Sikström C, Nylander P O, Beckman L
Department of Medical Genetics, University of Umeå, Sweden.
Hum Hered. 1988;38(6):341-52. doi: 10.1159/000153812.
The frequencies of transferrin C (TF C) subtypes were studied in 315 Finns, 222 Swedish Lapps and in 4,157 conscripts and blood donors from the counties of Norrbotten and Västerbotten in northern Sweden. The Swedish individuals were distributed according to place of birth into 23 subpopulations or regions. A significant heterogeneity between the 23 regions was observed for the TF C1, C2 and C3 genes and for rare genes. Clines were found for the TF C1 and C3 genes and for rare transferrin genes in northern Sweden. The frequencies of the C1 and C3 genes were increasing in the southwestern and northeastern direction, respectively, and the frequency of the rare transferrin genes was increasing in the northern direction. The geographical picture of the C3 gene and of rare transferrin genes could be interpreted in terms of Finnish influence. The frequency of the TF C3 gene in Finland and northern Sweden (14 and 15%) is the highest so far reported in the world. The overall picture of geographical variations of the C1 and C2 genes were not explainable in terms of ethnic influence and may be caused by random differentiation and/or selective forces.
在315名芬兰人、222名瑞典拉普人以及来自瑞典北部北博滕郡和西博滕郡的4157名应征入伍者和献血者中,研究了转铁蛋白C(TF C)亚型的频率。这些瑞典人根据出生地被分为23个亚群或地区。观察到TF C1、C2和C3基因以及稀有基因在这23个地区之间存在显著的异质性。在瑞典北部发现了TF C1和C3基因以及稀有转铁蛋白基因的渐变群。C1和C3基因的频率分别在西南和东北方向增加,稀有转铁蛋白基因的频率在北方增加。C3基因和稀有转铁蛋白基因的地理分布情况可以从芬兰的影响方面来解释。芬兰和瑞典北部TF C3基因的频率(分别为14%和15%)是迄今为止世界上报道的最高频率。C1和C2基因地理变异的总体情况无法用种族影响来解释,可能是由随机分化和/或选择力造成的。