Alu元件密度之间存在线性关系,而CpG岛与距离更远的L1元件之间存在反比关系,这表明Alu对L1甲基化传播具有抑制作用。然后,使用来自11种不同人类组织的DNA制剂,对16个基因上游的CpG岛与最近的逆转录元件之间的过渡性CpG位点进行甲基化分析。在所选择的基因和不同组织中观察到了甲基化可变的过渡性CpG。