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The response of early neural genes to FGF signaling or inhibition of BMP indicate the absence of a conserved neural induction module

BACKGROUND: The molecular mechanism that initiates the formation of the vertebrate central nervous system has long been debated. Studies in Xenopus and mouse demonstrate that inhibition of BMP signaling is sufficient to induce neural tissue in explants or ES cells respectively, whereas studies in ch...

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Autores principales: Rogers, Crystal D, Ferzli, George S, Casey, Elena S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3271986/
https://www.ncbi.nlm.nih.gov/pubmed/22172147
http://dx.doi.org/10.1186/1471-213X-11-74
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author Rogers, Crystal D
Ferzli, George S
Casey, Elena S
author_facet Rogers, Crystal D
Ferzli, George S
Casey, Elena S
author_sort Rogers, Crystal D
collection PubMed
description BACKGROUND: The molecular mechanism that initiates the formation of the vertebrate central nervous system has long been debated. Studies in Xenopus and mouse demonstrate that inhibition of BMP signaling is sufficient to induce neural tissue in explants or ES cells respectively, whereas studies in chick argue that instructive FGF signaling is also required for the expression of neural genes. Although additional signals may be involved in neural induction and patterning, here we focus on the roles of BMP inhibition and FGF8a. RESULTS: To address the question of necessity and sufficiency of BMP inhibition and FGF signaling, we compared the temporal expression of the five earliest genes expressed in the neuroectoderm and determined their requirements for induction at the onset of neural plate formation in Xenopus. Our results demonstrate that the onset and peak of expression of the genes vary and that they have different regulatory requirements and are therefore unlikely to share a conserved neural induction regulatory module. Even though all require inhibition of BMP for expression, some also require FGF signaling; expression of the early-onset pan-neural genes sox2 and foxd5α requires FGF signaling while other early genes, sox3, geminin and zicr1 are induced by BMP inhibition alone. CONCLUSIONS: We demonstrate that BMP inhibition and FGF signaling induce neural genes independently of each other. Together our data indicate that although the spatiotemporal expression patterns of early neural genes are similar, the mechanisms involved in their expression are distinct and there are different signaling requirements for the expression of each gene.
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spelling pubmed-32719862012-02-04 The response of early neural genes to FGF signaling or inhibition of BMP indicate the absence of a conserved neural induction module Rogers, Crystal D Ferzli, George S Casey, Elena S BMC Dev Biol Research Article BACKGROUND: The molecular mechanism that initiates the formation of the vertebrate central nervous system has long been debated. Studies in Xenopus and mouse demonstrate that inhibition of BMP signaling is sufficient to induce neural tissue in explants or ES cells respectively, whereas studies in chick argue that instructive FGF signaling is also required for the expression of neural genes. Although additional signals may be involved in neural induction and patterning, here we focus on the roles of BMP inhibition and FGF8a. RESULTS: To address the question of necessity and sufficiency of BMP inhibition and FGF signaling, we compared the temporal expression of the five earliest genes expressed in the neuroectoderm and determined their requirements for induction at the onset of neural plate formation in Xenopus. Our results demonstrate that the onset and peak of expression of the genes vary and that they have different regulatory requirements and are therefore unlikely to share a conserved neural induction regulatory module. Even though all require inhibition of BMP for expression, some also require FGF signaling; expression of the early-onset pan-neural genes sox2 and foxd5α requires FGF signaling while other early genes, sox3, geminin and zicr1 are induced by BMP inhibition alone. CONCLUSIONS: We demonstrate that BMP inhibition and FGF signaling induce neural genes independently of each other. Together our data indicate that although the spatiotemporal expression patterns of early neural genes are similar, the mechanisms involved in their expression are distinct and there are different signaling requirements for the expression of each gene. BioMed Central 2011-12-15 /pmc/articles/PMC3271986/ /pubmed/22172147 http://dx.doi.org/10.1186/1471-213X-11-74 Text en Copyright ©2011 Rogers et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Rogers, Crystal D
Ferzli, George S
Casey, Elena S
The response of early neural genes to FGF signaling or inhibition of BMP indicate the absence of a conserved neural induction module
title The response of early neural genes to FGF signaling or inhibition of BMP indicate the absence of a conserved neural induction module
title_full The response of early neural genes to FGF signaling or inhibition of BMP indicate the absence of a conserved neural induction module
title_fullStr The response of early neural genes to FGF signaling or inhibition of BMP indicate the absence of a conserved neural induction module
title_full_unstemmed The response of early neural genes to FGF signaling or inhibition of BMP indicate the absence of a conserved neural induction module
title_short The response of early neural genes to FGF signaling or inhibition of BMP indicate the absence of a conserved neural induction module
title_sort response of early neural genes to fgf signaling or inhibition of bmp indicate the absence of a conserved neural induction module
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3271986/
https://www.ncbi.nlm.nih.gov/pubmed/22172147
http://dx.doi.org/10.1186/1471-213X-11-74
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