Synergistic activation of the Atlantic salmon hepatocyte nuclear factor (HNF) 1 promoter by the orphan nuclear receptors HNF4 and chicken ovalbumin upstream promoter transcription factor I (COUP-TFI)

Citation
A. Mcnair et al., Synergistic activation of the Atlantic salmon hepatocyte nuclear factor (HNF) 1 promoter by the orphan nuclear receptors HNF4 and chicken ovalbumin upstream promoter transcription factor I (COUP-TFI), BIOCHEM J, 352, 2000, pp. 557-564
Citations number
37
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL JOURNAL
ISSN journal
02646021 → ACNP
Volume
352
Year of publication
2000
Part
2
Pages
557 - 564
Database
ISI
SICI code
0264-6021(200012)352:<557:SAOTAS>2.0.ZU;2-S
Abstract
Hepatocyte nuclear factor 1 (HNF1) is a liver-enriched transcription factor that plays an important role in transcriptional networks involved in liver function. The promoters of mammalian HNF1 genes contains a single binding site for another liver-enriched transcription factor, the nuclear hormone r eceptor HNF4. A transcriptional hierarchy involving HNF4-mediated activatio n of the HNF1 promoter has been proposed to be of crucial importance in mai ntaining the differentiated hepatocyte phenotype, Here we present evidence that the Atlantic salmon HNF1 promoter contains three nuclear-hormone-recep tor-binding sequences. Gel-shift assays showed that these motifs are recogn ized with different affinities by HNF4 and the orphan nuclear receptors chi cken ovalbumin upstream promoter transcription factors COUP-TFI and COUP-TF II. In hepatoma cells, the site showing highest affinity for HNF4 appears t o be crucial for promoter activity. Transfection experiments in nonhepatic cells indicated that the salmon HNF1 promoter was activated by both HNF4 an d COUP-TFs. We also identified a promoter fragment encompassing the two mor e distal nuclear-hormone-binding sites that was activated by HNF4, unaffect ed by COUP-TF and showed a strong synergistic activation by HNF4/COUP-TF. R esults are presented detailing these interactions in relation to the salmon HNF1 promoter architecture.