An analysis of POMC gene methylation and expression in patients with schizophrenia

IF 1.7 4区 医学 Q3 DEVELOPMENTAL BIOLOGY International Journal of Developmental Neuroscience Pub Date : 2024-02-11 DOI:10.1002/jdn.10319
Xuanyu Chen, Lili Qing, Tiantian Zou, Jia Wang, Wensa Yin, Zhiyong Wang, Tiantian Cheng, Yumei Lu, Liping Hu, Linlin Liu, Shengjie Nie
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Abstract

Schizophrenia is a chronic mental disorder that affects millions of people and is believed to be caused by both environmental and genetic factors. Despite extensive research, the exact mechanisms underlying schizophrenia are still unclear. Studies have shown that numerous psychiatric disorders are associated with methylation of the POMC gene, which encodes adrenocorticotropic hormone, a critical player in the hypothalamic–pituitary–adrenal axis. However, the association between DNA methylation in POMC patients and schizophrenia remains unclear. In this study, we evaluated three fragments of the POMC promoter region, including 51 CpG sites, in the peripheral blood of schizophrenia patients and healthy controls. The POMC protein level was measured via enzyme-linked immunosorbent assay (ELISA). The schizophrenia group exhibited significantly greater levels of methylation of the POMC gene than those in the control group. The methylation level of the POMC-2 fragment was significantly greater in the patient group than in the control group. There were 17 significantly hypermethylated CpG sites in the patient group. After stratification by sex, POMC methylation levels were found to be significantly greater in male schizophrenia patients than in healthy controls; the methylation levels of POMC-2 fragments were greater in the male patient group; nine CpG sites were significantly hypermethylated in the male patient group; and only one CpG site was significantly hypermethylated in the female patient group. The POMC protein level in patients was significantly lower than that in healthy controls. These findings demonstrate that the DNA methylation of POMC might be associated with the pathophysiology of schizophrenia. Overall, studying the correlation between POMC methylation and schizophrenia may contribute to the diagnosis and evaluation of neuropsychiatric disorders.

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精神分裂症患者 POMC 基因甲基化和表达分析。
精神分裂症是一种影响数百万人的慢性精神障碍,据信是由环境和遗传因素造成的。尽管进行了大量研究,但精神分裂症的确切发病机制仍不清楚。研究表明,许多精神疾病都与 POMC 基因的甲基化有关,POMC 基因编码促肾上腺皮质激素,是下丘脑-垂体-肾上腺轴的一个重要角色。然而,POMC 患者的 DNA 甲基化与精神分裂症之间的关系仍不清楚。在这项研究中,我们评估了精神分裂症患者和健康对照者外周血中 POMC 启动子区的三个片段,包括 51 个 CpG 位点。通过酶联免疫吸附试验(ELISA)测定了POMC蛋白水平。精神分裂症组 POMC 基因的甲基化水平明显高于对照组。患者组 POMC-2 片段的甲基化水平明显高于对照组。患者组中有17个CpG位点的甲基化水平明显偏高。按性别分层后发现,男性精神分裂症患者的POMC甲基化水平明显高于健康对照组;男性患者组中POMC-2片段的甲基化水平更高;男性患者组中有9个CpG位点存在明显的高甲基化;而女性患者组中只有一个CpG位点存在明显的高甲基化。患者体内的POMC蛋白水平明显低于健康对照组。这些发现表明,POMC 的 DNA 甲基化可能与精神分裂症的病理生理学有关。总之,研究 POMC 甲基化与精神分裂症之间的相关性可能有助于神经精神疾病的诊断和评估。
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来源期刊
CiteScore
3.30
自引率
5.60%
发文量
78
审稿时长
6-12 weeks
期刊介绍: International Journal of Developmental Neuroscience publishes original research articles and critical review papers on all fundamental and clinical aspects of nervous system development, renewal and regeneration, as well as on the effects of genetic and environmental perturbations of brain development and homeostasis leading to neurodevelopmental disorders and neurological conditions. Studies describing the involvement of stem cells in nervous system maintenance and disease (including brain tumours), stem cell-based approaches for the investigation of neurodegenerative diseases, roles of neuroinflammation in development and disease, and neuroevolution are also encouraged. Investigations using molecular, cellular, physiological, genetic and epigenetic approaches in model systems ranging from simple invertebrates to human iPSC-based 2D and 3D models are encouraged, as are studies using experimental models that provide behavioural or evolutionary insights. The journal also publishes Special Issues dealing with topics at the cutting edge of research edited by Guest Editors appointed by the Editor in Chief. A major aim of the journal is to facilitate the transfer of fundamental studies of nervous system development, maintenance, and disease to clinical applications. The journal thus intends to disseminate valuable information for both biologists and physicians. International Journal of Developmental Neuroscience is owned and supported by The International Society for Developmental Neuroscience (ISDN), an organization of scientists interested in advancing developmental neuroscience research in the broadest sense.
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