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法医尸检标本中生物钟基因启动子的甲基化分析

Methylation analysis of circadian clock gene promoters in forensic autopsy specimens.

作者信息

Nakatome Masato, Orii Minami, Hamajima Makoto, Hirata Yukari, Uemura Misato, Hirayama Sayaka, Isobe Ichiro

机构信息

Department of Legal Medicine, Fujita Health University School of Medicine, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi 470-1192, Japan.

出版信息

Leg Med (Tokyo). 2011 Jul;13(4):205-9. doi: 10.1016/j.legalmed.2011.03.001. Epub 2011 May 18.

DOI:10.1016/j.legalmed.2011.03.001
PMID:21596611
Abstract

DNA methylation in gene promoter regions influences gene expression. Circadian clock genes play an important role in the formation of a biological clock and aberrant methylation of these genes contributes to several disorders. In this study, we examined forensic autopsy specimens to determine whether DNA methylation status in the promoter regions of nine circadian clock genes (Per1, Per2, Per3, Cry1, Cry2, Bmal1, Clock, Tim, and Ck1e) is related to a change in acquired diathesis and/or causes of death. Methylation-specific PCR and direct sequencing methods revealed that the promoters of Per1, Cry2, Bmal1, Clock, and Ck1e were unmethylated in all the forensic autopsy specimens, while the promoters of Per2, Per3, Cry1, and Tim were partially methylated. Methylation status varied between individuals and between tissues in the same patient. A detailed analysis of methylation patterns in the Cry1 promoter region revealed that the patterns also varied between individuals and the Cry1 promoter had highly methylated patterns in two cases that had been exposed to methamphetamine. These results suggest that the methylation status of clock gene promoters varies between individuals. Methamphetamine use may influence methylation in the Cry1 gene promoter region and disturb circadian rhythmicity.

摘要

基因启动子区域的DNA甲基化影响基因表达。昼夜节律时钟基因在生物钟的形成中起重要作用,这些基因的异常甲基化会导致多种疾病。在本研究中,我们检查了法医尸检标本,以确定九个昼夜节律时钟基因(Per1、Per2、Per3、Cry1、Cry2、Bmal1、Clock、Tim和Ck1e)启动子区域的DNA甲基化状态是否与后天素质的变化和/或死因有关。甲基化特异性PCR和直接测序方法显示,在所有法医尸检标本中,Per1、Cry2、Bmal1、Clock和Ck1e的启动子未甲基化,而Per2、Per3、Cry1和Tim的启动子部分甲基化。甲基化状态在个体之间以及同一患者的不同组织之间存在差异。对Cry1启动子区域甲基化模式的详细分析表明,不同个体的甲基化模式也有所不同,并且在两例使用过甲基苯丙胺的病例中,Cry1启动子具有高度甲基化的模式。这些结果表明,时钟基因启动子的甲基化状态在个体之间存在差异。使用甲基苯丙胺可能会影响Cry1基因启动子区域的甲基化并扰乱昼夜节律。

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