Activation of β-catenin signaling by Rspo1 controls differentiation of the mammalian ovary
- Others:
- Génétique du développement normal et pathologique ; Université Nice Sophia Antipolis (1965 - 2019) (UNS) ; COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Institut National de la Santé et de la Recherche Médicale (INSERM)
- Utrecht University [Utrecht]
- Kyoto University [Kyoto]
- Università degli Studi di Pavia = University of Pavia (UNIPV)
- Institut de Biologie Valrose (IBV) ; Université Nice Sophia Antipolis (1965 - 2019) (UNS) ; COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Côte d'Azur (UCA)
Description
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 b-catenin signaling pathway. b-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 b-catenin activation determines the fate of the gonad, with Rspo1 acting as a crucial regulator of canonical b-catenin signaling required for female development.
Abstract
International audience
Additional details
- URL
- https://hal.archives-ouvertes.fr/hal-03746250
- URN
- urn:oai:HAL:hal-03746250v1
- Origin repository
- UNICA