کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2041101 | 1073145 | 2012 | 12 صفحه PDF | دانلود رایگان |

SummaryMost 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.
Graphical AbstractFigure optionsDownload as PowerPoint slideHighlights
► ATP4 is required during gastrulation/neurulation for cilia-driven leftward flow to occur
► ATP4 acts on canonical and noncanonical Wnt signaling
► Wnt/β-catenin is necessary and sufficient for gastrula Foxj1 expression
► Leftward flow is the conserved mode of symmetry breakage in Xenopus
Journal: - Volume 1, Issue 5, 31 May 2012, Pages 516–527