Varawalla N Y, Fitches A C, Old J M
Institute of Molecular Medicine, John Radcliffe Hospital, Oxford, UK.
Hum Genet. 1992 Dec;90(4):443-9. doi: 10.1007/BF00220475.
beta-globin gene haplotypes were determined for 196 normal (beta-A) and 419 thalassaemia (beta-Th) chromosomes of individuals from four different regions of the Indian subcontinent; North-west Pakistan, Gujarat, Punjab and Sindh. Analysis of beta-A and beta-Th haplotypes and haplotype-mutation associations in each regional group along with a consideration of Indian history provided information about the origin and spread of beta-thalassaemia mutations on the Indian subcontinent. The data are consistent with relatively recent and local origins for most beta-thalassaemia mutations. The frequencies of particular alleles differ markedly in various regions and these may be useful population markers. Of the high frequency alleles, intervening sequence 1 (IVS-1) nucleotide 5 (G-C) and codons 41/42 (-CTTT) appear to be older as suggested by multiple haplotype associations and a widespread geographical distribution. The microepidemiology of beta-thalassaemia in this region reflects considerable ethnic diversity, gene flow from population migration and natural selection by malaria infection.
对来自印度次大陆四个不同地区(巴基斯坦西北部、古吉拉特邦、旁遮普邦和信德省)的196条正常(β-A)染色体和419条地中海贫血(β-Th)染色体进行了β-珠蛋白基因单倍型测定。对每个区域组中的β-A和β-Th单倍型以及单倍型-突变关联进行分析,并结合印度历史,提供了有关β-地中海贫血突变在印度次大陆的起源和传播的信息。数据表明,大多数β-地中海贫血突变起源相对较近且具有局部性。特定等位基因的频率在不同地区有显著差异,这些可能是有用的群体标记。在高频等位基因中,如通过多个单倍型关联和广泛的地理分布所表明的,内含子序列1(IVS-1)第5位核苷酸(G-C)和密码子41/42(-CTTT)似乎更为古老。该地区β-地中海贫血的微观流行病学反映了相当大的种族多样性、人口迁移导致的基因流动以及疟疾感染引起的自然选择。