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A role for HOX13 proteins in the regulatory switch between TADs at the HoxD locus
During vertebrate limb development, Hoxd genes are regulated following a bimodal strategy involving two topologically associating domains (TADs) located on either side of the gene cluster. These regulatory landscapes alternatively control different subsets of Hoxd targets, first into the arm and sub...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4888838/ https://www.ncbi.nlm.nih.gov/pubmed/27198226 http://dx.doi.org/10.1101/gad.281055.116 |
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author | Beccari, Leonardo Yakushiji-Kaminatsui, Nayuta Woltering, Joost M. Necsulea, Anamaria Lonfat, Nicolas Rodríguez-Carballo, Eddie Mascrez, Benedicte Yamamoto, Shiori Kuroiwa, Atsushi Duboule, Denis |
author_facet | Beccari, Leonardo Yakushiji-Kaminatsui, Nayuta Woltering, Joost M. Necsulea, Anamaria Lonfat, Nicolas Rodríguez-Carballo, Eddie Mascrez, Benedicte Yamamoto, Shiori Kuroiwa, Atsushi Duboule, Denis |
author_sort | Beccari, Leonardo |
collection | PubMed |
description | During vertebrate limb development, Hoxd genes are regulated following a bimodal strategy involving two topologically associating domains (TADs) located on either side of the gene cluster. These regulatory landscapes alternatively control different subsets of Hoxd targets, first into the arm and subsequently into the digits. We studied the transition between these two global regulations, a switch that correlates with the positioning of the wrist, which articulates these two main limb segments. We show that the HOX13 proteins themselves help switch off the telomeric TAD, likely through a global repressive mechanism. At the same time, they directly interact with distal enhancers to sustain the activity of the centromeric TAD, thus explaining both the sequential and exclusive operating processes of these two regulatory domains. We propose a model in which the activation of Hox13 gene expression in distal limb cells both interrupts the proximal Hox gene regulation and re-enforces the distal regulation. In the absence of HOX13 proteins, a proximal limb structure grows without any sign of wrist articulation, likely related to an ancestral fish-like condition. |
format | Online Article Text |
id | pubmed-4888838 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48888382016-06-10 A role for HOX13 proteins in the regulatory switch between TADs at the HoxD locus Beccari, Leonardo Yakushiji-Kaminatsui, Nayuta Woltering, Joost M. Necsulea, Anamaria Lonfat, Nicolas Rodríguez-Carballo, Eddie Mascrez, Benedicte Yamamoto, Shiori Kuroiwa, Atsushi Duboule, Denis Genes Dev Research Paper During vertebrate limb development, Hoxd genes are regulated following a bimodal strategy involving two topologically associating domains (TADs) located on either side of the gene cluster. These regulatory landscapes alternatively control different subsets of Hoxd targets, first into the arm and subsequently into the digits. We studied the transition between these two global regulations, a switch that correlates with the positioning of the wrist, which articulates these two main limb segments. We show that the HOX13 proteins themselves help switch off the telomeric TAD, likely through a global repressive mechanism. At the same time, they directly interact with distal enhancers to sustain the activity of the centromeric TAD, thus explaining both the sequential and exclusive operating processes of these two regulatory domains. We propose a model in which the activation of Hox13 gene expression in distal limb cells both interrupts the proximal Hox gene regulation and re-enforces the distal regulation. In the absence of HOX13 proteins, a proximal limb structure grows without any sign of wrist articulation, likely related to an ancestral fish-like condition. Cold Spring Harbor Laboratory Press 2016-05-15 /pmc/articles/PMC4888838/ /pubmed/27198226 http://dx.doi.org/10.1101/gad.281055.116 Text en © 2016 Beccari et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by/4.0/ This article, published in Genes & Development, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Paper Beccari, Leonardo Yakushiji-Kaminatsui, Nayuta Woltering, Joost M. Necsulea, Anamaria Lonfat, Nicolas Rodríguez-Carballo, Eddie Mascrez, Benedicte Yamamoto, Shiori Kuroiwa, Atsushi Duboule, Denis A role for HOX13 proteins in the regulatory switch between TADs at the HoxD locus |
title | A role for HOX13 proteins in the regulatory switch between TADs at the HoxD locus |
title_full | A role for HOX13 proteins in the regulatory switch between TADs at the HoxD locus |
title_fullStr | A role for HOX13 proteins in the regulatory switch between TADs at the HoxD locus |
title_full_unstemmed | A role for HOX13 proteins in the regulatory switch between TADs at the HoxD locus |
title_short | A role for HOX13 proteins in the regulatory switch between TADs at the HoxD locus |
title_sort | role for hox13 proteins in the regulatory switch between tads at the hoxd locus |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4888838/ https://www.ncbi.nlm.nih.gov/pubmed/27198226 http://dx.doi.org/10.1101/gad.281055.116 |
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