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Tcf7l1 protects the anterior neural fold from adopting the neural crest fate
Author(s) -
J. Mašek,
Ondřej Machoň,
Vladimír Kořínek,
Makoto M. Taketo,
Zbyněk Kozmík
Publication year - 2016
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.15
H-Index - 36
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.132357
Subject(s) - biology , wnt signaling pathway , neural tube , neural plate , neuroepithelial cell , neuroectoderm , neural fold , neural crest , forebrain , microbiology and biotechnology , neural cell , neurulation , beta catenin , neural stem cell , neural development , mesoderm , genetics , embryonic stem cell , neuroscience , signal transduction , cell , central nervous system , gene , embryo , stem cell , gastrulation
The neural crest (NC) is crucial for the evolutionary diversification of vertebrates. NC cells are induced at the neural plate border by the coordinated action of several signaling pathways, including Wnt/β-catenin. NC cells are normally generated in the posterior neural plate border, whereas the anterior neural fold is devoid of NC cells. Using the mouse model, we show here that active repression of Wnt/β-catenin signaling is required for maintenance of neuroepithelial identity in the anterior neural fold and for inhibition of NC induction. Conditional inactivation of Tcf7l1, a transcriptional repressor of Wnt target genes, leads to aberrant activation of Wnt/β-catenin signaling in the anterior neuroectoderm and its conversion into NC. This reduces the developing prosencephalon without affecting the anterior-posterior neural character. Thus, Tcf7l1 defines the border between the NC and the prospective forebrain via restriction of the Wnt/β-catenin signaling gradient.

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