Mirnics K, Middleton F A, Marquez A, Lewis D A, Levitt P
Department of Neurobiology, University of Pittsburgh School of Medicine, Pennsylvania 15261, USA. karoly+@pitt.edu
Neuron. 2000 Oct;28(1):53-67. doi: 10.1016/s0896-6273(00)00085-4.
Microarray expression profiling of prefrontal cortex from matched pairs of schizophrenic and control subjects and hierarchical data analysis revealed that transcripts encoding proteins involved in the regulation of presynaptic function (PSYN) were decreased in all subjects with schizophrenia. Genes of the PSYN group showed a different combination of decreased expression across subjects. Over 250 other gene groups did not show altered expression. Selected PSYN microarray observations were verified by in situ hybridization. Two of the most consistently changed transcripts in the PSYN functional gene group, N-ethylmaleimide sensitive factor and synapsin II, were decreased in ten of ten and nine of ten subjects with schizophrenia, respectively. The combined data suggest that subjects with schizophrenia share a common abnormality in presynaptic function. We set forth a predictive, testable model.
对精神分裂症患者与对照受试者的配对前额叶皮质进行微阵列表达谱分析及分层数据分析,结果显示,在所有精神分裂症患者中,编码参与突触前功能(PSYN)调节的蛋白质的转录本减少。PSYN组的基因在不同受试者中表现出不同的表达降低组合。超过250个其他基因组未显示表达改变。通过原位杂交验证了所选的PSYN微阵列观察结果。PSYN功能基因组中变化最一致的两个转录本,即N - 乙基马来酰亚胺敏感因子和突触素II,在十名精神分裂症患者中的十名和十名中的九名中分别减少。综合数据表明,精神分裂症患者在突触前功能方面存在共同异常。我们提出了一个可预测、可检验的模型。