Sexually dimorphic transcription of estrogen receptors in cod gonads throughout a reproductive cycle
Author's accepted version (post-print). This manuscript has been accepted for publication in Journal of Molecular Endocrinology, but the version presented here has not yet been copy-edited, formatted or proofed. Consequently, BioScientifica accepts no responsibility for any errors or omissions...
| Published in: | Journal of Molecular Endocrinology |
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| Main Authors: | , , , , |
| Format: | Article in Journal/Newspaper |
| Language: | English |
| Published: |
BioScientifica
2015
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| Subjects: | |
| Online Access: | http://hdl.handle.net/11250/279299 https://doi.org/10.1530/JME-13-0187 |
| Summary: | Author's accepted version (post-print). This manuscript has been accepted for publication in Journal of Molecular Endocrinology, but the version presented here has not yet been copy-edited, formatted or proofed. Consequently, BioScientifica accepts no responsibility for any errors or omissions it may contain. The definitive version is now freely available at http://dx.doi.org/10.1530/JME-13-0187, 2014. The role of sex steroid regulation in gonadal maturation is a very complex process that is far from being fully understood. Hence, we have investigated seasonal changes in gonadal expression of estrogen receptors (ERs) in Atlantic cod (Gadus morhua L.), a batch spawner, throughout annual reproductive cycle. Three nuclear ER partial cDNA sequences (esr1, esr2a and esr2b) were cloned and all esr transcripts were detected mainly in liver and gonads of either sex. In situ hybridization of esrs along with germ cell (vasa) and gonadal somatic cell markers (gsdf, 3β-hsd and amh for testicular, or gsdf for ovarian somatic cells) showed that in testis all three esrs were preferentially localized within interstitial fibroblasts composed of immature and mature Leydig cells, whereas in ovary they were differentially expressed in both follicular cells and oocytes. Quantitative real-time PCR analysis revealed a sexually dimorphic expression pattern of the three esr paralogues in testis and ovary. A significant increase in esr2a expression was identified in testis and esr2b in ovary, whereas esr1 transcripts were elevated in both testis and ovary at February and March prior to the spawning period. The localization and sexually dimorphic expression of esr genes in gonads suggest a direct function of estrogen via ERs in gonadal somatic cell growth and differentiation for Leydig cell in testis and follicular cells in ovary throughout the annual reproductive cycle in Atlantic cod. |
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