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KLF4和Sp1对人妊娠特异性糖蛋白PSG-5启动子的激活作用。

Activation of the human pregnancy-specific glycoprotein PSG-5 promoter by KLF4 and Sp1.

作者信息

Blanchon Loïc, Nores Rodrigo, Gallot Denis, Marceau Geoffroy, Borel Valérie, Yang Vincent W, Bocco José Luis, Lémery Didier, Panzetta-Dutari Graciela, Sapin Vincent

机构信息

INSERM U.384, Laboratoire de Biochimie, Faculté de Médecine, F-63000 Clermont-Ferrand, France.

出版信息

Biochem Biophys Res Commun. 2006 May 12;343(3):745-53. doi: 10.1016/j.bbrc.2006.03.032. Epub 2006 Mar 20.

Abstract

Pregnancy-specific glycoproteins (PSGs) are major placental proteins thought to be essential for the maintenance of gestation. Little is known about the regulation of expression of the 11 genes encoding these proteins. It was previously demonstrated that Krüppel-like factor 6 (KLF6) and specific-protein 1 (Sp1) bind to conserved sequence within the PSG-5 gene promoter. Informatics analysis revealed the presence of one potential binding site for Krüppel-like factor 4 (KLF4), in the PSG-5 promoter, suggesting a potential transcriptional regulator role for KLF4. Using gene promoter-reporter transfections and X-ChIP assays, we demonstrated that KLF4 is an activator of the PSG-5 promoter by binding to a KLF consensus like binding which includes the Core Promoter Element region (-147/-140). Furthermore, we used previous data showing the binding of Sp1 transcription factor to a GT-box (-443/-437) and co-transfection assays with KLF4 and Sp1 to demonstrate the strong synergic activity of these two factors on the PSG-5 promoter.

摘要

妊娠特异性糖蛋白(PSG)是主要的胎盘蛋白,被认为对维持妊娠至关重要。关于编码这些蛋白的11个基因的表达调控知之甚少。先前已证明,Krüppel样因子6(KLF6)和特异性蛋白1(Sp1)与PSG-5基因启动子内的保守序列结合。信息学分析显示,在PSG-5启动子中存在一个潜在的Krüppel样因子4(KLF4)结合位点,提示KLF4可能具有转录调节作用。通过基因启动子-报告基因转染和X-ChIP分析,我们证明KLF4通过与一个包含核心启动子元件区域(-147/-140)的KLF共有样结合位点结合,从而成为PSG-5启动子的激活因子。此外,我们利用先前显示Sp1转录因子与GT盒(-443/-437)结合的数据以及KLF4和Sp1的共转染分析,证明这两个因子对PSG-5启动子具有强大的协同活性。

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