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We have localized a cell type-specific silencer element in the SCG10 gene by deletion analysis. This neural-restrictive silencer element (NRSE) selectively represses SCG10 expression in nonneuronal cells and tissues. The NRSE contains a 21 bp region with striking homology to a sequence present in a silencer domain of the rat type II sodium channel (NaII), another neuron-specific gene. We have identified a sequence-specific protein(s) that binds the SCG10 NRSE, as well as the homologous element in the NaII gene. A point mutation in the NRSE that abolishes binding of this neural-restrictive silencer-binding factor (NRSBF) in vitro also eliminates silencing activity in vivo. NRSBF is present in nuclear extracts from nonneuronal cells but not in extracts from neuronal cells, suggesting that the neuron-specific expression of SCG10 reflects, at least in part, the absence or inactivity of this protein. These data identify the NRSE as a potentially general DNA element for the control of neuron-specific gene expression in vertebrates. 相似文献
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NRSF慢病毒干涉载体的构建及功能初步检测 总被引:1,自引:0,他引:1
为研究神经元限制性沉默因子(NRSF)负调控神经元及胰岛细胞中神经特异性基因的表达,拟通过RNAi的方法降低NRSF表达以进一步观察其调控的下游基因的表达情况.构建含人胰岛素启动子-荧光素酶(HIP-LUC)的pcDNA3.1报告载体.通过RNAi序列设计软件进行NRSF干涉片段及脱靶对照片段的设计,然后构建慢病毒干涉载体.包装产生慢病毒干涉毒液,用其感染HeLa细胞获得稳定干涉NRSF的细胞株,利用RT-PCR、实时定量PCR、蛋白质免疫印迹、免疫荧光染色等方法检测NRSF的干涉效果及其下游基因的表达情况,观察干涉NRSF后胰岛素启动子报告载体荧光素酶活性的变化.构建具有NRSF干涉效果的慢病毒干涉载体成功,并获得了稳定干涉NRSF及脱靶对照的HeLa细胞株,RT-PCR及实时定量PCR检测结果表明,NRSF干涉片段的干涉效率为56%(n=6,P<0.01),蛋白质免疫印迹、免疫荧光染色方法检测证实干涉后NRSF蛋白表达水平明显降低.RT-PCR实验表明干涉NRSF后下游基因开始表达,荧光素酶活性分析表明,干涉NRSF后胰岛素启动子活性增强了2.4倍(n=3,P<0.01).上述结果表明,成功构建NRSF的慢病毒干涉载体并获得稳定干涉NRSF的HeLa细胞株,干涉NRSF后,其下游基因特别是胰岛素基因开始表达.这一研究工作有助于我们进一步了解NRSF在胰岛细胞发育分化中的调控作用. 相似文献
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Role of the microtubule destabilizing proteins SCG10 and stathmin in neuronal growth 总被引:7,自引:0,他引:7
The related proteins SCG10 and stathmin are highly expressed in the developing nervous system. Recently it was discovered that they are potent microtubule destabilizing factors. While stathmin is expressed in a variety of cell types and shows a cytosolic distribution, SCG10 is neuron-specific and membrane-associated. It contains an N-terminal targeting sequence that mediates its transport to the growing tips of axons and dendrites. SCG10 accumulates in the central domain of the growth cone, a region that also contains highly dynamic microtubules. These dynamic microtubules are known to be important for growth cone advance and responses to guidance cues. Because overexpression of SCG10 strongly enhances neurite outgrowth, SCG10 appears to be an important factor for the dynamic assembly and disassembly of growth cone microtubules during axonal elongation. Phosphorylation negatively regulates the microtubule destabilizing activity of SCG10 and stathmin, suggesting that these proteins may link extracellular signals to the rearrangement of the neuronal cytoskeleton. A role for these proteins in axonal elongation is also supported by their growth-associated expression pattern in nervous system development as well as during neuronal regeneration. 相似文献
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A CTCF-dependent silencer located in the differentially methylated area may regulate expression of a housekeeping gene overlapping a tissue-specific gene domain
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Klochkov D Rincón-Arano H Ioudinkova ES Valadez-Graham V Gavrilov A Recillas-Targa F Razin SV 《Molecular and cellular biology》2006,26(5):1589-1597