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Rapid screening for MTHFR gene 677C>T polymorphism in Down syndrome using high resolution melting curve and pyrosequencing / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 528-533, 2013.
Article Dans Chinois | WPRIM | ID: wpr-237213
ABSTRACT
<p><b>OBJECTIVE</b>To establish a rapid method for detecting MTHFR gene 677C>T polymorphisms with high-resolution melting curve method (HRM) and pyrosequencing.</p><p><b>METHODS</b>Peripheral blood samples were collected from 155 Down syndrome patients and 182 normal controls from Children's Hospital of Shanghai. The accuracy of three methods including regular HRM, internal control HRM and artificial heterozygosity HRM was compared. Meanwhile, allele frequencies in 10, 30 and 50 mixed samples were measured with pyrosequencing, and the results were compared with that of HRM.</p><p><b>RESULTS</b>Heterozygosity of 677C>T polymorphism could be distinguished by various HRM methods. However, homozygotes CC and TT were only identifiable by internal control HRM and artificial heterozygosity HRM. The accuracy of pyrosequencing for allele frequency has improved with increased sample number. When the number of mixed samples has exceeded 30, the difference between pyrosequencing results and actual values became less than 4%. TT genotype was more frequent in Down syndrome patients than controls (25.2% vs. 14.3%). No significant difference was found in T allele frequency between the two groups (44.9% vs. 40.1%).</p><p><b>CONCLUSION</b>Respectively, internal control HRM and pyrosequencing may be ideal methods for determination of genotypic and allelic frequencies.</p>
Sujets)
Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Analyse de séquence d&apos;ADN / Mutation ponctuelle / Syndrome de Down / Polymorphisme de nucléotide simple / Methylenetetrahydrofolate reductase (NADPH2) / Température de transition / Diagnostic / Génétique / Méthodes Type d'étude: Etude diagnostique / Étude de dépistage Limites du sujet: Enfant / Enfant d'âge préscolaire / Femelle / Humains / Mâle langue: Chinois Texte intégral: Chinese Journal of Medical Genetics Année: 2013 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Analyse de séquence d&apos;ADN / Mutation ponctuelle / Syndrome de Down / Polymorphisme de nucléotide simple / Methylenetetrahydrofolate reductase (NADPH2) / Température de transition / Diagnostic / Génétique / Méthodes Type d'étude: Etude diagnostique / Étude de dépistage Limites du sujet: Enfant / Enfant d'âge préscolaire / Femelle / Humains / Mâle langue: Chinois Texte intégral: Chinese Journal of Medical Genetics Année: 2013 Type: Article