Expression and methylation of BDNF in the human brain in schizophrenia

Sern-Yih Cheah, R. McLeay, L. Wockner, B. Lawford, R. Young, C. P. Morris, J. Voisey
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引用次数: 16

Abstract

Abstract Objectives: To examine the combined effect of the BDNF Val66Met (rs6265) polymorphism and BDNF DNA methylation on transcriptional regulation of the BDNF gene. Methods: DNA methylation profiles were generated for CpG sites proximal to Val66Met, within BDNF promoter I and exon V for prefrontal cortex samples from 25 schizophrenia and 25 control subjects. Val66Met genotypes and BDNF mRNA expression data were generated by transcriptome sequencing. Expression, methylation and genotype data were correlated and examined for association with schizophrenia. Results: There was 43% more of the BDNF V-VIII-IX transcript in schizophrenia samples. BDNF mRNA expression and DNA methylation of seven CpG sites were not associated with schizophrenia after accounting for age and PMI effects. BDNF mRNA expression and DNA methylation were not altered by Val66Met after accounting for age and PMI effects. DNA methylation of one CpG site had a marginally significant positive correlation with mRNA expression in schizophrenia subjects. Conclusions: Schizophrenia risk was not associated with differential BDNF mRNA expression and DNA methylation. A larger age-matched cohort with comprehensive clinical history is required to accurately identify the effects of genotype, mRNA expression and DNA methylation on schizophrenia risk.
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精神分裂症患者脑内BDNF的表达和甲基化
摘要目的:探讨BDNF Val66Met (rs6265)多态性和BDNF DNA甲基化对BDNF基因转录调控的联合影响。方法:对25名精神分裂症患者和25名对照患者的前额叶皮层样本,在BDNF启动子I和外显子V内,生成Val66Met附近CpG位点的DNA甲基化谱。转录组测序生成Val66Met基因型和BDNF mRNA表达数据。表达、甲基化和基因型数据相互关联,并检查与精神分裂症的关联。结果:精神分裂症样本中BDNF V-VIII-IX转录本增加43%。在考虑了年龄和PMI的影响后,BDNF mRNA表达和7个CpG位点的DNA甲基化与精神分裂症无关。在考虑年龄和PMI影响后,BDNF mRNA表达和DNA甲基化未被Val66Met改变。精神分裂症患者一个CpG位点的DNA甲基化与mRNA表达呈极显著正相关。结论:精神分裂症风险与BDNF mRNA表达和DNA甲基化差异无关。需要更大的具有全面临床病史的年龄匹配队列来准确识别基因型、mRNA表达和DNA甲基化对精神分裂症风险的影响。
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