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上游刺激因子参与人类钙周期蛋白(S100A6)基因的调控。

Upstream stimulatory factor is involved in the regulation of the human calcyclin (S100A6) gene.

作者信息

Leśniak W, Jezierska A, Kuźnicki J

机构信息

Department of Molecular and Cellular Neurobiology, Nencki Institute of Experimental Biology, 3 Pasteur Street, 02-093 Warsaw, Poland.

出版信息

Biochim Biophys Acta. 2000 Dec 15;1517(1):73-81. doi: 10.1016/s0167-4781(00)00259-1.

Abstract

Calcyclin (S100A6) is a calcium-binding protein overexpressed in several tumor cell lines including melanoma with high metastatic activity. The calcyclin gene promoter fragment -361/-167 activates transcription several fold when compared to the basal -167/+134 promoter fragment indicating the presence of enhancer element within -361/-167 bp region. By means of the electrophoretic mobility shift assay (EMSA) we found that this region contains a protein-binding site and mapped it to an E-box sequence at position -283/-278. Using antibodies against USF1 we identified the upstream stimulatory factor as the transcription factor bound to the E-box sequence in EMSA. This factor was also enriched in protein fractions obtained from Ehrlich ascites tumor cells nuclear extract by affinity chromatography using the E-box sequence as a ligand. Cotransfection of the USF1 expression vector with a plasmid carrying the luciferase gene under control of the -361/+134 calcyclin gene promoter fragment resulted in several fold activation of luciferase activity. On the other hand, mutations within the E-box led to a marked decrease in the efficiency of calcyclin gene promoter fragment. The results indicate that USF1 binds to an E-box sequence of the calcyclin gene promoter and enhances its transcription activity. This mechanism might be responsible for the upregulation of calcyclin gene expression in response to various stimuli and in tumors.

摘要

钙周期蛋白(S100A6)是一种钙结合蛋白,在包括具有高转移活性的黑色素瘤在内的多种肿瘤细胞系中过表达。与基础的-167/+134启动子片段相比,钙周期蛋白基因启动子片段-361/-167可使转录激活数倍,这表明在-361/-167 bp区域内存在增强子元件。通过电泳迁移率变动分析(EMSA),我们发现该区域包含一个蛋白质结合位点,并将其定位到-283/-278位置的一个E盒序列。使用针对USF1的抗体,我们在EMSA中鉴定出上游刺激因子是与E盒序列结合的转录因子。通过使用E盒序列作为配体的亲和色谱法,该因子也在从艾氏腹水肿瘤细胞核提取物中获得的蛋白质组分中得到富集。将USF1表达载体与携带在-361/+134钙周期蛋白基因启动子片段控制下的荧光素酶基因的质粒共转染,导致荧光素酶活性激活数倍。另一方面,E盒内的突变导致钙周期蛋白基因启动子片段的效率显著降低。结果表明,USF1与钙周期蛋白基因启动子的E盒序列结合并增强其转录活性。这种机制可能负责钙周期蛋白基因表达在对各种刺激和肿瘤中的上调。

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