机构地区:[1]贵阳医学院分子生物学重点实验室,550004 [2]贵州省毕节市疾病预防控制中心 [3]贵州省长顺县疾病预防控制中心
出 处:《中国地方病学杂志》2011年第2期148-151,共4页Chinese Jouranl of Endemiology
摘 要:目的探讨过氧化氢酶(CAT)基因启动子区-262C/T、-21A/T多态性与燃煤型氟中毒之间的关系。方法2007年,在贵州省毕节市鸭池镇燃煤型氟中毒非改灶村抽取150名村民作为非干预组,于该市长春镇燃煤型氟中毒改灶村抽取150名村民作为干预组,于非地方性氟中毒长顺县白云山镇抽取150名村民作对照组,应用聚合酶链反应限制性片段长度多态性(PCR—RFLP)分析方法,分别检测各组CAT-262C/T、-21A/T多态的基因型。结果非干预组、干预组和对照组CAT-262C/r、CAT-21A/T多态的基因型频率分布符合Hardy—weinberg遗传平衡定律(P〉0.05)。在研究人群中检测到CAT-262C/T多态的两种基因型CC和CT,未检测到TT基因型:检测到CAT-21A/T多态的三种基因型AA、AT和TT。对照组、干预组和非干预组CAT基因—262C/T多态位点的基因型(CC、CT)频率分别为89.33%(134/150)、10.67%(16/150)、88.67%(133/150)、11.33%(17/150)、93.33%(140/150)、6.67%(10/150);对照组、干预组和非干预组C等位基因频率分别为94.67%(284/300)、94.33%(283/300)、96.67%(290/300);T等位基因频率分别为5-33%(16/300)、5.67%(17/300)、3.33%(10/300)。对照组,干预组和非干预组CAT基因一21A/T多态位点基因型(AA、AT、TT)频率分别为48.67%(73/150)、46.00%(69/150)、5.33%(8/150)、52.67%(79/150)、38.00%(57/150)、9.33%(14/150)、51.33%(77/150)、38.00%(57/150)、10.67%(16/150);对照组、干预组和非干预组A等位基因频率分别为71.67%(215/300)、71.67%(215/300)、70.33%(211/300);T等位基因频率分别为28_33%(85/300)、28.33%(85/300)、29.67%(89/300)。CAT-262C/T和CAT-21A/T基因型频率及等位基因频率在对�Objective To explore the relationship between -262C/T and -21A/T polymorphisms of eatalase(CAT) gene and coal-burning borne fluorosis. Methods In 2007, 150 villagers were taken as a non- intervention group in Bijie city from the village of coal-burning borne fluorosis areas with unchanged cooking stoves ; 150 villagers were taken as the intervention group from the town of Changchun county where cooking stoves changed; 150 villagers were taken as control from non-endemic fluorosis areas in Baiyun town of Changshun county. PCR-restriction fragment length polymorphism were employed to detect genotypes of CAT-262C/T and CAT-21A/T polymorphism of CAT gene. Results The genotypic frequencies of CAT-262C/T and CAT-21A/T in non- intervention group,intervention group and control group were in line with Hardy-Weinberg equilibrium law(P 〉 0.05 ). The genotypes of CC and CT were detected while no TT were detected for CAT-262C/T polyinorphism; the genotypes of AA, AT and TT were detected for CAT-21A/T. The genotype frequencies of CAT-262 CC, CT in control group, intervention group and non-intervention group were (89.33% (134/150), 10.67%(16/150); 88.67% (133/150), 11.33% (17/150),93.33% (140/150),6.67% (10/150), respectively. The gene frequency of C in control group, intervention group and non-intervention group were (94.67% (284/300), 94.33% (283/300), 96.67% (290/300), respectively. The gene frequency of T in control group, intervention group and non-intervention group were 5.33% (16/300), 5.67% (17/300), 3.33% (10/300), respectively. The genotype frequencies of CAT-21 AA, AT and TF in control group, intervention group and non-intervention group were 48.67% (73/150),46.00% (69/150), 5.33% (8/150), 52.67% (79/150), 38.00% (57/150), 9.33% (14/150), 51.33% (77/150), 38.00% (57/150), 10.67% (16/150), respectively. The gene frequency of A in control group, intervention group and non-intervention group were 71.67% (215/300),71.67%
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