中国临床药理学与治疗学
中國臨床藥理學與治療學
중국림상약이학여치료학
CHINESE JOURNAL OF CLINICAL PHARMACOLOGY
2002年
2期
100-105
,共6页
严奉祥%廖端芳%CHOU Wen-Hwei%WEDLUND Peter-J%ROBBINS-WEILER Dorris-k%RYDER Thomas-B%LIU Wei-Wei%PERBOST Clotilde%FAIRCHILD Maureen%KOCH Walter-H
嚴奉祥%廖耑芳%CHOU Wen-Hwei%WEDLUND Peter-J%ROBBINS-WEILER Dorris-k%RYDER Thomas-B%LIU Wei-Wei%PERBOST Clotilde%FAIRCHILD Maureen%KOCH Walter-H
엄봉상%료단방%CHOU Wen-Hwei%WEDLUND Peter-J%ROBBINS-WEILER Dorris-k%RYDER Thomas-B%LIU Wei-Wei%PERBOST Clotilde%FAIRCHILD Maureen%KOCH Walter-H
CYP2D6%表型%基因型%PCR%寡核苷酸微陈列杂交
CYP2D6%錶型%基因型%PCR%寡覈苷痠微陳列雜交
CYP2D6%표형%기인형%PCR%과핵감산미진렬잡교
phenotype%genotype%PCR%oligonucleotide microarray hybridization
目的:为了评价CYP2D6的基因型和表型的联系以及基因芯片在CYP2D6多基因分析中的应用.方法:242健康志愿者,口服dextromethorphan后收集尿液测定其代谢率,收集20ml血提取DNA,并通过基因特异性PCR和/(或)基因芯片分析CYP2D6*2--*11,*17和多拷贝CYP2D6基因,其中5个基因(*3、*4、*6、*7和*9)用PCR和CYD450基因芯片同时分析.结果:CYP2D6基因型比表型更富有信息和更能反映CYP2D6酶的表达.CYP2D6*3、*4、*6、*7和*9的基因检测在CYP450基因芯片和基因特异性PCR中显示高度的一致性.结论:基因芯片在检测基因多位点的多基因中是一个有发展前途和可靠的方法.
目的:為瞭評價CYP2D6的基因型和錶型的聯繫以及基因芯片在CYP2D6多基因分析中的應用.方法:242健康誌願者,口服dextromethorphan後收集尿液測定其代謝率,收集20ml血提取DNA,併通過基因特異性PCR和/(或)基因芯片分析CYP2D6*2--*11,*17和多拷貝CYP2D6基因,其中5箇基因(*3、*4、*6、*7和*9)用PCR和CYD450基因芯片同時分析.結果:CYP2D6基因型比錶型更富有信息和更能反映CYP2D6酶的錶達.CYP2D6*3、*4、*6、*7和*9的基因檢測在CYP450基因芯片和基因特異性PCR中顯示高度的一緻性.結論:基因芯片在檢測基因多位點的多基因中是一箇有髮展前途和可靠的方法.
목적:위료평개CYP2D6적기인형화표형적련계이급기인심편재CYP2D6다기인분석중적응용.방법:242건강지원자,구복dextromethorphan후수집뇨액측정기대사솔,수집20ml혈제취DNA,병통과기인특이성PCR화/(혹)기인심편분석CYP2D6*2--*11,*17화다고패CYP2D6기인,기중5개기인(*3、*4、*6、*7화*9)용PCR화CYD450기인심편동시분석.결과:CYP2D6기인형비표형경부유신식화경능반영CYP2D6매적표체.CYP2D6*3、*4、*6、*7화*9적기인검측재CYP450기인심편화기인특이성PCR중현시고도적일치성.결론:기인심편재검측기인다위점적다기인중시일개유발전전도화가고적방법.
To evaluate association of genotype and phenotype of CYP2D6 and the application of oligonucleotide microarray hybridization genetic testing in CYP2D6 multiple alleles analyses. METHODS: Two hundred forty-two healthy volunteers were recruited, and a 60 mg oral dose of dextromethorphan (DXT) was administered to each for assessment of the DXT metabolic ratio [ MR]. A 20 ml blood sample was also collected for DNA isolation and testing. CYP2D6 alleles * 2-*11; * 17 and multiple CYP2D6 gene copies were tested by allele-specific PCR and/or the affymetrix CYP450 gene chip assay. Five of the CYP2D6 alleles ( * 3, * 4, *6, * 7, and * 9) were evaluated by both PCR and the CYP450 gene chip assay. RESULTS: The CYP2D6genotype was more informative and reflective in CYP2D6 enzyme expression than a phenotype. Genetic tests for the CYP2D6 * 3, * 4, * 6, * 7 and * 9 alleles showed a high degree of concordance between the CYP450 gene chip and AS-PCR methods. CONCLUSION: Oligonucleotide microarray hybridization is a promising and reliable approach for detecting multiple alleles at gene loci.