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首页> 外文期刊>Molecular and Cellular Endocrinology >CpG methylation and the methyl CpG binding protein 2 (MeCP2) are required for restraining corticotropin releasing hormone (CRH) gene expression
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CpG methylation and the methyl CpG binding protein 2 (MeCP2) are required for restraining corticotropin releasing hormone (CRH) gene expression

机译:CpG甲基化和甲基CpG结合蛋白2(MECP2)需要抑制皮质激素释放激素(CRH)基因表达

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摘要

The hypothalamic-pituitary-adrenal (HPA) axis plays a critical role in mounting a stress response and maintaining homeostasis. A dysregulated HPA axis and elevated levels of CRH are associated with a number of disorders. Although extensive research has been devoted to understanding molecular events associated with stimulated CRH gene, less is known about the mechanisms that restrain CRH expression. Using a cell culture system, we report here two molecular aspects of CRH gene regulation that are required for maintenance of basal level of CRH gene expression. These are a specific CpG methylation at a single CpG, and adequate levels of the methyl CpG binding protein 2 (MeCP2). The single site methylation allows the recruitment of MeCP2 to the CRH gene promoter region, and MeCP2 knockdown leads to increased expression of CRH gene. Taken together, the results indicate that site-specific methylation and MeCP2 are required for maintenance of basal levels of CRH gene expression. (C) 2017 Published by Elsevier Ireland Ltd.
机译:下丘脑 - 垂体 - 肾上腺(HPA)轴在安装应力响应和维持稳态方面发挥着关键作用。具有疑难解的HPA轴和升高的CRH水平与许多疾病有关。虽然已经致力于了解与刺激的CRH基因相关的分子事件的广泛研究,但是抑制CRH表达的机制较少。使用细胞培养系统,我们在此报告了CRH基因调控的两个分子方面,用于维持CRH基因表达的基础水平。这些是单个CPG的特异性CpG甲基化,并且足够水平的甲基CpG结合蛋白2(MECP2)。单位甲基化允许募集MECP2至CRH基因启动子区,MECP2敲低导致CRH基因的表达增加。占据,结果表明,培养基因水平的CRH基因表达的基础水平需要特异性甲基化和MECP2。 (c)2017年由elsevier爱尔兰有限公司出版

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