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Mutations in capillary morphogenesis gene-2 result in the allelic disorders juvenile hyaline fibromatosis and infantile systemic hyalinosis.

http://www.ncbi.nlm.nih.gov/pubmed/12973667

Juvenile hyaline fibromatosis (JHF) and infantile systemic hyalinosis (ISH) are autosomal recessive syndromes of unknown etiology characterized by multiple, recurring subcutaneous tumors, gingival hypertrophy, joint contractures, osteolysis, and osteoporosis. Both are believed to be allelic disorders; ISH is distinguished from JHF by its more severe phenotype, which includes hyaline deposits in multiple organs, recurrent infections, and death within the first 2 years of life. Using the previously reported chromosome 4q21 JHF disease locus as a guide for candidate-gene identification, we identified and characterized JHF and ISH disease-causing mutations in the capillary morphogenesis factor-2 gene (CMG2). Although CMG2 encodes a protein upregulated in endothelial cells during capillary formation and was recently shown to function as an anthrax-toxin receptor, its physiologic role is unclear. Two ISH family-specific truncating mutations, E220X and the 1-bp insertion P357insC that results in translation of an out-of-frame stop codon, were generated by site-directed mutagenesis and were shown to delete the CMG-2 transmembrane and/or cytosolic domains, respectively. An ISH compound mutation, I189T, is predicted to create a novel and destabilizing internal cavity within the protein. The JHF family-specific homoallelic missense mutation G105D destabilizes a von Willebrand factor A extracellular domain alpha-helix, whereas the other mutation, L329R, occurs within the transmembrane domain of the protein. Finally, and possibly providing insight into the pathophysiology of these diseases, analysis of fibroblasts derived from patients with JHF or ISH suggests that CMG2 mutations abrogate normal cell interactions with the extracellular matrix.

Pubmed ID: 12973667 RIS Download

Mesh terms: Amino Acid Sequence | Base Sequence | Child | Chromosome Mapping | Exons | Female | Fibroma | Genes, Recessive | Genetic Markers | Glomerulosclerosis, Focal Segmental | Humans | Infant | Male | Membrane Proteins | Models, Molecular | Mutation, Missense | Pedigree | Protein Conformation | Protein Structure, Secondary | Receptors, Peptide | Syndrome

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Associated grants

  • Agency: NHLBI NIH HHS, Id: HL59373
  • Agency: NCRR NIH HHS, Id: S10 RR 015935

Comparative Toxicogenomics Database (Data, Disease Annotation)

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