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A Systematic Survey of Expression and Function of Zebrafish frizzled Genes

Wnt signaling is crucial for the regulation of numerous processes in development. Consistent with this, the gene families for both the ligands (Wnts) and receptors (Frizzleds) are very large. Surprisingly, while we have a reasonable understanding of the Wnt ligands likely to mediate specific Wnt-dep...

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Autores principales: Nikaido, Masataka, Law, Edward W. P., Kelsh, Robert N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551900/
https://www.ncbi.nlm.nih.gov/pubmed/23349976
http://dx.doi.org/10.1371/journal.pone.0054833
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author Nikaido, Masataka
Law, Edward W. P.
Kelsh, Robert N.
author_facet Nikaido, Masataka
Law, Edward W. P.
Kelsh, Robert N.
author_sort Nikaido, Masataka
collection PubMed
description Wnt signaling is crucial for the regulation of numerous processes in development. Consistent with this, the gene families for both the ligands (Wnts) and receptors (Frizzleds) are very large. Surprisingly, while we have a reasonable understanding of the Wnt ligands likely to mediate specific Wnt-dependent processes, the corresponding receptors usually remain to be elucidated. Taking advantage of the zebrafish model's excellent genomic and genetic properties, we undertook a comprehensive analysis of the expression patterns of frizzled (fzd) genes in zebrafish. To explore their functions, we focused on testing their requirement in several developmental events known to be regulated by Wnt signaling, convergent extension movements of gastrulation, neural crest induction, and melanocyte specification. We found fourteen distinct fzd genes in the zebrafish genome. Systematic analysis of their expression patterns between 1-somite and 30 hours post-fertilization revealed complex, dynamic and overlapping expression patterns. This analysis demonstrated that only fzd3a, fzd9b, and fzd10 are expressed in the dorsal neural tube at stages corresponding to the timing of melanocyte specification. Surprisingly, however, morpholino knockdown of these, alone or in combination, gave no indication of reduction of melanocytes, suggesting the important involvement of untested fzds or another type of Wnt receptor in this process. Likewise, we found only fzd7b and fzd10 expressed at the border of the neural plate at stages appropriate for neural crest induction. However, neural crest markers were not reduced by knockdown of these receptors. Instead, these morpholino knockdown studies showed that fzd7a and fzd7b work co-operatively to regulate convergent extension movement during gastrulation. Furthermore, we show that the two fzd7 genes function together with fzd10 to regulate epiboly movements and mesoderm differentiation.
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spelling pubmed-35519002013-01-24 A Systematic Survey of Expression and Function of Zebrafish frizzled Genes Nikaido, Masataka Law, Edward W. P. Kelsh, Robert N. PLoS One Research Article Wnt signaling is crucial for the regulation of numerous processes in development. Consistent with this, the gene families for both the ligands (Wnts) and receptors (Frizzleds) are very large. Surprisingly, while we have a reasonable understanding of the Wnt ligands likely to mediate specific Wnt-dependent processes, the corresponding receptors usually remain to be elucidated. Taking advantage of the zebrafish model's excellent genomic and genetic properties, we undertook a comprehensive analysis of the expression patterns of frizzled (fzd) genes in zebrafish. To explore their functions, we focused on testing their requirement in several developmental events known to be regulated by Wnt signaling, convergent extension movements of gastrulation, neural crest induction, and melanocyte specification. We found fourteen distinct fzd genes in the zebrafish genome. Systematic analysis of their expression patterns between 1-somite and 30 hours post-fertilization revealed complex, dynamic and overlapping expression patterns. This analysis demonstrated that only fzd3a, fzd9b, and fzd10 are expressed in the dorsal neural tube at stages corresponding to the timing of melanocyte specification. Surprisingly, however, morpholino knockdown of these, alone or in combination, gave no indication of reduction of melanocytes, suggesting the important involvement of untested fzds or another type of Wnt receptor in this process. Likewise, we found only fzd7b and fzd10 expressed at the border of the neural plate at stages appropriate for neural crest induction. However, neural crest markers were not reduced by knockdown of these receptors. Instead, these morpholino knockdown studies showed that fzd7a and fzd7b work co-operatively to regulate convergent extension movement during gastrulation. Furthermore, we show that the two fzd7 genes function together with fzd10 to regulate epiboly movements and mesoderm differentiation. Public Library of Science 2013-01-22 /pmc/articles/PMC3551900/ /pubmed/23349976 http://dx.doi.org/10.1371/journal.pone.0054833 Text en © 2013 Nikaido et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Nikaido, Masataka
Law, Edward W. P.
Kelsh, Robert N.
A Systematic Survey of Expression and Function of Zebrafish frizzled Genes
title A Systematic Survey of Expression and Function of Zebrafish frizzled Genes
title_full A Systematic Survey of Expression and Function of Zebrafish frizzled Genes
title_fullStr A Systematic Survey of Expression and Function of Zebrafish frizzled Genes
title_full_unstemmed A Systematic Survey of Expression and Function of Zebrafish frizzled Genes
title_short A Systematic Survey of Expression and Function of Zebrafish frizzled Genes
title_sort systematic survey of expression and function of zebrafish frizzled genes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551900/
https://www.ncbi.nlm.nih.gov/pubmed/23349976
http://dx.doi.org/10.1371/journal.pone.0054833
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