OBJECTIVES: To study the variability at the myotonic dystrophy protein kinase (DMPK) gene in a Chilean sample of healthy people. DM1 is an autosomal dominant disorder caused by an expansion of a (CTG) repeat at the 3'-UTR of the gene DMPK. Healthy individuals have alleles under 35 repeats and diseased individuals have over 50. METHODS: Genotyping the number of (CTG) repeats at this gene in a sample of healthy Chilean people. RESULTS: Allele frequencies were significantly different from those of other populations. The most frequent allele was with five repeats. The frequency of larger alleles (>18 CTG repeats) was 11%, close to the European frequency (12%) and higher than the Japanese (8%) and Aboriginal Pehuenche samples (8%). CONCLUSIONS: Allelic frequencies in the Chilean sample studied were intermediate between those of the two ancestral populations (European and Pehuenche).
OBJECTIVES: To study the variability at the myotonic dystrophy protein kinase (DMPK) gene in a Chilean sample of healthy people. DM1 is an autosomal dominant disorder caused by an expansion of a (CTG) repeat at the 3'-UTR of the gene DMPK. Healthy individuals have alleles under 35 repeats and diseased individuals have over 50. METHODS: Genotyping the number of (CTG) repeats at this gene in a sample of healthy Chilean people. RESULTS: Allele frequencies were significantly different from those of other populations. The most frequent allele was with five repeats. The frequency of larger alleles (>18 CTG repeats) was 11%, close to the European frequency (12%) and higher than the Japanese (8%) and Aboriginal Pehuenche samples (8%). CONCLUSIONS: Allelic frequencies in the Chilean sample studied were intermediate between those of the two ancestral populations (European and Pehuenche).
Authors: J J Magaña; P Cortés-Reynosa; R Escobar-Cedillo; R Gómez; N Leyva-García; B Cisneros Journal: Mol Biol Rep Date: 2010-07-16 Impact factor: 2.316