The transcription factor hepatocyte nuclear factor 3 (HNF-3) is involved in the coordinate expression of several liver genes. HNF-3 DNA binding activity is composed of three different liver proteins which recognize the same DNA site. The HNF-3 proteins (designated α, β, and γ) possess homology in the DNA binding domain and in several additional regions. To understand the cell-type-specific expression of HNF-3β, we have defined the regulatory sequences that elicit hepatoma-specific expression. Promoter activity requires -134 bp of HNF-3β proximal sequences and binds four nuclear proteins, including two ubiquitous factors. One of these promoter sites interacts with a novel cell-specific factor, LF-H3β, whose binding activity correlates with the HNF-3β tissue expression pattern. Furthermore, there is a binding site for the HNF-3 protein within its own promoter, suggesting that an autoactivation mechanism is involved in the establishment of HNF-3β expression. We propose that both the LF-H3β and HNF-3 sites play an important role in the cell-type-specific expression of the HNF-3β transcription factor.
The restricted promoter activity of the liver transcription factor hepatocyte nuclear factor 3β involves a cell-specific factor and positive autoactivation / Pani, L.; Qian, X.; Clevidence, D.; Costa, R. H.. - In: MOLECULAR AND CELLULAR BIOLOGY. - ISSN 0270-7306. - 12:2(1992), pp. 552-562. [10.1128/MCB.12.2.552]
The restricted promoter activity of the liver transcription factor hepatocyte nuclear factor 3β involves a cell-specific factor and positive autoactivation
Pani L.;
1992
Abstract
The transcription factor hepatocyte nuclear factor 3 (HNF-3) is involved in the coordinate expression of several liver genes. HNF-3 DNA binding activity is composed of three different liver proteins which recognize the same DNA site. The HNF-3 proteins (designated α, β, and γ) possess homology in the DNA binding domain and in several additional regions. To understand the cell-type-specific expression of HNF-3β, we have defined the regulatory sequences that elicit hepatoma-specific expression. Promoter activity requires -134 bp of HNF-3β proximal sequences and binds four nuclear proteins, including two ubiquitous factors. One of these promoter sites interacts with a novel cell-specific factor, LF-H3β, whose binding activity correlates with the HNF-3β tissue expression pattern. Furthermore, there is a binding site for the HNF-3 protein within its own promoter, suggesting that an autoactivation mechanism is involved in the establishment of HNF-3β expression. We propose that both the LF-H3β and HNF-3 sites play an important role in the cell-type-specific expression of the HNF-3β transcription factor.Pubblicazioni consigliate
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