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Promoter methylation analysis of seven clock genes in Parkinson's disease

机译:帕金森氏病中七个时钟基因的启动子甲基化分析

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摘要

The expression of clock genes is altered in leukocytes from patients with Parkinson's disease (PD). However, the underlying mechanisms are unknown. To determine whether abnormal CpG methylation contributes to the dysregulated expression of these genes, the methylation status of the promoters of seven major human clock genes, PER1, PER2, CRY1, CRY2, Clock, NPAS2, and BMAL1, was examined using methylation-specific PCR (MSP) and sequencing in 206 PD patients and 181 healthy controls. This analysis revealed that most clock gene promoters were devoid of methylation. Methylation was only detectable in the CRY1 and NPAS2 promoters. Interestingly, the methylation frequency of the NPAS2 promoter was significantly decreased in PD patients. These results suggest that altered promoter methylation may contribute to the abnormal expression of clock genes in PD.
机译:帕金森氏病(PD)患者的白细胞中时钟基因的表达发生了改变。但是,其潜在机制尚不清楚。为了确定异常的CpG甲基化是否导致这些基因的表达失调,使用甲基化特异性PCR检查了七个主要人类时钟基因PER1,PER2,CRY1,CRY2,Clock,NPAS2和BMAL1的启动子的甲基化状态。 (MSP)和测序在206名PD患者和181名健康对照中进行。这项分析表明,大多数时钟基因启动子都没有甲基化。甲基化只能在CRY1和NPAS2启动子中检测到。有趣的是,PD患者中NPAS2启动子的甲基化频率显着降低。这些结果表明,启动子甲基化的改变可能与PD中Clock基因的异常表达有关。

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