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This version published online on October 4, 2007
Endocrinology, doi:10.1210/en.2007-0938
A more recent version of this article appeared on January 1, 2008
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*Nucleotide*Protein

Submitted on July 11, 2007
Accepted on September 25, 2007

Molecular cloning and characterization of estrogen, androgen and progesterone nuclear receptors from a freshwater turtle (Pseudemys nelsoni)

Yoshinao Katsu, Rie Ichikawa, Toshitaka Ikeuchi, Satomi Kohno, Louis J. Guillette Jr., and Taisen Iguchi*

Okazaki Institute for Integrative Bioscience (Y.K., R.I., Ta.I.), National Institutes of Natural Sciences, 5–1 Higashiyama, Myodaiji, Okazaki, Aichi, 444-8787, Japan; Department of Basic Biology (Y.K., Ta.I.), the Graduate University for Advanced Studies (SOKENDAI), 5–1 Higashiyama, Myodaiji, Okazaki, Aichi, 444-8787, Japan; Department of Bioscience (To.I.), Nagahama Institute of Bio-Science and Technology 1266 Tamura, Nagahama, 526-0829, Shiga, Japan; Department of Zoology (S.K., L.J.G.), Box 118525, University of Florida, Gainesville FL 32611, USA

* To whom correspondence should be addressed. E-mail: taisen{at}nibb.ac.jp.

Steroid hormones are essential for the normal function of many organ systems in vertebrates. Reproductive activity in females and males, such as the differentiation, growth and maintenance of the reproductive system, requires signaling by the sex steroids. Although extensively studied in mammals and a few fish, amphibians and bird species, the molecular mechanisms of sex steroid hormone (estrogens, androgens and progestins) action are poorly understood in reptiles. Here we evaluate hormone receptor ligand interactions in a freshwater turtle, the Red belly slider (Pseudemys nelsoni), following the isolation of cDNAs encoding an estrogen receptor alpha (ER{alpha}), an androgen receptor (AR) and a progesterone receptor (PR). The full-length Red belly slider ER{alpha} (tER{alpha}), tAR and tPR cDNAs were obtained using 5' and 3' rapid amplification cDNA ends (RACE). The deduced amino acid sequences showed high identity to the chicken orthologs (tER{alpha}: 90%; tAR: 71%; tPR: 71%). Using transient transfection assays of mammalian cells, tER{alpha} protein displayed estrogen-dependent activation of transcription from an estrogen-responsive-element containing promoter. The other receptor proteins, tAR and tPR, also displayed androgen- or progestin-dependent activation of transcription from androgen- and progestin-responsive murine mammary tumor virus promoters. We further examined the transactivation of tER{alpha}, tAR and tPR by ligands using a modified GAL4-transactivation system. We found that the GAL4-transactivation system was not suitable for the measurement of tAR and tPR transactivations. This is the first report of the full-coding regions of a reptilian AR and PR, and the examination of their transactivation by steroid hormones.


Key words: reptile • turtle • estrogen receptor • androgen receptor • progesterone receptor • cloning • transactivation







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