This Article Full Text Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Request Copyright Permission Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Toda, K. Articles by Okada, T. Search for Related Content PubMed PubMed Citation Articles by Toda, K. Articles by Okada, T.

Aromatase-Knockout Mouse Carrying an Estrogen-Inducible Enhanced Green Fluorescent Protein Gene Facilitates Detection of Estrogen Actions in Vivo

Departments of Molecular Genetics (K.T.), Animal Laboratory for Investigation (Y.O.), Gastroenterology and Hepatology (T.S.), and Anatomy and Cell Biology (T.O.), Kochi Medical School, Nankoku, Kochi 783-8505, Japan; Division of Cell Differentiation, National Institute for Basic Biology (M.Z., K.M.), Okazaki, Aichi 444-0085, Japan; and Core Research for Evolutional Science and Technology, Japan Science and Technology Corp. (M.Z., K.M.), Kawaguchi 332-0012, Japan

Address all correspondence and requests for reprints to: Dr. Katsumi Toda, Department of Molecular Genetics, Kochi Medical School, Nankoku, Kochi 783-8505, Japan. E-mail: todak{at}kochi-ms.ac.jp.

Aromatase is an enzyme that converts androgen to estrogen in the gonads and also at extragonadal sites, including the brain. In this study we developed a transgenic mouse that carries an enhanced green fluorescent protein (EGFP) gene inducible by estrogen through an estrogen response element to facilitate detection of estrogen actions in vivo. The expression of EGFP in aromatase-deficient (Ar^-/-) female mice was significantly suppressed at the pituitary gland, ovary, uterus, and gonadal fat pad and was induced by dietary 17ß-estradiol to wild-type (Ar^+/+) levels or higher. These results demonstrate that the expression of the EGFP gene is tissue selective and estrogen dependent in vivo. Employing this transgenic mouse, we examined whether estrogen synthesis in the extragonadal sites is necessary for reproduction in female mice. When ovaries of Ar^-/- mice were replaced with Ar^+/+ ovaries, a significant induction of EGFP expression in the pituitary gland and uterus was observed. Histological examinations showed the presence of antral follicles in the replaced ovaries, indicating that the transplants are functional in Ar^-/- mice. After crossing with males, three of 10 Ar^-/-females with Ar^+/+ ovaries became pregnant and fed their pups. Collectively, these observations indicate that estrogen synthesis in the ovary is sufficient for supporting female reproduction, and that infertility of Ar^-/- females is primarily due to a defect in estrogen synthesis in the ovary.

This article has been cited by other articles:

				S. H. Windahl, M. K. Lagerquist, N. Andersson, C. Jochems, A. Kallkopf, C. Hakansson, J. Inzunza, J.-A. Gustafsson, P. T. van der Saag, H. Carlsten, et al. Identification of Target Cells for the Genomic Effects of Estrogens in Bone Endocrinology, December 1, 2007; 148(12): 5688 - 5695. [Abstract] [Full Text] [PDF]