Interaction of nuclear factors with the cAMP response elements of the human β3-adrenoceptor gene
- 28 Downloads
Four potential cyclic adenosine 3′,5′-monophosphate (cAMP) response elements (CREs), each having at most two mismatches from the classical canonical sequence, have been identified in the 5′UTR of the human β3-adrenoceptor gene by Liggett and Schwinn (1991). Recently, three of these CREs were shown to confer responsiveness to cAMP when cloned into a CAT reporter vector (Thomas et al., 1992). In this study, in vitro gel-retardation assays have shown that recombinant human CRE binding protein-1 (CREB-1) or activating transcription factor-1 (ATF-1) can interact specifically with these four putative CREs (termed β3CRE2), although with different affinities. Nuclear extracts from human brown or white adipose tissue contain proteins interacting with β3CRE3 and β3CRE2. These adipose nuclear factors were shown by competition assays and the use of antibodies to differ from CREB-1 or ATF-1. The nuclear factor(s) interacting with β3CRE2 was found in human and rat brown and white adipose tissues, but not in the other nonadipose tissues examined, i.e., rat lung, liver, kidney, and heart, suggesting an adipose tissue-specific DNA binding or expression pattern. β3CRE2 is found to constitute a hexameric element that is highly homologous to the binding site for members of the nuclear hormone receptor superfamily, and a competition assay using this site has provided evidence that an adipose tissuespecific orphan member of this superfamily may bind to β3CRE2. Reporter gene assays have indicated that β3CRE2 and β3CRE3 slightly repress the basal level of transcription and that β3CRE2 confers cAMP responsiveness, whereas β3CRE3 does not.
Key Wordsβ3-adrenoceptor cAMP transcription CREB adipose tissue
Unable to display preview. Download preview PDF.
- Alksnis, M., Barkhem, T., Stromsted, P.-E., Ahola, H., Kutoh, E., Gustafsson, J.-A., Poellinger, L., and Nilsson, S. (1991).J. Biol. Chem. 266, 10,078–10,085Google Scholar
- Chawla, A. and Lazar, M. A. (1993).J. Biol. Chem. 268, 16,265–16,269.Google Scholar
- Howe, R. (1993).Drug Future 18, 529–549.Google Scholar
- Orten, D., Strawhecker, J., Sanderson, S., Huang, D., Prystowsky, M., and Hinrichs, S. (1994).J. Biol. Chem. 269, 32,254–32,263.Google Scholar
- Pestell, R., Hollenberg, A., Albanese, C., and Jameson, J. L. (1994).J. Biol. Chem. 269, 31,090–31,096.Google Scholar
- Sambrook, J., Fritsch, E. F., and Maniatis, T. (1989).Molecular Cloning: A Laboratory Manual, 2nd ed. Cold Spring Harbor Laboratory Press: Cold Spring Harbor, NY.Google Scholar