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Activation of haptoglobin gene expression by cAMP involves CCAAT/enhancer‐binding protein isoforms in intestinal epithelial cells
Author(s) -
Pelletier Nadine,
Boudreau François,
Yu Shun-Jiang,
Zani Sonia,
Boulanger Véronique,
Asselin Claude
Publication year - 1998
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/s0014-5793(98)01388-x
Subject(s) - microbiology and biotechnology , ccaat enhancer binding proteins , forskolin , gene isoform , activator (genetics) , biology , transfection , haptoglobin , gene expression , messenger rna , enhancer , electrophoretic mobility shift assay , transcription factor , adenylate kinase , gene , nuclear protein , cell culture , biochemistry , enzyme , endocrinology , genetics
CCAAT/enhancer‐binding protein (C/EBP) isoforms are expressed in rodent intestine and in the rat intestinal epithelial cell line IEC‐6 but their role remains to be determined. Treatment of IEC‐6 cells with the adenylate cyclase activator forskolin led to coordinate induction of C/EBP isoforms α, β and δ at the mRNA and protein levels. Transient transfection assays showed that their expression is controlled at the transcriptional level. Forskolin treatment induced haptoglobin mRNA levels. Electrophoretic mobility shift and supershift assays demonstrated an increase in DNA‐binding activities of the three C/EBP isoforms to the haptoA and haptoC C/EBP DNA‐binding sites of the proximal haptoglobin promoter. Site‐specific mutations of both sites led to a decrease in transcriptional induction by forskolin, suggesting that C/EBP isoforms are involved in the cAMP‐dependent regulation of the acute‐phase protein gene haptoglobin in intestinal epithelial cells.