TY - JOUR
T1 - The cut-homeodomain transcriptional activator HNF-6 is coexpressed with its target gene HNF-3β in the developing murine liver and pancreas
AU - Rausa, Francisco
AU - Samadani, Uzma
AU - Ye, Honggang
AU - Lim, Lorena
AU - Fletcher, Colin F.
AU - Jenkins, Nancy A.
AU - Copeland, Neal G.
AU - Costa, Robert H.
N1 - Funding Information:
We thank Robert Storti, Pradip Raychaudhuri, Heping Zhou, and Chris Tebeau for critically reviewing the manuscript. We also thank Guy Rousseau and Frederic Lemaigre for sharing their HNF-6 data prior to publication and Roland Stein for sharing his submitted manuscript on the pdx-1 promoter. We are grateful to David Over-dier for his advice with the yeast one-hybrid system, Graeme Bell for the rat insulin cDNA and Debra Gilbert for excellent technical assistance. The DNA sequence for the human and mouse HNF-6 cDNA was determined by the DNA Sequencing and Synthesis Facility at Iowa State University of Science and Technology. This work was supported by Public Health Service Grant R01 GM43241-08 from the National Institute of General Medical Sciences (R.H.C.) and in part by the National Cancer Institute, DHHS, under Contract NO1-CO-74101 with ABL (N.A.J. and N.G.C.). R.H.C. is an Established Investigator of the American Heart Association/Bristol-Myers Squibb. U.S. is the Charlotte Webster Barnes, Helen T. Barnes, and Broda O. Barnes Scholar in Molecular Medicine.
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 1997/12/15
Y1 - 1997/12/15
N2 - Murine hepatocyte nuclear factor-3β (HNF-3β) 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-3β 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-3β 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-3β 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- 3β, are coexpressed in the pancreatic and hepatic diverticulum. More detailed analysis of HNF-6 and HNF-3β'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-3β transcripts colocalize in the exocrine acinar cells, but their expression patterns diverge in other pancreatic epithelium. HNF-6, but not HNF-3β, expression continues in the pancreatic ductal epithelium, whereas only HNF-3β 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.
AB - Murine hepatocyte nuclear factor-3β (HNF-3β) 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-3β 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-3β 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-3β 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- 3β, are coexpressed in the pancreatic and hepatic diverticulum. More detailed analysis of HNF-6 and HNF-3β'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-3β transcripts colocalize in the exocrine acinar cells, but their expression patterns diverge in other pancreatic epithelium. HNF-6, but not HNF-3β, expression continues in the pancreatic ductal epithelium, whereas only HNF-3β 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.
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U2 - 10.1006/dbio.1997.8744
DO - 10.1006/dbio.1997.8744
M3 - Article
C2 - 9441664
AN - SCOPUS:0031573810
VL - 192
SP - 228
EP - 246
JO - Developmental Biology
JF - Developmental Biology
SN - 0012-1606
IS - 2
ER -