Previous Article | Next Article 
Mol Cell Biol. 1993 October; 13(10): 6416-6426
Elements and factors involved in tissue-specific and embryonic expression of the liver transcription factor LFB1 in Xenopus laevis.
D Zapp,
S Bartkowski,
B Holewa,
C Zoidl,
L Klein-Hitpass and
G U Ryffel
Institut für Zellbiologie (Tumorforschung), Universitätsklinikum Essen, Germany.
ABSTRACT
LFB1 (HNF1) is a tissue-specific transcription factor found in the livers, stomachs, intestines, and kidneys of vertebrates. By analyzing the promoter of the Xenopus LFB1 gene, we identified potential autoregulation by LFB1 and regulation by HNF4, a transcription factor with a tissue distribution similar to that of LFB1. Injection of LFB1 promoter-chloramphenicol acetyltransferase constructs into Xenopus eggs revealed embryonic activation that is restricted to the region of the developing larvae expressing endogeneous LFB1. Proper embryonic activation was also observed with a rat LFB1 promoter. Deletion analysis of the Xenopus and rat promoters revealed that in both promoters embryonic activation is absolutely dependnet on the presence of an element that contains CCNCTCTC as the core consensus sequence. Since this element is recognized by the maternal factor OZ-1 previously described by N. Ovsenek, A. M. Zorn, and P. A. Krieg (Development 115:649-655, 1992), we might have identified the main constituents of a hierarchy that leads via LFB1 to the activation of tissue-specific genes during embryogenesis.
Mol Cell Biol. 1993 October; 13(10): 6416-6426
This article has been cited by other articles:
-
Bailly, A., Torres-Padilla, M. E., Tinel, A. P., Weiss, M. C.
(2001). An enhancer element 6 kb upstream of the mouse HNF4{alpha}1 promoter is activated by glucocorticoids and liver-enriched transcription factors. Nucleic Acids Res
29: 3495-3505
[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]
-
Bailly, A, Spath, G, Bender, V, Weiss, M.
(1998). Phenotypic effects of the forced expression of HNF4 and HNF1alpha are conditioned by properties of the recipient cell. J. Cell Sci.
111: 2411-2421
[Abstract]
-
Shi, Y., Sullivan, S. K., Pitterle, D. M., Kennington, E. A., Graff, J. M., Blackshear, P. J.
(1997). Mechanisms of MARCKS Gene Activation during Xenopus Development. J. Biol. Chem.
272: 29290-29300
[Abstract]
[Full Text]
-
Klotzbücher, M., Schwerk, C., Holewa, B., Klein-Hitpass, L.
(1997). Activation of Transcription by Progesterone Receptor Involves Derepression of Activation Functions by a Cofactor. Mol. Endocrinol.
11: 768-778
[Abstract]
[Full Text]
-
Weber, H, Holewa, B, Jones, E., Ryffel, G.
(1996). Mesoderm and endoderm differentiation in animal cap explants: identification of the HNF4-binding site as an activin A responsive element in the Xenopus HNF1alpha promoter. Development
122: 1975-1984
[Abstract]
-
Schwerk, C., Klotzbücher, M., Sachs, M., Ulber, V., Klein-Hitpass, L.
(1995). Identification of a Transactivation Function in the Progesterone Receptor That Interacts with the TAF[IMAGE]110 Subunit of the TFIID Complex. J. Biol. Chem.
270: 21331-21338
[Abstract]
[Full Text]
-
Pogge yon Strandmann, E, Ryffel, G.
(1995). Developmental expression of the maternal protein XDCoH, the dimerization cofactor of the homeoprotein LFB1 (HNF1). Development
121: 1217-1226
[Abstract]
-
Pare, J.-F., Roy, S., Galarneau, L., Belanger, L.
(2001). The Mouse Fetoprotein Transcription Factor (FTF) Gene Promoter Is Regulated by Three GATA Elements with Tandem E Box and Nkx Motifs, and FTF in Turn Activates the Hnf3beta , Hnf4alpha , and Hnf1alpha Gene Promoters. J. Biol. Chem.
276: 13136-13144
[Abstract]
[Full Text]