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通过聚合酶链反应-单链构象多态性技术鉴定希腊β地中海贫血患者和携带者中四种最常见的β珠蛋白基因突变:该方法的优点和局限性

Identification of the four most common beta-globin gene mutations in Greek beta-thalassemic patients and carriers by PCR-SSCP: advantages and limitations of the method.

作者信息

Kakavas Konstantinos V, Noulas Argiris, Chalkias Christos, Hadjichristodoulou Christos, Georgiou Ioannis, Georgatsou Elena, Bonanou Sophia

机构信息

Department of Biochemistry, School of Medicine, Faculty of Health Sciences, University of Thessaly, Larissa, Greece.

出版信息

J Clin Lab Anal. 2006;20(1):1-7. doi: 10.1002/jcla.20091.

DOI:10.1002/jcla.20091
PMID:16470532
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6807422/
Abstract

In the present study we investigated whether the single-strand conformational polymorphism (SSCP) method could be employed to identify (rather than simply detect) the four most common beta-globin gene mutations in the Greek population: IVS-I-110, Cd39, IVS-I-1, and IVS-I-6. Using DNA from 50 beta-thalassemic patients and carriers, we amplified by PCR the appropriate 238-bp region of the human beta-globin gene, analyzed the reaction products by nondenaturing polyacrylamide gel electrophoresis, and visualized the bands by silver staining. Single-stranded DNA (ssDNA) fragments showed a reproducible pattern of bands that was characteristic of the mutations present. With the use of control samples containing six of the 10 possible combinations of the four most common beta-globin gene mutations, we were able to predict the mutations present in a quarter of the patients studied. Our predictions were confirmed independently by the amplification refractory mutation system (ARMS) method. We conclude that this non-radioactive PCR-SSCP method can be used to reliably identify mutations in patients, provided that suitable controls are available. Moreover, the method is easy to apply to the identification of mutations in carriers, which makes it particularly useful for population screening.

摘要

在本研究中,我们调查了单链构象多态性(SSCP)方法是否可用于鉴定(而非仅仅检测)希腊人群中四种最常见的β-珠蛋白基因突变:IVS-I-110、Cd39、IVS-I-1和IVS-I-6。我们使用来自50名β地中海贫血患者和携带者的DNA,通过聚合酶链反应(PCR)扩增人β-珠蛋白基因的适当238 bp区域,通过非变性聚丙烯酰胺凝胶电泳分析反应产物,并通过银染使条带可视化。单链DNA(ssDNA)片段显示出可重复的条带模式,这是存在的突变的特征。通过使用包含四种最常见β-珠蛋白基因突变的10种可能组合中的六种的对照样品,我们能够预测所研究患者中四分之一患者存在的突变。我们的预测通过扩增阻滞突变系统(ARMS)方法得到独立证实。我们得出结论,这种非放射性PCR-SSCP方法可用于可靠地鉴定患者中的突变,前提是有合适的对照。此外,该方法易于应用于携带者突变的鉴定,这使其对于人群筛查特别有用。

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