Cargando…
Uncoupling Time and Space in the Collinear Regulation of Hox Genes
During development of the vertebrate body axis, Hox genes are transcribed sequentially, in both time and space, following their relative positions within their genomic clusters. Analyses of animal genomes support the idea that Hox gene clustering is essential for coordinating the various times of ge...
Autores principales: | , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2642670/ https://www.ncbi.nlm.nih.gov/pubmed/19266017 http://dx.doi.org/10.1371/journal.pgen.1000398 |
_version_ | 1782164638870274048 |
---|---|
author | Tschopp, Patrick Tarchini, Basile Spitz, François Zakany, Jozsef Duboule, Denis |
author_facet | Tschopp, Patrick Tarchini, Basile Spitz, François Zakany, Jozsef Duboule, Denis |
author_sort | Tschopp, Patrick |
collection | PubMed |
description | During development of the vertebrate body axis, Hox genes are transcribed sequentially, in both time and space, following their relative positions within their genomic clusters. Analyses of animal genomes support the idea that Hox gene clustering is essential for coordinating the various times of gene activations. However, the eventual collinear ordering of the gene specific transcript domains in space does not always require genomic clustering. We analyzed these complex regulatory relationships by using mutant alleles at the mouse HoxD locus, including one that splits the cluster into two pieces. We show that both positive and negative regulatory influences, located on either side of the cluster, control an early phase of collinear expression in the trunk. Interestingly, this early phase does not systematically impact upon the subsequent expression patterns along the main body axis, indicating that the mechanism underlying temporal collinearity is distinct from those acting during the second phase. We discuss the potential functions and evolutionary origins of these mechanisms, as well as their relationship with similar processes at work during limb development. |
format | Text |
id | pubmed-2642670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-26426702009-03-06 Uncoupling Time and Space in the Collinear Regulation of Hox Genes Tschopp, Patrick Tarchini, Basile Spitz, François Zakany, Jozsef Duboule, Denis PLoS Genet Research Article During development of the vertebrate body axis, Hox genes are transcribed sequentially, in both time and space, following their relative positions within their genomic clusters. Analyses of animal genomes support the idea that Hox gene clustering is essential for coordinating the various times of gene activations. However, the eventual collinear ordering of the gene specific transcript domains in space does not always require genomic clustering. We analyzed these complex regulatory relationships by using mutant alleles at the mouse HoxD locus, including one that splits the cluster into two pieces. We show that both positive and negative regulatory influences, located on either side of the cluster, control an early phase of collinear expression in the trunk. Interestingly, this early phase does not systematically impact upon the subsequent expression patterns along the main body axis, indicating that the mechanism underlying temporal collinearity is distinct from those acting during the second phase. We discuss the potential functions and evolutionary origins of these mechanisms, as well as their relationship with similar processes at work during limb development. Public Library of Science 2009-03-06 /pmc/articles/PMC2642670/ /pubmed/19266017 http://dx.doi.org/10.1371/journal.pgen.1000398 Text en Tschopp 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Tschopp, Patrick Tarchini, Basile Spitz, François Zakany, Jozsef Duboule, Denis Uncoupling Time and Space in the Collinear Regulation of Hox Genes |
title | Uncoupling Time and Space in the Collinear Regulation of Hox Genes |
title_full | Uncoupling Time and Space in the Collinear Regulation of Hox Genes |
title_fullStr | Uncoupling Time and Space in the Collinear Regulation of Hox Genes |
title_full_unstemmed | Uncoupling Time and Space in the Collinear Regulation of Hox Genes |
title_short | Uncoupling Time and Space in the Collinear Regulation of Hox Genes |
title_sort | uncoupling time and space in the collinear regulation of hox genes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2642670/ https://www.ncbi.nlm.nih.gov/pubmed/19266017 http://dx.doi.org/10.1371/journal.pgen.1000398 |
work_keys_str_mv | AT tschopppatrick uncouplingtimeandspaceinthecollinearregulationofhoxgenes AT tarchinibasile uncouplingtimeandspaceinthecollinearregulationofhoxgenes AT spitzfrancois uncouplingtimeandspaceinthecollinearregulationofhoxgenes AT zakanyjozsef uncouplingtimeandspaceinthecollinearregulationofhoxgenes AT dubouledenis uncouplingtimeandspaceinthecollinearregulationofhoxgenes |