This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Holewa, B.
Right arrow Articles by Ryffel, G. U.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Holewa, B.
Right arrow Articles by Ryffel, G. U.

 Previous Article  |  Next Article 

Mol. Cell. Biol., 02 1997, 687-694, Vol 17, No. 2
Copyright © 1997, American Society for Microbiology

HNF4beta, a new gene of the HNF4 family with distinct activation and expression profiles in oogenesis and embryogenesis of Xenopus laevis

B Holewa, D Zapp, T Drewes, S Senkel and GU Ryffel
Institut fur Zellbiologie (Tumorforschung), Universitatsklinikum Essen, Germany.

The transcription factor hepatocyte nuclear factor 4 (HNF4) is an orphan member of the nuclear receptor superfamily expressed in mammals in liver, kidney, and the digestive tract. Recently, we isolated the Xenopus homolog of mammalian HNF4 and revealed that it is not only a tissue-specific transcription factor but also a maternal component of the Xenopus egg and distributed within an animal-to-vegetal gradient. We speculate that this gradient cooperates with the vegetally localized embryonic induction factor activin A to activate expression of HNF1alpha, a tissue-specific transcription factor with an expression pattern overlapping that of HNF4. We have now identified a second Xenopus HNF4 gene, which is more distantly related to mammalian HNF4 than the previously isolated gene. This new gene was named HNF4beta to distinguish it from the known HNF4 gene, which is now called HNF4alpha. By reverse transcription-PCR, we detected within the 5' untranslated region of HNF4beta two splice variants (HNF4beta2 and HNF4beta3) with additional exons, which seem to affect RNA stability. HNF4beta is a functional transcription factor acting sequence specifically on HNF4 binding sites known for HNF4alpha, but it seems to have a lower DNA binding activity and is a weaker transactivator than the alpha isoform. Furthermore, the two factors differ with respect to tissue distribution in adult frogs: whereas HNF4alpha is expressed in liver and kidney, HNF4beta is expressed in addition in stomach, intestine, lung, ovary, and testis. Both factors are maternal proteins and present at constant levels throughout embryogenesis. However, using reverse transcription- PCR, we found the RNA levels to change substantially: whereas HNF4alpha is expressed early during oogenesis and is absent in the egg, HNF4beta is first detected in the latest stage of oogenesis, and transcripts are present in the egg and early cleavage stages. Furthermore, zygotic HNF4alpha transcripts appear in early gastrula and accumulate during further embryogenesis, whereas HNF4beta mRNA transiently appears during gastrulation before it accumulates again at the tail bud stage. All of these distinct characteristics of the newly identified HNF4 protein imply that the alpha and beta isoform have different functions in development and in adult tissues.


This article has been cited by other articles:

  • Fustin, J.M., O'Neill, J.S., Hastings, M.H., Hazlerigg, D.G., Dardente, H. (2009). Cry1 Circadian Phase in vitro: Wrapped Up with an E-Box. J Biol Rhythms 24: 16-24 [Abstract]  
  • Bertrand, S., Brunet, F. G., Escriva, H., Parmentier, G., Laudet, V., Robinson-Rechavi, M. (2004). Evolutionary Genomics of Nuclear Receptors: From Twenty-Five Ancestral Genes to Derived Endocrine Systems. Mol Biol Evol 21: 1923-1937 [Abstract] [Full Text]  
  • Bohn, S., Thomas, H., Turan, G., Ellard, S., Bingham, C., Hattersley, A. T., Ryffel, G. U. (2003). Distinct Molecular and Morphogenetic Properties of Mutations in the Human HNF1{beta} Gene That Lead to Defective Kidney Development. J. Am. Soc. Nephrol. 14: 2033-2041 [Abstract] [Full Text]  
  • Stolze, I., Berchner-Pfannschmidt, U., Freitag, P., Wotzlaw, C., Rossler, J., Frede, S., Acker, H., Fandrey, J. (2002). Hypoxia-inducible erythropoietin gene expression in human neuroblastoma cells. Blood 100: 2623-2628 [Abstract] [Full Text]  
  • Schrem, H., Klempnauer, J., Borlak, J. (2002). Liver-Enriched Transcription Factors in Liver Function and Development. Part I: The Hepatocyte Nuclear Factor Network and Liver-Specific Gene Expression. Pharmacol. Rev. 54: 129-158 [Abstract] [Full Text]  
  • v. Strandmann, E. P., Senkel, S., Ryffel, G., Hengge, U. R. (2001). Dimerization Co-Factor of Hepatocyte Nuclear Factor 1/Pterin-4{{alpha}}-Carbinolamine Dehydratase Is Necessary for Pigmentation in Xenopus and Overexpressed in Primary Human Melanoma Lesions. Am. J. Pathol. 158: 2021-2029 [Abstract] [Full Text]  
  • Peiler, G., Böckmann, B., Nakhei, H., Ryffel, G. U. (2000). Inhibitor of the Tissue-Specific Transcription Factor HNF4, a Potential Regulator in Early Xenopus Development. Mol. Cell. Biol. 20: 8676-8683 [Abstract] [Full Text]  
  • Lausen, J., Thomas, H., Lemm, I., Bulman, M., Borgschulze, M., Lingott, A., Hattersley, A. T., Ryffel, G. U. (2000). Naturally occurring mutations in the human HNF4{alpha} gene impair the function of the transcription factor to a varying degree. Nucleic Acids Res 28: 430-437 [Abstract] [Full Text]  
  • Giguère, V. (1999). Orphan Nuclear Receptors: From Gene to Function. Endocr. Rev. 20: 689-725 [Abstract] [Full Text]  
  • Sladek, F. M., Ruse, M. D. Jr., Nepomuceno, L., Huang, S.-M., Stallcup, M. R. (1999). Modulation of Transcriptional Activation and Coactivator Interaction by a Splicing Variation in the F Domain of Nuclear Receptor Hepatocyte Nuclear Factor 4alpha 1. Mol. Cell. Biol. 19: 6509-6522 [Abstract] [Full Text]  
  • Dell, H., Hadzopoulou-Cladaras, M. (1999). CREB-binding Protein Is a Transcriptional Coactivator for Hepatocyte Nuclear Factor-4 and Enhances Apolipoprotein Gene Expression. J. Biol. Chem. 274: 9013-9021 [Abstract] [Full Text]