Tanaka Shinya, Kamachi Yusuke, Tanouchi Aki, Hamada Hiroshi, Jing Naihe, Kondoh Hisato
Graduate School of Frontier Biosciences, Osaka University, 1-3 Yamadaoka, Suita, Osaka 565-0871, Japan.
Mol Cell Biol. 2004 Oct;24(20):8834-46. doi: 10.1128/MCB.24.20.8834-8846.2004.
Intermediate-filament Nestin and group B1 SOX transcription factors (SOX1/2/3) are often employed as markers for neural primordium, suggesting their regulatory link. We have identified adjacent and essential SOX and POU factor binding sites in the Nestin neural enhancer. The 30-bp sequence of the enhancer including these sites (Nes30) showed a nervous system-specific and SOX-POU-dependent enhancer activity in multimeric forms in transfection assays and was utilized in assessing the specificity of the synergism; combinations of either group B1 or group C SOX (SOX11) with class III POU proved effective. In embryonic day 13.5 mouse spinal cord, Nestin was expressed in the cells with nuclei in the ventricular and subventricular zones. SOX1/2/3 expression was confined to the nuclei of the ventricular zone; SOX11 localized to the nuclei of both subventricular (high-level expression) and intermediate (low-level expression) zones. Class III POU (Brn2) was expressed at high levels, localizing to the nucleus in the ventricular and subventricular zones; moderate expression was observed in the intermediate zone, distributed in the cytoplasm. These data support the model that synergic interactions between group B1/C SOX and class III POU within the nucleus determine Nestin expression. Evidence also suggests that such interactions are involved in the regulation of neural primordial cells.
中间丝蛋白巢蛋白和B1组SOX转录因子(SOX1/2/3)常被用作神经原基的标志物,这表明它们之间存在调控联系。我们在巢蛋白神经增强子中鉴定出相邻且关键的SOX和POU因子结合位点。包含这些位点的增强子30碱基序列(Nes30)在转染实验中以多聚体形式表现出神经系统特异性和SOX-POU依赖性增强子活性,并用于评估协同作用的特异性;B1组或C组SOX(SOX11)与III类POU的组合被证明是有效的。在胚胎第13.5天的小鼠脊髓中,巢蛋白在室管膜区和室管膜下区有细胞核的细胞中表达。SOX1/2/3的表达局限于室管膜区的细胞核;SOX11定位于室管膜下区(高水平表达)和中间区(低水平表达)的细胞核。III类POU(Brn2)高水平表达,定位于室管膜区和室管膜下区的细胞核;在中间区观察到中等水平表达,分布于细胞质中。这些数据支持了细胞核内B1/C组SOX与III类POU之间的协同相互作用决定巢蛋白表达的模型。证据还表明,这种相互作用参与了神经原细胞的调控。