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Segregation of brain and organizer precursors is differentially regulated by Nodal signaling at blastula stage
Author(s) -
Aitana M. Castro Colabianchi,
María B. Tavella,
Laura E. Boyadjián López,
Marcelo Rubinstein,
Lucía F. Franchini,
Silvia L. López
Publication year - 2021
Publication title -
biology open
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.936
H-Index - 41
ISSN - 2046-6390
DOI - 10.1242/bio.051797
Subject(s) - blastula , chordin , biology , nodal , gastrulation , nodal signaling , polarity in embryogenesis , sox2 , population , noggin , microbiology and biotechnology , neuroscience , embryonic stem cell , anatomy , embryo , genetics , embryogenesis , gene , demography , sociology , bone morphogenetic protein
The blastula Chordin- and Noggin-expressing (BCNE) center comprises animal-dorsal and marginal-dorsal cells of the amphibian blastula and contains the precursors of the brain and the gastrula organizer. Previous findings suggested that the BCNE behaves as a homogeneous cell population that only depends on nuclear β-catenin activity but does not require Nodal and later segregates into its descendants during gastrulation. In contrast to previous findings, in this work, we show that the BCNE does not behave as a homogeneous cell population in response to Nodal antagonists. In fact, we found that chordin.1 expression in a marginal subpopulation of notochordal precursors indeed requires Nodal input. We also establish that an animal BCNE subpopulation of cells that express both, chordin.1 and sox2 (a marker of pluripotent neuroectodermal cells), and gives rise to most of the brain, persisted at blastula stage after blocking Nodal. Therefore, Nodal signaling is required to define a population of chordin.1+ cells and to restrict the recruitment of brain precursors within the BCNE as early as at blastula stage. We discuss our findings in Xenopus in comparison to other vertebrate models, uncovering similitudes in early brain induction and delimitation through Nodal signaling.

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