Activation of β-catenin signaling by Rspo1 controls differentiation of the mammalian ovary

被引:343
作者
Chassot, Anne-Amandine [1 ,2 ]
Ranc, Fariba [1 ,2 ]
Gregoire, Elodie P. [1 ,2 ]
Roepers-Gajadien, Hermien L. [3 ,4 ]
Taketo, Makoto M. [5 ]
Camerino, Giovanna [6 ]
de Rooij, Dirk G. [3 ]
Schedl, Andreas [1 ,2 ]
Chaboissier, Marie-Christine [1 ,2 ]
机构
[1] INSERM, U636, F-06108 Nice, France
[2] Univ Nice, Lab Genet Dev Normal & Pathol, F-06108 Nice, France
[3] Univ Utrecht, Dept Endocrinol, NL-3584 CH Utrecht, Netherlands
[4] Acad Med Ctr, Ctr Reprod Med, NL-1105 AZ Amsterdam, Netherlands
[5] Kyoto Univ, Dept Pharmacol, Grad Sch Med, Kyoto 6068501, Japan
[6] Univ Pavia, Dipartimento Patol Umana & Ereditaria, Sez Biol Gen & Genet Med, I-27100 Pavia, Italy
关键词
D O I
10.1093/hmg/ddn016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The sex of an individual is determined by the fate of the gonad. While the expression of Sry and Sox9 is sufficient to induce male development, we here show that female differentiation requires activation of the canonical beta-catenin signaling pathway. beta-catenin activation is controlled by Rspo1 in XX gonads and Rspo1 knockout mice show masculinized gonads. Molecular analyses demonstrate an absence of female-specific activation of Wnt4 and as a consequence XY-like vascularization and steroidogenesis. Moreover, germ cells of XX knockout embryos show changes in cellular adhesions and a failure to enter XX specific meiosis. Sex cords develop around birth, when Sox9 becomes strongly activated. Thus, a balance between Sox9 and beta-catenin activation determines the fate of the gonad, with Rspo1 acting as a crucial regulator of canonical beta-catenin signaling required for female development.
引用
收藏
页码:1264 / 1277
页数:14
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