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.