Constitutive expression of the gene for the cell-specific p48 DNA-binding subunit of pancreas transcription factor 1 in cultured cells is under control of binding sites for transcription factors Sp1 and alphaCbf.

Détails

ID Serval
serval:BIB_4528
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Constitutive expression of the gene for the cell-specific p48 DNA-binding subunit of pancreas transcription factor 1 in cultured cells is under control of binding sites for transcription factors Sp1 and alphaCbf.
Périodique
Journal of Biological Chemistry
Auteur⸱e⸱s
Knöfler M., Krapp A., Hagenbüchle O., Wellauer P.K.
ISSN
0021-9258
Statut éditorial
Publié
Date de publication
1996
Volume
271
Numéro
36
Pages
21993-2002
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't - Publication Status: ppublish
Résumé
We have cloned and characterized the rat gene that encodes the p48 DNA-binding subunit of pancreas transcription factor 1 (Ptf1), a cell-specific basic region helix-loop-helix (bHLH) protein. The ptf1-p48 gene measures 1.8 kilobases in size and occurs as a single copy in the haploid genome. Run-on transcription assays suggest that this gene is subject to transcriptional control since no activity of its promoter is detected in nonproducing cells. The gene specifies two mRNAs that encode the same protein and originate from transcription initiation at alternative sites. Expression analysis of hybrid genes bearing deletions of the gene's 5'-flanking region fused to a reporter gene defines a promoter region within the gene-proximal 260 base pairs of DNA. The cis-acting elements that control promoter activity include binding sites for transcription factors Sp1 and alphaCbf, a 60-kDa CCAAT box-binding protein. The gene promoter, however, functions not only in exocrine pancreatic cells but also in cells of other origin. No cell-specific transcriptional control element was detected in as much as 10 kilobases of 5'-flanking region. We discuss models of how the cell-specific expression of the endogenous ptf1-p48 gene might be established during development of the animal.
Mots-clé
Animals, Base Sequence, Binding Sites, CCAAT-Enhancer-Binding Proteins, Cloning, Molecular, DNA Footprinting, DNA-Binding Proteins/genetics, DNA-Binding Proteins/metabolism, Deoxyribonuclease I/metabolism, Electrophoresis, Polyacrylamide Gel, Molecular Sequence Data, Rats, Rats, Sprague-Dawley, Sp1 Transcription Factor/metabolism, Transcription Factors/genetics
Pubmed
Web of science
Création de la notice
19/11/2007 13:40
Dernière modification de la notice
20/08/2019 14:49
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