Timed Collinear Activation of Hox Genes during Gastrulation Controls the Avian Forelimb Position

Limb position along the body is highly consistent within one species but very variable among vertebrates. Despite major advances in our understanding of limb patterning in three dimensions, how limbs reproducibly form along the antero-posterior axis remains largely unknown. Hox genes have long been...

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Veröffentlicht in:Current biology 2019-01, Vol.29 (1), p.35-50.e4
Hauptverfasser: Moreau, Chloe, Caldarelli, Paolo, Rocancourt, Didier, Roussel, Julian, Denans, Nicolas, Pourquie, Olivier, Gros, Jerome
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container_end_page 50.e4
container_issue 1
container_start_page 35
container_title Current biology
container_volume 29
creator Moreau, Chloe
Caldarelli, Paolo
Rocancourt, Didier
Roussel, Julian
Denans, Nicolas
Pourquie, Olivier
Gros, Jerome
description Limb position along the body is highly consistent within one species but very variable among vertebrates. Despite major advances in our understanding of limb patterning in three dimensions, how limbs reproducibly form along the antero-posterior axis remains largely unknown. Hox genes have long been suspected to control limb position; however, supporting evidences are mostly correlative and their role in this process is unclear. Here, we show that limb position is determined early in development through the action of Hox genes. Dynamic lineage analysis revealed that, during gastrulation, the forelimb, interlimb, and hindlimb fields are progressively generated and concomitantly patterned by the collinear activation of Hox genes in a two-step process. First, the sequential activation of Hoxb genes controls the relative position of their own collinear domains of expression in the forming lateral plate mesoderm, as demonstrated by functional perturbations during gastrulation. Then, within these collinear domains, we show that Hoxb4 anteriorly and Hox9 genes posteriorly, respectively, activate and repress the expression of the forelimb initiation gene Tbx5 and instruct the definitive position of the forelimb. Furthermore, by comparing the dynamics of Hoxb genes activation during zebra finch, chicken, and ostrich gastrulation, we provide evidences that changes in the timing of collinear Hox gene activation might underlie natural variation in forelimb position between different birds. Altogether, our results that characterize the cellular and molecular mechanisms underlying the regulation and natural variation of forelimb positioning in avians show a direct and early role for Hox genes in this process. [Display omitted] •Forelimb, interlimb, and hindlimb domains are sequentially laid during gastrulation•Temporal collinear activation controls Hox sequential expression in these domains•Hox domains differentially instruct (Hox4) or repress (Hox9) limb formation•Changes in collinear activation underlie bird natural variation in limb position How limbs reproducibly form along the vertebrate body remains largely unknown. Whereas Hox genes have long been suspected to regulate limb position, their role in this process is unclear. Here, Moreau et al. show a direct and early role for Hox genes in the regulation and natural variation of the forelimb position in birds.
doi_str_mv 10.1016/j.cub.2018.11.009
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Despite major advances in our understanding of limb patterning in three dimensions, how limbs reproducibly form along the antero-posterior axis remains largely unknown. Hox genes have long been suspected to control limb position; however, supporting evidences are mostly correlative and their role in this process is unclear. Here, we show that limb position is determined early in development through the action of Hox genes. Dynamic lineage analysis revealed that, during gastrulation, the forelimb, interlimb, and hindlimb fields are progressively generated and concomitantly patterned by the collinear activation of Hox genes in a two-step process. First, the sequential activation of Hoxb genes controls the relative position of their own collinear domains of expression in the forming lateral plate mesoderm, as demonstrated by functional perturbations during gastrulation. Then, within these collinear domains, we show that Hoxb4 anteriorly and Hox9 genes posteriorly, respectively, activate and repress the expression of the forelimb initiation gene Tbx5 and instruct the definitive position of the forelimb. Furthermore, by comparing the dynamics of Hoxb genes activation during zebra finch, chicken, and ostrich gastrulation, we provide evidences that changes in the timing of collinear Hox gene activation might underlie natural variation in forelimb position between different birds. Altogether, our results that characterize the cellular and molecular mechanisms underlying the regulation and natural variation of forelimb positioning in avians show a direct and early role for Hox genes in this process. 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Despite major advances in our understanding of limb patterning in three dimensions, how limbs reproducibly form along the antero-posterior axis remains largely unknown. Hox genes have long been suspected to control limb position; however, supporting evidences are mostly correlative and their role in this process is unclear. Here, we show that limb position is determined early in development through the action of Hox genes. Dynamic lineage analysis revealed that, during gastrulation, the forelimb, interlimb, and hindlimb fields are progressively generated and concomitantly patterned by the collinear activation of Hox genes in a two-step process. First, the sequential activation of Hoxb genes controls the relative position of their own collinear domains of expression in the forming lateral plate mesoderm, as demonstrated by functional perturbations during gastrulation. Then, within these collinear domains, we show that Hoxb4 anteriorly and Hox9 genes posteriorly, respectively, activate and repress the expression of the forelimb initiation gene Tbx5 and instruct the definitive position of the forelimb. Furthermore, by comparing the dynamics of Hoxb genes activation during zebra finch, chicken, and ostrich gastrulation, we provide evidences that changes in the timing of collinear Hox gene activation might underlie natural variation in forelimb position between different birds. Altogether, our results that characterize the cellular and molecular mechanisms underlying the regulation and natural variation of forelimb positioning in avians show a direct and early role for Hox genes in this process. [Display omitted] •Forelimb, interlimb, and hindlimb domains are sequentially laid during gastrulation•Temporal collinear activation controls Hox sequential expression in these domains•Hox domains differentially instruct (Hox4) or repress (Hox9) limb formation•Changes in collinear activation underlie bird natural variation in limb position How limbs reproducibly form along the vertebrate body remains largely unknown. Whereas Hox genes have long been suspected to regulate limb position, their role in this process is unclear. Here, Moreau et al. show a direct and early role for Hox genes in the regulation and natural variation of the forelimb position in birds.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>30554902</pmid><doi>10.1016/j.cub.2018.11.009</doi><orcidid>https://orcid.org/0000-0002-2264-2851</orcidid><oa>free_for_read</oa></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals Complete; Cell Press Free Archives; EZB-FREE-00999 freely available EZB journals
subjects Animals
birds
Body Patterning
Chick Embryo - embryology
chicken
Chickens
collinearity
Forelimb - embryology
gastrulation
Gastrulation - genetics
Gene Expression Regulation, Developmental
Genes, Homeobox
Hox genes
lateral plate mesoderm
limb
patterning
Songbirds - embryology
Struthioniformes - embryology
Tbx5
Transcriptional Activation
Wings, Animal - embryology
title Timed Collinear Activation of Hox Genes during Gastrulation Controls the Avian Forelimb Position
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