会议专题

ASSESSMENT OF TaqMan-MGBPROBES USEFULNESS IN THE GENOTYPING OF GSTP1 EXON 5 SNP:COMPARISON TO THE PCR-RFLP METHOD

A high-throughput genotyping method has been developed to detect single-nucleotide polymorphisms(SNP). This method utilizes the 5 -nuclease activity of Taq polymerase in conjunction with fluorogenic TaqMan-MGB Probes. GSTP1 exon 5 gene presents a single-nucleotide polymorphism (A to G) that results into an amino-acid substitution (Ile to Val). This polymorphism affects enzyme activity and widely studied in the context of SNP related to cancer susceptibility. The goal was to evaluate TaqMan-MGB Probes genotyping method usefulness in detecting a wellknown SNP in comparison to PCR-RFLP. In 321 unrelated individuals who were ethnic minority from Guizhout GSTP1 exon 5 SNP was analyzed by TaqMan-MGB probes genotyping method and PCR-RFLP method. The genotyping using both methods resulted in the characterization of 226 (70.4%) homozygous wild-type (AA), 92 (28. 7%) heterozygote (AG) and 3 (0.9%) homozygous mutant (GG). All samples were also identically genotyped by the two methods. Results show that TaqMan-MGB Probes genotyping method is a good alternative to classical PCR-RFLP method in genotyping SNPs. It is rapid, reproducible, and highly sensitive and could be applied toward fully automated large-scale genotyping

TaqMan-MGB Probes SNP GSTP1 PCR-RFLP

Wei Zhang Xilin Ren Keren Shan Changxue Wu Yi Li Yan Xiao Yan Zhao Xiaolan Qi Yan He Zhizhong Guan

The Key Lab of Molecular Biology, Guiyang Medical College, Guiyang 550004, China

国际会议

The 4th International Forum on Post-genome Technologies(4IFPT)(第四届国际后基因组生命科学技术学术论坛)

杭州

英文

81-85

2006-09-25(万方平台首次上网日期,不代表论文的发表时间)