Proceedings of the National Academy of Sciences · 2012 · 117 citations · 42 references
Life SciencesDevelopmental BiologyGeneticsCraniofacial DevelopmentEmbryogenesisOrganogenesisCardiovascular DevelopmentCongenital Heart DiseaseHeart DevelopmentMesoderm SpecificationMuscle DevelopmentMuscle DifferentiationCardiac Development GeneticsCardiac Development PathwaysCardiac Developmental Gene RegulationCardiac SpecificationCardiogenic Mesoderm DifferentiationCraniofacial Muscle DevelopmentDevelopmental Transcription FactorsDigeorge Syndrome
The search for developmental mechanisms driving vertebrate organogenesis has paved the way toward a deeper understanding of birth defects. During embryogenesis, parts of the heart and craniofacial muscles arise from pharyngeal mesoderm (PM) progenitors. Here, we reveal a hierarchical regulatory network of a set of transcription factors expressed in the PM that initiates heart and craniofacial organogenesis. Genetic perturbation of this network in mice resulted in heart and craniofacial muscle defects, revealing robust cross-regulation between its members. We identified Lhx2 as a previously undescribed player during cardiac and pharyngeal muscle development. Lhx2 and Tcf21 genetically interact with Tbx1, the major determinant in the etiology of DiGeorge/velo-cardio-facial/22q11.2 deletion syndrome. Furthermore, knockout of these genes in the mouse recapitulates specific cardiac features of this syndrome. We suggest that PM-derived cardiogenesis and myogenesis are network properties rather than properties specific to individual PM members. These findings shed new light on the developmental underpinnings of congenital defects.
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TBX1 Is Responsible for Cardiovascular Defects in Velo-Cardio-Facial/DiGeorge Syndrome
Sandra Merscher, Birgit Funke, Jonathan A. Epstein et al. · Cell · 2001 · 988 citations
Medicine, Cardiology, Physiology +9