DAX-1 functions as an LXXLL-containing corepressor for activated estrogen receptors

We have discovered that the orphan receptor DAX-1 (NROB1) interacts with th e estrogen receptors ER alpha and ER beta. Interaction occurs with ligand-a ctivated ERs in solution and on DNA and is mediated by the unique DAX-1 N-t erminal repeat domain. Each of the three repeats contains a leucine-rich re ceptor-binding motif, known as the LXXLL motif, which is usually found in n uclear receptor coactivators. We have demonstrated that DAX-1 functions as an inhibitor of ER activation in mammalian cells and suggest a mechanism in volving two sequential events, occupation of the ligand-induced coactivator -binding surface and subsequent recruitment of corepressors. Accordingly, w e propose that DAX-1 itself acts as a corepressor for ERs. Because DAX-1 is coexpressed with ERs in reproductive tissues, these interactions could pla y significant roles by influencing estrogen signaling pathways. Our results point at functional similarities between DAX-1 and the orphan receptor SHP (NROB2) in that they have acquired features of transcriptional coregulator s that are unique for members of the nuclear receptor family.