中国医药
中國醫藥
중국의약
CHINA MEDICINE
2013年
4期
472-474
,共3页
李杰%刘双%郭伟%陈勇%高元明
李傑%劉雙%郭偉%陳勇%高元明
리걸%류쌍%곽위%진용%고원명
荧光聚合酶链反应%维生素K环氧化物还原酶%细胞色素P450 2C9
熒光聚閤酶鏈反應%維生素K環氧化物還原酶%細胞色素P450 2C9
형광취합매련반응%유생소K배양화물환원매%세포색소P450 2C9
Fluorescence polymerase chain reaction%Vitamin K epoxide reductase complex subunt 1%Cytochrome P450 2C9
目的 建立一种快速、准确、简便、经济的检测维生素K环氧化物还原酶复合体亚单位1(VKORC1)和细胞色素P450 2C9(CYP2C9)基因型的方法.方法 提取220例肺栓塞患者外周血的DNA,针对2个基因的SNP位点设计特异性引物,并进行荧光聚合酶链反应(PCR),根据荧光PCR的熔解曲线分析样本的基因型.同时对样本进行传统的限制性酶切片段长度多态性(PCR-RFLP)基因分型,从时间、通量、费用、准确性等方面对2种方法进行比较.结果 VKORC1 1693G>A和CYP2C9 1075A>C两个SNP位点的不同基因型具有不同的熔解曲线峰型.220例样本中,VKORC1基因AA型184例,AG型34例,GG型2例,各占83.6%、15.5%、0.9%;CYP2C9基因*1/*1型201例,*1/*3型19例,各占91.4,%、8.6%,无*3/*3型纯合子.PCR-RFLP检测结果与上述结果基本相同.2种方法相比,前者较后者操作步骤少,用时少,费用相当,结果更准确.结论 利用荧光PCR检测VKORC1及CYP2C9的SNP分型操作简便、快速、经济、准确,适用于临床实验室开展基因分型.
目的 建立一種快速、準確、簡便、經濟的檢測維生素K環氧化物還原酶複閤體亞單位1(VKORC1)和細胞色素P450 2C9(CYP2C9)基因型的方法.方法 提取220例肺栓塞患者外週血的DNA,針對2箇基因的SNP位點設計特異性引物,併進行熒光聚閤酶鏈反應(PCR),根據熒光PCR的鎔解麯線分析樣本的基因型.同時對樣本進行傳統的限製性酶切片段長度多態性(PCR-RFLP)基因分型,從時間、通量、費用、準確性等方麵對2種方法進行比較.結果 VKORC1 1693G>A和CYP2C9 1075A>C兩箇SNP位點的不同基因型具有不同的鎔解麯線峰型.220例樣本中,VKORC1基因AA型184例,AG型34例,GG型2例,各佔83.6%、15.5%、0.9%;CYP2C9基因*1/*1型201例,*1/*3型19例,各佔91.4,%、8.6%,無*3/*3型純閤子.PCR-RFLP檢測結果與上述結果基本相同.2種方法相比,前者較後者操作步驟少,用時少,費用相噹,結果更準確.結論 利用熒光PCR檢測VKORC1及CYP2C9的SNP分型操作簡便、快速、經濟、準確,適用于臨床實驗室開展基因分型.
목적 건립일충쾌속、준학、간편、경제적검측유생소K배양화물환원매복합체아단위1(VKORC1)화세포색소P450 2C9(CYP2C9)기인형적방법.방법 제취220례폐전새환자외주혈적DNA,침대2개기인적SNP위점설계특이성인물,병진행형광취합매련반응(PCR),근거형광PCR적용해곡선분석양본적기인형.동시대양본진행전통적한제성매절편단장도다태성(PCR-RFLP)기인분형,종시간、통량、비용、준학성등방면대2충방법진행비교.결과 VKORC1 1693G>A화CYP2C9 1075A>C량개SNP위점적불동기인형구유불동적용해곡선봉형.220례양본중,VKORC1기인AA형184례,AG형34례,GG형2례,각점83.6%、15.5%、0.9%;CYP2C9기인*1/*1형201례,*1/*3형19례,각점91.4,%、8.6%,무*3/*3형순합자.PCR-RFLP검측결과여상술결과기본상동.2충방법상비,전자교후자조작보취소,용시소,비용상당,결과경준학.결론 이용형광PCR검측VKORC1급CYP2C9적SNP분형조작간편、쾌속、경제、준학,괄용우림상실험실개전기인분형.
Objective To establish a rapid,accurate,simple and economical method for detecting gene polymorphisms of vitamin K epoxide reductase complex subunit 1 (VKORC1) and cytochrome P450 2C9 (CYP2C9).Methods The DNA extracted from the peripheral blood from 220 patients with pulmonary embolism were examined.The specific primers were designed regarding of the two gene SNP sites,and the real tiem PCR was performed.According to the fluorescence PCR melting curve,sample genotypes were analyzed.At the same time,the genotypes of these samples were detected by the traditional restriction enzyme fragment length polymorphism (PCR-RFLP).The expense of the time,the cost and the accuracy of two methods were compared.Results Different genotypes of VKORC1-1693 G > A and CYP2C9 1075 A > C has different melt curve peak patterns.Among 220 samples,there were 177 cases VKORC1 AA of 34 cases,AG 2cases GG,which represente 83.6%,15.5%,0.9% respectively; CYP2C9 * 1/* 1 201 cases,19 cases * 1/* 3 type,each accounted for 91.4 %,8.6%,no * 3/* 3 homozygote.The testing results of PCR-RFLP were basically the same with the former.Comparing the two kinds of methods,the PCR method need less operation steps,spent less time,cost equal,and the results are more accurate than the latter.Conclusion Fluorescence PCR is the fast,simple,economic and accurate method to detect the genotypes of VKORC1 and CYP2C9 which is suitable for the genotyping in clinical laboratory.