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Polarized regulatory landscape and Wnt responsiveness underlie Hox activation in embryos

Sequential 3′-to-5′ activation of the Hox gene clusters in early embryos is a most fascinating issue in developmental biology. Neither the trigger nor the regulatory elements involved in the transcriptional initiation of the 3′-most Hox genes have been unraveled in any organism. We demonstrate that...

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Autores principales: Neijts, Roel, Amin, Shilu, van Rooijen, Carina, Tan, Sander, Creyghton, Menno P., de Laat, Wouter, Deschamps, Jacqueline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066237/
https://www.ncbi.nlm.nih.gov/pubmed/27633012
http://dx.doi.org/10.1101/gad.285767.116
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author Neijts, Roel
Amin, Shilu
van Rooijen, Carina
Tan, Sander
Creyghton, Menno P.
de Laat, Wouter
Deschamps, Jacqueline
author_facet Neijts, Roel
Amin, Shilu
van Rooijen, Carina
Tan, Sander
Creyghton, Menno P.
de Laat, Wouter
Deschamps, Jacqueline
author_sort Neijts, Roel
collection PubMed
description Sequential 3′-to-5′ activation of the Hox gene clusters in early embryos is a most fascinating issue in developmental biology. Neither the trigger nor the regulatory elements involved in the transcriptional initiation of the 3′-most Hox genes have been unraveled in any organism. We demonstrate that a series of enhancers, some of which are Wnt-dependent, is located within a HoxA 3′ subtopologically associated domain (subTAD). This subTAD forms the structural basis for multiple layers of 3′-polarized features, including DNA accessibility and enhancer activation. Deletion of the cassette of Wnt-dependent enhancers proves its crucial role in initial transcription of HoxA at the 3′ side of the cluster.
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spelling pubmed-50662372016-10-28 Polarized regulatory landscape and Wnt responsiveness underlie Hox activation in embryos Neijts, Roel Amin, Shilu van Rooijen, Carina Tan, Sander Creyghton, Menno P. de Laat, Wouter Deschamps, Jacqueline Genes Dev Research Communication Sequential 3′-to-5′ activation of the Hox gene clusters in early embryos is a most fascinating issue in developmental biology. Neither the trigger nor the regulatory elements involved in the transcriptional initiation of the 3′-most Hox genes have been unraveled in any organism. We demonstrate that a series of enhancers, some of which are Wnt-dependent, is located within a HoxA 3′ subtopologically associated domain (subTAD). This subTAD forms the structural basis for multiple layers of 3′-polarized features, including DNA accessibility and enhancer activation. Deletion of the cassette of Wnt-dependent enhancers proves its crucial role in initial transcription of HoxA at the 3′ side of the cluster. Cold Spring Harbor Laboratory Press 2016-09-01 /pmc/articles/PMC5066237/ /pubmed/27633012 http://dx.doi.org/10.1101/gad.285767.116 Text en © 2016 Neijts et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article, published in Genes & Development, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Research Communication
Neijts, Roel
Amin, Shilu
van Rooijen, Carina
Tan, Sander
Creyghton, Menno P.
de Laat, Wouter
Deschamps, Jacqueline
Polarized regulatory landscape and Wnt responsiveness underlie Hox activation in embryos
title Polarized regulatory landscape and Wnt responsiveness underlie Hox activation in embryos
title_full Polarized regulatory landscape and Wnt responsiveness underlie Hox activation in embryos
title_fullStr Polarized regulatory landscape and Wnt responsiveness underlie Hox activation in embryos
title_full_unstemmed Polarized regulatory landscape and Wnt responsiveness underlie Hox activation in embryos
title_short Polarized regulatory landscape and Wnt responsiveness underlie Hox activation in embryos
title_sort polarized regulatory landscape and wnt responsiveness underlie hox activation in embryos
topic Research Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066237/
https://www.ncbi.nlm.nih.gov/pubmed/27633012
http://dx.doi.org/10.1101/gad.285767.116
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