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沉默元件调节神经胶质细胞黏附分子Ng-CAM的基因表达。

Silencer elements modulate the expression of the gene for the neuron-glia cell adhesion molecule, Ng-CAM.

作者信息

Kallunki P, Jenkinson S, Edelman G M, Jones F S

机构信息

Department of Neurobiology, Scripps Research Institute, La Jolla, California 92037, USA.

出版信息

J Biol Chem. 1995 Sep 8;270(36):21291-8. doi: 10.1074/jbc.270.36.21291.

Abstract

The combined factors that regulate the expression of cell adhesion molecules (CAMs) during development of the nervous system are largely unknown. To identify such factors for Ng-CAM, the neuron-glia CAM, constructs containing portions of the 5' end of the Ng-CAM gene were examined for activity after transfection into N2A neuroblastoma and NIH3T3 cells. Positive regulatory elements active in both cell types included an Ng-CAM proximal promoter with SP1 and cAMP response element motifs extending 447 base pairs upstream of a single RNA start site and a region within the first exon corresponding to 5'-untranslated sequences. Negative regulatory elements included five neuron-restrictive silencer elements (NRSEs) and a binding site for Pax gene products in a 305-base pair segment of the first intron. Constructs containing the promoter together with the entire first intron were active in N2A cells but were silenced in NIH3T3 cells. This silencer activity was mapped to the NRSEs. In contrast, the Pax motif inhibited activity of Ng-CAM constructs in both cell types. The DNA elements defined in these transfection experiments were examined for their ability to bind nuclear factors. The region within the first exon formed a DNA-protein complex after exposure to nuclear extracts prepared from both NIH3T3 and N2A cells. The NRSE region formed a more prominent complex with proteins prepared from NIH3T3 cells than it did with extracts from N2A cells. A member of the Pax protein family, Pax-3 bound to the Pax motif. Mutations introduced within the Pax motif in its ATTA sequence eliminated this binding whereas mutations in its GTTCC sequence did not, suggesting that paired homeodomain interactions are important for the recognition of Pax-3 by this DNA target sequence. The combined data suggest that negative regulation by NRSEs and Pax proteins may play a key role in the place-dependent expression patterns of Ng-CAM during development.

摘要

在神经系统发育过程中调节细胞黏附分子(CAMs)表达的综合因素在很大程度上尚不清楚。为了确定神经细胞黏附分子(Ng-CAM)的此类因素,将含有Ng-CAM基因5'端部分的构建体转染到N2A神经母细胞瘤细胞和NIH3T3细胞中后,检测其活性。在两种细胞类型中均具有活性的正调控元件包括一个Ng-CAM近端启动子,其具有SP1和cAMP反应元件基序,该基序在单个RNA起始位点上游延伸447个碱基对,以及第一外显子内对应于5'-非翻译序列的区域。负调控元件包括五个神经元限制性沉默元件(NRSEs)和第一内含子305个碱基对片段中Pax基因产物的结合位点。含有启动子和整个第一内含子的构建体在N2A细胞中具有活性,但在NIH3T3细胞中沉默。这种沉默活性定位于NRSEs。相反,Pax基序在两种细胞类型中均抑制Ng-CAM构建体的活性。检测了这些转染实验中确定的DNA元件结合核因子的能力。第一外显子内的区域在与从NIH3T3细胞和N2A细胞制备的核提取物接触后形成了DNA-蛋白质复合物。NRSE区域与从NIH3T3细胞制备的蛋白质形成的复合物比与从N2A细胞制备的提取物形成的复合物更显著。Pax蛋白家族的一个成员Pax-3与Pax基序结合。在Pax基序的ATTA序列中引入的突变消除了这种结合,而其GTTCC序列中的突变则没有,这表明配对的同源结构域相互作用对于该DNA靶序列识别Pax-3很重要。综合数据表明,NRSEs和Pax蛋白的负调控可能在发育过程中Ng-CAM的位置依赖性表达模式中起关键作用。

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