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[中国福建省类孟买血型个体的Fut1基因突变]

[Fut1 gene mutation for para-bombay blood type individual in Fujian Province of China].

作者信息

Huang Hao-Bou, Fan Li-Ping, Wai Shi-Jin, Zeng Feng, Lin Hai-Yan, Zhang Rong

机构信息

Department of Blood Transfusion, Fujian Institute of Hematology, Union Hospital, Fujian Medical University, Fuzhou 350001, Fujian Province, China.

出版信息

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2010 Oct;18(5):1338-40.

Abstract

This study was aimed to investigate the molecular mechanisms for para-Bombay blood type individual in Fujian Province of China. The para-Bombay blood type of this individual was identified by routine serological techniques. The full coding region of alpha (1,2) fucosyltransferase (FUT1) gene of this individual was amplified by polymerase chain reaction (PCR), then the PCR product was cloned into T vector. The mutation in coding region of fut1 gene was identified by TA cloning, so as to explore the molecular mechanisms for para-Bombay blood type individual. The results indicated that the full coding region of fut1 gene was successfully amplified by PCR. AG deletion at position 547-552 on 2 homologous chromosomes was detected by TA cloning method, leading to a reading frame shift and a premature stop codon. It is concluded that genetic mutation of fut1 gene in this para-bombay blood type individual was h1h1 homozygotic type.

摘要

本研究旨在探讨中国福建省类孟买血型个体的分子机制。通过常规血清学技术鉴定该个体的类孟买血型。采用聚合酶链反应(PCR)扩增该个体α(1,2)岩藻糖基转移酶(FUT1)基因的完整编码区,然后将PCR产物克隆到T载体中。通过TA克隆鉴定fut1基因编码区的突变,以探讨类孟买血型个体的分子机制。结果表明,通过PCR成功扩增了fut1基因的完整编码区。采用TA克隆方法检测到2条同源染色体上第547-552位的AG缺失,导致读框移位和提前终止密码子。结论是该类孟买血型个体的fut1基因发生了h1h1纯合型基因突变。

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