Hertzberg Libi, Zohar Ada H, Yitzhaky Assif
Department of Physics of Complex Systems, Weizmann Institute of Science, 76100 Rehovot, Israel.
Shalvata Mental Health Center, Affiliated with the Sackler School of Medicine, Tel-Aviv University, 69978 Tel Aviv, Israel.
Life (Basel). 2021 Feb 27;11(3):190. doi: 10.3390/life11030190.
One of the most studied molecular models of gene-environment interactions is that of FKBP5, which has been shown to interact with childhood adversity to increase the risk of psychiatric disorders, and has been implicated in schizophrenia. While the model predicts up-regulation of FKBP5, previous brain samples gene expression studies yielded inconsistent results.
We performed a systematic gene expression meta-analysis of FKBP5 and NR3C1, a glucocorticoid receptor inhibited by FKBP5, in cerebellum samples of patients with schizophrenia. The gene expression databases GEO, SMRI and those of NIMH were searched, and out of six screened datasets, three were eligible for the meta-analysis (overall 69 with schizophrenia and 78 controls).
We detected up-regulation of FKBP5 and down-regulation of NR3C1 in schizophrenia, and a negative correlation between their expression patterns. Correlation analysis suggested that the detected differential expression did not result from potential confounding factors.
Our results give significant support to the FKBP5 gene-environment interaction model for schizophrenia, which provides a molecular mechanism by which childhood adversity is involved in the development of the disorder. To explore FKBP5's potential as a therapeutic target, a mapping of its differential expression patterns in different brain regions of schizophrenia patients is needed.
FKBP5是研究最多的基因-环境相互作用分子模型之一,已证明其与童年逆境相互作用会增加精神疾病风险,并与精神分裂症有关。虽然该模型预测FKBP5会上调,但先前对脑样本的基因表达研究结果并不一致。
我们对精神分裂症患者小脑样本中的FKBP5和NR3C1(一种受FKBP5抑制的糖皮质激素受体)进行了系统的基因表达荟萃分析。搜索了基因表达数据库GEO、SMRI以及美国国立精神卫生研究所的数据库,在筛选出的6个数据集中,有3个符合荟萃分析的条件(共69例精神分裂症患者和78例对照)。
我们检测到精神分裂症患者中FKBP5上调,NR3C1下调,且它们的表达模式呈负相关。相关性分析表明,检测到的差异表达并非由潜在的混杂因素导致