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[类孟买型中国人FUT1和FUT2基因的分子遗传学分析:鉴定出一种新型FUT1等位基因]

[Molecular genetic analysis of FUT1 and FUT2 gene in para-Bombay Chinese: a novel FUT1 allele is identified].

作者信息

Su Yu qing, Wei Tian-li, Yu Qiong, Liang Yan-lian, Li Da-cheng

机构信息

Shenzhen Blood Center, Shenzhen Institute of Transfusion Medicine, Shenzhen, Guangdong, 518035 PR China.

出版信息

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Oct;24(5):520-3.

Abstract

OBJECTIVE

Molecular genetic analysis of FUT1 and FUT2 gene was performed for seven Chinese Han individuals serologically typed as para-Bombay.

METHODS

Seven DNA samples were studied by polymerase chain reaction and then by direct sequencing. Molecular cloning sequencing was done for an individual with a novel FUT1 allele. Family segregation analysis of the novel FUT1 allele was done to explore whether the allele was responsible for the fucosyltransferase defects of H.

RESULTS

The FUT1 genotypes of seven para-Bombay individuals were h1h1 (four individuals), h2h2 (two individuals), h328hnew (one individual), alleles h1 lost one of the three AG repeats located at the nucleotides 547-552 of the FUT1 gene, h2 lost two of the three T repeats located at the nucleotides 880-882, h328 (nt328G>A) was a missense mutation, all of them were known mutations, while allele hnew deleted GGTATTCCGCATCACCCTGCCCGTGCTGGCCCC at nt360-400, total 33 bases, and the frame-shift mutation was not previously reported. The segregation of the hnew allele in his family showed that his father genotype was Hh328, and his mother was Hhnew, while two brother were h328hnew. The FUT2 genotypes of seven para-Bombay individuals were Se357 Se357 (three individuals), Se357 Se357,385 (three individuals), Se357,716Se357,716(one individual), the functional Se357(nt357C>T), Se716(nt716G>A) and the weakly functional Se385(nt385A>T) were known. The seven para-Bombay individuals carried at least one copy of a functional FUT2 allele was consistent with their secretor status.

CONCLUSION

A novel FUT1 allele was identified in a para-Bombay Chinese individual, which was responsible for the inactivation of the FUT1-encoded enzyme activity.

摘要

目的

对7名血清学鉴定为类孟买型的中国汉族个体进行FUT1和FUT2基因的分子遗传学分析。

方法

采用聚合酶链反应对7份DNA样本进行研究,随后进行直接测序。对携带新型FUT1等位基因的个体进行分子克隆测序。对新型FUT1等位基因进行家系分离分析,以探究该等位基因是否导致H抗原岩藻糖基转移酶缺陷。

结果

7名类孟买型个体的FUT1基因型分别为h1h1(4例)、h2h2(2例)、h328hnew(1例),等位基因h1在FUT1基因第547 - 552位核苷酸处的3个AG重复序列中缺失1个,h2在第880 - 882位核苷酸处的3个T重复序列中缺失2个,h328(nt328G>A)为错义突变,均为已知突变,而等位基因hnew在第360 - 400位核苷酸处缺失GGTATTCCGCATCACCCTGCCCGTGCTGGCCCC,共33个碱基,此移码突变未见先前报道。其家系中hnew等位基因的分离情况显示,其父亲基因型为Hh328,母亲为Hhnew,两个兄弟为h328hnew。7名类孟买型个体的FUT2基因型分别为Se357Se357(3例);Se357Se357,385(3例);Se357,716Se357,716(1例),功能性的Se357(nt357C>T)、Se716(nt716G>A)以及弱功能性的Se385(nt385A>T)均为已知。7名类孟买型个体携带至少1个功能性FUT贰等位基因,这与他们的分泌型状态相符。

结论

在1名中国类孟买型个体中鉴定出1个新型FUT1等位基因,该等位基因导致FUT1编码的酶活性失活。

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