Kan Y W, Dozy A M
Science. 1980 Jul 18;209(4454):388-91. doi: 10.1126/science.7384810.
A polymorphic HpaI endonuclease recognition site on the 3' side of the beta-globin gene was used to analyze the evolution of the beta-globin gene mutants S and C. Study of the world wide distribution of the normal and variant HpaI sites showed that the mutation which resulted in the variant 13.0-kilobase fragment arose in a localized region in West Africa. It predated the hemoglobin S and C mutations, both of which arose separately from a chromosome with the variant 13.0-kilobase HpaI site. In contrast, the sickle genes in other parts of Africa and in Asia are associated with the normal 7.6-kilobase HpaI fragment, indicating that the sickle mutations in these other areas arose separately from that in West Africa.
利用β-珠蛋白基因3'端的一个多态性HpaI核酸内切酶识别位点来分析β-珠蛋白基因突变体S和C的进化。对正常和变异HpaI位点的全球分布研究表明,导致变异的13.0千碱基片段的突变发生在西非的一个局部地区。它早于血红蛋白S和C突变,这两种突变均分别起源于带有变异的13.0千碱基HpaI位点的染色体。相比之下,非洲其他地区和亚洲的镰状基因与正常的7.6千碱基HpaI片段相关,这表明这些其他地区的镰状突变是与西非的镰状突变分别发生的。