RESUMO
Polymorphism of highly polymorphic triplet repeats CTG of the 3'-untranslated region of the myotonin protein kinase gene and CAG of the genes associated with dentatorobral-pallidoluysian atrophy (DRPLA, or Hew River syndrome) and spinocerebellar ataxia type 1 (SCA1) was analyzed in several ethnic populations of Russia. A difference in allele spectra of the three genes was demonstrated for populations differing in ethnic origin.
Assuntos
Genética Populacional , Proteínas do Tecido Nervoso/genética , Proteínas Nucleares/genética , Polimorfismo Genético , Proteínas Serina-Treonina Quinases/genética , Repetições de Trinucleotídeos , Regiões 3' não Traduzidas , Alelos , Ataxina-1 , Ataxinas , Humanos , Miotonina Proteína Quinase , Sibéria/etnologiaRESUMO
Frequencies of the wild-type and null genotypes of the GSTM1 and GSTT1 genes were established in healthy donors from several Russian populations (ethnic Russians from the towns of Oshevensk and Kholmogory, Arkhangel'sk oblast; ethnic Khants; ethnic Kalmyks; and ethnic Buryats) in order to identify the ethnic group with the maximal frequency of the null genotype. The highest frequency of individuals with the null genotype of both genes was observed in the Kalmyk and Buryat populations. The results may be used to study the effect of climatic and ecological conditions on multifactorial disease incidence in populations.