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Collinear Hox-Hox interactions are involved in patterning the vertebrate anteroposterior (A-P) axis
Investigating regulation and function of the Hox genes, key regulators of positional identity in the embryo, opened a new vista in developmental biology. One of their most striking features is collinearity: the temporal and spatial orders of expression of these clustered genes each match their 3’ to...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388487/ https://www.ncbi.nlm.nih.gov/pubmed/28399140 http://dx.doi.org/10.1371/journal.pone.0175287 |
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author | Zhu, Kongju Spaink, Herman P. Durston, Antony J. |
author_facet | Zhu, Kongju Spaink, Herman P. Durston, Antony J. |
author_sort | Zhu, Kongju |
collection | PubMed |
description | Investigating regulation and function of the Hox genes, key regulators of positional identity in the embryo, opened a new vista in developmental biology. One of their most striking features is collinearity: the temporal and spatial orders of expression of these clustered genes each match their 3’ to 5’ order on the chromosome. Despite recent progress, the mechanisms underlying collinearity are not understood. Here we show that ectopic expression of 4 different single Hox genes predictably induces and represses expression of others, leading to development of different predictable specific sections of the body axis. We use ectopic expression in wild-type and noggin—dorsalised (Hox-free) Xenopus embryos, to show that two Hox-Hox interactions are important. Posterior induction (induction of posterior Hox genes by anterior ones: PI), drives Hox temporal collinearity (Hox timer), which itself drives anteroposterior (A-P) patterning. Posterior prevalence (repression of anterior Hox genes by posterior ones: PP) is important in translating temporal to spatial collinearity. We thus demonstrate for the first time that two collinear Hox interactions are important for vertebrate axial patterning. These findings considerably extend and clarify earlier work suggesting the existence and importance of PP and PI, and provide a major new insight into genesis of the body axis. |
format | Online Article Text |
id | pubmed-5388487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-53884872017-05-03 Collinear Hox-Hox interactions are involved in patterning the vertebrate anteroposterior (A-P) axis Zhu, Kongju Spaink, Herman P. Durston, Antony J. PLoS One Research Article Investigating regulation and function of the Hox genes, key regulators of positional identity in the embryo, opened a new vista in developmental biology. One of their most striking features is collinearity: the temporal and spatial orders of expression of these clustered genes each match their 3’ to 5’ order on the chromosome. Despite recent progress, the mechanisms underlying collinearity are not understood. Here we show that ectopic expression of 4 different single Hox genes predictably induces and represses expression of others, leading to development of different predictable specific sections of the body axis. We use ectopic expression in wild-type and noggin—dorsalised (Hox-free) Xenopus embryos, to show that two Hox-Hox interactions are important. Posterior induction (induction of posterior Hox genes by anterior ones: PI), drives Hox temporal collinearity (Hox timer), which itself drives anteroposterior (A-P) patterning. Posterior prevalence (repression of anterior Hox genes by posterior ones: PP) is important in translating temporal to spatial collinearity. We thus demonstrate for the first time that two collinear Hox interactions are important for vertebrate axial patterning. These findings considerably extend and clarify earlier work suggesting the existence and importance of PP and PI, and provide a major new insight into genesis of the body axis. Public Library of Science 2017-04-11 /pmc/articles/PMC5388487/ /pubmed/28399140 http://dx.doi.org/10.1371/journal.pone.0175287 Text en © 2017 Zhu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Zhu, Kongju Spaink, Herman P. Durston, Antony J. Collinear Hox-Hox interactions are involved in patterning the vertebrate anteroposterior (A-P) axis |
title | Collinear Hox-Hox interactions are involved in patterning the vertebrate anteroposterior (A-P) axis |
title_full | Collinear Hox-Hox interactions are involved in patterning the vertebrate anteroposterior (A-P) axis |
title_fullStr | Collinear Hox-Hox interactions are involved in patterning the vertebrate anteroposterior (A-P) axis |
title_full_unstemmed | Collinear Hox-Hox interactions are involved in patterning the vertebrate anteroposterior (A-P) axis |
title_short | Collinear Hox-Hox interactions are involved in patterning the vertebrate anteroposterior (A-P) axis |
title_sort | collinear hox-hox interactions are involved in patterning the vertebrate anteroposterior (a-p) axis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388487/ https://www.ncbi.nlm.nih.gov/pubmed/28399140 http://dx.doi.org/10.1371/journal.pone.0175287 |
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