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Molecular insights into the origin of the Hox-TALE patterning system

Despite tremendous body form diversity in nature, bilaterian animals share common sets of developmental genes that display conserved expression patterns in the embryo. Among them are the Hox genes, which define different identities along the anterior–posterior axis. Hox proteins exert their function...

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Autores principales: Hudry, Bruno, Thomas-Chollier, Morgane, Volovik, Yael, Duffraisse, Marilyne, Dard, Amélie, Frank, Dale, Technau, Ulrich, Merabet, Samir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3957477/
https://www.ncbi.nlm.nih.gov/pubmed/24642410
http://dx.doi.org/10.7554/eLife.01939
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author Hudry, Bruno
Thomas-Chollier, Morgane
Volovik, Yael
Duffraisse, Marilyne
Dard, Amélie
Frank, Dale
Technau, Ulrich
Merabet, Samir
author_facet Hudry, Bruno
Thomas-Chollier, Morgane
Volovik, Yael
Duffraisse, Marilyne
Dard, Amélie
Frank, Dale
Technau, Ulrich
Merabet, Samir
author_sort Hudry, Bruno
collection PubMed
description Despite tremendous body form diversity in nature, bilaterian animals share common sets of developmental genes that display conserved expression patterns in the embryo. Among them are the Hox genes, which define different identities along the anterior–posterior axis. Hox proteins exert their function by interaction with TALE transcription factors. Hox and TALE members are also present in some but not all non-bilaterian phyla, raising the question of how Hox–TALE interactions evolved to provide positional information. By using proteins from unicellular and multicellular lineages, we showed that these networks emerged from an ancestral generic motif present in Hox and other related protein families. Interestingly, Hox-TALE networks experienced additional and extensive molecular innovations that were likely crucial for differentiating Hox functions along body plans. Together our results highlight how homeobox gene families evolved during eukaryote evolution to eventually constitute a major patterning system in Eumetazoans. DOI: http://dx.doi.org/10.7554/eLife.01939.001
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spelling pubmed-39574772014-03-27 Molecular insights into the origin of the Hox-TALE patterning system Hudry, Bruno Thomas-Chollier, Morgane Volovik, Yael Duffraisse, Marilyne Dard, Amélie Frank, Dale Technau, Ulrich Merabet, Samir eLife Developmental Biology and Stem Cells Despite tremendous body form diversity in nature, bilaterian animals share common sets of developmental genes that display conserved expression patterns in the embryo. Among them are the Hox genes, which define different identities along the anterior–posterior axis. Hox proteins exert their function by interaction with TALE transcription factors. Hox and TALE members are also present in some but not all non-bilaterian phyla, raising the question of how Hox–TALE interactions evolved to provide positional information. By using proteins from unicellular and multicellular lineages, we showed that these networks emerged from an ancestral generic motif present in Hox and other related protein families. Interestingly, Hox-TALE networks experienced additional and extensive molecular innovations that were likely crucial for differentiating Hox functions along body plans. Together our results highlight how homeobox gene families evolved during eukaryote evolution to eventually constitute a major patterning system in Eumetazoans. DOI: http://dx.doi.org/10.7554/eLife.01939.001 eLife Sciences Publications, Ltd 2014-03-18 /pmc/articles/PMC3957477/ /pubmed/24642410 http://dx.doi.org/10.7554/eLife.01939 Text en Copyright © 2014, Hudry et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology and Stem Cells
Hudry, Bruno
Thomas-Chollier, Morgane
Volovik, Yael
Duffraisse, Marilyne
Dard, Amélie
Frank, Dale
Technau, Ulrich
Merabet, Samir
Molecular insights into the origin of the Hox-TALE patterning system
title Molecular insights into the origin of the Hox-TALE patterning system
title_full Molecular insights into the origin of the Hox-TALE patterning system
title_fullStr Molecular insights into the origin of the Hox-TALE patterning system
title_full_unstemmed Molecular insights into the origin of the Hox-TALE patterning system
title_short Molecular insights into the origin of the Hox-TALE patterning system
title_sort molecular insights into the origin of the hox-tale patterning system
topic Developmental Biology and Stem Cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3957477/
https://www.ncbi.nlm.nih.gov/pubmed/24642410
http://dx.doi.org/10.7554/eLife.01939
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