INSERM, U575, Université de Strasbourg, Centre de Neurochimie, 67084 Strasbourg, France.
Neurobiol Dis. 2010 Jun;38(3):414-24. doi: 10.1016/j.nbd.2010.02.014. Epub 2010 Mar 6.
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.
雷特综合征及其“早发性癫痫”变异型是与 MECP2 和 CDKL5 基因内突变相关的严重神经发育障碍。抗抑郁药和滥用药物诱导表观遗传因子 MeCP2 的表达,从而影响染色质重塑。我们表明,在可卡因作用下,或在暴露于血清素的细胞中,或在过表达 MeCP2 的情况下,增加的 MeCP2 水平导致 Cdkl5 在大鼠脑结构中的抑制。相比之下,通过 siRNA 介导的 Mecp2 敲低和 DNA-甲基转移酶抑制剂诱导 Cdkl5 的表达,表明其受 MeCP2 和 DNA 甲基化的调控。在可卡因处理的大鼠纹状体中,Cdkl5 基因的甲基化及其与 MeCP2 的甲基化依赖性结合增加。我们的数据表明,Cdkl5 是 MeCP2 抑制的靶基因,为产生重叠症状的基因突变之间提供了联系。它们强调了 DNA 甲基化变化作为参与药物触发的长期可塑性的潜在机制。