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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2014
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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 |
format | Online Article Text |
id | pubmed-3957477 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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