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β-Catenin directly regulates Islet1 expression in cardiovascular progenitors and is required for multiple aspects of cardiogenesis

β-Catenin directly regulates Islet1 expression in cardiovascular progenitors and is required for multiple aspects of cardiogenesis
Recent studies have demonstrated that the LIM homeodomain transcription factor Islet1 (Isl1) marks pluripotent cardiovascular progenitor cells and is required for proliferation, survival, and migration of recently defined second heart field progenitors. Factors that are upstream of Isl1 in cardiovascular progenitors have not yet been defined. Here we demonstrate that β-catenin is required for Isl1 expression in cardiac progenitors, directly regulating the Isl1 promoter. Ablation of β- catenin in Isl1-expressing progenitors disrupts multiple aspects of cardiogenesis, resulting in embryonic lethality at E13. β-Catenin is also required upstream of a number of genes required for pharyngeal arch, outflow tract, and/or atrial septal morphogenesis, including Tbx2 , Tbx3 , Wnt11 , Shh , and Pitx2 . Our findings demonstrate that β-catenin signaling regulates proliferation and survival of cardiac progenitors.
- University of California, San Diego United States
- Max Planck Institute of Neurobiology Germany
- University of Hong Kong China (People's Republic of)
- University of Montana United States
- Max Planck Society Germany
Cardiac progenitors, 572, LIM-Homeodomain Proteins, Molecular Sequence Data, Apoptosis, Mice, Transgenic, Cardiovascular System, Mice, Cell Movement, Animals, Humans, Cell Proliferation, Direct target, Homeodomain Proteins, Cardiac morphogenesis, Base Sequence, Myocardium, Stem Cells, Gene Expression Regulation, Developmental, Cell Differentiation, Heart, Isl1, Embryo, Mammalian, Mutation, Pharyngeal Muscles
Cardiac progenitors, 572, LIM-Homeodomain Proteins, Molecular Sequence Data, Apoptosis, Mice, Transgenic, Cardiovascular System, Mice, Cell Movement, Animals, Humans, Cell Proliferation, Direct target, Homeodomain Proteins, Cardiac morphogenesis, Base Sequence, Myocardium, Stem Cells, Gene Expression Regulation, Developmental, Cell Differentiation, Heart, Isl1, Embryo, Mammalian, Mutation, Pharyngeal Muscles
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