NF kappa B interacts with serum amyloid A3 enhancer factor to synergistically activate mouse serum amyloid A3 gene transcription

Citation
Zy. Bing et al., NF kappa B interacts with serum amyloid A3 enhancer factor to synergistically activate mouse serum amyloid A3 gene transcription, J BIOL CHEM, 275(41), 2000, pp. 31616-31623
Citations number
61
Categorie Soggetti
Biochemistry & Biophysics
Journal title
JOURNAL OF BIOLOGICAL CHEMISTRY
ISSN journal
00219258 → ACNP
Volume
275
Issue
41
Year of publication
2000
Pages
31616 - 31623
Database
ISI
SICI code
0021-9258(20001013)275:41<31616:NKBIWS>2.0.ZU;2-0
Abstract
We had previously identified a distal regulatory element (DRE) in the mouse serum amyloid A3 (SAA3) promoter that functions as a cytokine-inducible tr anscription enhancer. Within this DRE, three functional elements interact w ith CCAAT/enhancer-binding protein (C/EBP) and SAA3 enhancer factor (SEF) t ranscription factors. In this study, we show that cotransfection of the SEF expression plasmid with an SAA3/luciferase reporter resulted in 3-5-fold a ctivation of the SAA3 promoter. When SEF-transfected cells were further sti mulated with conditioned medium or interleukin-l, SAA3 promoter activity wa s dramatically increased, suggesting that SEF may cooperate functionally wi th other interleukin-l-inducible transcription factors to synergistically u p-regulate SAA3 gene transcription. Indeed, cotransfection of SEF and NF ka ppa Bp65 expression DNAs resulted in synergistic activation of the SAA3 pro moter. Intriguingly, no consensus NF kappa B-binding site was found in the SAA3 promoter region; rather a putative NF kappa B-binding sequence with 3- base pair mismatches was identified in the DRE, When this sequence was used in an electrophoretic mobility shift assay, it interacted with NF kappa Bp 50, albeit with binding affinities that were several hundredfold lower than that with the consensus NF kappa B probe. Functional cooperation between S EF and NF kappa B was further strengthened by the finding that SEF and NF k appa B formed stable cytokine-inducible protein-protein complexes. Finally, despite its weak binding, mutation of this NF kappa B-binding site neverth eless dramatically reduced both NF kappa Bp65- and cytokine-mediated induct ion of SAA3 promoter. Therefore, the molecular basis for the functional syn ergy between SEF and NF kappa B may, in part, be the ability of SEF to recr uit NF kappa B through physical interactions that lead to enhancement or st abilization of NF kappa B binding to the SAA3 promoter element.