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Ets-1与小鼠细胞角蛋白EndoA基因增强子的序列特异性结合。

Sequence specific binding of Ets-1 to the mouse cytokeratin EndoA gene enhancer.

作者信息

Hamazato F, Fujimura Y, Tamai Y, Takemoto Y, Matsushiro A, Nozaki M

机构信息

Department of Microbial Genetics, Osaka University, Japan.

出版信息

Biochem Biophys Res Commun. 1993 Apr 30;192(2):430-8. doi: 10.1006/bbrc.1993.1433.

Abstract

Expression of the mouse cytokeratin EndoA gene is regulated by an enhancer that is located 1 kilobases (kb) 3' downstream from the gene. The EndoA enhancer consists of six direct repeats with homology to the PEA3 motif in the polyoma virus enhancer core. The PEA3 motif binds to the proto-oncogene Ets product. In this report we show that GST-c-Ets-1 fusion protein binds specifically to the EndoA enhancer unit sequence by gel shift analysis. Footprinting showed that the Ets-1 binding site consisted of 20 bases in each repeat. Ets-1 also moderately activated the EndoA enhancer. These results demonstrate that Ets-1 binds in a sequence specific fashion to the mouse EndoA enhancer and suggest that c-Ets-1 or other related Ets family genes function in regulating EndoA gene expression.

摘要

小鼠细胞角蛋白EndoA基因的表达受一个增强子调控,该增强子位于基因下游1千碱基(kb)处。EndoA增强子由六个直接重复序列组成,与多瘤病毒增强子核心中的PEA3基序具有同源性。PEA3基序与原癌基因Ets产物结合。在本报告中,我们通过凝胶迁移分析表明,GST-c-Ets-1融合蛋白与EndoA增强子单位序列特异性结合。足迹分析表明,Ets-1结合位点在每个重复序列中由20个碱基组成。Ets-1也适度激活了EndoA增强子。这些结果表明,Ets-1以序列特异性方式与小鼠EndoA增强子结合,并提示c-Ets-1或其他相关Ets家族基因在调节EndoA基因表达中起作用。

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