Huang Hsien-Sung, Matevossian Anouch, Whittle Catheryne, Kim Se Young, Schumacher Armin, Baker Stephen P, Akbarian Schahram
Brudnick Neuropsychiatric Research Institute, Department of Psychiatry, University of Massachusetts Medical School, Worcester, Massachusetts 01604, USA.
J Neurosci. 2007 Oct 17;27(42):11254-62. doi: 10.1523/JNEUROSCI.3272-07.2007.
Alterations in GABAergic mRNA expression play a key role for prefrontal dysfunction in schizophrenia and other neurodevelopmental disease. Here, we show that histone H3-lysine 4 methylation, a chromatin mark associated with the transcriptional process, progressively increased at GAD1 and other GABAergic gene promoters (GAD2, NPY, SST) in human prefrontal cortex (PFC) from prenatal to peripubertal ages and throughout adulthood. Alterations in schizophrenia included decreased GAD1 expression and H3K4-trimethylation, predominantly in females and in conjunction with a risk haplotype at the 5' end of GAD1. Heterozygosity for a truncated, lacZ knock-in allele of mixed-lineage leukemia 1 (Mll1), a histone methyltransferase expressed in GABAergic and other cortical neurons, resulted in decreased H3K4 methylation at GABAergic gene promoters. In contrast, Gad1 H3K4 (tri)methylation and Mll1 occupancy was increased in cerebral cortex of mice after treatment with the atypical antipsychotic, clozapine. These effects were not mimicked by haloperidol or genetic ablation of dopamine D2 and D3 receptors, suggesting that blockade of D2-like signaling is not sufficient for clozapine-induced histone methylation. Therefore, chromatin remodeling mechanisms at GABAergic gene promoters, including MLL1-mediated histone methylation, operate throughout an extended period of normal human PFC development and play a role in the neurobiology of schizophrenia.
γ-氨基丁酸能(GABAergic)信使核糖核酸(mRNA)表达的改变在精神分裂症和其他神经发育疾病的前额叶功能障碍中起关键作用。在此,我们表明,组蛋白H3赖氨酸4甲基化,一种与转录过程相关的染色质标记,在人类前额叶皮质(PFC)中,从产前到青春期前后以及整个成年期,在谷氨酸脱羧酶1(GAD1)和其他GABA能基因启动子(GAD2、神经肽Y、促生长抑素)处逐渐增加。精神分裂症中的改变包括GAD1表达和H3K4三甲基化降低,主要发生在女性中,并且与GAD1 5'端的一个风险单倍型相关。混合谱系白血病1(Mll1)的截短型lacZ敲入等位基因杂合性,Mll1是一种在GABA能和其他皮质神经元中表达的组蛋白甲基转移酶,导致GABA能基因启动子处的H3K4甲基化降低。相反,用非典型抗精神病药物氯氮平治疗后,小鼠大脑皮质中Gad1 H3K4(三)甲基化和Mll1占有率增加。这些效应未被氟哌啶醇或多巴胺D2和D3受体的基因敲除所模拟,表明D2样信号的阻断不足以引起氯氮平诱导的组蛋白甲基化。因此,GABA能基因启动子处的染色质重塑机制,包括MLL1介导的组蛋白甲基化,在正常人类PFC发育的延长时期内起作用,并在精神分裂症的神经生物学中发挥作用。