We have investigated the proteins binding the E-selectin promoter NF-k
appaB element in its natural DNA context, using probes extending beyon
d the NF-kappaB recognition decamer. In band shift assays, we detected
two distinct NF-kappaB complexes using nuclear extracts from several
cytokine-induced cells. Subunit-specific antisera as blockers of compl
ex formation plus DNA - protein cross-linking experiments revealed the
faster migrating form to contain the NF-kappaB p50 plus p65 subunits.
In contrast, the slower migrating form is composed of p50 plus the p6
5-related p75 protein. We show as the crucial determinant in generatio
n of the larger complex the presence of more than five basepairs extra
DNA sequence downstream of the NF-kappaB-site. Although no specific s
equence is required in this 3' extended DNA to bind the larger complex
, an intact kappaB binding site is. This may be explained by a require
ment for activated p50 as part of this complex. The potential for a re
gulatory role for the p75 containing complex on the E-selectin promote
r is discussed.