Publication | Open Access
ATP4a Is Required for Wnt-Dependent Foxj1 Expression and Leftward Flow in Xenopus Left-Right Development
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Citations
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References
2012
Year
Molecular RegulationGeneticsMolecular GeneticsWnt-dependent Foxj1 ExpressionCellular PhysiologyEmbryologyTranscriptional RegulationSymmetry BreakageLeftward FlowMolecular PhysiologyXenopus Left-right DevelopmentDevelopmental GeneticsMedicineIon ChannelsMorphogenesisEmbryonic DevelopmentOrganogenesisGene ExpressionNervous SystemCell BiologyBiologySignal TransductionDevelopmental BiologyEvolutionary Developmental BiologyGap JunctionsPhysiologyGene RegulationCell Fate DeterminationCell PolarityCilia-driven Leftward Flow
Most vertebrate embryos break symmetry by a cilia-driven leftward flow during neurulation. In the frog Xenopus asymmetric expression of the ion pump ATP4a was reported at the 4-cell stage. The "ion-flux" model postulates that symmetry is broken flow-independently through an ATP4-generated asymmetric voltage gradient that drives serotonin through gap junctions to one side of the embryo. Here, we show that ATP4a is symmetrically expressed. Gene knockdown or pharmacological inhibition compromised organ situs, asymmetric marker gene expression, and leftward flow. The gastrocoel roof plate (GRP), where flow in frog occurs, revealed fewer, shortened, and misaligned cilia. Foxj1, a master control gene of motile cilia, was downregulated in the superficial mesoderm, from which the GRP develops. Specifically, ATP4 was required for Wnt/β-catenin-regulated Foxj1 induction and Wnt/PCP-dependent cilia polarization. Our work argues for evolutionary conservation of symmetry breakage in the vertebrates.
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