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CDKL5 is a brain MeCP2 target gene regulated by DNA methylation.

机译:CDKL5是受DNA甲基化调节的大脑MeCP2靶基因。

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Rett syndrome and its "early-onset seizure" variant are severe neurodevelopmental disorders associated with mutations within the MECP2 and the CDKL5 genes. Antidepressants and drugs of abuse induce the expression of the epigenetic factor MeCP2, thereby influencing chromatin remodeling. We show that increased MeCP2 levels resulted in the repression of Cdkl5 in rat brain structures in response to cocaine, as well as in cells exposed to serotonin, or overexpressing MeCP2. In contrast, Cdkl5 was induced by siRNA-mediated knockdown of Mecp2 and by DNA-methyltransferase inhibitors, demonstrating its regulation by MeCP2 and by DNA methylation. Cdkl5 gene methylation and its methylation-dependent binding to MeCP2 were increased in the striatum of cocaine-treated rats. Our data demonstrate that Cdkl5 is a MeCP2-repressed target gene providing a link between genes the mutation of which generates overlapping symptoms. They highlight DNA methylation changes as a potential mechanism participating in the long-term plasticity triggered by pharmacological agents.
机译:Rett综合征及其“早期发作”变异是与MECP2和CDKL5基因内的突变相关的严重神经发育障碍。抗抑郁药和滥用药物会诱导表观遗传因子MeCP2的表达,从而影响染色质重塑。我们显示,增加的MeCP2水平导致可卡因以及暴露于血清素或过表达MeCP2的细胞对大鼠脑结构中Cdkl5的抑制。相反,Cdkl5是由siRNA介导的Mecp2敲低和DNA-甲基转移酶抑制剂诱导的,证明了其由MeCP2和DNA甲基化的调控。在可卡因治疗的大鼠纹状体中,Cdkl5基因甲基化及其与MeCP2的甲基化依赖性结合增加。我们的数据表明Cdkl5是一种MeCP2抑制的靶基因,提供其突变产生重叠症状的基因之间的链接。他们强调了DNA甲基化变化是参与由药理剂触发的长期可塑性的潜在机制。

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