Distinct properties of the cAMP-responsive element of the rat insulin I gene

• Published in: The Journal of biological chemistry Vol. 269; no. 43; pp. 27036 - 27044
• Main Authors: Oetjen, E, Diedrich, T, Eggers, A, Eckert, B, Knepel, W
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 28-10-1994; American Society for Biochemistry and Molecular Biology
• Subjects: Animals; Blotting, Southern; Blotting, Western; Calcium - metabolism; Cell Nucleus - metabolism; Cyclic AMP - pharmacology; Cyclic AMP Response Element-Binding Protein - genetics; Cyclic AMP Response Element-Binding Protein - metabolism; Gene Expression Regulation - drug effects; Glucagon - metabolism; Insulin - genetics; Islets of Langerhans - metabolism; Membrane Potentials; Protein Binding; Rats - genetics; Regulatory Sequences, Nucleic Acid; Signal Transduction; Somatostatin - metabolism; Subcellular Fractions - metabolism; Transcription, Genetic
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/S0021-9258(18)47122-0

The cAMP response element (CRE)-binding transcription factor CREB can mediate induction of gene transcription in response to calcium as well as to cAMP. Since the rat insulin I gene 5'-flanking region contains a CRE with an octamer-like motif (TGACGTCC), CREB binding and cAMP/calcium responsiveness of the insulin CRE were investigated. In an electrophoretic mobility shift assay and in Southwestern blot experiments, bacterially expressed recombinant CREB bound to the insulin CRE as it did to the rat glucagon and rat somatostatin gene CREs. However, in nuclear extracts of the pancreatic islet cell line HIT, protein complexes binding to the insulin CRE did not contain proteins with CREB-like immunoreactivity, although these bound to the glucagon and somatostatin CREs. When reporter fusion genes were transfected into HIT cells, the isolated insulin CRE increased basal activity and mediated transcriptional activation by cAMP. However, cAMP stimulation of transcription through the insulin CRE was weak when compared with the response through the glucagon and somatostatin CREs. Furthermore, the insulin CRE did not confer responsiveness to membrane depolarization and calcium influx, in contrast to the glucagon and somatostatin CREs. These results demonstrate that the functional properties of the rat insulin I gene CRE are different from those of the rat glucagon and somatostatin CREs which may be explained by a distinct pattern of nuclear protein binding and suggest the existence of post-translational mechanisms that decrease the binding of cellular CREB to the insulin CRE.