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[外周血中Reelin基因启动子甲基化及其与精神分裂症患者认知功能的关系]

[Methylation of the Reelin Gene Promoter in Peripheral Blood and Its Relationship with the Cognitive Function of Schizophrenia Patients].

作者信息

Alfimova M V, Kondratiev N V, Golov A K, Golimbet V E

机构信息

Mental Health Research Center, Moscow, 115522 Russia.

出版信息

Mol Biol (Mosk). 2018 Sep-Oct;52(5):782-792. doi: 10.1134/S0026898418050026.

Abstract

There is a decrease in the expression of the reelin gene (RELN) in the brain of schizophrenia patients, which can underlie observed cognitive abnormalities. It is suggested that this decrease is caused by the hypermethylation of the RELN promoter. The aim of the study was to investigate methylation of the RELN promoter in the peripheral blood of schizophrenia patients and its association with their cognitive deficits. A modified SMRT-BS (single-molecule real-time bisulfite sequencing) was used. We determined the methylation rate of 170 CpG sites within a 1465 bp DNA region containing the entire CpG island in the RELN promoter in 51 schizophrenia patients and 52 healthy controls. All subjects completed a battery of neuropsychological tests. There were no DNA methylation changes associated with schizophrenia. Most CpGs sites were unmethylated in both groups. At the same time, there was a variability in the methylation level of different regions within the promoter. The methylation level in the area from -258 to -151 bp relative to RELN transcription start site was a significant predictor of the index of patients' cognitive functioning if sex, age, smoking, education, and polymorphism rsl858815 had been considered. The positive correlation between the methylation rate in this region and cognitive index suggests that the hypomethylation of the RELN promoter could contribute to the development of cognitive deficits in schizophrenia.

摘要

精神分裂症患者大脑中reelin基因(RELN)的表达下降,这可能是观察到的认知异常的基础。有人认为这种下降是由RELN启动子的高甲基化引起的。本研究的目的是调查精神分裂症患者外周血中RELN启动子的甲基化情况及其与认知缺陷的关系。使用了改良的SMRT-BS(单分子实时亚硫酸氢盐测序)。我们测定了51名精神分裂症患者和52名健康对照者中包含RELN启动子中整个CpG岛的1465 bp DNA区域内170个CpG位点的甲基化率。所有受试者都完成了一系列神经心理学测试。未发现与精神分裂症相关的DNA甲基化变化。两组中大多数CpG位点均未甲基化。同时,启动子内不同区域的甲基化水平存在差异。如果考虑性别、年龄、吸烟、教育程度和多态性rsl858815,相对于RELN转录起始位点-258至-151 bp区域的甲基化水平是患者认知功能指数的重要预测指标。该区域甲基化率与认知指数之间的正相关表明,RELN启动子的低甲基化可能导致精神分裂症认知缺陷的发展。

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