Rapid genotyping of the OATP1B1 polymorphisms A388G and T521C with real-time PCR FRET assays

被引:6
作者
den Buijsch, RAMO
Bekers, O
Wijnen, PAHM
van Dieijen-Visser, MP
de Vries, JE
机构
[1] Univ Hosp Maastricht, Dept Clin Chem, NL-6202 AZ Maastricht, Netherlands
[2] Univ Hosp Maastricht, Dept Biochem & Clin Genet, NL-6202 AZ Maastricht, Netherlands
关键词
FRET assays; LightCycler; OATP-C; polymorphisms;
D O I
10.1517/14622416.6.4.393
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The polymorphisms (OATP)1B1 A388G and T521C of the solute carrier organic anion-transporter family member 1131 gene (SLCO1B1), previously known as OATP-C, have potential impacts on drug metabolism. In order to establish a fast and consistent assay for these polymorphisms, rapid speed polymerase chain reaction (PCR) fluorescence resonance energy transfer (FRET) assays on the LightCycler (R) were developed for both OATP1B1 polymorphisms. A locked nucleic acid (LNA) on the polymorphic location within the sensor probe was necessary to discriminate both alleles of the OATP1B1 T521C polymorphism. To confirm the reliability of both real-time PCR FRET assays, these new methods were validated by genotyping 120 samples using a PCR restriction fragment length polymorphism (RFLP) assay and an allele-specific PCR. The results of the real-time PCR FRET assays were completely in line with conventional PCR methods, indicating that the real-time PCR FRET assays are appropriate for clinical settings.
引用
收藏
页码:393 / 397
页数:5
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