High resolution melting analysis for gene scanning

被引:149
作者
Erali, Maria [2 ]
Wittwer, Carl T. [1 ,2 ]
机构
[1] Univ Utah, Sch Med, Dept Pathol, Salt Lake City, UT 84132 USA
[2] ARUP Inst Clin & Expt Pathol, Salt Lake City, UT 84108 USA
关键词
High resolution melting; Heteroduplex scanning; Genotyping; LCGreen Plus; LightScanner; CONDUCTANCE REGULATOR GENE; CURVE ANALYSIS; CLOSED-TUBE; SINGLE; ELECTROPHORESIS; MUTATIONS; VARIANTS;
D O I
10.1016/j.ymeth.2010.01.013
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
High resolution melting is a new method of genotyping and variant scanning that can be seamlessly appended to PCR amplification. Limitations of genotyping by amplicon melting can be addressed by unlabeled probe or snapback primer analysis, all performed without labeled probes. High resolution melting can also be used to scan for rare sequence variants in large genes with multiple exons and is the focus of this article. With the simple addition of a heteroduplex-detecting dye before PCR, high resolution melting is performed without any additions, processing or separation steps. Heterozygous variants are identified by atypical melting curves of a different shape compared to wild-type homozygotes. Homozygous or hemizygous variants are detected by prior mixing with wild-type DNA. Design, optimization, and performance considerations for high resolution scanning assays are presented for rapid turnaround of gene scanning. Design concerns include primer selection and predicting melting profiles in silico. Optimization includes temperature gradient selection of the annealing temperature, random population screening for common variants, and batch preparation of primer plates with robotically deposited and dried primer pairs. Performance includes rapid DNA preparation, PCR, and scanning by high resolution melting that require, in total, only 3 h when no variants are present. When variants are detected, they can be identified in an additional 3 h by rapid cycle sequencing and capillary electrophoresis. For each step in the protocol, a general overview of principles is provided, followed by an in depth analysis of one example, scanning of CYBB, the gene that is mutated in X-linked chronic granulomatous disease. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:250 / 261
页数:12
相关论文
共 42 条
[1]   Comparison of High-Resolution Melting Analysis with Denaturing High-Performance Liquid Chromatography for Mutation Scanning in the ABCA4 Gene [J].
Aguirre-Lamban, Jana ;
Riveiro-Alvarez, Rosa ;
Garcia-Hoyos, Maria ;
Cantalapiedra, Diego ;
Avila-Fernandez, Almudena ;
Villaverde-Montero, Cristina ;
Jose Trujillo-Tiebas, Maria ;
Ramos, Carmen ;
Ayuso, Carmen .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2010, 51 (05) :2615-2619
[2]   Thermal stability of DNA [J].
Blake, RD ;
Delcourt, SG .
NUCLEIC ACIDS RESEARCH, 1998, 26 (14) :3323-3332
[3]   Complete gene scanning by temperature gradient capillary electrophoresis using the cystic fibrosis transmembrane conductance regulator gene as a model [J].
Chou, LS ;
Gedge, F ;
Lyon, E .
JOURNAL OF MOLECULAR DIAGNOSTICS, 2005, 7 (01) :111-120
[4]   Mutations in the phenflalanine hydroxylase gene identified in 95 patients with phenylketonuria using novel systems of mutation scanning and specific genotyping based upon thermal melt profiles [J].
Dobrowolski, Steven F. ;
Ellingson, Clinton ;
Coyne, Thomas ;
Grey, Jesse ;
Martin, Ranae ;
Naylor, Edwin W. ;
Koch, Richard ;
Levy, Harvey L. .
MOLECULAR GENETICS AND METABOLISM, 2007, 91 (03) :218-227
[5]   High resolution melting applications for clinical laboratory medicine [J].
Erali, Maria ;
Voelkerding, Karl V. ;
Wittwer, Carl T. .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 2008, 85 (01) :50-58
[6]  
Farrar JS, 2010, MOLECULAR DIAGNOSTICS, 2ND EDITION, P229, DOI 10.1016/B978-0-12-374537-8.00015-8
[7]   THEORY OF DNA MELTING CURVES [J].
FIXMAN, M ;
FREIRE, JJ .
BIOPOLYMERS, 1977, 16 (12) :2693-2704
[8]   Base-pair neutral homozygotes can be discriminated by calibrated high-resolution melting of small amplicons [J].
Gundry, Cameron N. ;
Dobrowolski, Steven F. ;
Martin, Y. Ranae ;
Robbins, Thomas C. ;
Nay, Lyle M. ;
Boyd, Nathan ;
Coyne, Thomas ;
Wall, Mikeal D. ;
Wittwer, Carl T. ;
Teng, David H. -F. .
NUCLEIC ACIDS RESEARCH, 2008, 36 (10) :3401-3408
[9]   Expanded instrument comparison of amplicon DNA melting analysis for mutation scanning and genotyping [J].
Herrmann, Mark G. ;
Durtschi, Jacob D. ;
Wittwer, Carl T. ;
Voelkerding, Karl V. .
CLINICAL CHEMISTRY, 2007, 53 (08) :1544-1548
[10]   Instrument comparison for heterozygote scanning of single and double heterozygotes:: A correction and extension of Herrmann et al., Clin Chem 2006;52:494-503 [J].
Herrmann, Mark G. ;
Durtschi, Jacob D. ;
Bromley, L. Kathryn ;
Wittwer, Carl T. ;
Voelkerding, Karl V. .
CLINICAL CHEMISTRY, 2007, 53 (01) :150-152