Yusoff Narazah Mohd, Shirakawa Taku, Nishiyama Kaoru, Ghazali Selamah, Ee Choo Keng, Orita Ayako, Abdullah Wan Zaidah, Isa Mohd Nizam, Van Rostenberghe Hans, Matsuo Masafumi
Haematology Department, School of Medical Sciences, University Science Malaysia, Kelantan.
Int J Hematol. 2002 Aug;76(2):149-52. doi: 10.1007/BF02982577.
Multiplex polymerase chain reaction (PCR) using multiple tandem forward primers and a common reverse primer (MPTP) was recently established as a comprehensive screening method for mutations in X-linked recessive diseases. In the work reported here, MPTP was used to scan for mutations of the glucose-6-phosphate dehydrogenase (G6PD) gene. Mutations in exons 3,4,5,6,7,9, 11, and 12 of the G6PD gene were screened by MPTP in 93 unrelated Malaysian patients with G6PD deficiency. Of the 93 patients, 80 (86%) had identified mutations. Although all of these were missense mutations, identified nucleotide changes were heterogeneous, with 9 mutations involving various parts of the exons. These 9 mutations were G-to-A nucleotide changes at nucleotide 871 of the G6PD gene (G871A), corresponding to G6PD Viangchan, G6PD Mediterranean (C563T), G6PD Vanua Lava (T383C), G6PD Coimbra (C592T), G6PD Kaiping (G1388A), G6PD Orissa (C131G), G6PD Mahidol (G487A), G6PD Canton (G1376T), and G6PD Chatham (G1003A). Our results document heterogeneous mutations of the G6PD gene in the Malaysian population.
使用多个串联正向引物和一个通用反向引物的多重聚合酶链反应(PCR)(MPTP)最近被确立为一种用于筛查X连锁隐性疾病突变的综合方法。在本文报道的研究中,MPTP被用于扫描葡萄糖-6-磷酸脱氢酶(G6PD)基因的突变。通过MPTP对93名无亲缘关系的马来西亚G6PD缺乏症患者的G6PD基因外显子3、4、5、6、7、9、11和12进行了突变筛查。在这93名患者中,80名(86%)检测到了突变。尽管所有这些都是错义突变,但检测到的核苷酸变化是异质性的,有9种突变涉及外显子的不同部位。这9种突变分别是G6PD基因第871位核苷酸处的G到A的核苷酸变化(G871A),对应于G6PD万象型、G6PD地中海型(C563T)、G6PD瓦努阿熔岩型(T383C)、G6PD科英布拉型(C592T)、G6PD开平型(G1388A)、G6PD奥里萨邦型(C131G)、G6PD马希多尔型(G487A)、G6PD广州型(G1376T)和G6PD查塔姆型(G1003A)。我们的结果证明了马来西亚人群中G6PD基因的异质性突变。