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Published on: February 16, 2017
Identification of the genes regulated by Wnt-4, a critical signal for commitment of the ovary
Florence Naillat1, Wenying Yan2, Riikka Karjalainen3
1Academy of Finland, Centre of Excellence of Cell-Extracellular Matrix Research, Biocenter Oulu & Infotech Oulu, Faculty of Biochemistry and Molecular Medicine, University of Oulu, Finland.
Abstract:
The indifferent mammalian embryonic gonad generates an ovary or testis, but the factors involved are still poorly known. The Wnt-4 signal represents one critical female determinant, since its absence leads to partial female-to-male sex reversal in mouse, but its signalling is as well implicated in the testis development. We used the Wnt-4 deficient mouse as a model to identify candidate gonadogenesis genes, and found that the Notum, Phlda2, Runx-1 and Msx1 genes are typical of the wild-type ovary and the Osr2, Dach2, Pitx2 and Tacr3 genes of the testis. Strikingly, the expression of these latter genes becomes reversed in the Wnt-4 knock-out ovary, suggesting a role in ovarian development. We identified the transcription factor Runx-1 as a Wnt-4 signalling target gene, since it is expressed in the ovary and is reduced upon Wnt-4 knock-out. Consistent with this, introduction of the Wnt-4 signal into early ovary cells ex vivo induces Runx-1 expression, while conversely Wnt-4 expression is down-regulated in the absence of Runx-1. We conclude that the Runx-1 gene can be a Wnt-4 signalling target, and that Runx-1 and Wnt-4 are mutually interdependent in their expression. The changes in gene expression due to the absence of Wnt-4 in gonads reflect the sexually dimorphic role of this signal and its complex gene network in mammalian gonad development.
Insights
Wnt-4 signaling is crucial for mammalian gonad development. Its absence in mice alters gene expression, revealing a complex network essential for ovary and testis formation, with Runx-1 identified as a key target gene.
Area of Science:
- Developmental Biology
- Genetics
- Reproductive Biology
Background:
- Mammalian embryonic gonads differentiate into ovaries or testes through poorly understood mechanisms.
- Wnt-4 signaling is a known female determinant, but also plays a role in testis development.
Purpose of the Study:
- To identify candidate gonadogenesis genes using Wnt-4 deficient mice.
- To elucidate the role of Wnt-4 signaling in the gene regulatory network of mammalian gonad development.
Main Methods:
- Utilized Wnt-4 deficient mice as a model system.
- Analyzed gene expression patterns in wild-type and Wnt-4 knock-out gonads.
- Investigated the regulatory relationship between Wnt-4 and Runx-1 using ex vivo cell culture.
Main Results:
- Identified distinct gene expression profiles for wild-type ovaries (Notum, Phlda2, Runx-1, Msx1) and testes (Osr2, Dach2, Pitx2, Tacr3).
- Observed reversed expression of testis-associated genes in Wnt-4 knock-out ovaries.
- Established Runx-1 as a Wnt-4 signaling target gene, with interdependent expression between Wnt-4 and Runx-1.
Conclusions:
- Wnt-4 signaling is essential for establishing normal ovarian gene expression patterns.
- Runx-1 is a direct target of Wnt-4 signaling and is mutually regulated with Wnt-4.
- These findings highlight the sexually dimorphic role of Wnt-4 and its complex gene network in mammalian gonadogenesis.
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