Department of Medicine, Centre of Excellence in Neuromics of Université de Montréal, Centre Hospitalier de l'Université de Montréal Research Center, Université de Montréal, Montréal, QC H2L 2W5, Canada
Proc Natl Acad Sci U S A. 2010 Apr 27;107(17):7863-8. doi: 10.1073/pnas.0906232107. Epub 2010 Apr 12.
Schizophrenia likely results from poorly understood genetic and environmental factors. We studied the gene encoding the synaptic protein SHANK3 in 285 controls and 185 schizophrenia patients with unaffected parents. Two de novo mutations (R1117X and R536W) were identified in two families, one being found in three affected brothers, suggesting germline mosaicism. Zebrafish and rat hippocampal neuron assays revealed behavior and differentiation defects resulting from the R1117X mutant. As mutations in SHANK3 were previously reported in autism, the occurrence of SHANK3 mutations in subjects with a schizophrenia phenotype suggests a molecular genetic link between these two neurodevelopmental disorders.
精神分裂症可能是由尚未完全了解的遗传和环境因素引起的。我们研究了编码突触蛋白 SHANK3 的基因,在 285 名对照者和 185 名无患病父母的精神分裂症患者中进行了研究。在两个家族中发现了两个从头突变(R1117X 和 R536W),一个家族中发现了三个受影响的兄弟,提示种系嵌合体。斑马鱼和大鼠海马神经元测定显示,R1117X 突变导致行为和分化缺陷。由于先前在自闭症中报道了 SHANK3 突变,因此在具有精神分裂症表型的受试者中发生 SHANK3 突变表明这两种神经发育障碍之间存在分子遗传学联系。