Martinson J J, Excoffier L, Swinburn C, Boyce A J, Harding R M, Langaney A, Clegg J B
MRC Molecular Haematology Unit, Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford, United Kingdom.
Am J Hum Genet. 1995 Nov;57(5):1186-98.
RFLP haplotypes at the alpha-globin gene complex have been examined in 190 individuals from the Niokolo Mandenka population of Senegal: haplotypes were assigned unambiguously for 210 chromosomes. The Mandenka share with other African populations a sample size-independent haplotype diversity that is much greater than that in any non-African population: the number of haplotypes observed in the Mandenka is typically twice that seen in the non-African populations sampled to date. Of these haplotypes, 17.3% had not been observed in any previous surveys, and a further 19.1% have previously been reported only in African populations. The haplotype distribution shows clear differences between African and non-African peoples, but this is on the basis of population-specific haplotypes combined with haplotypes common to all. The relationship of the newly reported haplotypes to those previously recorded suggests that several mutation processes, particularly recombination as homologous exchange or gene conversion, have been involved in their production. A computer program based on the expectation-maximization (EM) algorithm was used to obtain maximum-likelihood estimates of haplotype frequencies for the entire data set: good concordance between the unambiguous and EM-derived sets was seen for the overall haplotype frequencies. Some of the low-frequency haplotypes reported by the estimation algorithm differ greatly, in structure, from those haplotypes known to be present in human populations, and they may not represent haplotypes actually present in the sample.
在来自塞内加尔尼奥科洛曼丁卡人群的190名个体中,对α-珠蛋白基因复合体的限制性片段长度多态性(RFLP)单倍型进行了检测:明确确定了210条染色体的单倍型。曼丁卡人与其他非洲人群一样,具有与样本量无关的单倍型多样性,这种多样性远大于任何非非洲人群:在曼丁卡人群中观察到的单倍型数量通常是迄今为止所采样的非非洲人群的两倍。在这些单倍型中,17.3%在以往任何调查中均未被观察到,另有19.1%此前仅在非洲人群中被报道过。单倍型分布显示非洲人和非非洲人之间存在明显差异,但这是基于特定人群的单倍型以及所有人群共有的单倍型。新报道的单倍型与先前记录的单倍型之间的关系表明,其产生涉及多种突变过程,特别是作为同源交换或基因转换的重组。使用基于期望最大化(EM)算法的计算机程序来获得整个数据集单倍型频率的最大似然估计:对于总体单倍型频率,明确确定的数据集与基于EM算法得出的数据集之间具有良好的一致性。估计算法报告的一些低频单倍型在结构上与已知存在于人类群体中的单倍型有很大差异,它们可能并不代表样本中实际存在的单倍型。