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Genetic insights into the mechanisms of Fgf signaling
The fibroblast growth factor (Fgf) family of ligands and receptor tyrosine kinases is required throughout embryonic and postnatal development and also regulates multiple homeostatic functions in the adult. Aberrant Fgf signaling causes many congenital disorders and underlies multiple forms of cancer...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4826393/ https://www.ncbi.nlm.nih.gov/pubmed/27036966 http://dx.doi.org/10.1101/gad.277137.115 |
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author | Brewer, J. Richard Mazot, Pierre Soriano, Philippe |
author_facet | Brewer, J. Richard Mazot, Pierre Soriano, Philippe |
author_sort | Brewer, J. Richard |
collection | PubMed |
description | The fibroblast growth factor (Fgf) family of ligands and receptor tyrosine kinases is required throughout embryonic and postnatal development and also regulates multiple homeostatic functions in the adult. Aberrant Fgf signaling causes many congenital disorders and underlies multiple forms of cancer. Understanding the mechanisms that govern Fgf signaling is therefore important to appreciate many aspects of Fgf biology and disease. Here we review the mechanisms of Fgf signaling by focusing on genetic strategies that enable in vivo analysis. These studies support an important role for Erk1/2 as a mediator of Fgf signaling in many biological processes but have also provided strong evidence for additional signaling pathways in transmitting Fgf signaling in vivo. |
format | Online Article Text |
id | pubmed-4826393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48263932016-10-01 Genetic insights into the mechanisms of Fgf signaling Brewer, J. Richard Mazot, Pierre Soriano, Philippe Genes Dev Review The fibroblast growth factor (Fgf) family of ligands and receptor tyrosine kinases is required throughout embryonic and postnatal development and also regulates multiple homeostatic functions in the adult. Aberrant Fgf signaling causes many congenital disorders and underlies multiple forms of cancer. Understanding the mechanisms that govern Fgf signaling is therefore important to appreciate many aspects of Fgf biology and disease. Here we review the mechanisms of Fgf signaling by focusing on genetic strategies that enable in vivo analysis. These studies support an important role for Erk1/2 as a mediator of Fgf signaling in many biological processes but have also provided strong evidence for additional signaling pathways in transmitting Fgf signaling in vivo. Cold Spring Harbor Laboratory Press 2016-04-01 /pmc/articles/PMC4826393/ /pubmed/27036966 http://dx.doi.org/10.1101/gad.277137.115 Text en © 2016 Brewer et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Review Brewer, J. Richard Mazot, Pierre Soriano, Philippe Genetic insights into the mechanisms of Fgf signaling |
title | Genetic insights into the mechanisms of Fgf signaling |
title_full | Genetic insights into the mechanisms of Fgf signaling |
title_fullStr | Genetic insights into the mechanisms of Fgf signaling |
title_full_unstemmed | Genetic insights into the mechanisms of Fgf signaling |
title_short | Genetic insights into the mechanisms of Fgf signaling |
title_sort | genetic insights into the mechanisms of fgf signaling |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4826393/ https://www.ncbi.nlm.nih.gov/pubmed/27036966 http://dx.doi.org/10.1101/gad.277137.115 |
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