| First Author | Tremblay GB | Year | 1997 |
| Journal | Mol Endocrinol | Volume | 11 |
| Issue | 3 | Pages | 353-65 |
| PubMed ID | 9058381 | Mgi Jnum | J:38785 |
| Mgi Id | MGI:86169 | Doi | 10.1210/mend.11.3.9902 |
| Citation | Tremblay GB, et al. (1997) Cloning, chromosomal localization, and functional analysis of the murine estrogen receptor beta. Mol Endocrinol 11(3):353-65 |
| abstractText | Estrogen receptor beta (ER beta) is a novel steroid receptor that is expressed in rat prostate and ovary. We have cloned the mouse homolog of ER beta and mapped the gene, designated Estrb, to the central region of chromosome 12. The cDNA encodes a protein of 485 amino acids that shares, respectively, 97% and 60% identity with the DNA- and ligand-binding domains of mouse (m) ER alpha. Mouse ER beta binds to an inverted repeat spaced by three nucleotides in a gel mobility shift assay and transactivates promoters containing synthetic or natural estrogen response elements in an estradiol (E(2))- dependent manner. Scatchard analysis indicates that mER beta has slightly lower affinity for E(2) [dissociation constant (K-d) = 0.5 nM] when compared with mER alpha (K-d = 0.2 nM). Antiestrogens, including 4-hydroxytamoxifen (OHT), ICI 182,780, and a novel compound, EM-800, inhibit E(2)-dependent transactivation efficiently. However, while OHT displays partial agonistic activity with ER alpha on a basal promoter linked to estrogen response elements in Cos- 1 cells, this effect is not observed with mER beta. Cotransfection of mER beta and H-Ras(V12) causes enhanced activation in the presence of E(2). Mutagenesis of a serine residue (position 60), located within a mitogen- activated protein kinase consensus phosphorylation site abolishes the stimulatory effect of Ras, suggesting that the activity of mER beta is also regulated by the mitogen- activated protein kinase pathway. Surprisingly, the coactivator SRC-1 up-regulates mER beta transactivation both in the absence and presence of E(2), and in vitro interaction between SRC-1 and the ER beta ligand-binding domain is enhanced by E(2). Moreover, the ligand- independent stimulatory effect of SRC-1 on ER beta transcriptional activity is abolished by ICI 182,780, but not by OHT. Our results demonstrate that while ER beta shares many of the functional characteristics of ER alpha, the molecular mechanisms regulating the transcriptional activity of mER beta may be distinct from those of ER alpha. |
