Todo T, Adachi S, Yamauchi K
Department of Biology, Faculty of Fisheries, Hokkaido University, Japan.
Mol Cell Endocrinol. 1996 May 17;119(1):37-45. doi: 10.1016/0303-7207(96)03792-6.
A cDNA encoding the Japanese eel, Anguilla japonica, estrogen receptor (ER) was isolated and sequenced. This cDNA contains a complete open reading frame encoding 573 amino acid residues, and the molecular weight of this protein is calculated to be 63417. The amino acid sequence of the eel ER shows high homology of the DNA binding (80%) and ligand binding (55%) domains with those of other species. However, the other domains show greatly reduced homology (10-20%). When the cDNA was ligated to the pSVL vector and transfected into COS7 cells, a protein was produced that had high affinity for estradiol-17 beta (E2) and specifically bound estrogens. Northern analysis showed that three ER mRNAs with lengths of 5.6, 3.8 and 1.2 kb were expressed in eel liver. Their expression was E2 inducible, with the 5.6 kb mRNA being strongly dependent on E2 stimulation.
分离并测序了编码日本鳗鲡(Anguilla japonica)雌激素受体(ER)的cDNA。该cDNA包含一个完整的开放阅读框,编码573个氨基酸残基,此蛋白的分子量经计算为63417。鳗鲡ER的氨基酸序列在DNA结合结构域(80%)和配体结合结构域(55%)与其他物种的相应结构域具有高度同源性。然而,其他结构域的同源性则大幅降低(10 - 20%)。当将该cDNA连接到pSVL载体并转染到COS7细胞中时,产生了一种对17β - 雌二醇(E2)具有高亲和力且能特异性结合雌激素的蛋白质。Northern分析表明,鳗鲡肝脏中表达了三种长度分别为5.6、3.8和1.2 kb的ER mRNA。它们的表达是E2诱导型的,其中5.6 kb的mRNA强烈依赖于E2刺激。