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SETDB1 在大脑中的表观遗传机制:对神经精神疾病的影响。

Epigenetic mechanism of SETDB1 in brain: implications for neuropsychiatric disorders.

机构信息

Institutes of Brain Science, State Key Laboratory of Medical Neurobiology and MOE Frontier Center for Brain Science, Fudan University, 200032, Shanghai, China.

Department of Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Munich, Germany.

出版信息

Transl Psychiatry. 2020 Apr 22;10(1):115. doi: 10.1038/s41398-020-0797-7.

Abstract

Neuropsychiatric disorders are a collective of cerebral conditions with a multifactorial and polygenetic etiology. Dysregulation of epigenetic profiles in the brain is considered to play a critical role in the development of neuropsychiatric disorders. SET domain, bifurcate 1 (SETDB1), functioning as a histone H3K9 specific methyltransferase, is not only critically involved in transcriptional silencing and local heterochromatin formation, but also affects genome-wide neuronal epigenetic profiles and is essential for 3D genome integrity. Here, we provide a review of recent advances towards understanding the role of SETDB1 in the central nervous system during early neurodevelopment as well as in the adult brain, with a particular focus on studies that link its functions to neuropsychiatric disorders and related behavioral changes, and the exploration of novel therapeutic strategies targeting SETDB1.

摘要

神经精神疾病是一组具有多因素和多基因病因的脑部疾病。大脑中表观遗传谱的失调被认为在神经精神疾病的发展中起着关键作用。SET 结构域,二分体 1(SETDB1),作为一种组蛋白 H3K9 特异性甲基转移酶,不仅与转录沉默和局部异染色质形成密切相关,而且还影响全基因组神经元表观遗传谱,并对 3D 基因组完整性至关重要。在这里,我们综述了近年来在理解 SETDB1 在早期神经发育以及成年大脑中的作用方面的进展,特别关注将其功能与神经精神疾病和相关行为变化联系起来的研究,并探讨了针对 SETDB1 的新型治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6c0/7176658/0cc151bf80ff/41398_2020_797_Fig1_HTML.jpg

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