Molecular Characterization of the Xenopus CCAAT-Enhancer Binding Protein β Gene Promoter

2001 ◽  
Vol 285 (2) ◽  
pp. 430-436 ◽  
Author(s):  
Pelagia Foka ◽  
Stavroula Kousteni ◽  
Dipak P. Ramji
Keyword(s):  
Molecular Characterization ◽  
Binding Protein ◽  
Gene Promoter ◽  
Enhancer Binding Protein ◽  
Ccaat Enhancer Binding Protein

Molecular cloning and characterization of rainbow trout (Oncorhynchus mykiss) CCAAT/enhancer binding protein ?

2003 ◽  
Vol 55 (4) ◽  
pp. 253-261 ◽  
Author(s):  
Kazuhiro Fujiki ◽  
Lena Gerwick ◽  
Christopher J. Bayne ◽  
Leslie Mitchell ◽  
Julie Gauley ◽  
...  
Keyword(s):  
Rainbow Trout ◽  
Oncorhynchus Mykiss ◽  
Molecular Cloning ◽  
Binding Protein ◽  
Rainbow Trout Oncorhynchus Mykiss ◽  
Enhancer Binding Protein ◽  
Ccaat Enhancer Binding Protein

scholarly journals Interaction of CCAAT/enhancer-binding protein α and β with the rat caeruloplasmin gene promoter

1993 ◽  
Vol 294 (2) ◽  
pp. 473-479 ◽  
Author(s):  
C D Bingle ◽  
R E Fleming ◽  
J D Gitlin
Keyword(s):  
Rat Liver ◽  
Specific Binding ◽  
Binding Protein ◽  
Specific Interaction ◽  
Gene Promoter ◽  
Nuclear Extract ◽  
Mobility Shift ◽  
Specific Expression ◽  
Enhancer Binding Protein ◽  
Ccaat Enhancer Binding Protein

To determine the mechanisms of expression of the rat caeruloplasmin gene, the promoter region was analysed by DNAase I footprinting. Using nuclear extract from rat liver, a prominent site of protein-DNA interaction was detected from -93 to -48 upstream of the caeruloplasmin gene transcription start and sequence analysis of this region revealed three potential CCAAT/enhancer-binding protein (C/EBP) consensus elements. Mobility-shift analysis using an oligonucleotide encoding this region identified specific binding of proteins from rat liver nuclear extract, and some of these complexes were supershifted using antisera to the C/EBP alpha and beta family members. Mobility-shift studies using a polypeptide encoding the DNA-binding domain of C/EBP alpha also revealed a specific interaction with this region of the caeruloplasmin promoter, and DNAase I footprinting using this polypeptide protected the identical region from -93 to -48. Co-transfection of expression plasmids encoding C/EBP alpha or a related leucine-zipper factor D-binding protein (DBP) revealed a C/EBP-specific increase in reporter gene activity in HepG2 cells transfected with caeruloplasmin-chloramphenicol acetyltransferase containing the -93 to -48 region. A similar result was obtained when these constructs were co-transfected into mouse L cells which were shown not to express the endogenous caeruloplasmin gene. Taken together, these data indicate a role for C/EBP alpha and beta in mediating transcription from the caeruloplasmin gene promoter and suggest that this region of the promoter is not responsible for tissue-specific expression.

scholarly journals A Role for CCAAT/Enhancer-Binding Protein β in the Basal Regulation of the Distal-Less 3 Gene Promoter in Placental Cells

Endocrinology ◽  
2004 ◽  
Vol 145 (3) ◽  
pp. 1096-1105 ◽  
Author(s):  
Manja P. Holland ◽  
Stuart P. Bliss ◽  
Kathie A. Berghorn ◽  
Mark S. Roberson
Keyword(s):  
Binding Protein ◽  
Gene Promoter ◽  
Enhancer Binding Protein ◽  
Placental Cells ◽  
Ccaat Enhancer Binding Protein
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