Fifty percent of the infantile malignant osteopetrosis (IMO) cases reported in the literature present mutations in the TCIRG1 gene encoding the 116-kDa osteoclast specific subunit of the vacuolar proton ATPase (ATP6I). In this study, we identified four novel mutations in a series of six IMO patients. All of these mutations correspond to single nucleotide changes and affect splice acceptor or donor sites, resulting in aberrant transcription products. We report also a missense mutation, G405R, previously described in several Costa Rican patients. This independent finding suggests that the highly conserved residue at amino acid 405 plays a critical role in the a3 subunit function. Finally, the results of this study were used to provide a prenatal diagnosis to one of the families.
Pubmed ID: 12552563 RIS Download
Mesh terms: Chromosomes, Human, Pair 11 | Female | Genes, Recessive | Genetic Markers | Genotype | Haplotypes | Humans | Infant | Infant, Newborn | Infant, Newborn, Diseases | Male | Mutation | Organ Specificity | Osteoclasts | Osteopetrosis | Pedigree | Prenatal Diagnosis | Protein Subunits | Vacuolar Proton-Translocating ATPases
Publication data is provided by the National Library of Medicine ® and PubMed ®. Data is retrieved from PubMed ® on a weekly schedule. For terms and conditions see the National Library of Medicine Terms and Conditions.