High-throughput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: Validation of the method

被引:45
作者
Andersen, PS [1 ]
Jespersgaard, C [1 ]
Vuust, J [1 ]
Christiansen, M [1 ]
Larsen, LA [1 ]
机构
[1] Statens Serum Inst, Dept Clin Biochem, DK-2300 Copenhagen S, Denmark
关键词
SSCP; mutation analysis; single strand conformation polymorphism; KCNQ1; TNNI3; method; validation; capillary electrophoresis; capillary array electrophoresis; mutation detection; CAE; MYH7; MYL2; MYL3;
D O I
10.1002/humu.10161
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Capillary array electrophoresis (CAE) is a novel technique, which allows for high throughput analysis of DNA fragments. When screening for mutations in whole populations or large patient groups it is necessary to have robust and well. characterized setups for high throughput analysis. For large,scale mutation screening, we have developed procedures for single strand conformation polymorphism (SSCP) assays using CAE (CAE-SSCP) whereby we may increase both the sensitivity and the throughput compared to conventional SSCP analysis. In this study we have validated CAE-SSCP by 1) comparing detection by slab,gel based SSCP with CAE,SSCP of mutations in the MYH7, MYL2, and MYL3 genes encoding sarcomere proteins from patients suffering from hypertrophic cardiomyopathy; and 2) by constructing a series of 185 mutants having substitution mutations, as well as insertion/deletion mutations, or some combinations of these, in different sequence contexts in four exons and different positions relative to the end of the amplicon (three from the KCNQ1 gene, encoding a cardiac potassium channel, and one from the TNNI3 gene encoding cardiac troponin I). The method identified 181 out of 185 mutations (98%), and the data suggest that the position of mutation in the fragment had no effect on the sensitivity. Analysis of the specificity of the method showed that only very few mutants could not be distinguished from each other and there were no false positives.
引用
收藏
页码:116 / 122
页数:7
相关论文
共 27 条
[1]   Prediction of DNA single-strand conformation polymorphism: analysis by capillary electrophoresis and computerized DNA modeling [J].
Atha, DH ;
Kasprzak, W ;
O'Connell, CD ;
Shapiro, BA .
NUCLEIC ACIDS RESEARCH, 2001, 29 (22) :4643-4653
[2]  
Bugge M, 2000, J MED GENET, V37, P858, DOI 10.1136/jmg.37.11.858
[3]   Comparison of fluorescent single-strand conformation polymorphism analysis and denaturing high-performance liquid chromatography for detection of EXT1 and EXT2 mutations in hereditary multiple exostoses [J].
Dobson-Stone, C ;
Cox, RD ;
Lonie, L ;
Southam, L ;
Fraser, M ;
Wise, C ;
Bernier, F ;
Hodgson, S ;
Porter, DE ;
Simpson, AHRW ;
Monaco, AP .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2000, 8 (01) :24-32
[4]  
Ellis LA, 2000, HUM MUTAT, V15, P556, DOI 10.1002/1098-1004(200006)15:6<556::AID-HUMU7>3.0.CO
[5]  
2-C
[6]   LIMITATIONS IN THE USE OF SSCP ANALYSIS [J].
FAN, E ;
LEVIN, DB ;
GLICKMAN, BW ;
LOGAN, DM .
MUTATION RESEARCH, 1993, 288 (01) :85-92
[7]   Fluorescence-based single-strand conformation polymorphism analysis of the low density lipoprotein receptor gene by capillary electrophoresis [J].
Geisel, J ;
Walz, T ;
Bodis, M ;
Nauck, M ;
Oette, K ;
Herrmann, W .
JOURNAL OF CHROMATOGRAPHY B, 1999, 724 (02) :239-247
[8]   Correlation of MFOLD-predicted DNA secondary structures with separation patterns obtained by capillary electrophoresis single-strand conformation polymorphism (CE-SSCP) analysis [J].
Glavac, D ;
Potocnik, U ;
Podpecnik, D ;
Zizek, T ;
Smerkolj, S ;
Ravnik-Glavac, M .
HUMAN MUTATION, 2002, 19 (04) :384-394
[9]   HOW SENSITIVE IS PCR-SSCP [J].
HAYASHI, K ;
YANDELL, DW .
HUMAN MUTATION, 1993, 2 (05) :338-346
[10]   A streamlined mutation detection system: Multicolor post-PCR fluorescence labeling and single-strand conformational polymorphism analysis by capillary electrophoresis [J].
Inazuka, M ;
Wenz, HM ;
Sakabe, M ;
Tahira, T ;
Hayashi, K .
GENOME RESEARCH, 1997, 7 (11) :1094-1103