Prince Henry's Institute of Medical Research, Monash Medical Centre, P.O. Box 5152, Clayton, Melbourne 3168, Australia.
Endocrinology. 2012 Feb;153(2):901-12. doi: 10.1210/en.2011-1347. Epub 2011 Nov 29.
Genome analysis of patients with disorders of sex development, and gain- and loss-of-function studies in mice indicate that gonadal development is regulated by opposing signals. In females, the Wnt/β-catenin canonical pathway blocks testicular differentiation by repressing the expression of the Sertoli cell-specific gene Sox9 by an unknown mechanism. Using cell and embryonic gonad culture models, we show that activation of the Wnt/β-catenin pathway inhibits the expression of Sox9 and Amh, whereas mRNA and protein levels of Sry and steroidogenic factor 1 (Sf1), two key transcriptional regulators of Sox9, are not altered. Ectopic activation of Wnt/β-catenin signaling in male gonads led to a loss of Sf1 binding to the Tesco enhancer and absent Sox9 expression that we also observed in wild-type ovaries. Moreover, ectopic Wnt/β-catenin signaling induced the expression of the female somatic cell markers, Bmp2 and Rspo1, as a likely consequence of Sox9 loss. Wnt/β-catenin signaling in XY gonads did not, however, affect gene expression of the steroidogenic Leydig cell Sf1 target gene, Cyp11a1, or Sf1 binding to the Cyp11a1 promoter. Our data support a model in ovary development whereby activation of β-catenin prevents Sf1 binding to the Sox9 enhancer, thereby inhibiting Sox9 expression and Sertoli cell differentiation.
对患有性别发育障碍的患者进行基因组分析,并在小鼠中进行增益和缺失功能研究表明,性腺发育受相反信号的调节。在女性中,Wnt/β-catenin 经典途径通过未知机制抑制 Sertoli 细胞特异性基因 Sox9 的表达来阻止睾丸分化。使用细胞和胚胎性腺培养模型,我们表明 Wnt/β-catenin 途径的激活抑制 Sox9 和 Amh 的表达,而 Sox9 和类固醇生成因子 1 (Sf1) 的两个关键转录调节因子的 mRNA 和蛋白水平没有改变。雄性性腺中 Wnt/β-catenin 信号的异位激活导致 Tesco 增强子结合的 Sf1 丧失和 Sox9 表达缺失,我们也在野生型卵巢中观察到这种缺失。此外,异位 Wnt/β-catenin 信号诱导女性体细胞标志物 Bmp2 和 Rspo1 的表达,这可能是 Sox9 缺失的结果。然而,XY 性腺中的 Wnt/β-catenin 信号并未影响类固醇生成细胞 Leydig 细胞 Sf1 靶基因 Cyp11a1 的基因表达,也未影响 Sf1 与 Cyp11a1 启动子的结合。我们的数据支持卵巢发育的模型,即β-catenin 的激活阻止 Sf1 结合 Sox9 增强子,从而抑制 Sox9 的表达和 Sertoli 细胞分化。