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抵消表观遗传机制调节人类神经元中神经元回路的结构发育。

Counteracting epigenetic mechanisms regulate the structural development of neuronal circuitry in human neurons.

机构信息

Department of Biological Sciences, University of South Carolina, Columbia, SC, USA.

Center for Childhood Neurotherapeutics, University of South Carolina, Columbia, SC, USA.

出版信息

Mol Psychiatry. 2022 Apr;27(4):2291-2303. doi: 10.1038/s41380-022-01474-1. Epub 2022 Feb 24.

Abstract

Autism spectrum disorders (ASD) are associated with defects in neuronal connectivity and are highly heritable. Genetic findings suggest that there is an overrepresentation of chromatin regulatory genes among the genes associated with ASD. ASH1 like histone lysine methyltransferase (ASH1L) was identified as a major risk factor for ASD. ASH1L methylates Histone H3 on Lysine 36, which is proposed to result primarily in transcriptional activation. However, how mutations in ASH1L lead to deficits in neuronal connectivity associated with ASD pathogenesis is not known. We report that ASH1L regulates neuronal morphogenesis by counteracting the catalytic activity of Polycomb Repressive complex 2 group (PRC2) in stem cell-derived human neurons. Depletion of ASH1L decreases neurite outgrowth and decreases expression of the gene encoding the neurotrophin receptor TrkB whose signaling pathway is linked to neuronal morphogenesis. The neuronal morphogenesis defect is overcome by inhibition of PRC2 activity, indicating that a balance between the Trithorax group protein ASH1L and PRC2 activity determines neuronal morphology. Thus, our work suggests that ASH1L may epigenetically regulate neuronal morphogenesis by modulating pathways like the BDNF-TrkB signaling pathway. Defects in neuronal morphogenesis could potentially impair the establishment of neuronal connections which could contribute to the neurodevelopmental pathogenesis associated with ASD in patients with ASH1L mutations.

摘要

自闭症谱系障碍 (ASD) 与神经元连接缺陷有关,且具有高度遗传性。遗传研究结果表明,与 ASD 相关的基因中,染色质调控基因的代表性过高。ASH1 样组蛋白赖氨酸甲基转移酶 (ASH1L) 被确定为 ASD 的主要危险因素之一。ASH1L 对组蛋白 H3 赖氨酸 36 进行甲基化,这主要导致转录激活。然而,ASH1L 突变如何导致与 ASD 发病机制相关的神经元连接缺陷尚不清楚。我们报告称,ASH1L 通过抵消多梳抑制复合物 2 组 (PRC2) 在干细胞衍生的人类神经元中的催化活性来调节神经元形态发生。ASH1L 的耗竭会减少神经突的生长,并降低编码神经营养因子受体 TrkB 的基因的表达,其信号通路与神经元形态发生有关。PRC2 活性的抑制克服了神经元形态发生缺陷,表明 Trithorax 组蛋白 ASH1L 和 PRC2 活性之间的平衡决定了神经元形态。因此,我们的工作表明,ASH1L 可以通过调节 BDNF-TrkB 信号通路等途径来表观遗传调控神经元形态发生。神经元形态发生缺陷可能会损害神经元连接的建立,这可能导致与 ASD 相关的神经发育发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e69/9133078/073cdf18bc9b/nihms-1777239-f0001.jpg

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