Cargando…

Competition between Jagged-Notch and Endothelin1 Signaling Selectively Restricts Cartilage Formation in the Zebrafish Upper Face

The intricate shaping of the facial skeleton is essential for function of the vertebrate jaw and middle ear. While much has been learned about the signaling pathways and transcription factors that control facial patterning, the downstream cellular mechanisms dictating skeletal shapes have remained u...

Descripción completa

Detalles Bibliográficos
Autores principales: Barske, Lindsey, Askary, Amjad, Zuniga, Elizabeth, Balczerski, Bartosz, Bump, Paul, Nichols, James T., Crump, J. Gage
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4825933/
https://www.ncbi.nlm.nih.gov/pubmed/27058748
http://dx.doi.org/10.1371/journal.pgen.1005967
_version_ 1782426269630070784
author Barske, Lindsey
Askary, Amjad
Zuniga, Elizabeth
Balczerski, Bartosz
Bump, Paul
Nichols, James T.
Crump, J. Gage
author_facet Barske, Lindsey
Askary, Amjad
Zuniga, Elizabeth
Balczerski, Bartosz
Bump, Paul
Nichols, James T.
Crump, J. Gage
author_sort Barske, Lindsey
collection PubMed
description The intricate shaping of the facial skeleton is essential for function of the vertebrate jaw and middle ear. While much has been learned about the signaling pathways and transcription factors that control facial patterning, the downstream cellular mechanisms dictating skeletal shapes have remained unclear. Here we present genetic evidence in zebrafish that three major signaling pathways − Jagged-Notch, Endothelin1 (Edn1), and Bmp − regulate the pattern of facial cartilage and bone formation by controlling the timing of cartilage differentiation along the dorsoventral axis of the pharyngeal arches. A genomic analysis of purified facial skeletal precursors in mutant and overexpression embryos revealed a core set of differentiation genes that were commonly repressed by Jagged-Notch and induced by Edn1. Further analysis of the pre-cartilage condensation gene barx1, as well as in vivo imaging of cartilage differentiation, revealed that cartilage forms first in regions of high Edn1 and low Jagged-Notch activity. Consistent with a role of Jagged-Notch signaling in restricting cartilage differentiation, loss of Notch pathway components resulted in expanded barx1 expression in the dorsal arches, with mutation of barx1 rescuing some aspects of dorsal skeletal patterning in jag1b mutants. We also identified prrx1a and prrx1b as negative Edn1 and positive Bmp targets that function in parallel to Jagged-Notch signaling to restrict the formation of dorsal barx1+ pre-cartilage condensations. Simultaneous loss of jag1b and prrx1a/b better rescued lower facial defects of edn1 mutants than loss of either pathway alone, showing that combined overactivation of Jagged-Notch and Bmp/Prrx1 pathways contribute to the absence of cartilage differentiation in the edn1 mutant lower face. These findings support a model in which Notch-mediated restriction of cartilage differentiation, particularly in the second pharyngeal arch, helps to establish a distinct skeletal pattern in the upper face.
format Online
Article
Text
id pubmed-4825933
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-48259332016-04-22 Competition between Jagged-Notch and Endothelin1 Signaling Selectively Restricts Cartilage Formation in the Zebrafish Upper Face Barske, Lindsey Askary, Amjad Zuniga, Elizabeth Balczerski, Bartosz Bump, Paul Nichols, James T. Crump, J. Gage PLoS Genet Research Article The intricate shaping of the facial skeleton is essential for function of the vertebrate jaw and middle ear. While much has been learned about the signaling pathways and transcription factors that control facial patterning, the downstream cellular mechanisms dictating skeletal shapes have remained unclear. Here we present genetic evidence in zebrafish that three major signaling pathways − Jagged-Notch, Endothelin1 (Edn1), and Bmp − regulate the pattern of facial cartilage and bone formation by controlling the timing of cartilage differentiation along the dorsoventral axis of the pharyngeal arches. A genomic analysis of purified facial skeletal precursors in mutant and overexpression embryos revealed a core set of differentiation genes that were commonly repressed by Jagged-Notch and induced by Edn1. Further analysis of the pre-cartilage condensation gene barx1, as well as in vivo imaging of cartilage differentiation, revealed that cartilage forms first in regions of high Edn1 and low Jagged-Notch activity. Consistent with a role of Jagged-Notch signaling in restricting cartilage differentiation, loss of Notch pathway components resulted in expanded barx1 expression in the dorsal arches, with mutation of barx1 rescuing some aspects of dorsal skeletal patterning in jag1b mutants. We also identified prrx1a and prrx1b as negative Edn1 and positive Bmp targets that function in parallel to Jagged-Notch signaling to restrict the formation of dorsal barx1+ pre-cartilage condensations. Simultaneous loss of jag1b and prrx1a/b better rescued lower facial defects of edn1 mutants than loss of either pathway alone, showing that combined overactivation of Jagged-Notch and Bmp/Prrx1 pathways contribute to the absence of cartilage differentiation in the edn1 mutant lower face. These findings support a model in which Notch-mediated restriction of cartilage differentiation, particularly in the second pharyngeal arch, helps to establish a distinct skeletal pattern in the upper face. Public Library of Science 2016-04-08 /pmc/articles/PMC4825933/ /pubmed/27058748 http://dx.doi.org/10.1371/journal.pgen.1005967 Text en © 2016 Barske 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Barske, Lindsey
Askary, Amjad
Zuniga, Elizabeth
Balczerski, Bartosz
Bump, Paul
Nichols, James T.
Crump, J. Gage
Competition between Jagged-Notch and Endothelin1 Signaling Selectively Restricts Cartilage Formation in the Zebrafish Upper Face
title Competition between Jagged-Notch and Endothelin1 Signaling Selectively Restricts Cartilage Formation in the Zebrafish Upper Face
title_full Competition between Jagged-Notch and Endothelin1 Signaling Selectively Restricts Cartilage Formation in the Zebrafish Upper Face
title_fullStr Competition between Jagged-Notch and Endothelin1 Signaling Selectively Restricts Cartilage Formation in the Zebrafish Upper Face
title_full_unstemmed Competition between Jagged-Notch and Endothelin1 Signaling Selectively Restricts Cartilage Formation in the Zebrafish Upper Face
title_short Competition between Jagged-Notch and Endothelin1 Signaling Selectively Restricts Cartilage Formation in the Zebrafish Upper Face
title_sort competition between jagged-notch and endothelin1 signaling selectively restricts cartilage formation in the zebrafish upper face
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4825933/
https://www.ncbi.nlm.nih.gov/pubmed/27058748
http://dx.doi.org/10.1371/journal.pgen.1005967
work_keys_str_mv AT barskelindsey competitionbetweenjaggednotchandendothelin1signalingselectivelyrestrictscartilageformationinthezebrafishupperface
AT askaryamjad competitionbetweenjaggednotchandendothelin1signalingselectivelyrestrictscartilageformationinthezebrafishupperface
AT zunigaelizabeth competitionbetweenjaggednotchandendothelin1signalingselectivelyrestrictscartilageformationinthezebrafishupperface
AT balczerskibartosz competitionbetweenjaggednotchandendothelin1signalingselectivelyrestrictscartilageformationinthezebrafishupperface
AT bumppaul competitionbetweenjaggednotchandendothelin1signalingselectivelyrestrictscartilageformationinthezebrafishupperface
AT nicholsjamest competitionbetweenjaggednotchandendothelin1signalingselectivelyrestrictscartilageformationinthezebrafishupperface
AT crumpjgage competitionbetweenjaggednotchandendothelin1signalingselectivelyrestrictscartilageformationinthezebrafishupperface