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</script>The bHLH regulator pMesogenin1 is required for maturation and segmentation of paraxial mesoderm
The bHLH regulator pMesogenin1 is required for maturation and segmentation of paraxial mesoderm
Paraxial mesoderm in vertebrates gives rise to all trunk and limb skeletal muscles, the trunk skeleton, and portions of the trunk dermis and vasculature. We show here that germline deletion of mousepMesogenin1, a bHLH class gene specifically expressed in developmentally immature unsegmented paraxial mesoderm, causes complete failure of somite formation and segmentation of the body trunk and tail. At the molecular level, the phenotype features dramatic loss of expression within the presomitic mesoderm of Notch/Deltapathway components and oscillating somitic clock genes that are thought to control segmentation and somitogenesis. Subsequent patterning and specification steps for paraxial mesoderm also fail, leading to a complete absence of all trunk paraxial mesoderm derivatives, which include skeletal muscle, vertebrae, and ribs. We infer thatpMesogenin1 is an essential upstream regulator of trunk paraxial mesoderm development and segmentation.
- California Institute of Technology United States
Fetal Proteins, Male, Receptors, Notch, Helix-Loop-Helix Motifs, Homozygote, Gene Expression Regulation, Developmental, Glycosyltransferases, Membrane Proteins, Proteins, Cell Differentiation, Mice, Inbred Strains, Mice, Mutant Strains, Fungal Proteins, Mesoderm, Embryonic and Fetal Development, Mice, Basic Helix-Loop-Helix Transcription Factors, Animals, Abnormalities, Multiple, Female
Fetal Proteins, Male, Receptors, Notch, Helix-Loop-Helix Motifs, Homozygote, Gene Expression Regulation, Developmental, Glycosyltransferases, Membrane Proteins, Proteins, Cell Differentiation, Mice, Inbred Strains, Mice, Mutant Strains, Fungal Proteins, Mesoderm, Embryonic and Fetal Development, Mice, Basic Helix-Loop-Helix Transcription Factors, Animals, Abnormalities, Multiple, Female
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