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Abstract / Description of output
The ciliary margin (CM) develops in the peripheral retina and gives rise to the iris and the ciliary body. The Wnt/β-catenin signalling pathway has been implicated in ciliary margin development. Here, we tested the hypothesis that in the developing mouse retina Foxg1 is responsible for suppressing the Wnt/β-catenin pathway and restricting CM development. We showed that there is excess CM tissue in Foxg1(-/-) null embryos and this expansion is more pronounced in the nasal retina where Foxg1 normally shows its highest expression levels. Results on expression of a reporter allele for Wnt/β-catenin signalling and of Lef1, a target of Wnt/β-catenin signalling, displayed significant upregulation of this pathway in Foxg1(-/-) nulls at embryonic days 12.5 and 14.5. Interestingly, this upregulation was observed specifically in the nasal retina, where normally very few Wnt-responsive cells are observed. These results indicate a suppressive role of Foxg1 on this signalling pathway. Our results reveal a new role of Foxg1 in limiting CM development in the nasal peripheral retina and add a new molecular player in the developmental network involved in CM specification.
Original language | English |
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Pages (from-to) | 299-313 |
Number of pages | 15 |
Journal | Developmental Biology |
Volume | 380 |
Issue number | 2 |
DOIs | |
Publication status | Published - 15 Aug 2013 |
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Dive into the research topics of 'Foxg1 is required to limit the formation of ciliary margin tissue and Wnt/β-catenin signalling in the developing nasal retina of the mouse'. Together they form a unique fingerprint.Projects
- 1 Finished
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Deciphering molecular pathways and cellular events involved in uveal coloboma
Fotaki, V., Pratt, T. & Price, D.
1/06/12 → 30/09/16
Project: Research