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      WNT signaling, in synergy with T/TBX6, controls Notch signaling by regulating Dll1 expression in the presomitic mesoderm of mouse embryos.

      Genes & development
      Animals, Body Patterning, CHO Cells, Cells, Cultured, Cricetinae, DNA-Binding Proteins, genetics, metabolism, Drug Synergism, Gene Expression Regulation, Developmental, Homeodomain Proteins, Humans, Intracellular Signaling Peptides and Proteins, Ligands, Luciferases, Lymphoid Enhancer-Binding Factor 1, Membrane Proteins, Mesoderm, Mice, Mice, Transgenic, Promoter Regions, Genetic, Proto-Oncogene Proteins, pharmacology, Receptors, Notch, Signal Transduction, Somites, Tail, cytology, embryology, physiology, Transcription Factors, Transcription, Genetic, Wnt Proteins

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          Abstract

          Notch signaling in the presomitic mesoderm (psm) is critical for somite formation and patterning. Here, we show that WNT signals regulate transcription of the Notch ligand Dll1 in the tailbud and psm. LEF/TCF factors cooperate with TBX6 to activate transcription from the Dll1 promoter in vitro. Mutating either T or LEF/TCF sites in the Dll1 promoter abolishes reporter gene expression in vitro as well as in the tail bud and psm of transgenic embryos. Our results indicate that WNT activity, in synergy with TBX6, regulates Dll1 transcription and thereby controls Notch activity, somite formation, and patterning.

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