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Spatio-temporal dynamics of gene expression of the Edn1-Dlx5/6 pathway during development of the lower jaw

The morphogenesis of the vertebrate skull results from highly dynamic integrated processes involving the exchange of signals between the ectoderm, the endoderm, and cephalic neural crest cells (CNCCs). Before migration CNCCs are not committed to form any specific skull element, molecular signals exc...

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Published in:Genesis (New York, N.Y. : 2000) N.Y. : 2000), 2010-06, Vol.48 (6), p.262-373
Main Authors: Vieux-Rochas, Maxence, Mantero, Stefano, Heude, Eglantine, Barbieri, Ottavia, Astigiano, Simonetta, Couly, Gérard, Kurihara, Hiroki, Levi, Giovanni, Merlo, Giorgio R.
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cited_by cdi_FETCH-LOGICAL-c5295-f485b73f87ef685cd7dcc992e650536df3fef965fa4d17c590794822cf28db6e3
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container_title Genesis (New York, N.Y. : 2000)
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creator Vieux-Rochas, Maxence
Mantero, Stefano
Heude, Eglantine
Barbieri, Ottavia
Astigiano, Simonetta
Couly, Gérard
Kurihara, Hiroki
Levi, Giovanni
Merlo, Giorgio R.
description The morphogenesis of the vertebrate skull results from highly dynamic integrated processes involving the exchange of signals between the ectoderm, the endoderm, and cephalic neural crest cells (CNCCs). Before migration CNCCs are not committed to form any specific skull element, molecular signals exchanged in restricted regions of tissue interaction are crucial in providing positional identity to the CNCCs mesenchyme and activate the specific morphogenetic process of different skeletal components of the head. In particular, the endothelin‐1 (Edn1)‐dependent activation of Dlx5 and Dlx6 in CNCCs that colonize the first pharyngeal arch (PA1) is necessary and sufficient to specify maxillo‐mandibular identity. Here, to better analyze the spatio‐temporal dynamics of this process, we associate quantitative gene expression analysis with detailed examination of skeletal phenotypes resulting from combined allelic reduction of Edn1, Dlx5, and Dlx6. We show that Edn1‐dependent and ‐independent regulatory pathways act at different developmental times in distinct regions of PA1. The Edn1→Dlx5/6→Hand2 pathway is already active at E9.5 during early stages of CNCCs colonization. At later stages (E10.5) the scenario is more complex: we propose a model in which PA1 is subdivided into four adjacent territories in which distinct regulations are taking place. This new developmental model may provide a conceptual framework to interpret the craniofacial malformations present in several mouse mutants and in human first arch syndromes. More in general, our findings emphasize the importance of quantitative gene expression in the fine control of morphogenetic events. genesis 48:362–373, 2010. © 2010 Wiley‐Liss, Inc.
doi_str_mv 10.1002/dvg.20625
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At later stages (E10.5) the scenario is more complex: we propose a model in which PA1 is subdivided into four adjacent territories in which distinct regulations are taking place. This new developmental model may provide a conceptual framework to interpret the craniofacial malformations present in several mouse mutants and in human first arch syndromes. 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subjects allelic dosage
Animals
Basic Helix-Loop-Helix Transcription Factors - genetics
cranial neural crest cells
craniofacial development
Development Biology
Dlx
Embryo, Mammalian - cytology
Embryo, Mammalian - metabolism
Embryology and Organogenesis
endothelin-1
Endothelin-1 - genetics
first arch syndromes
Gene Expression Regulation, Developmental - physiology
Homeodomain Proteins - genetics
Humans
In Situ Hybridization
Jaw - embryology
Life Sciences
Mandible - metabolism
Mice
Mice, Knockout
Morphogenesis
Neurobiology
Neurons and Cognition
pharyngeal arches
Phenotype
Reproductive Biology
Reverse Transcriptase Polymerase Chain Reaction
RNA, Messenger - genetics
Sexual reproduction
Signal Transduction
title Spatio-temporal dynamics of gene expression of the Edn1-Dlx5/6 pathway during development of the lower jaw
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