Institute of Molecular Pathology and Immunology of University of Porto (IPATIMUP), Porto, Portugal.
Braz J Med Biol Res. 2010 Jul;43(7):677-80. doi: 10.1590/s0100-879x2010007500056. Epub 2010 Jun 11.
A 3-bp insertion/deletion polymorphism in intron 6 of GSTM3 (rs1799735, GSTM3A/B) affects the activity of the phase 2 xenobiotic metabolizing enzyme GSTM3 and has been associated with increased cancer risk. The GSTM3B allele is rare or absent in Southeast Asians, occurs in 5-20% of Europeans but was detected in 80% of Bantu from South Africa. The wide genetic diversity among Africans led us to investigate whether the high frequency of GSTM3B prevailed in other sub-Saharan African populations. In 168 healthy individuals from Angola, Mozambique and the São Tomé e Príncipe islands, the GSTM3B allele was three times more frequent (0.74-0.78) than the GSTM3A allele (0.22-0.26), with no significant differences in allele frequency across the three groups. We combined these data with previously published results to carry out a multidimensional scaling analysis, which provided a visualization of the worldwide population affinities based on the GSTM3 *A/*B polymorphism.
GSTM3 基因 6 号内含子中的 3 个碱基插入/缺失多态性(rs1799735,GSTM3A/B)影响 2 期外源性代谢酶 GSTM3 的活性,并与癌症风险增加相关。GSTM3B 等位基因在东南亚人群中罕见或缺失,在 5-20%的欧洲人群中出现,但在南非的班图人中检测到 80%。非洲人群中的遗传多样性广泛,这促使我们研究 GSTM3B 的高频率是否在其他撒哈拉以南非洲人群中普遍存在。在来自安哥拉、莫桑比克和圣多美和普林西比岛的 168 名健康个体中,GSTM3B 等位基因的频率(0.74-0.78)是 GSTM3A 等位基因(0.22-0.26)的三倍,三个群体之间的等位基因频率没有显著差异。我们将这些数据与之前发表的结果相结合,进行多维尺度分析,根据 GSTM3*A/*B 多态性提供了全球人群亲缘关系的可视化。