Koda Yoshiro, Ishida Takafumi, Tachida Hidenori, Wang Baojie, Pang Hao, Soejima Mikiko, Soemantri Augustinus, Kimura Hiroshi
Division of Human Genetics, Department of Forensic Medicine, Kurume University School of Medicine, 830-0011 Kurume, Japan.
Hum Genet. 2003 Nov;113(6):534-41. doi: 10.1007/s00439-003-1013-6. Epub 2003 Sep 3.
We have investigated the allelic polymorphism of the human ABO-secretor locus ( FUT2) in 90 unrelated Papuan-speaking New Guineans (Dani group), 101 admixed New Guineans from Irian Jaya, Indonesia, and 32 New Guineans from Papua New Guinea by DNA sequencing analysis. Whereas the total frequency of various nonfunctional alleles at the FUT2 locus in the worldwide populations so far examined is around 0.5, we have found only one individual heterozygous for a nonfunctional allele in the 90 Dani group members and a frequency of nonfunctional alleles of 0.1-0.2 in the admixed New Guineans. Admixed New Guineans had the Asian-specific null allele se(385) and the characteristic nonfunctional allele se(del2) found in Polynesians. In addition, both New Guinean populations had unique functional alleles ( Se(375) and Se(400)) with high frequencies (0.11-0.37); these are absent in other populations of the world except for African and Samoan populations. The Se(375) allele had G and C at positions 1009 and 1011 of the 3' untranslated region, respectively, whereas all other FUT2 alleles found so far in the world, except for se(428), have 1009A and 1011T. The Se(375) allele found in Africans has 1009G and 1011T, or 1009A and 1011T. Corresponding positions of nonhuman primates have G and C, suggesting that the Se(375) allele is one of the ancestral alleles, reflecting the early human migration from Africa to New Guinea and the long isolation of Dani populations from neighboring populations.
我们通过DNA测序分析,对90名讲巴布亚语的新几内亚人(丹尼族)、101名来自印度尼西亚伊里安查亚的混血新几内亚人以及32名来自巴布亚新几内亚的新几内亚人进行了人类ABO分泌型基因座(FUT2)的等位基因多态性研究。在迄今为止所检测的全球人群中,FUT2基因座各种无功能等位基因的总频率约为0.5,而在90名丹尼族成员中,我们仅发现1例无功能等位基因杂合个体,在混血新几内亚人中无功能等位基因的频率为0.1 - 0.2。混血新几内亚人具有亚洲特有的无效等位基因se(385)以及在波利尼西亚人中发现的特征性无功能等位基因se(del2)。此外,两个新几内亚人群都有频率较高(0.11 - 0.37)的独特功能性等位基因(Se(375)和Se(400));除非洲人和萨摩亚人群外,世界上其他人群中不存在这些等位基因。Se(375)等位基因在3'非翻译区的第1009和1011位分别为G和C,而迄今为止在世界上发现的所有其他FUT2等位基因,除了se(428),在这两个位置均为1009A和1011T。在非洲人中发现的Se(375)等位基因在这两个位置为1009G和1011T,或者1009A和1011T。非人类灵长类动物的相应位置为G和C,这表明Se(375)等位基因是祖先等位基因之一,反映了人类早期从非洲迁移到新几内亚以及丹尼人群与邻近人群长期隔离的情况。