Transcriptional targets shared by estrogen receptor-related receptors (ERRs) and estrogen receptor (ER) α, but not by ERβ

The physiological activities of estrogens are thought to be mediated by specific nuclear receptors, ER alpha and ERP, However, certain tissues, such as the bone, that are highly responsive to estrogens only express a low level of these receptors, Starting from this apparent contradiction, we have evaluated the potentials of two related receptors ERR alpha and ERR beta to intervene in estrogen signaling. ER alpha ERR alpha and ERR beta bind to and activate transcription through both the classical estrogen response element (ERE) and the SF-1 response element (SFRE), In contrast, ER beta DNA-binding and transcriptional activity is restricted to the ERE, Accordingly, the osteopontin gene promoter is stimulated through SFRE sequences, by ERRa as well as by ERa, but not by ERP. Analysis of the cross-talk within the ER/ERR subgroup of nuclear receptors thus revealed common targets but also functional differences between the two ERs.