Weickert Cynthia Shannon, Straub Richard E, McClintock Benjamin W, Matsumoto Mitsuyuki, Hashimoto Ryota, Hyde Thomas M, Herman Mary M, Weinberger Daniel R, Kleinman Joel E
Clinical Brain Disorders Branch, Intramural Research Program, National Institute of Mental Health, National Institutes of Health, Bethesda, MD, USA.
Arch Gen Psychiatry. 2004 Jun;61(6):544-55. doi: 10.1001/archpsyc.61.6.544.
The schizophrenia-susceptibility gene dysbindin (DTNBP1 on 6p22.3) encodes a neuronal protein that binds to beta-dystrobrevin and may be part of the dystrophin protein complex. Little is known about dysbindin expression in normal or schizophrenic brain.
To determine whether brain regions implicated in schizophrenia express dysbindin and whether abnormal levels of dysbindin messenger RNA (mRNA) may be found in this disorder and to test whether sequence variations in the dysbindin gene in the promoter region, 5' and 3' untranslated regions, or introns would affect dysbindin mRNA levels.
In patients with schizophrenia and controls, we compared dysbindin, synaptophysin, spinophilin, and cyclophilin mRNA levels in the dorsolateral prefrontal cortex and dysbindin mRNA levels in the midbrain by in situ hybridization. We genotyped brain DNA at 11 single nucleotide polymorphisms to determine whether genetic variation in the dysbindin gene affects cortical dysbindin mRNA levels.
Quantitative assessment of dysbindin mRNA levels across various brain regions and comparative studies of dysbindin mRNA levels in brains of patients with schizophrenia compared with normal controls.
Dysbindin mRNA was detected in the frontal cortex, temporal cortex, hippocampus, caudate, putamen, nucleus accumbens, amygdala, thalamus, and midbrain of the adult brain. Patients with schizophrenia had statistically significantly reduced dysbindin mRNA levels in multiple layers of the dorsolateral prefrontal cortex, whereas synaptophysin, spinophilin, and cyclophilin mRNA levels were unchanged. Dysbindin mRNA levels were quantitatively reduced in the midbrain of patients with schizophrenia, but not statistically significantly. Cortical dysbindin mRNA levels varied statistically significantly according to dysbindin genotype.
Dysbindin mRNA is expressed widely in the brain, and its expression is reduced in schizophrenia. Variation in dysbindin mRNA levels may be determined in part by variation in the promoter and the 5' and 3' untranslated regions. These data add to the evidence that dysbindin is an etiologic factor in schizophrenia risk.
精神分裂症易感基因dysbindin(位于6p22.3的DTNBP1)编码一种与β - 肌营养不良蛋白结合的神经元蛋白,可能是肌营养不良蛋白复合物的一部分。关于dysbindin在正常或精神分裂症大脑中的表达情况知之甚少。
确定与精神分裂症相关的脑区是否表达dysbindin,以及在这种疾病中是否能发现dysbindin信使核糖核酸(mRNA)水平异常,并测试dysbindin基因启动子区域、5'和3'非翻译区或内含子中的序列变异是否会影响dysbindin mRNA水平。
在精神分裂症患者和对照组中,我们通过原位杂交比较了背外侧前额叶皮质中dysbindin、突触素、亲环蛋白和棘状蛋白的mRNA水平以及中脑中dysbindin的mRNA水平。我们对脑DNA的11个单核苷酸多态性进行基因分型,以确定dysbindin基因的遗传变异是否会影响皮质dysbindin mRNA水平。
对不同脑区dysbindin mRNA水平进行定量评估,并对精神分裂症患者与正常对照者大脑中dysbindin mRNA水平进行比较研究。
在成人大脑的额叶皮质、颞叶皮质、海马体、尾状核、壳核、伏隔核、杏仁核、丘脑和中脑中检测到dysbindin mRNA。精神分裂症患者背外侧前额叶皮质多层中的dysbindin mRNA水平在统计学上显著降低,而突触素、棘状蛋白和亲环蛋白的mRNA水平未发生变化。精神分裂症患者中脑的dysbindin mRNA水平在数量上有所降低,但无统计学意义。皮质dysbindin mRNA水平根据dysbindin基因型在统计学上有显著差异。
dysbindin mRNA在大脑中广泛表达,其在精神分裂症中表达降低。dysbindin mRNA水平的变化可能部分由启动子以及5'和3'非翻译区的变异决定。这些数据进一步证明dysbindin是精神分裂症风险的一个病因因素。