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亨廷顿病患者自我中心记忆过程中,TGF-β信号基因的活性调节 H3K9 乙酰化改变。

Altered activity-regulated H3K9 acetylation at TGF-beta signaling genes during egocentric memory in Huntington's disease.

机构信息

Laboratoire de Neurosciences Cognitives et Adaptatives (LNCA), Université de Strasbourg, Strasbourg 67000, France; Centre National de la Recherche Scientifique (CNRS, UMR 7364), Strasbourg 67000, France.

Université Paris-Saclay, Commissariat à l'Energie Atomique et aux Energies Alternatives (CEA), Centre National de la Recherche Scientifique (CNRS), Molecular Imaging Research Center (MIRCen), Laboratoire des Maladies Neurodégénératives, Fontenay aux Roses, France.

出版信息

Prog Neurobiol. 2022 Dec;219:102363. doi: 10.1016/j.pneurobio.2022.102363. Epub 2022 Sep 27.

DOI:10.1016/j.pneurobio.2022.102363
PMID:36179935
Abstract

Molecular mechanisms underlying cognitive deficits in Huntington's disease (HD), a striatal neurodegenerative disorder, are unknown. Here, we generated ChIPseq, 4Cseq and RNAseq data on striatal tissue of HD and control mice during striatum-dependent egocentric memory process. Multi-omics analyses showed altered activity-dependent epigenetic gene reprogramming of neuronal and glial genes regulating striatal plasticity in HD mice, which correlated with memory deficit. First, our data reveal that spatial chromatin re-organization and transcriptional induction of BDNF-related markers, regulating neuronal plasticity, were reduced since memory acquisition in the striatum of HD mice. Second, our data show that epigenetic memory implicating H3K9 acetylation, which established during late phase of memory process (e.g. during consolidation/recall) and contributed to glia-mediated, TGFβ-dependent plasticity, was compromised in HD mouse striatum. Specifically, memory-dependent regulation of H3K9 acetylation was impaired at genes controlling extracellular matrix and myelination. Our study investigating the interplay between epigenetics and memory identifies H3K9 acetylation and TGFβ signaling as new targets of striatal plasticity, which might offer innovative leads to improve HD.

摘要

亨廷顿病(HD)是一种纹状体神经退行性疾病,其认知缺陷的分子机制尚不清楚。在这里,我们在亨廷顿病和对照小鼠的纹状体组织中生成了 ChIPseq、4Cseq 和 RNAseq 数据,以研究纹状体依赖的自我中心记忆过程。多组学分析显示,HD 小鼠中神经元和神经胶质基因的活性依赖性表观遗传基因重编程发生改变,这些基因调节纹状体可塑性,与记忆缺陷相关。首先,我们的数据表明,BDNF 相关标志物的空间染色质重组织和转录诱导,调节神经元可塑性,在 HD 小鼠纹状体的记忆获得过程中就已经减少。其次,我们的数据表明,涉及 H3K9 乙酰化的表观遗传记忆,在记忆过程的晚期(例如在巩固/回忆期间)建立,并有助于神经胶质介导的 TGFβ 依赖性可塑性,在 HD 小鼠纹状体中受到损害。具体而言,控制细胞外基质和髓鞘形成的基因的 H3K9 乙酰化的记忆依赖性调节受损。我们研究了表观遗传学和记忆之间的相互作用,确定 H3K9 乙酰化和 TGFβ 信号作为纹状体可塑性的新靶点,这可能为改善 HD 提供新的思路。

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Altered activity-regulated H3K9 acetylation at TGF-beta signaling genes during egocentric memory in Huntington's disease.亨廷顿病患者自我中心记忆过程中,TGF-β信号基因的活性调节 H3K9 乙酰化改变。
Prog Neurobiol. 2022 Dec;219:102363. doi: 10.1016/j.pneurobio.2022.102363. Epub 2022 Sep 27.
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Acetylome analyses provide novel insights into the effects of chronic intermittent hypoxia on hippocampus-dependent cognitive impairment.
乙酰化蛋白质组分析为慢性间歇性缺氧对海马体依赖性认知障碍的影响提供了新的见解。
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Unlocking the epigenetic symphony: histone acetylation's impact on neurobehavioral change in neurodegenerative disorders.揭开表观遗传交响乐的面纱:组蛋白乙酰化对神经退行性疾病中神经行为改变的影响。
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