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Molecular cloning and characterization of a nuclear androgen receptor activated by 11-ketotestosterone
Umeå University, Faculty of Medicine, Department of Molecular Biology (Faculty of Medicine).
Umeå University, Faculty of Medicine, Department of Molecular Biology (Faculty of Medicine).
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2005 (English)In: Reproductive Biology and Endocrinology, ISSN 1477-7827, E-ISSN 1477-7827, Vol. 3, 37Article in journal (Refereed) PublishedText
Abstract [en]

Although 11-ketotestosterone is a potent androgen and induces male secondary sex characteristics in many teleosts, androgen receptors with high binding affinity for 11-ketotestosterone or preferential activation by 11-ketotestosterone have not been identified. So, the mechanism by which 11-ketotestosterone exhibits such high potency remains unclear. Recently we cloned the cDNA of an 11-ketotestosterone regulated protein, spiggin, from three-spined stickleback renal tissue. As spiggin is the only identified gene product regulated by 11-ketotestosterone, the stickleback kidney is ideal for determination of the mechanism of 11-ketotestosterone gene regulation. A single androgen receptor gene with two splicing variants, belonging to the androgen receptor-beta subfamily was cloned from stickleback kidney. A high affinity, saturable, single class of androgen specific binding sites, with the characteristics of an androgen receptor, was identified in renal cytosolic and nuclear fractions. Measurement of ligand binding moieties in the cytosolic and nuclear fractions as well as to the recombinant receptor revealed lower affinity for 11-ketotestosterone than for dihydrotestosterone. Treatment with different androgens did not upregulate androgen receptor mRNA level or increase receptor abundance, suggesting that autoregulation is not involved in differential ligand activation. However, comparison of the transactivation potential of the stickleback androgen receptor with the human androgen receptor, in both human HepG2 cells and zebrafish ZFL cells, revealed preferential activation by 11-ketotestosterone of the stickleback receptor, but not of the human receptor. These findings demonstrate the presence of a receptor preferentially activated by 11-ketotestosterone in the three-spined stickleback, so far the only one known in any animal.

Place, publisher, year, edition, pages
London: BioMed Central, 2005. Vol. 3, 37
Keyword [en]
male 3-spined stickleback, steroid-binding protein, croaker micropogonias undulatus, gasterosteus-aculeatus, atlantic croaker, rainbow trout, messenger RNA, response elements, up-regulation, cDNA cloning
National Category
Endocrinology and Diabetes Obstetrics, Gynecology and Reproductive Medicine
Identifiers
URN: urn:nbn:se:umu:diva-120406DOI: 10.1186/1477-7827-3-37ISI: 000231508500001PubMedID: 16107211OAI: oai:DiVA.org:umu-120406DiVA: diva2:935313
Available from: 2016-06-10 Created: 2016-05-16 Last updated: 2016-06-10Bibliographically approved

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von Hofsten, JonasGrahn, Birgitta
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Department of Molecular Biology (Faculty of Medicine)
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Reproductive Biology and Endocrinology
Endocrinology and DiabetesObstetrics, Gynecology and Reproductive Medicine

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