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Analysis of methionine synthase reductase polymorphism (A66G) in Indian Muslim population.
Indian J Hum Genet ; 2013 Apr; 19(2): 183-187
Artigo em Inglês | IMSEAR | ID: sea-149427
ABSTRACT
BACKGROUND AND

OBJECTIVES:

Methionine synthase reductase (MTRR) is a vital enzyme of homocysteine/methionine metabolic pathway and is required for the conversion of inactive form of methionine synthase (MTR) to its active form. A clinically important allelic variant of MTRR A66G, with less enzymatic activity is reported with worldwide prevalence rate of ~ 30%. The present study was designed to determine the frequency of MTRR A66G polymorphism in rural Sunni Muslim population of Eastern Uttar Pradesh. MATERIALS AND

METHODS:

Total 56 subjects were analyzed for MTRR A66G polymorphism. A66G mutation analysis was carried out according to the polymerase chain reaction-restriction fragment length polymorphism method of Wilson et al. [1] amplification with MTRR specific primers followed by amplicon digestion with NdeI enzyme was used for the identification of different MTRR genotypes in subjects. RESULTS AND

DISCUSSION:

The AA genotype was found in 5 subjects, AG in 23 subjects, and GG genotype in 28 subjects. Genotype frequencies of AA, AG, and GG were 0.089, 0.41, and 0.5 respectively. The allele frequency of A allele was found to be 0.298 and G allele was 0.705.

CONCLUSION:

It is evident from the present study that the percentage of homozygous genotype GG and frequency of G allele is high in the target Muslim population.
Assuntos

Texto completo: DisponíveL Índice: IMSEAR (Sudeste Asiático) Assunto principal: Polimorfismo Genético / Idoso / Humanos / Adolescente / Adulto / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Códigos de Ética / Grupos Populacionais / Alelos País/Região como assunto: Ásia Idioma: Inglês Revista: Indian J Hum Genet Ano de publicação: 2013 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: IMSEAR (Sudeste Asiático) Assunto principal: Polimorfismo Genético / Idoso / Humanos / Adolescente / Adulto / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Códigos de Ética / Grupos Populacionais / Alelos País/Região como assunto: Ásia Idioma: Inglês Revista: Indian J Hum Genet Ano de publicação: 2013 Tipo de documento: Artigo