Philibert R A, Winfield S L, Sandhu H K, Martin B M, Ginns E I
Department of Psychiatry, University of Iowa, Rm 2-126b Psychiatry Research/MEB, Iowa City, IA 52242-1000, USA.
Gene. 2000 Apr 4;246(1-2):303-10. doi: 10.1016/s0378-1119(00)00049-4.
The neuroligins are a family of proteins that are thought to mediate cell to cell interactions between neurons. During the sequencing at an Xq13 locus associated with a mental retardation syndrome in some studies, we discovered a portion of the human orthologue of the rat neuroligin-3 gene. We now report the structure and the expression of that gene. The gene spans approximately 30kb and contains eight exons. Unlike the rat gene, it codes for at least two mRNAs and at least one of which is expressed outside the CNS. Interestingly, the putative promoter for the gene overlaps the last exon of the neighboring HOPA gene and is located less than 1kb from an OPA element in which a polymorphism associated with mental retardation is found. These findings suggest a possible role for the neuroligin gene in mental retardation and that the role of the gene in humans may differ from its role in rats.
神经连接蛋白是一类蛋白质,被认为可介导神经元之间的细胞间相互作用。在一些研究中,于与智力发育迟缓综合征相关的Xq13位点进行测序时,我们发现了大鼠神经连接蛋白3基因的部分人类同源物。我们现在报告该基因的结构和表达情况。该基因跨度约30kb,包含8个外显子。与大鼠基因不同,它编码至少两种mRNA,其中至少一种在中枢神经系统外表达。有趣的是,该基因的推定启动子与相邻的HOPA基因的最后一个外显子重叠,且距离发现与智力发育迟缓相关多态性的OPA元件不到1kb。这些发现表明神经连接蛋白基因在智力发育迟缓中可能发挥作用,且该基因在人类中的作用可能与其在大鼠中的作用不同。