Sackler Program for Epigenetics and Developmental Psychobiology at McGill University, Douglas Mental Health University Institute, McGill University, Montreal, Quebec H4H 1R3, Canada.
J Neurosci. 2010 Sep 29;30(39):13130-7. doi: 10.1523/JNEUROSCI.1039-10.2010.
Parenting and the early environment influence the risk for various psychopathologies. Studies in the rat suggest that variations in maternal care stably influence DNA methylation, gene expression, and neural function in the offspring. Maternal care affects neural development, including the GABAergic system, the function of which is linked to the pathophysiology of diseases including schizophrenia and depression. Postmortem studies of human schizophrenic brains have revealed decreased forebrain expression of glutamic acid decarboxylase 1 (GAD1) accompanied by increased methylation of a GAD1 promoter. We examined whether maternal care affects GAD1 promoter methylation in the hippocampus of adult male offspring of high and low pup licking/grooming (high-LG and low-LG) mothers. Compared with the offspring of low-LG mothers, those reared by high-LG dams showed enhanced hippocampal GAD1 mRNA expression, decreased cytosine methylation, and increased histone 3-lysine 9 acetylation (H3K9ac) of the GAD1 promoter. DNA methyltransferase 1 expression was significantly higher in the offspring of low- compared with high-LG mothers. Pup LG increases hippocampal serotonin (5-HT) and nerve growth factor-inducible factor A (NGFI-A) expression. Chromatin immunoprecipitation assays revealed enhanced NGFI-A association with and H3K9ac of the GAD1 promoter in the hippocampus of high-LG pups after a nursing bout. Treatment of hippocampal neuronal cultures with either 5-HT or an NGFI-A expression plasmid significantly increased GAD1 mRNA levels. The effect of 5-HT was blocked by a short interfering RNA targeting NGFI-A. These results suggest that maternal care influences the development of the GABA system by altering GAD1 promoter methylation levels through the maternally induced activation of NGFI-A and its association with the GAD1 promoter.
养育方式和早期环境会影响各种精神病理学的风险。大鼠研究表明,母体照顾的变化会稳定地影响后代的 DNA 甲基化、基因表达和神经功能。母体照顾会影响神经发育,包括 GABA 能系统,其功能与包括精神分裂症和抑郁症在内的疾病的病理生理学有关。对人类精神分裂症大脑的尸检研究表明,谷氨酸脱羧酶 1(GAD1)的前脑表达减少,同时 GAD1 启动子的甲基化增加。我们研究了母体照顾是否会影响海马体中成年雄性后代的 GAD1 启动子甲基化,这些雄性后代来自高舔/理(高 LG)和低舔/理(低 LG)母亲的后代。与低 LG 母亲的后代相比,由高 LG 母亲抚养的后代表现出增强的海马体 GAD1mRNA 表达、降低的胞嘧啶甲基化和 GAD1 启动子的组蛋白 3-赖氨酸 9 乙酰化(H3K9ac)增加。低 LG 母亲后代的 DNA 甲基转移酶 1 表达明显高于高 LG 母亲后代。幼仔 LG 增加了海马体 5-羟色胺(5-HT)和神经生长因子诱导因子 A(NGFI-A)的表达。染色质免疫沉淀分析显示,在哺乳后,高 LG 幼仔的海马体中,NGFI-A 与 GAD1 启动子的结合增强,以及 H3K9ac 增加。用 5-HT 或 NGFI-A 表达质粒处理海马神经元培养物可显著增加 GAD1mRNA 水平。5-HT 的作用被靶向 NGFI-A 的短发夹 RNA 阻断。这些结果表明,母体照顾通过母体诱导的 NGFI-A 激活及其与 GAD1 启动子的结合,改变 GAD1 启动子甲基化水平,从而影响 GABA 系统的发育。