Roberts Rebecca L, Kennedy Martin A
Department of Pathology, Christchurch School of Medicine and Health Sciences, PO Box 4345, Christchurch, New Zealand.
Clin Chim Acta. 2006 Apr;366(1-2):348-51. doi: 10.1016/j.cca.2005.11.008. Epub 2005 Dec 20.
CYP2D6 is a highly polymorphic enzyme that mediates the metabolism of around 20% of all currently prescribed drugs. Genetic variability within CYP2D6 results in poor (PM), intermediate (IM), extensive (EM) and ultra-rapid metabolisers (UM) of CYP2D6 substrates. Here we describe an assay which is able to detect the major PM (CYP2D6*3, *4, *5, 6), IM (CYP2D69, *10, 41) and UM (CYP2D6nxn) alleles found in Caucasians. This assay is performed in two stages. The first stage is a multiplex long-range PCR which is used to simultaneously screen for whole gene deletions and duplications while isolating CYP2D6 from the CYP2D gene cluster to avoid pseudogene contamination. In the second stage, individuals with one or more copies of CYP2D6 are genotyped for PM and IM alleles using a two-tube multiplex Amplification Refractory Mutation System (ARMS). The specificity and reliability of the multiplex long-range PCR and subsequent ARMS were confirmed using a panel of positive controls that had been previously validated by PCR-RFLPs and DNA sequencing. This two-stage assay offers a robust and cheap alternative to many currently available CYP2D6 genotyping approaches. Our entire assay, once patient DNA has been extracted, can be run within 7 h using 10 microl PCRs.
细胞色素P450 2D6(CYP2D6)是一种高度多态性的酶,介导目前约20%的处方药的代谢。CYP2D6基因的变异性导致CYP2D6底物的代谢能力差(PM)、中等(IM)、广泛(EM)和超快速代谢者(UM)。在此,我们描述了一种能够检测高加索人群中主要的PM(CYP2D6*3、*4、*5、6)、IM(CYP2D69、*10、41)和UM(CYP2D6nxn)等位基因的检测方法。该检测分两个阶段进行。第一阶段是多重长程PCR,用于同时筛查全基因缺失和重复,同时从CYP2D基因簇中分离CYP2D6,以避免假基因污染。在第二阶段,使用两管多重扩增不应突变系统(ARMS)对具有一个或多个CYP2D6拷贝的个体进行PM和IM等位基因基因分型。使用一组先前已通过PCR-限制性片段长度多态性(RFLP)和DNA测序验证的阳性对照,确认了多重长程PCR和随后的ARMS的特异性和可靠性。这种两阶段检测方法为许多目前可用的CYP2D6基因分型方法提供了一种强大且廉价的替代方案。一旦提取了患者DNA,我们的整个检测可以在7小时内使用10微升PCR进行。