Abstract
The promoter of the cholecystokinin (CCK) gene possesses evolutionary conserved juxtaposed E-box and cAMP/TPA responsive elements (CRE/TRE). We have examined the functional interaction of these two sites. As previously noted, c-Jun/c-Fos heterodimers greatly increase promoter activity through association with the CRE/TRE. Mutation of the E-box enhanced the activation by c-Jun/c-Fos, as well as stimulation by forskolin and bFGF, that acts through the CRE/TRE site. Moreover, c-Jun/c-Fos stimulation was inhibited by co-expression of c-Myc and Max. The results indicate that factors associating with the E-box exhibit a negative cooperative effect on the activation via the CRE/TRE element. We propose that this mechanism plays a significant role in CCK gene transcription and other genes with juxtaposed E-box and CRE/TRE.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Base Sequence
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Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
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Basic-Leucine Zipper Transcription Factors
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Cholecystokinin / genetics*
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Cyclic AMP / metabolism*
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Cyclic AMP / pharmacology
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Cyclic AMP Response Element-Binding Protein / genetics
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Cyclic AMP Response Element-Binding Protein / metabolism
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DNA-Binding Proteins / genetics
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DNA-Binding Proteins / metabolism
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Gene Expression Regulation*
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Helix-Loop-Helix Motifs*
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Humans
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Leucine Zippers*
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Mice
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Molecular Sequence Data
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Mutagenesis
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Promoter Regions, Genetic*
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Proto-Oncogene Proteins c-fos / genetics
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Proto-Oncogene Proteins c-fos / metabolism
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Proto-Oncogene Proteins c-jun / genetics
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Proto-Oncogene Proteins c-jun / metabolism
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Proto-Oncogene Proteins c-myc / genetics
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Proto-Oncogene Proteins c-myc / metabolism
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Response Elements*
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Tetradecanoylphorbol Acetate / metabolism*
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Tetradecanoylphorbol Acetate / pharmacology
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Transcription Factors / genetics
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Transcription Factors / metabolism
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Tumor Cells, Cultured
Substances
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Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
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Basic-Leucine Zipper Transcription Factors
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Cyclic AMP Response Element-Binding Protein
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DNA-Binding Proteins
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MAX protein, human
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Myc associated factor X
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Proto-Oncogene Proteins c-fos
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Proto-Oncogene Proteins c-jun
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Proto-Oncogene Proteins c-myc
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Transcription Factors
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Max protein, mouse
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Cholecystokinin
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Cyclic AMP
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Tetradecanoylphorbol Acetate