Literaturdatenbank
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Barske, L. A., & Capel, B. (2010). Estrogen represses sox9 during sex determination in the red-eared slider turtle trachemys scripta. Developmental Biology, 341(1), 305–314.
Added by: Admin (25 Aug 2010 21:58:41 UTC) |
| Resource type: Journal Article DOI: 10.1016/j.ydbio.2010.02.010 BibTeX citation key: Barske2010 View all bibliographic details  |
Categories: General Keywords: Emydidae, Schildkröten = turtles + tortoises, Trachemys, Trachemys scripta, Zeitigung = incubation Creators: Barske, Capel Collection: Developmental Biology |
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| Abstract |
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Production of male offspring in viviparous eutherian mammals requires a sex-determining mechanism resistant to maternal hormones. This constraint is relaxed in egg-laying species, which are sensitive to hormones during sex determination and often use an increase in aromatase, the estrogen-synthesizing enzyme, as a key feminizing signal. In the turtle Trachemys scripta, sex is normally determined by temperature, but estrogen treatment overrides this cue and leads exclusively to female development. We assessed whether the expression of SOX9, a central male sex-determining gene in mammals, or three other conserved transcription factors (WT1, GATA4, and LHX9) was regulated by estrogen signaling in the turtle. As in mice, all somatic cell types in the immature turtle gonad initially expressed WT1 and GATA4, whereas SOX9 was restricted to the Sertoli precursors and LHX9 to the coelomic epithelium and interstitium. After the bipotential period, SOX9 was abruptly down-regulated at the female temperature. Strikingly, embryos treated with β-estradiol at the male temperature lost SOX9 expression more than two stages earlier than controls, though WT1, GATA4, and LHX9 were unaffected. Conversely, inhibition of estrogen synthesis and signaling prevented or delayed SOX9 down-regulation at the female temperature. These results suggest that endogenous estrogen feminizes the medulla of the bipotential turtle gonad by inhibiting SOX9 expression. This mechanism may be involved in the male-to-female sex reversal in wild populations exposed to environmental estrogens, and is consistent with results showing that the estrogen receptor represses Sox9 to block transdifferentiation of granulosa cells into Sertoli-like cells in the adult mouse ovary.
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