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Contributions of Noncanonical Smoothened Signaling During Embryonic Development

The Sonic Hedgehog (Shh) signaling pathway is active during embryonic development in metazoans, and provides instructional cues necessary for proper tissue patterning. The pathway signal transducing component, Smoothened (Smo), is a G protein-coupled receptor (GPCR) that has been demonstrated to sig...

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Detalles Bibliográficos
Autores principales: Pandit, Tanushree, Ogden, Stacey K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5794034/
https://www.ncbi.nlm.nih.gov/pubmed/29399514
http://dx.doi.org/10.3390/jdb5040011
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author Pandit, Tanushree
Ogden, Stacey K.
author_facet Pandit, Tanushree
Ogden, Stacey K.
author_sort Pandit, Tanushree
collection PubMed
description The Sonic Hedgehog (Shh) signaling pathway is active during embryonic development in metazoans, and provides instructional cues necessary for proper tissue patterning. The pathway signal transducing component, Smoothened (Smo), is a G protein-coupled receptor (GPCR) that has been demonstrated to signal through at least two effector routes. The first is a G protein–independent canonical route that signals to Gli transcriptional effectors to establish transcriptional programs specifying cell fate during early embryonic development. The second, commonly referred to as the noncanonical Smo signal, induces rapid, transcription-independent responses that are essential for establishing and maintaining distinct cell behaviors during development. Herein, we discuss contributions of this noncanonical route during embryonic development. We also highlight important open questions regarding noncanonical Smo signal route selection during development, and consider implications of noncanonical signal corruption in disease.
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spelling pubmed-57940342018-02-01 Contributions of Noncanonical Smoothened Signaling During Embryonic Development Pandit, Tanushree Ogden, Stacey K. J Dev Biol Review The Sonic Hedgehog (Shh) signaling pathway is active during embryonic development in metazoans, and provides instructional cues necessary for proper tissue patterning. The pathway signal transducing component, Smoothened (Smo), is a G protein-coupled receptor (GPCR) that has been demonstrated to signal through at least two effector routes. The first is a G protein–independent canonical route that signals to Gli transcriptional effectors to establish transcriptional programs specifying cell fate during early embryonic development. The second, commonly referred to as the noncanonical Smo signal, induces rapid, transcription-independent responses that are essential for establishing and maintaining distinct cell behaviors during development. Herein, we discuss contributions of this noncanonical route during embryonic development. We also highlight important open questions regarding noncanonical Smo signal route selection during development, and consider implications of noncanonical signal corruption in disease. MDPI 2017-10-17 /pmc/articles/PMC5794034/ /pubmed/29399514 http://dx.doi.org/10.3390/jdb5040011 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Pandit, Tanushree
Ogden, Stacey K.
Contributions of Noncanonical Smoothened Signaling During Embryonic Development
title Contributions of Noncanonical Smoothened Signaling During Embryonic Development
title_full Contributions of Noncanonical Smoothened Signaling During Embryonic Development
title_fullStr Contributions of Noncanonical Smoothened Signaling During Embryonic Development
title_full_unstemmed Contributions of Noncanonical Smoothened Signaling During Embryonic Development
title_short Contributions of Noncanonical Smoothened Signaling During Embryonic Development
title_sort contributions of noncanonical smoothened signaling during embryonic development
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5794034/
https://www.ncbi.nlm.nih.gov/pubmed/29399514
http://dx.doi.org/10.3390/jdb5040011
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