Kurdi-Haidar B, Mason P J, Berrebi A, Ankra-Badu G, al-Ali A, Oppenheim A, Luzzatto L
Department of Haematology, Royal Post-graduate Medical School, London, England.
Am J Hum Genet. 1990 Dec;47(6):1013-9.
A common glucose-6-phosphate dehydrogenase (G6PD) variant characterized by severe enzyme deficiency and B-like electrophoretic mobility is called "G6PD-Mediterranean" because it is found in different populations around the Mediterranean Sea. Sequence analysis of Italian subjects has revealed that the molecular basis of G6PD-Mediterranean is a single C-T transition at nucleotide position 563, causing a serine phenylalanine replacement at amino acid position 188. Most G6PD-Mediterranean subjects also have a silent C-T transition (without amino acid replacement) at nucleotide position 1311. Twenty-one unrelated individuals from Saudi Arabia, Iraq, Iran, Jordan, Lebanon, and Israel with both severe G6PD deficiency and B-like electrophoretic mobility were tested for both mutations by using amplification followed by digestion with appropriate restriction enzymes. All but one had the 563 mutation, and, of these, all but one had the 1311 mutation. Another 24 unrelated Middle Eastern individuals with normal G6PD activity or not known to be G6PD deficient were similarly tested. Four had the silent mutation at position 1311 in the absence of the deficiency mutation at position 563. We conclude that (1) the large majority of Middle Eastern subjects with the G6PD-Mediterranean phenotype have the same mutation found in Italy, (2) the silent mutation is an independent polymorphism in the Middle East, with a frequency of about .13, and (3) the mutation leading to the G6PD-Mediterranean deficiency has probably arisen on a chromosome that already carried the silent mutation.
一种常见的葡萄糖-6-磷酸脱氢酶(G6PD)变体,其特征为严重的酶缺乏和B样电泳迁移率,被称为“G6PD-地中海型”,因为它在地中海周边的不同人群中被发现。对意大利受试者的序列分析表明,G6PD-地中海型的分子基础是核苷酸位置563处的单个C-T转换,导致氨基酸位置188处的丝氨酸被苯丙氨酸取代。大多数G6PD-地中海型受试者在核苷酸位置1311处也有一个沉默的C-T转换(无氨基酸取代)。通过扩增后用适当的限制酶消化,对来自沙特阿拉伯、伊拉克、伊朗、约旦、黎巴嫩和以色列的21名患有严重G6PD缺乏和B样电泳迁移率的无关个体进行了两种突变的检测。除一人外,所有人都有563突变,其中除一人外,所有人都有1311突变。另外24名G6PD活性正常或未知是否缺乏G6PD的中东无关个体也进行了类似检测。四人在位置1311处有沉默突变,而在位置563处没有缺陷突变。我们得出结论:(1)绝大多数具有G6PD-地中海型表型的中东受试者具有在意大利发现的相同突变;(2)沉默突变是中东地区一种独立的多态性,频率约为0.13;(3)导致G6PD-地中海型缺乏的突变可能发生在已经携带沉默突变的染色体上。