Power S C, Cereghini S
URA Centre National de la Recherche Scientifique, Institut Pasteur, Paris, France.
Mol Cell Biol. 1996 Mar;16(3):778-91. doi: 10.1128/MCB.16.3.778.
vHNF1 (also termed HNF1 beta) is a member of the hepatocyte nuclear fa ctor 1 (HNF1; also termed HNF1 alpha) family of homeodomain-containing transcription factors that interact with a sequence motif found in the regulatory regions of a large number of genes expressed mainly in the liver. It has been suggested that vHNF1 plays a role in early differentiation of specialized epithelia of several endoderm- and mesoderm-derived organs, with HNF1 playing a role in later stages. In support of this idea, expression of vHNF1 but not HNF1 is induced upon treatment of the embryonal carcinoma cell line F9 with retinoic acid. We have cloned and analyzed the vHNF1 promoter to gain a better understanding of the regulation of vHNF1 expression and how it relates to the expression of HNF1. We have identified five sites of DNA-protein interaction within the first 260 bp upstream of the transcription start site, which involve at least three different families of transcription factors. Two sites, a distal DR-1 motif and a proximal octamer motif, are the most important for promoter activity. The DR-1 motif interacts with several members of the steroid hormone receptor superfamily including HNF4, COUP-TFI/Ear3, COUP-TFII/Arp1, and RAR alpha/RXR alpha heterodimers. The vHNF1 promoter is transactivated by COUP-TFI/Ear3 and COUP-TFII/Arp1 and, unlike the HNF1 promoter, is virtually unaffected by HNF4. Interestingly, the proximal octamer site and not the DR-1 site is required for COUP-TFI/Ear3 and COUP-TFII/Arp1 transactivation of the vHNF1 promoter. COUP-TFI/Ear3 does not bind directly to this proximal octamer site. We present evidence of an interaction between COUP-TFI/Ear3 and the octamer-binding proteins in vitro and in the cell, suggesting that COUP-TFI and COUP-TFII activate the vHNF1 promoter via an indirect mechanism.
vHNF1(也称为HNF1β)是含同源结构域的转录因子肝细胞核因子1(HNF1;也称为HNF1α)家族的成员,该家族与在大量主要在肝脏中表达的基因的调控区域中发现的序列基序相互作用。有人提出,vHNF1在几个内胚层和中胚层衍生器官的特化上皮细胞的早期分化中起作用,而HNF1在后期起作用。支持这一观点的是,在用视黄酸处理胚胎癌细胞系F9时,诱导了vHNF1的表达,但未诱导HNF1的表达。我们克隆并分析了vHNF1启动子,以更好地了解vHNF1表达的调控及其与HNF1表达的关系。我们在转录起始位点上游的前260 bp内鉴定出五个DNA-蛋白质相互作用位点,这些位点涉及至少三个不同的转录因子家族。两个位点,一个远端DR-1基序和一个近端八聚体基序,对启动子活性最为重要。DR-1基序与类固醇激素受体超家族的几个成员相互作用,包括HNF4、COUP-TFI/Ear3、COUP-TFII/Arp1和RARα/RXRα异二聚体。vHNF1启动子被COUP-TFI/Ear3和COUP-TFII/Arp1反式激活,与HNF1启动子不同,它实际上不受HNF4的影响。有趣的是,vHNF1启动子的COUP-TFI/Ear3和COUP-TFII/Arp1反式激活需要近端八聚体位点而不是DR-1位点。COUP-TFI/Ear3不直接结合到这个近端八聚体位点。我们提供了COUP-TFI/Ear3与八聚体结合蛋白在体外和细胞内相互作用的证据,表明COUP-TFI和COUP-TFII通过间接机制激活vHNF1启动子。