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精神分裂症的表观遗传调控:重点关注人类研究中的甲基化和组蛋白修饰。

Epigenetic Regulation in Schizophrenia: Focus on Methylation and Histone Modifications in Human Studies.

机构信息

School of Health and Behavioural Sciences, Faculty of Health Sciences, Australian Catholic University, 1100 Nudgee Rd, Banyo, QLD 4014, Australia.

Centre for Genomics and Personalised Health, School of Biomedical Sciences, Queensland University of Technology, 60 Musk Ave, Kelvin Grove, QLD 4059, Australia.

出版信息

Genes (Basel). 2024 Feb 21;15(3):272. doi: 10.3390/genes15030272.

Abstract

Despite extensive research over the last few decades, the etiology of schizophrenia (SZ) remains unclear. SZ is a pathological disorder that is highly debilitating and deeply affects the lifestyle and minds of those affected. Several factors (one or in combination) have been reported as contributors to SZ pathogenesis, including neurodevelopmental, environmental, genetic and epigenetic factors. Deoxyribonucleic acid (DNA) methylation and post-translational modification (PTM) of histone proteins are potentially contributing epigenetic processes involved in transcriptional activity, chromatin folding, cell division and apoptotic processes, and DNA damage and repair. After establishing a summary of epigenetic processes in the context of schizophrenia, this review aims to highlight the current understanding of the role of DNA methylation and histone PTMs in this disorder and their potential roles in schizophrenia pathophysiology and pathogenesis.

摘要

尽管在过去几十年中进行了广泛的研究,但精神分裂症 (SZ) 的病因仍不清楚。SZ 是一种病理性疾病,它使人衰弱,并深深影响着受影响者的生活方式和思维。有报道称,多种因素(一种或多种组合)可导致 SZ 的发病机制,包括神经发育、环境、遗传和表观遗传因素。脱氧核糖核酸 (DNA) 甲基化和组蛋白的翻译后修饰 (PTM) 是参与转录活性、染色质折叠、细胞分裂和凋亡过程以及 DNA 损伤和修复的潜在表观遗传过程。在概述了 SZ 背景下的表观遗传过程后,本综述旨在强调 DNA 甲基化和组蛋白 PTM 在该疾病中的作用及其在 SZ 病理生理学和发病机制中的潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae1f/10970389/907c3dbbca8d/genes-15-00272-g001.jpg

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