Sorbonne Université, Gene Regulation and Adaptive Behaviors, Neuroscience Paris-Seine, IBPS. CNRS UMR8246, INSERM, Paris, France.
Sorbonne Université, Neurophysiology and Behaviors, Neuroscience Paris-Seine, IBPS. CNRS UMR8246, INSERM, UPMC, Paris, France.
Nat Commun. 2022 Apr 4;13(1):1807. doi: 10.1038/s41467-022-29380-8.
Enduring behavioral changes upon stress exposure involve changes in gene expression sustained by epigenetic modifications in brain circuits, including the mesocorticolimbic pathway. Brahma (BRM) and Brahma Related Gene 1 (BRG1) are ATPase subunits of the SWI/SNF complexes involved in chromatin remodeling, a process essential to enduring plastic changes in gene expression. Here, we show that in mice, social defeat induces changes in BRG1 nuclear distribution. The inactivation of the Brg1/Smarca4 gene within dopamine-innervated regions or the constitutive inactivation of the Brm/Smarca2 gene leads to resilience to repeated social defeat and decreases the behavioral responses to cocaine without impacting midbrain dopamine neurons activity. Within striatal medium spiny neurons, Brg1 gene inactivation reduces the expression of stress- and cocaine-induced immediate early genes, increases levels of heterochromatin and at a global scale decreases chromatin accessibility. Altogether these data demonstrate the pivotal function of SWI/SNF complexes in behavioral and transcriptional adaptations to salient environmental challenges.
在应激暴露下持久的行为改变涉及到脑回路中表观遗传修饰维持的基因表达变化,包括中脑边缘奖赏通路。Brahma(BRM)和Brahma 相关基因 1(BRG1)是 SWI/SNF 复合物的 ATP 酶亚基,参与染色质重塑,这是基因表达持久可塑性变化所必需的过程。在这里,我们表明,在小鼠中,社交挫败会引起 BRG1 核分布的变化。在多巴胺能神经支配区域内失活 Brg1/Smarca4 基因或组成型失活 Brm/Smarca2 基因会导致对重复社交挫败的弹性,并减少对可卡因的行为反应,而不影响中脑多巴胺神经元的活动。在纹状体中间神经元中,Brg1 基因失活会降低应激和可卡因诱导的即刻早期基因的表达,增加异染色质的水平,并在全局范围内降低染色质可及性。总的来说,这些数据表明 SWI/SNF 复合物在行为和转录适应显著环境挑战中的关键作用。