经典型苯丙酮尿症苯丙氨酸羟化酶基因的新突变鉴定  

Identification of novel mutations in the phenylalanine hydroxylase gene of classical phenylketonuria

作　　者：张军力[1] 孟峻[1] 翟晓萍[2] 方根[2] 高建钢[1] 史珉[1] 王永祥[1] 

机构地区：[1]内蒙古医学院第一附属医院检验科,呼和浩特010050 [2]内蒙古血液中心

出　　处：《中华医学遗传学杂志》2005年第2期134-137,共4页Chinese Journal of Medical Genetics

基　　金：内蒙古自治区卫生厅医药卫生科研基金会(981118)~~

摘　　要：目的　研究经典型苯丙酮尿症(phenylketonuria,PKU)基因突变。方法　应用聚合酶链反应,单链构象多态分析和DNA直接测序等技术,对内蒙古地区32个PKU家系苯丙氨酸羟化酶(phenylalanine hydroxylase,PAH )基因第3～12外显子进行了鉴定分析。结果　检出14种PAH基因点突变:R2 4 3Q (12 / 6 4 )、Y35 6 X(6 / 6 4 )、Y2 0 4 C(5 / 6 4 )、R2 6 1Q(2 / 6 4 )、Y16 1S(2 / 6 4 )、R2 5 2 Q(1/ 6 4 )、R111X (2 / 6 4 )、D2 82 G (1/ 6 4 )、S30 3P(1/ 6 4 )、G2 39D(1/ 6 4 )、R4 13P(1/ 6 4 )、IVS7nt+2 (2 / 6 4 )、IVS4 nt+3(1/ 6 4 )、IVS9nt+34(2 / 6 4 ) ,经检索国际PAH基因突变数据统计库(截至到2 0 0 4年7月) ,确认IVS4 nt+3(G>C)、IVS9nt+34(G>A)为国际首次发现的新突变,S30 3P(T>C)、D2 82 G(A>G)为国内首次报道的新突变。结论　内蒙古人群苯丙氨酸羟化酶基因存在突变的多样性,R2 4 3Q、Y35 6 X、Y2 0 4 C是PAH基因的突变热点。Objective To investigate the mutations of phenylalanine hydroxylase ( PAH ) gene in the cases of classical phenylketonuria (PKU). Methods The exons 3-12 of the PAH gene in 32 PKU patients from Inner Mongolia were studied by using PCR-single strand conformation polymorphism technique and DNA direct sequencing. Results Fourteen point mutations were identified. The frequencies of mutations were R243Q(12/64), Y356X(6/64), Y204C(5/64), R261Q(2/64), Y161S(2/64), R252Q(1/64), R111X(2/64), D282G(1/64), S303P(1/64), G239D(1/64), R413P(1/64), IVS7nt+2(2/64), IVS4nt+3(1/64) and IVS9nt+34(2/64). Two novel mutations IVS4nt+3(G>C) and IVS9nt+34(G>A) were first found. The S303P(T>C) and D282G(A>G) were first documented in Chinese PAH gene. Conclusion This study demonstrated the variety of the mutation type PAH gene of PKU in Inner Mongolia population, and confirmed that R243Q, Y356X, Y204C were the hot spots of PAH gene mutation.

关 键 词：苯丙氨酸羟化酶基因 经典型苯丙酮尿症 单链构象多态分析 DNA直接测序 聚合酶链反应 基因突变 内蒙古地区 基因点突变 2004年 PAH基因 方法应用 鉴定分析 数据统计 首次发现 首次报道 突变热点 PKU 外显子 多样性 国际 

分 类 号：R725.8[医药卫生—儿科]