Novel mutations in theTCIRG1gene encoding the a3 subunit of the vacuolar proton pump in patients affected by infantile malignant osteopetrosis
doi: 10.1002/humu.10165
pmid: 12552563
Novel mutations in theTCIRG1gene encoding the a3 subunit of the vacuolar proton pump in patients affected by infantile malignant osteopetrosis
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.
- French National Centre for Scientific Research France
- Necker-Enfants Malades Hospital France
- Hôpital de la Timone France
- Nice Sophia Antipolis University France
- Université Côte d'Azur France
Genetic Markers, Male, Vacuolar Proton-Translocating ATPases, Genotype, Osteoclasts, Genes, Recessive, [SDV.BC.IC] Life Sciences [q-bio]/Cellular Biology/Cell Behavior [q-bio.CB], [SDV.BBM.BM] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology, Infant, Newborn, Diseases, [SDV.CAN] Life Sciences [q-bio]/Cancer, Prenatal Diagnosis, Humans, [SDV.BBM.BC] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Biochemistry [q-bio.BM], [SDV.MHEP.RSOA] Life Sciences [q-bio]/Human health and pathology/Rhumatology and musculoskeletal system, Chromosomes, Human, Pair 11, Infant, Newborn, Infant, Pedigree, [SDV.IB.BIO] Life Sciences [q-bio]/Bioengineering/Biomaterials, Protein Subunits, Haplotypes, Organ Specificity, Osteopetrosis, Mutation, [SDV.BBM.GTP] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], Female
Genetic Markers, Male, Vacuolar Proton-Translocating ATPases, Genotype, Osteoclasts, Genes, Recessive, [SDV.BC.IC] Life Sciences [q-bio]/Cellular Biology/Cell Behavior [q-bio.CB], [SDV.BBM.BM] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology, Infant, Newborn, Diseases, [SDV.CAN] Life Sciences [q-bio]/Cancer, Prenatal Diagnosis, Humans, [SDV.BBM.BC] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Biochemistry [q-bio.BM], [SDV.MHEP.RSOA] Life Sciences [q-bio]/Human health and pathology/Rhumatology and musculoskeletal system, Chromosomes, Human, Pair 11, Infant, Newborn, Infant, Pedigree, [SDV.IB.BIO] Life Sciences [q-bio]/Bioengineering/Biomaterials, Protein Subunits, Haplotypes, Organ Specificity, Osteopetrosis, Mutation, [SDV.BBM.GTP] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], Female
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