Iwata Atsushi
Department of Molecular Neuroscience on Neurodegeneration, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
Nihon Shinkei Seishin Yakurigaku Zasshi. 2012 Nov;32(5-6):269-73.
Alpha-synuclein (SNCA) gene expression is an important factor in the pathogenesis of Parkinson's disease (PD). Gene multiplication can cause inherited PD, and promoter polymorphisms that increase SNCA expression are associated with sporadic PD. CpG methylation in the promoter region may also influence SNCA expression. By using cultured cells, we identified a region of the SNCA CpG island in which the methylation status altered along with increased SNCA expression. Postmortem brain analysis revealed regional non-specific methylation differences in this CpG region in the anterior cingulate and putamen among controls and PD; however, in the substantia nigra of PD, methylation was significantly decreased. This CpG region may function as an intronic regulatory element for the SNCA gene. Our findings suggest that a novel epigenetic regulatory mechanism controlling SNCA expression influences PD pathogenesis.
α-突触核蛋白(SNCA)基因表达是帕金森病(PD)发病机制中的一个重要因素。基因倍增可导致遗传性PD,而增加SNCA表达的启动子多态性与散发性PD相关。启动子区域的CpG甲基化也可能影响SNCA表达。通过使用培养细胞,我们确定了SNCA CpG岛的一个区域,其中甲基化状态随SNCA表达增加而改变。尸检脑分析显示,对照组和PD患者前扣带回和壳核中该CpG区域存在区域非特异性甲基化差异;然而,在PD患者的黑质中,甲基化显著降低。该CpG区域可能作为SNCA基因的内含子调控元件发挥作用。我们的研究结果表明,一种控制SNCA表达的新型表观遗传调控机制影响PD的发病机制。