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Ancient Pbx-Hox signatures define hundreds of vertebrate developmental enhancers
BACKGROUND: Gene regulation through cis-regulatory elements plays a crucial role in development and disease. A major aim of the post-genomic era is to be able to read the function of cis-regulatory elements through scrutiny of their DNA sequence. Whilst comparative genomics approaches have identifie...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3261376/ https://www.ncbi.nlm.nih.gov/pubmed/22208168 http://dx.doi.org/10.1186/1471-2164-12-637 |
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author | Parker, Hugo J Piccinelli, Paul Sauka-Spengler, Tatjana Bronner, Marianne Elgar, Greg |
author_facet | Parker, Hugo J Piccinelli, Paul Sauka-Spengler, Tatjana Bronner, Marianne Elgar, Greg |
author_sort | Parker, Hugo J |
collection | PubMed |
description | BACKGROUND: Gene regulation through cis-regulatory elements plays a crucial role in development and disease. A major aim of the post-genomic era is to be able to read the function of cis-regulatory elements through scrutiny of their DNA sequence. Whilst comparative genomics approaches have identified thousands of putative regulatory elements, our knowledge of their mechanism of action is poor and very little progress has been made in systematically de-coding them. RESULTS: Here, we identify ancient functional signatures within vertebrate conserved non-coding elements (CNEs) through a combination of phylogenetic footprinting and functional assay, using genomic sequence from the sea lamprey as a reference. We uncover a striking enrichment within vertebrate CNEs for conserved binding-site motifs of the Pbx-Hox hetero-dimer. We further show that these predict reporter gene expression in a segment specific manner in the hindbrain and pharyngeal arches during zebrafish development. CONCLUSIONS: These findings evoke an evolutionary scenario in which many CNEs evolved early in the vertebrate lineage to co-ordinate Hox-dependent gene-regulatory interactions that pattern the vertebrate head. In a broader context, our evolutionary analyses reveal that CNEs are composed of tightly linked transcription-factor binding-sites (TFBSs), which can be systematically identified through phylogenetic footprinting approaches. By placing a large number of ancient vertebrate CNEs into a developmental context, our findings promise to have a significant impact on efforts toward de-coding gene-regulatory elements that underlie vertebrate development, and will facilitate building general models of regulatory element evolution. |
format | Online Article Text |
id | pubmed-3261376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32613762012-01-20 Ancient Pbx-Hox signatures define hundreds of vertebrate developmental enhancers Parker, Hugo J Piccinelli, Paul Sauka-Spengler, Tatjana Bronner, Marianne Elgar, Greg BMC Genomics Research Article BACKGROUND: Gene regulation through cis-regulatory elements plays a crucial role in development and disease. A major aim of the post-genomic era is to be able to read the function of cis-regulatory elements through scrutiny of their DNA sequence. Whilst comparative genomics approaches have identified thousands of putative regulatory elements, our knowledge of their mechanism of action is poor and very little progress has been made in systematically de-coding them. RESULTS: Here, we identify ancient functional signatures within vertebrate conserved non-coding elements (CNEs) through a combination of phylogenetic footprinting and functional assay, using genomic sequence from the sea lamprey as a reference. We uncover a striking enrichment within vertebrate CNEs for conserved binding-site motifs of the Pbx-Hox hetero-dimer. We further show that these predict reporter gene expression in a segment specific manner in the hindbrain and pharyngeal arches during zebrafish development. CONCLUSIONS: These findings evoke an evolutionary scenario in which many CNEs evolved early in the vertebrate lineage to co-ordinate Hox-dependent gene-regulatory interactions that pattern the vertebrate head. In a broader context, our evolutionary analyses reveal that CNEs are composed of tightly linked transcription-factor binding-sites (TFBSs), which can be systematically identified through phylogenetic footprinting approaches. By placing a large number of ancient vertebrate CNEs into a developmental context, our findings promise to have a significant impact on efforts toward de-coding gene-regulatory elements that underlie vertebrate development, and will facilitate building general models of regulatory element evolution. BioMed Central 2011-12-30 /pmc/articles/PMC3261376/ /pubmed/22208168 http://dx.doi.org/10.1186/1471-2164-12-637 Text en Copyright ©2011 Parker et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Parker, Hugo J Piccinelli, Paul Sauka-Spengler, Tatjana Bronner, Marianne Elgar, Greg Ancient Pbx-Hox signatures define hundreds of vertebrate developmental enhancers |
title | Ancient Pbx-Hox signatures define hundreds of vertebrate developmental enhancers |
title_full | Ancient Pbx-Hox signatures define hundreds of vertebrate developmental enhancers |
title_fullStr | Ancient Pbx-Hox signatures define hundreds of vertebrate developmental enhancers |
title_full_unstemmed | Ancient Pbx-Hox signatures define hundreds of vertebrate developmental enhancers |
title_short | Ancient Pbx-Hox signatures define hundreds of vertebrate developmental enhancers |
title_sort | ancient pbx-hox signatures define hundreds of vertebrate developmental enhancers |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3261376/ https://www.ncbi.nlm.nih.gov/pubmed/22208168 http://dx.doi.org/10.1186/1471-2164-12-637 |
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