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Distribution of race-specific null alleles of the FUT2 in Africa, European and Asian populations.

Distribution of race-specific null alleles of the FUT2 in Africa, European and Asian populations.
FUT2 种族特异性无效等位基因在非洲、欧洲和亚洲人群中的分布。
批准号:
10041209
负责人:
KIMURA Hiroshi
金额:
$2.37万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B).
财政年份:
1998
资助国家:
日本
项目状态:
已结题
起止时间:
1998 至 1999

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项目成果

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中文摘要
翻译
ABO (H)抗原在保密中的表达,如saliva是由秘书基因(FUT 2)-编码α (1, 2) fucosyltransferase (Se enzyme)调节的。ABO秘书小组至少有一个功能性的Se Allele,而非Secretors,谁未能在Saliva中表达ABH抗原,对非功能性的Se Allele都是一致的。我们对各种人口中FUT 2的分子分析提出了一项建议,即无迹象是特定的。null allele se D1428 D1 was found to be common in African (Xhosa) and Caucasians (European and Iranian), while the null allele D1357,385 D1 was found to be common in Asian populations (Chinese、Korean、Japanese、Indonesian an Samoan)。Frequency of se D1428,D1 and of se D1375,385,D1 in each population was 0.4 ~ 0.5。However, we found both se D1428 y D1 and se D1375,385 y D1 in a Bangrad?population。The presence of both seイD1428エD1 (0. 234) and seイD1375,385エD1 (0. 074) suggests the admixture of Aryans and Asians in Bangrad\。In addition, we found se D1 fus D1 as one of null alleles in Japanese (0.05 ~ 0.08) and the absence of the se D1 fus D1 in Chinese, suggesting that the se D1 fuus D1 emerged from within Japanese。
英文摘要
The expression of ABO (H) antigens in secretions such as saliva is regulated by the Secretor gene (FUT2)-encoded α (1, 2) fucosyltransferase (Se enzyme). The ABO secretor group has at least one functional Se allele, and nonsecretors, who fail to express ABH antigens in saliva, are homozygous for the nonfunctional se allele. Our molecular analysis of the FUT2 in various population has suggested that null alleles were race-specific. The null allele seィイD1428ィエD1 was found to be common in African (Xhosa) and Caucasians (European and Iranian), while the null allele seィイD1357,385ィエD1 was found to be common in Asian populations (Chinese, Korean, Japanese, Indonesian an Samoan). Frequency of seィイD1428ィエD1 and of seィイD1375,385ィエD1 in each population was 0.4〜0.5. However, we found both seィイD1428ィエD1 and seィイD1375,385ィエD1 in a Bangladesh population. The presence of both seィイD1428ィエD1 (0.234) and seィイD1375,385ィエD1 (0.074) suggests the admixture of Aryans and Asians in Bangladesh. In addition, we found seィイD1fusィエD1 as one of null alleles in Japanese (0.05〜0.08) and the absence of the seィイD1fusィエD1 in Chinese, suggesting that the seィイD1fusィエD1 emerged from within Japanese.
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会议论文
H. Pang, Y. Koda, M. Soejima, T. Schlaphoff, ED du Toit, H. Kimura: "Allelic diversity of the human plasma α(1,3)fucosyltransferase gene(FUT6)"Ann Hum Genet. 63. 277-284 (1999)
H. Pang、Y. Koda、M. Soejima、T. Schlaphoff、ED du Toit、H. Kimura:“人血浆 α(1,3) 岩藻糖基转移酶基因 (FUT6) 的等位基因多样性”Ann Hum Genet。 -284 (1999)
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通讯作者:
Koda Y, Soejima M, Kimura H.: "Structure and expression of H type GDP-L-fucose : β-D-galactoside2-α-L-fucosyltransferase gene (FUT1). Two transcription start sites and alternative splicing generate several forms of FUT1 mRNA." J Biol Chem. 272. 7501-7505
Koda Y、Soejima M、Kimura H.:“H 型 GDP-L-岩藻糖的结构和表达:β-D-半乳糖苷 2-α-L-岩藻糖基转移酶基因 (FUT1)。两个转录起始位点和选择性剪接产生多种形式的FUT1 mRNA。”《生物化学杂志》。272. 7501-7505
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Pang H, Liu YH, Koda Y, Soejima M, Jia JT, Schlaphoff T, du Toit ED, Kimura H.: "Five novel missense mutations of the Lewis gene (FUT3) in African (Xhosa) and Caucasian populations in South Africa." Hum Genet. 102. 675-680 (1998)
Pang H、Liu YH、Koda Y、Soejima M、Jia JT、Schlaphoff T、du Toit ED、Kimura H.:“南非非洲(科萨)和高加索人群中 Lewis 基因 (FUT3) 的五种新错义突变。
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