Differential distribution of splice variants of estrogen receptor beta in human testicular cells suggests specific functions in spermatogenesis

• Published in: The Journal of steroid biochemistry and molecular biology Vol. 92; no. 1; pp. 97 - 106
• Main Authors: Aschim, E.L., Sæther, T., Wiger, R., Grotmol, T., Haugen, T.B.
• Format: Journal Article
• Language: English
• Published: Oxford Elsevier Ltd 01.09.2004; Elsevier Science
• Subjects: Adolescent; Adult; Alternative Splicing - genetics; Biological and medical sciences; Cells, Cultured; Estrogen receptor beta; Estrogen Receptor beta - genetics; Estrogens - pharmacology; Fundamental and applied biological sciences. Psychology; Gene Expression; Human testis; Humans; Male; Middle Aged; RNA, Messenger - analysis; RNA, Messenger - genetics; RNA, Messenger - metabolism; Sequence Deletion - genetics; Spermatogenesis; Spermatogenesis - physiology; Splice variant; Testis - cytology; Testis - metabolism; Transsexual; Transsexualism; Vertebrates: endocrinology; Human testis; Splice variant; Spermatogenesis; Estrogen receptor beta; Transsexual; Human; Variant; Estrogen receptor; Cell function; Distribution; Testicle; Male genital system
• ISSN: 0960-0760; 1879-1220
• DOI: 10.1016/j.jsbmb.2004.05.008

A growing number of estrogen receptor beta (ERβ) splice variants are reported. Several of these have been discovered in testis, but with few exceptions little is known about their cellular localization. The aim of this study was to identify and elucidate the mRNA expression pattern of the different ERβ splice variants in human testicular cells. Northern analysis was performed on whole testis and fractions enriched in germ cells from untreated men and from estrogen-treated men undergoing sex change surgery. Probes were constructed in order to systematically screen for and identify various ERβ splice variants. Several ERβ bands were observed in the human testis, in which splice variants constituted the major part of total ERβ transcripts. Interestingly, only two ERβ wild-type transcripts were detected. These seem to be virtually absent from the haploid germ cells and are probably mainly located in somatic cells and/or primary spermatocytes. Several novel ERβ deletion variants were found in high levels in the haploid germ cell fractions and were nearly absent in testicular cells from the estrogen-treated men. The cell-dependent distribution raises the question whether splice variants may have specific functions in spermatogenesis, and whether the differential splicing of ERβ is regulated in a cell-specific manner.