A rapid screening method for a single nucleotide polymorphism (SNP) in the human MOR gene

被引:23
作者
Grösch, S [1 ]
Niederberger, E [1 ]
Lötsch, J [1 ]
Skarke, C [1 ]
Geisslinger, G [1 ]
机构
[1] Univ Frankfurt Klinikum, Inst Klin Pharmakol, Pharmazentrum Frankfurt, D-60590 Frankfurt, Germany
关键词
mu opioid receptor (MOR); fluorescence resonance energy transfer (FRET); LightCycler; polymorphism; SNP;
D O I
10.1046/j.0306-5251.2001.01504.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aims Genetic association Studies have suggested chat the single nucleotide polymorphism (SNP) at position 118 of the human mu -opioid receptor (MOR) gene could be a potential risk Factor For drug treatment variability in patients. Therefore, we wanted to develop a fast and reliable detection method for this SNP which is applicable in a clinical setting. Methods To detect the polymorphism at position A118-->G in the human MOR, gene we used the fluorescence resonance energy transfer (FRET)-PCR technique with subsequent melting curve analysis. Results The polymorphism at position A118-->G in the human MOR gene could be clearly discriminated with melting peak temperatures of 69.8 degrees C and 63.8 degrees C, corresponding to the wild type and mutated MOR allele, respectively. The results from FRET-PCR were validated by sequencing and restriction-fragment length polymorphism (RFLP). Screening of blood samples from 100 subjects showed an allelic distribution for the human MOR alleles of 79% homozygous wild type). 20% (heterozygous) and 0.9% (homozygous mutated). Conclusions The FRET-PCR protocol for detection of the human MOR gene polymorphism at position 118 offers a rapid and reliable method which could be used for population screening of this and other genes.
引用
收藏
页码:711 / 714
页数:4
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