摘要
本文报道应用DNA扩增技术对国内首例镰状细胞特征患者(Hb s杂合子)进行基因诊断。方法是从患者干血标本中微量抽提基因组DNA,通过聚合酶链反应(PCR)扩增其β珠蛋白基因,经限制性内切酶MstⅡ消化后作电泳分析直接检测Hb S基因。本文介绍的DNA诊断技术快速、灵敏、简便,它不需要放射性同位素标记的探针,可以采用干血抽提的DNA,因此,对遗传病基因诊断和携带者的筛查具有重要价值。
This paper describes a technique of DNA amplification in vitro and its application on detection of sickle cell (Hb S) gene.Genomic DNA was microextracted from dried blood specimen of the first patient with sickle cell trait in China.Target DNA sequence was amplified by the polymerase chain reaction (PCR) with the primers β(5'-ACACAACTGTGTT-CACTAGC-3') and β,(5'-CAACTTCATCCACGTTCACC-3') that primed amplification of an 110-base-pair (bp) segment of βglobin gene.The amplified DNA was digested with a restriction endonuclease Mst II,which has a recegnition site at codon 6 in the normal β globin gene,and cleaved the normal amplified (3 globin DNA into two fragments of 54bp and 56 bp which was as an overlap band in agarose gel electrophoresis,while the 110bp fragment amplified from DNA of sickle cell mutation remained uncleaved owing to a single base substitution (A→T) at codon 6 in the mutation.DNA amplification method is rapid,sensitive and simple,and does not require radioactive probes.Besides,the PCR amplification can be carried out on the DNA extracted from dried blood samples.So the technique is very useful for gene diagnosis and carier screening of genetic disease.
基金
美国国立卫生研究院科学基金(USPHS Research Grant HLB-29623)
关键词
DNA扩增
Hbs基因
聚合酶链反应
Chinese HbS gene,DNA amplification,Polymerase chain reaction
