Cloning and expression of the estrogen receptor-a (Esr1) from the Harderian gland of the sea turtle (Lepidochelys olivacea)

• Published in: General and comparative endocrinology 2009-06, Vol.162 (2), p.203-209
• Main Authors: Chavez, B, Ramos, L, Merchant-Larios, H, Vilchis, F
• Format: Article
• Language: English
• Subjects: Lepidochelys olivacea; Marine
• ISSN: 0016-6480
• DOI: 10.1016/j.ygcen.2009.02.010

The effects of estradiol on the Harderian gland (HG) are believed to be partially regulated by the transcriptional regulation of the estrogen-related genes via estrogen receptor (ER). In reptiles, however, it has not been well established whether the HG contains or expresses steroid nuclear receptors. As a first step toward investigating the molecular mechanisms of estrogen signalling in the HG, we isolated the cDNA for ERa in the sea turtle Lepidochelys olivacea. ERa was cloned using RT-PCR coupled with 5' and 3' RACE procedures. The cDNA contains a complete open reading frame encoding 588 amino acid residues. Comparative analysis of this amino acid sequence showed moderate to strong conservation of the ERa (Esr1) gene within divergent vertebrate groups. In transfection studies, the cloned ER displayed high affinity K sub(d)=0.25nM and high specificity for 17b-estradiol. Binding assays using sucrose density gradients demonstrated a specific 7-7.5 S binding component in the HG cytosolic fractions. RT-qPCR analysis showed significant ERa mRNA expression in the liver, HG, lung and brain. Altogether, these results provide evidence for the expression of intracellular ERs in the HG of the sea turtle and suggest that ERa may be an important modulator of the estrogen-mediated response in the HG of reptiles.