Description and Validation of High-Throughput Simultaneous Genotyping and Mutation Scanning by High-Resolution Melting Curve Analysis

被引:32
|
作者
Nguyen-Dumont, Tu
Le Calvez-Kelm, Florence
Forey, Nathalie
McKay-Chopin, Sandrine
Garritano, Sonia
Gioia-Patricola, Lydie
De Silva, Deepika [2 ]
Weigel, Ron [2 ]
Sangrajrang, Suleeporn [3 ]
Lesueur, Fabienne
Tavtigian, Sean V. [1 ]
机构
[1] Int Agcy Res Canc, Genet Susceptibil Grp, F-69372 Lyon 08, France
[2] Idaho Technol Inc, Salt Lake City, UT USA
[3] NCI, Div Res, Bangkok, Thailand
基金
澳大利亚国家健康与医学研究理事会; 美国国家卫生研究院;
关键词
high-resolution melting curve analysis; HR-melt; high throughput mutation scanning; genotyping; ATM; BREAST-CANCER PATIENTS; PERFORMANCE LIQUID-CHROMATOGRAPHY; ATM MUTATIONS; ATAXIA-TELANGIECTASIA; MISSENSE MUTATIONS; GENE; VARIANTS; POLYMORPHISMS; ASSOCIATION; POPULATION;
D O I
10.1002/humu.20949
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Mutation scanning using high-resolution melting curve analysis (HR-melt) is an effective and sensitive method to detect sequence variations. However, the presence of a common SNP within a mutation scanning amplicon may considerably complicate the interpretation of results and increase the number of samples flagged for sequencing by interfering with the clustering of samples according to melting profiles. A protocol describing simultaneous high-resolution gene scanning and genotyping has been reported. Here, we show that it can improve the sensitivity and the efficiency of large-scale case-control mutation screening. Two exons of ATM, both containing an SNP interfering with standard mutation scanning, were selected for screening of 1,356 subjects from an international breast cancer genetics study. Asymmetric PCR was performed in the presence of an SNP-specific unlabeled probe. Stratification of the samples according to their probe-target melting was aided by customized HR-melt software. This approach improved identification of rare known and unknown variants, while dramatically reducing the sequencing effort. It even allowed genotyping of tandem SNPs using a single probe. Hence, HR-melt is a rapid, efficient, and cost-effective tool that can be used for high-throughput mutation screening for research, as well as for molecular diagnostic and clinical purposes. Hum Mutat 30, 884-890, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:884 / 890
页数:7
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