Division of Neurobiology, The M. S. University of Baroda, Vadodara, Gujarat, 390002, India.
Department of Zoology, The M. S. University of Baroda, Vadodara, Gujarat, 390002, India.
J Mol Neurosci. 2018 Jul;65(3):343-350. doi: 10.1007/s12031-018-1112-4. Epub 2018 Jul 10.
MeCP2 (methyl-CpG binding protein 2), an epigenetic regulator, has been shown to regulate the function of neurons and glial cells. Our previous study has demonstrated that MeCP2 repress the myelin gene expression in rat oligodendrocytes but whether MeCP2 bind to myelin gene MBP and PLP is not yet known. Besides oligodendrocytes, C6 glioma also expresses myelin genes and could be used as a model system to study myelin gene expression. In the present study, we determined that MeCP2 directly bind to MBP, PLP, and BDNF promoter in oligodendrocytes. Further, it was found that MeCP2 differentially regulates the myelin gene expression in oligodendrocytes and C6 glioma. In contrast to oligodendrocytes, MeCP2 does not bind to promoter region of MBP and PLP in C6 glioma suggest that MeCP2 differentially regulates the gene expression in different cell types.
MeCP2(甲基化CpG 结合蛋白 2)是一种表观遗传调节剂,已被证明可以调节神经元和神经胶质细胞的功能。我们之前的研究表明,MeCP2 抑制大鼠少突胶质细胞中的髓鞘基因表达,但尚不清楚 MeCP2 是否与髓鞘基因 MBP 和 PLP 结合。除了少突胶质细胞,C6 神经胶质瘤也表达髓鞘基因,可作为研究髓鞘基因表达的模型系统。在本研究中,我们确定 MeCP2 可直接结合少突胶质细胞中的 MBP、PLP 和 BDNF 启动子。此外,还发现 MeCP2 可在少突胶质细胞和 C6 神经胶质瘤中差异调节髓鞘基因的表达。与少突胶质细胞相反,MeCP2 不与 C6 神经胶质瘤中的 MBP 和 PLP 启动子区域结合,表明 MeCP2 可在不同细胞类型中差异调节基因表达。