Rausa F, Samadani U, Ye H, Lim L, Fletcher C F, Jenkins N A, Copeland N G, Costa R H
Department of Biochemistry and Molecular Biology, University of Illinois at Chicago 60612-7334, USA.
Dev Biol. 1997 Dec 15;192(2):228-46. doi: 10.1006/dbio.1997.8744.
Murine hepatocyte nuclear factor-3 beta (HNF-3 beta) protein is a member of a large family of developmentally regulated transcription factors that share homology in the winged helix/fork head DNA binding domain and that participate in embryonic pattern formation. HNF-3 beta also mediates cell-specific transcription of genes important for the function of hepatocytes, intestinal and bronchiolar epithelial, and pancreatic acinar cells. We have previously identified a liver-enriched transcription factor, HNF-6, which is required for HNF-3 beta promoter activity and also recognizes the regulatory region of numerous hepatocyte-specific genes. In this study we used the yeast one-hybrid system to isolate the HNF-6 cDNA, which encodes a cut-homeodomain-containing transcription factor that binds with the same specificity as the liver HNF-6 protein. Cotransfection assays demonstrate that HNF-6 activates expression of a reporter gene driven by the HNF-6 binding site from either the HNF-3 beta or transthyretin (TTR) promoter regions. We used interspecific backcross analysis to determine that murine Hnf6 gene is located in the middle of mouse chromosome 9. In situ hybridization studies of staged specific embryos demonstrate that HNF-6 and its potential target gene, HNF-3 beta, are coexpressed in the pancreatic and hepatic diverticulum. More detailed analysis of HNF-6 and HNF-3 beta's developmental expression patterns provides evidence of colocalization in hepatocytes, intestinal epithelial, and in the pancreatic ductal epithelial and exocrine acinar cells. The expression patterns of these two transcription factors do not overlap in other endoderm-derived tissues or the neurotube. We also found that HNF-6 is also abundantly expressed in the dorsal root ganglia, the marginal layer, and the midbrain. At day 18 of gestation and in the adult pancreas, HNF-6 and HNF-3 beta transcripts colocalize in the exocrine acinar cells, but their expression patterns diverge in other pancreatic epithelium. HNF-6, but not HNF-3 beta, expression continues in the pancreatic ductal epithelium, whereas only HNF-3 beta becomes restricted to the endocrine cells of the islets of Langerhans. We discuss these expression patterns with respect to specification of hepatocytes and differentiation of the endocrine and exocrine pancreas.
小鼠肝细胞核因子3β(HNF-3β)蛋白是一大类发育调控转录因子家族的成员,这些转录因子在翼状螺旋/叉头DNA结合域具有同源性,并参与胚胎模式形成。HNF-3β还介导对肝细胞、肠和细支气管上皮细胞以及胰腺腺泡细胞功能重要的基因的细胞特异性转录。我们之前鉴定出一种肝脏富集转录因子HNF-6,它是HNF-3β启动子活性所必需的,并且还识别许多肝细胞特异性基因的调控区域。在本研究中,我们使用酵母单杂交系统分离出HNF-6 cDNA,其编码一种含切割型同源结构域的转录因子,该转录因子与肝脏HNF-6蛋白具有相同的结合特异性。共转染实验表明,HNF-6可激活由HNF-3β或甲状腺转运蛋白(TTR)启动子区域的HNF-6结合位点驱动的报告基因的表达。我们使用种间回交分析确定小鼠Hnf6基因位于小鼠9号染色体的中部。对特定发育阶段胚胎的原位杂交研究表明,HNF-6及其潜在靶基因HNF-3β在胰腺和肝憩室中共表达。对HNF-6和HNF-3β发育表达模式的更详细分析提供了它们在肝细胞、肠上皮细胞、胰腺导管上皮细胞和外分泌腺泡细胞中共定位的证据。这两种转录因子的表达模式在其他内胚层来源的组织或神经管中不重叠。我们还发现HNF-6在背根神经节、边缘层和中脑中也大量表达。在妊娠第18天和成年胰腺中,HNF-6和HNF-3β转录本在胰腺外分泌腺泡细胞中共定位,但它们在其他胰腺上皮细胞中的表达模式不同。HNF-6(而非HNF-3β)在胰腺导管上皮细胞中持续表达,而只有HNF-3β局限于胰岛的内分泌细胞中表达。我们结合肝细胞的特化以及胰腺内分泌和外分泌的分化来讨论这些表达模式。