The GST domain of GDAP1 is a frequent target of mutations in the dominant form of axonal Charcot Marie Tooth type 2K
| Autor: | Luciana Losito, C Baschirotto, Nereo Bresolin, Giovanni Airoldi, Sara Bonato, Maria Grazia D'Angelo, Antonio Trabacca, Alessandra Tonelli, M. T. Bassi, Claudia Crimella |
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| Přispěvatelé: | E. Medea Scientific Institute, Laboratory of Molecular Biology, Bosisio Parini., E. Medea Scientific Institute, 1Laboratory of Molecular Biology, Bosisio Parini., E. Medea Scientific Institute, Neuromuscular and Neurorehabilitation Unit, Bosisio Parini, E. Medea Scientific Institute, Unit of Neurorehabilitation I, Developmental Neurology and Functiona, Centro Dino Ferrari [Milano], Università degli Studi di Milano [Milano] (UNIMI)-Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico |
| Jazyk: | angličtina |
| Rok vydání: | 2010 |
| Předmět: |
Adult
medicine.medical_specialty Adolescent DNA Mutational Analysis Molecular Sequence Data Mutation Missense Nerve Tissue Proteins Disease Biology medicine.disease_cause Young Adult 03 medical and health sciences 0302 clinical medicine Degenerative disease Charcot-Marie-Tooth Disease Molecular genetics Peripheral nerve disease medicine Genetics Humans Missense mutation Age of Onset Mutation frequency Child Gene Genetics (clinical) Genes Dominant Glutathione Transferase 030304 developmental biology 0303 health sciences Mutation Sequence Analysis DNA medicine.disease Phenotype Axons Pedigree Electrophysiology Italy Neurology Child Preschool Diagnostics tests Gene Deletion 030217 neurology & neurosurgery |
| Zdroj: | Journal of Medical Genetics Journal of Medical Genetics, BMJ Publishing Group, 2010, 47 (10), pp.712. ⟨10.1136/jmg.2010.077909⟩ |
| ISSN: | 0022-2593 1468-6244 |
| DOI: | 10.1136/jmg.2010.077909⟩ |
| Popis: | International audience; Background: Mutations in GDAP1 associate with both demyelinating (CMT4A) and axonal (CMT2K) forms of CMT. While CMT4A shows recessive inheritance, CMT2K can present with either recessive (AR-CMT2K) or dominant segregation pattern (AD-CMT2K), the latter being characterized by milder phenotypes and later onset. The majority of the GDAP1 mutations are associated with CMT4A and AR-CMT2K, with only 4 heterozygous mutations identified in AD-CMT2K. Methods: We screened GDAP1 gene in a series of 43 index patients, 39 with CMT2 and 4 with intermediate CMT, with both sporadic and familial occurrence of the disease. Results: Three novel mutations were identified in three families with dominant segregation of the disease: two missense changes, p.Arg226Ser and p.Ser34Cys, affecting the GST domain of the GDAP1 protein and a novel deletion (c.23delAG) leading to early truncation of the protein upstream the GST domain. Wide variability in clinical presentation is shared by all three families mostly in terms of age at onset and disease severity. A rare variant p.Gly269Arg, located within the GST domain, apparently acts as phenotype modulator in the family carrying the deletion. Conclusion: The results obtained reveal a GDAP1 mutation frequency of 27% in the dominant families analyzed, a figure still unreported for this gene, thus suggesting that GDAP1 involvement in dominant CMT2 might be higher than expected. |
| Databáze: | OpenAIRE |
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