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Neuronal activity-induced BRG1 phosphorylation regulates enhancer activation

机译:神经元活性诱导的BRG1磷酸化调节增强剂活化

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Neuronal activity-induced enhancers drive gene activation. We demonstrate that BRG1, the core subunit of SWI/SNF-like BAF ATP-dependent chromatin remodeling complexes, regulates neuronal activity-induced enhancers. Upon stimulation, BRG1 is recruited to enhancers in an H3K27Ac-dependent manner. BRG1 regulates enhancer basal activities and inducibility by affecting cohesin binding, enhancer-promoter looping, RNA polymerase II recruitment, and enhancer RNA expression. We identify a serine phosphorylation site in BRG1 that is induced by neuronal stimulations and is sensitive to CaMKII inhibition. BRG1 phosphorylation affects its interaction with several transcription co-factors, including the NuRD repressor complex and cohesin, possibly modulating BRG1-mediated transcription outcomes. Using mice with knockin mutations, we show that non-phosphorylatable BRG1 fails to efficiently induce activity-dependent genes, whereas phosphomimic BRG1 increases enhancer activity and inducibility. These mutant mice display anxiety-like phenotypes and altered responses to stress. Therefore, we reveal a mechanism connecting neuronal signaling to enhancer activities through BRG1 phosphorylation.
机译:神经元活性诱导的增强剂驱动基因活化。我们证明BRG1,SWI / SNF样BAF ATP依赖性染色质重塑复合物的核心亚基,调节神经元活性诱导的增强剂。在刺激后,BRG1以H3K27AC依赖性方式募集到增强剂。 BRG1通过影响Cohonein结合,增强子 - 启动子循环,RNA聚合酶II募集和增强子RNA表达来调节增强剂基础活性和诱导性。我们鉴定由神经元刺激诱导的BRG1中的丝氨酸磷酸化位点,并且对CaMKII抑制敏感。 BRG1磷酸化影响其与几种转录共同因子的相互作用,包括Nurd阻遏物复合体和休尼蛋白,可能调节BRG1介导的转录结果。使用小鼠具有敲蛋白突变,我们表明不可磷酸化BRG1未能有效地诱导活性依赖性基因,而磷酸化BRG1增加增强剂活性和诱导性。这些突变小鼠显示出焦虑的表型并改变对压力的反应。因此,我们揭示了通过BRG1磷酸化连接神经元信号传导至增强剂活性的机制。

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