Cargando…

In vivo Hox binding specificity revealed by systematic changes to a single cis regulatory module

Hox proteins belong to a family of transcription factors with similar DNA binding specificities that control animal differentiation along the antero-posterior body axis. Hox proteins are expressed in partially overlapping regions where each one is responsible for the formation of particular organs a...

Descripción completa

Detalles Bibliográficos
Autores principales: Sánchez-Higueras, Carlos, Rastogi, Chaitanya, Voutev, Roumen, Bussemaker, Harmen J., Mann, Richard S., Hombría, James C.-G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6689074/
https://www.ncbi.nlm.nih.gov/pubmed/31399572
http://dx.doi.org/10.1038/s41467-019-11416-1
_version_ 1783442982672793600
author Sánchez-Higueras, Carlos
Rastogi, Chaitanya
Voutev, Roumen
Bussemaker, Harmen J.
Mann, Richard S.
Hombría, James C.-G.
author_facet Sánchez-Higueras, Carlos
Rastogi, Chaitanya
Voutev, Roumen
Bussemaker, Harmen J.
Mann, Richard S.
Hombría, James C.-G.
author_sort Sánchez-Higueras, Carlos
collection PubMed
description Hox proteins belong to a family of transcription factors with similar DNA binding specificities that control animal differentiation along the antero-posterior body axis. Hox proteins are expressed in partially overlapping regions where each one is responsible for the formation of particular organs and structures through the regulation of specific direct downstream targets. Thus, explaining how each Hox protein can selectively control its direct targets from those of another Hox protein is fundamental to understand animal development. Here we analyse a cis regulatory module directly regulated by seven different Drosophila Hox proteins and uncover how different Hox class proteins differentially control its expression. We find that regulation by one or another Hox protein depends on the combination of three modes: Hox-cofactor dependent DNA-binding specificity; Hox-monomer binding sites; and interaction with positive and negative Hox-collaborator proteins. Additionally, we find that similar regulation can be achieved by Amphioxus orthologs, suggesting these three mechanisms are conserved from insects to chordates.
format Online
Article
Text
id pubmed-6689074
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-66890742019-08-12 In vivo Hox binding specificity revealed by systematic changes to a single cis regulatory module Sánchez-Higueras, Carlos Rastogi, Chaitanya Voutev, Roumen Bussemaker, Harmen J. Mann, Richard S. Hombría, James C.-G. Nat Commun Article Hox proteins belong to a family of transcription factors with similar DNA binding specificities that control animal differentiation along the antero-posterior body axis. Hox proteins are expressed in partially overlapping regions where each one is responsible for the formation of particular organs and structures through the regulation of specific direct downstream targets. Thus, explaining how each Hox protein can selectively control its direct targets from those of another Hox protein is fundamental to understand animal development. Here we analyse a cis regulatory module directly regulated by seven different Drosophila Hox proteins and uncover how different Hox class proteins differentially control its expression. We find that regulation by one or another Hox protein depends on the combination of three modes: Hox-cofactor dependent DNA-binding specificity; Hox-monomer binding sites; and interaction with positive and negative Hox-collaborator proteins. Additionally, we find that similar regulation can be achieved by Amphioxus orthologs, suggesting these three mechanisms are conserved from insects to chordates. Nature Publishing Group UK 2019-08-09 /pmc/articles/PMC6689074/ /pubmed/31399572 http://dx.doi.org/10.1038/s41467-019-11416-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sánchez-Higueras, Carlos
Rastogi, Chaitanya
Voutev, Roumen
Bussemaker, Harmen J.
Mann, Richard S.
Hombría, James C.-G.
In vivo Hox binding specificity revealed by systematic changes to a single cis regulatory module
title In vivo Hox binding specificity revealed by systematic changes to a single cis regulatory module
title_full In vivo Hox binding specificity revealed by systematic changes to a single cis regulatory module
title_fullStr In vivo Hox binding specificity revealed by systematic changes to a single cis regulatory module
title_full_unstemmed In vivo Hox binding specificity revealed by systematic changes to a single cis regulatory module
title_short In vivo Hox binding specificity revealed by systematic changes to a single cis regulatory module
title_sort in vivo hox binding specificity revealed by systematic changes to a single cis regulatory module
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6689074/
https://www.ncbi.nlm.nih.gov/pubmed/31399572
http://dx.doi.org/10.1038/s41467-019-11416-1
work_keys_str_mv AT sanchezhiguerascarlos invivohoxbindingspecificityrevealedbysystematicchangestoasinglecisregulatorymodule
AT rastogichaitanya invivohoxbindingspecificityrevealedbysystematicchangestoasinglecisregulatorymodule
AT voutevroumen invivohoxbindingspecificityrevealedbysystematicchangestoasinglecisregulatorymodule
AT bussemakerharmenj invivohoxbindingspecificityrevealedbysystematicchangestoasinglecisregulatorymodule
AT mannrichards invivohoxbindingspecificityrevealedbysystematicchangestoasinglecisregulatorymodule
AT hombriajamescg invivohoxbindingspecificityrevealedbysystematicchangestoasinglecisregulatorymodule