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Smoothened mutants reveal redundant roles for Shh and Ihh signaling including regulation of L/R symmetry by the mouse node.

Cell | Jul 27, 2001

Genetic analyses in Drosophila have demonstrated that the multipass membrane protein Smoothened (Smo) is essential for all Hedgehog signaling. We show that Smo acts epistatic to Ptc1 to mediate Shh and Ihh signaling in the early mouse embryo. Smo and Shh/Ihh compound mutants have identical phenotypes: embryos fail to turn, arresting at somite stages with a small, linear heart tube, an open gut and cyclopia. The absence of visible left/right (L/R) asymmetry led us to examine the pathways controlling L/R situs. We present evidence consistent with a model in which Hedgehog signaling within the node is required for activation of Gdf1, and induction of left-side determinants. Further, we demonstrate an absolute requirement for Hedgehog signaling in sclerotomal development and a role in cardiac morphogenesis.

Pubmed ID: 11517919 RIS Download

Mesh terms: Animals | Body Patterning | DNA-Binding Proteins | Drosophila Proteins | Embryo, Mammalian | Embryonic Induction | Epistasis, Genetic | Gene Expression Regulation, Developmental | Growth Differentiation Factor 1 | Growth Substances | Heart | Hedgehog Proteins | Homeobox Protein Nkx-2.5 | Homeodomain Proteins | In Situ Hybridization | Intercellular Signaling Peptides and Proteins | Membrane Proteins | Mice | Models, Biological | Muscle Proteins | Mutation | Myogenic Regulatory Factor 5 | Nerve Tissue Proteins | Patched Receptors | Patched-1 Receptor | Proteins | RNA, Messenger | Receptors, Cell Surface | Receptors, G-Protein-Coupled | Signal Transduction | Smoothened Receptor | Somites | Trans-Activators | Transcription Factors | Xenopus Proteins

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Associated grants

  • Agency: NINDS NIH HHS, Id: NS33642

Gene Ontology (Data, Gene Annotation)

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