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All rights reserved. http://resource.belframework.org/belframework/20131211/knowledge/large_corpus.bel http://purl.org/dc/elements/1.1/title BEL Framework Large Corpus Document http://resource.belframework.org/belframework/20131211/knowledge/large_corpus.bel http://purl.org/pav/authoredBy http://www.tkuhn.ch/bel2nanopub/RATyWqw1ApRbMuBJrM9JGXaoyYCmCIPH4634WUH6o79e0#_5 http://resource.belframework.org/belframework/20131211/knowledge/large_corpus.bel http://purl.org/pav/version 20131211 http://www.tkuhn.ch/bel2nanopub/RATyWqw1ApRbMuBJrM9JGXaoyYCmCIPH4634WUH6o79e0#_4 http://www.w3.org/ns/prov#value Luciferase reporters carrying 1.8 kb of 5'-flanking region of the mouse CYP8B gene or 0.9 kb of 5'-flanking region of the rat CYP51 gene were constructed (Fig. 5A). The basal transcriptional activity of the CYP8B promoter (Fig. 5B, left panel) was high as compared with that of CYP7A. The addition of hDEC1 had little effect on the basal activity of the CYP8B promoter (Fig. 5B, left panel), whereas hDEC2 and mDEC2 suppressed the basal transcriptional activity of the CYP8B promoter. DBP expression plasmid enhanced the promoter activity by 4-fold (Fig. 5B, right panel). The enhanced transcriptional activity by rDBP was markedly suppressed by hDEC2 or mDEC2, but not by hDEC1. 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