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A Hox-TALE regulatory circuit for neural crest patterning is conserved across vertebrates

In jawed vertebrates (gnathostomes), Hox genes play an important role in patterning head and jaw formation, but mechanisms coupling Hox genes to neural crest (NC) are unknown. Here we use cross-species regulatory comparisons between gnathostomes and lamprey, a jawless extant vertebrate, to investiga...

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Autores principales: Parker, Hugo J., De Kumar, Bony, Green, Stephen A., Prummel, Karin D., Hess, Christopher, Kaufman, Charles K., Mosimann, Christian, Wiedemann, Leanne M., Bronner, Marianne E., Krumlauf, Robb
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6416258/
https://www.ncbi.nlm.nih.gov/pubmed/30867425
http://dx.doi.org/10.1038/s41467-019-09197-8
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author Parker, Hugo J.
De Kumar, Bony
Green, Stephen A.
Prummel, Karin D.
Hess, Christopher
Kaufman, Charles K.
Mosimann, Christian
Wiedemann, Leanne M.
Bronner, Marianne E.
Krumlauf, Robb
author_facet Parker, Hugo J.
De Kumar, Bony
Green, Stephen A.
Prummel, Karin D.
Hess, Christopher
Kaufman, Charles K.
Mosimann, Christian
Wiedemann, Leanne M.
Bronner, Marianne E.
Krumlauf, Robb
author_sort Parker, Hugo J.
collection PubMed
description In jawed vertebrates (gnathostomes), Hox genes play an important role in patterning head and jaw formation, but mechanisms coupling Hox genes to neural crest (NC) are unknown. Here we use cross-species regulatory comparisons between gnathostomes and lamprey, a jawless extant vertebrate, to investigate conserved ancestral mechanisms regulating Hox2 genes in NC. Gnathostome Hoxa2 and Hoxb2 NC enhancers mediate equivalent NC expression in lamprey and gnathostomes, revealing ancient conservation of Hox upstream regulatory components in NC. In characterizing a lamprey hoxα2 NC/hindbrain enhancer, we identify essential Meis, Pbx, and Hox binding sites that are functionally conserved within Hoxa2/Hoxb2 NC enhancers. This suggests that the lamprey hoxα2 enhancer retains ancestral activity and that Hoxa2/Hoxb2 NC enhancers are ancient paralogues, which diverged in hindbrain and NC activities. This identifies an ancestral mechanism for Hox2 NC regulation involving a Hox-TALE regulatory circuit, potentiated by inputs from Meis and Pbx proteins and Hox auto-/cross-regulatory interactions.
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spelling pubmed-64162582019-03-15 A Hox-TALE regulatory circuit for neural crest patterning is conserved across vertebrates Parker, Hugo J. De Kumar, Bony Green, Stephen A. Prummel, Karin D. Hess, Christopher Kaufman, Charles K. Mosimann, Christian Wiedemann, Leanne M. Bronner, Marianne E. Krumlauf, Robb Nat Commun Article In jawed vertebrates (gnathostomes), Hox genes play an important role in patterning head and jaw formation, but mechanisms coupling Hox genes to neural crest (NC) are unknown. Here we use cross-species regulatory comparisons between gnathostomes and lamprey, a jawless extant vertebrate, to investigate conserved ancestral mechanisms regulating Hox2 genes in NC. Gnathostome Hoxa2 and Hoxb2 NC enhancers mediate equivalent NC expression in lamprey and gnathostomes, revealing ancient conservation of Hox upstream regulatory components in NC. In characterizing a lamprey hoxα2 NC/hindbrain enhancer, we identify essential Meis, Pbx, and Hox binding sites that are functionally conserved within Hoxa2/Hoxb2 NC enhancers. This suggests that the lamprey hoxα2 enhancer retains ancestral activity and that Hoxa2/Hoxb2 NC enhancers are ancient paralogues, which diverged in hindbrain and NC activities. This identifies an ancestral mechanism for Hox2 NC regulation involving a Hox-TALE regulatory circuit, potentiated by inputs from Meis and Pbx proteins and Hox auto-/cross-regulatory interactions. Nature Publishing Group UK 2019-03-13 /pmc/articles/PMC6416258/ /pubmed/30867425 http://dx.doi.org/10.1038/s41467-019-09197-8 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Parker, Hugo J.
De Kumar, Bony
Green, Stephen A.
Prummel, Karin D.
Hess, Christopher
Kaufman, Charles K.
Mosimann, Christian
Wiedemann, Leanne M.
Bronner, Marianne E.
Krumlauf, Robb
A Hox-TALE regulatory circuit for neural crest patterning is conserved across vertebrates
title A Hox-TALE regulatory circuit for neural crest patterning is conserved across vertebrates
title_full A Hox-TALE regulatory circuit for neural crest patterning is conserved across vertebrates
title_fullStr A Hox-TALE regulatory circuit for neural crest patterning is conserved across vertebrates
title_full_unstemmed A Hox-TALE regulatory circuit for neural crest patterning is conserved across vertebrates
title_short A Hox-TALE regulatory circuit for neural crest patterning is conserved across vertebrates
title_sort hox-tale regulatory circuit for neural crest patterning is conserved across vertebrates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6416258/
https://www.ncbi.nlm.nih.gov/pubmed/30867425
http://dx.doi.org/10.1038/s41467-019-09197-8
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