The p.R1109X mutation in SH3TC2 gene is predominant in Spanish Gypsies with Charcot-Marie-Tooth disease type 4

• Published in: Clinical genetics 2007-04, Vol.71 (4), p.343-349
• Main Authors: Claramunt, R, Sevilla, T, Lupo, V, Cuesta, A, Millán, JM, Vílchez, JJ, Palau, F, Espinós, C
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; Charcot-Marie-Tooth Disease - classification; Charcot-Marie-Tooth Disease - genetics; Charcot-Marie-Tooth disease type 4; Chromosome Mapping; Chromosomes, Human, Pair 10 - genetics; Chromosomes, Human, Pair 5 - genetics; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases; Evolution, Molecular; Female; Founder Effect; Fundamental and applied biological sciences. Psychology; General aspects. Genetic counseling; Genes, Recessive; Genetics of eukaryotes. Biological and molecular evolution; gypsy population; Haplotypes; Human; Humans; Male; Medical genetics; Medical sciences; Molecular and cellular biology; Neurology; Pedigree; Point Mutation; Population genetics, reproduction patterns; Proteins - genetics; Roma - genetics; SH3TC2 gene; Spain
• ISSN: 0009-9163; 1399-0004
• DOI: 10.1111/j.1399-0004.2007.00774.x

Charcot–Marie–Tooth (CMT) disease type 4 (CMT4) is the name given to autosomal recessive forms of hereditary motor and sensory neuropathy (HMSN). When we began this study, three genes or loci associated with inherited peripheral neuropathies had already been identified in the European Gypsy population: HMSN‐Lom (MIM 601455), HMSN‐Russe (MIM 605285) and the congenital cataracts facial dysmorphism neuropathy syndrome (MIM 604168). We have carried out genetic analyses in a series of 20 Spanish Gypsy families diagnosed with a demyelinating CMT disease compatible with an autosomal recessive trait. We found the p.R148X mutation in the N‐myc downstream‐regulated gene 1 gene to be responsible for the HMSN‐Lom in four families and also possible linkage to the HMSN‐Russe locus in three others. We have also studied the CMT4C locus because of the clinical similarities and showed that in 10 families, the disease is caused by mutations located on the SH3 domain and tetratricopeptide repeats 2 (SH3TC2) gene: p.R1109X in 20 out of 21 chromosomes and p.C737_P738delinsX in only one chromosome. Moreover, the SH3TC2 p.R1109X mutation is associated with a conserved haplotype and, therefore, may be a private founder mutation for the Gypsy population. Estimation of the allelic age revealed that the SH3TC2 p.R1109X mutation may have arisen about 225 years ago, probably as the consequence of a bottleneck.