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Cas9-mediated excision of Nematostella brachyury disrupts endoderm development, pharynx formation and oral-aboral patterning

The mesoderm is a key novelty in animal evolution, although we understand little of how the mesoderm arose. brachyury, the founding member of the T-box gene family, is a key gene in chordate mesoderm development. However, the brachyury gene was present in the common ancestor of fungi and animals lon...

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Autores principales: Servetnick, Marc D., Steinworth, Bailey, Babonis, Leslie S., Simmons, David, Salinas-Saavedra, Miguel, Martindale, Mark Q.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5592810/
https://www.ncbi.nlm.nih.gov/pubmed/28705897
http://dx.doi.org/10.1242/dev.145839
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author Servetnick, Marc D.
Steinworth, Bailey
Babonis, Leslie S.
Simmons, David
Salinas-Saavedra, Miguel
Martindale, Mark Q.
author_facet Servetnick, Marc D.
Steinworth, Bailey
Babonis, Leslie S.
Simmons, David
Salinas-Saavedra, Miguel
Martindale, Mark Q.
author_sort Servetnick, Marc D.
collection PubMed
description The mesoderm is a key novelty in animal evolution, although we understand little of how the mesoderm arose. brachyury, the founding member of the T-box gene family, is a key gene in chordate mesoderm development. However, the brachyury gene was present in the common ancestor of fungi and animals long before mesoderm appeared. To explore ancestral roles of brachyury prior to the evolution of definitive mesoderm, we excised the gene using CRISPR/Cas9 in the diploblastic cnidarian Nematostella vectensis. Nvbrachyury is normally expressed in precursors of the pharynx, which separates endoderm from ectoderm. In knockout embryos, the pharynx does not form, embryos fail to elongate, and endoderm organization, ectodermal cell polarity and patterning along the oral-aboral axis are disrupted. Expression of many genes both inside and outside the Nvbrachyury expression domain is affected, including downregulation of Wnt genes at the oral pole. Our results point to an ancient role for brachyury in morphogenesis, cell polarity and the patterning of both ectodermal and endodermal derivatives along the primary body axis.
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spelling pubmed-55928102017-09-15 Cas9-mediated excision of Nematostella brachyury disrupts endoderm development, pharynx formation and oral-aboral patterning Servetnick, Marc D. Steinworth, Bailey Babonis, Leslie S. Simmons, David Salinas-Saavedra, Miguel Martindale, Mark Q. Development Research Article The mesoderm is a key novelty in animal evolution, although we understand little of how the mesoderm arose. brachyury, the founding member of the T-box gene family, is a key gene in chordate mesoderm development. However, the brachyury gene was present in the common ancestor of fungi and animals long before mesoderm appeared. To explore ancestral roles of brachyury prior to the evolution of definitive mesoderm, we excised the gene using CRISPR/Cas9 in the diploblastic cnidarian Nematostella vectensis. Nvbrachyury is normally expressed in precursors of the pharynx, which separates endoderm from ectoderm. In knockout embryos, the pharynx does not form, embryos fail to elongate, and endoderm organization, ectodermal cell polarity and patterning along the oral-aboral axis are disrupted. Expression of many genes both inside and outside the Nvbrachyury expression domain is affected, including downregulation of Wnt genes at the oral pole. Our results point to an ancient role for brachyury in morphogenesis, cell polarity and the patterning of both ectodermal and endodermal derivatives along the primary body axis. The Company of Biologists Ltd 2017-08-15 /pmc/articles/PMC5592810/ /pubmed/28705897 http://dx.doi.org/10.1242/dev.145839 Text en © 2017. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Servetnick, Marc D.
Steinworth, Bailey
Babonis, Leslie S.
Simmons, David
Salinas-Saavedra, Miguel
Martindale, Mark Q.
Cas9-mediated excision of Nematostella brachyury disrupts endoderm development, pharynx formation and oral-aboral patterning
title Cas9-mediated excision of Nematostella brachyury disrupts endoderm development, pharynx formation and oral-aboral patterning
title_full Cas9-mediated excision of Nematostella brachyury disrupts endoderm development, pharynx formation and oral-aboral patterning
title_fullStr Cas9-mediated excision of Nematostella brachyury disrupts endoderm development, pharynx formation and oral-aboral patterning
title_full_unstemmed Cas9-mediated excision of Nematostella brachyury disrupts endoderm development, pharynx formation and oral-aboral patterning
title_short Cas9-mediated excision of Nematostella brachyury disrupts endoderm development, pharynx formation and oral-aboral patterning
title_sort cas9-mediated excision of nematostella brachyury disrupts endoderm development, pharynx formation and oral-aboral patterning
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5592810/
https://www.ncbi.nlm.nih.gov/pubmed/28705897
http://dx.doi.org/10.1242/dev.145839
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