Characterization of Estrogen Receptor- (ER ) Messenger Ribonucleic Acid and Protein Expression in Rat Granulosa Cells

Abstract

We have examined estrogen-responsiveness of ovarian granulosa cells by focusing on estrogen receptor (ER) expression. Estrogen responsiveness was determined by examining the effect of 17β-estradiol (1–10 nm) on luciferase reporter activity in rat granulosa cells transfected with an ERE-luciferase construct. The results demonstrate an estrogen-induced (approximately 3-fold) increase in luciferase reporter activity, indicating that granulosa cells contain functional estrogen response element (ERE)-binding transcriptional activators. Gel mobility shift assays in combination with ER antibodies show that ERβ is the predominant ERE-binding protein in granulosa cells. Western blotting results show that granulosa cells contain ERβ-immunoreactive protein(s) migrating at a size substantially larger than the recombinant protein generated from the originally proposed 485 amino acid open-reading frame. This size discrepancy is not due to granulosa cell expression of ERβ isoforms with insertions within the coding region because RT-PCR assays revealed products with sizes expected for ERβ, ERβB, and δ3 isoforms. This size discrepancy appears to be due to usage of a well-conserved, upstream in-frame translation initiation codon (ATG436) leading to a 530 amino acid open reading frame. ERβ messenger RNA (mRNA) characterization using 5′-rapid amplification of complementary DNA ends (5′-RACE) show the presence of two different (P1- and P2-) 5′-ends of rat ERβ mRNA encoding the full-length ERβ protein. The generation of the P2-specific exon is likely due to initiation of transcription from an alternative promoter. Both P1- and P2-specific exon-containing ERβ mRNAs are expressed in granulosa cells, and they are rapidly down-regulated by the cAMP-mediated intracellular signaling pathway in cultured granulosa cells. Taken together, our results show that rat granulosa cells produce two different 3′,5′-cAMP-regulated ERβ mRNA species and that these mRNA species are capable of encoding the full-length ERβ protein.