Integrated allele-specific polymerase chain reaction-capillary electrophoresis microdevice for single nucleotide polymorphism genotyping

被引:23
作者
Choi, Jong Young [1 ,2 ]
Kim, Yong Tae [1 ,2 ]
Ahn, Jinwoo [3 ]
Kim, Kwan Suk [4 ]
Gweon, Dae-Gab [3 ]
Seo, Tae Seok [1 ,2 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, Program BK21, Taejon 305701, South Korea
[2] Korea Adv Inst Sci & Technol, KAIST Inst BioCentury, Taejon 305701, South Korea
[3] Korea Adv Inst Sci & Technol, Dept Mech Engn, Taejon 305701, South Korea
[4] Chungbuk Natl Univ, Coll Agr Life & Environm Sci, Cheongju 361763, South Korea
关键词
Integrated microdevice; Single nucleotide polymorphism; Allele-specific polymerase chain reaction; Capillary electrophoresis; On-site detection; DNA; SNP; PCR; MARKERS;
D O I
10.1016/j.bios.2012.03.009
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
An integrated allele-specific (AS) polymerase chain reaction (PCR) and capillary electrophoresis (CE) microdevice has been developed for multiplex single nucleotide polymorphism (SNP) genotyping on a portable instrumentation, which was applied for on-site identification of HANWOO (Korean indigenous beef cattle). Twelve sets of primers were designed for targeting beef cattle's eleven SNP loci for HANWOO verification and one primer set for a positive PCR control, and tie success rate for identification of HANWOO was demonstrated statistically. The AS PCR and CE separation for multiplex SNP typing was carried out on a glass-based microchip consisting of four layers: a microchannel plate for microfluidic control, a Pt-electrode plate for a resistance temperature detector (RID), a poly(dimethylsiloxane) (PDMS) membrane and a manifold glass for microvalve function. The operation of the sample loading, AS PCR, microvalve, and CE on a chip was automated with a portable genetic analyzer, and the laser-induced fluorescence detection was performed on a miniaturized fluorescence detector. The blind samples were correctly identified as a HANWOO by showing one or two amplicon peaks in the electropherogram, while the imported beef cattle revealed more than five peaks. Our genetic analysis platform provides rapid, accurate, and on-site multiplex SNP typing. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:327 / 334
页数:8
相关论文
共 30 条
[1]   Miniaturized isothermal nucleic acid amplification, a review [J].
Asiello, Peter J. ;
Baeumner, Antje J. .
LAB ON A CHIP, 2011, 11 (08) :1420-1430
[2]   MUTATION IN BLOOD-COAGULATION FACTOR-V ASSOCIATED WITH RESISTANCE TO ACTIVATED PROTEIN-C [J].
BERTINA, RM ;
KOELEMAN, BPC ;
KOSTER, T ;
ROSENDAAL, FR ;
DIRVEN, RJ ;
DERONDE, H ;
VANDERVELDEN, PA ;
REITSMA, PH .
NATURE, 1994, 369 (6475) :64-67
[3]   Microfabricated bioprocessor for integrated nanoliter-scale Sanger DNA sequencing [J].
Blazej, Robert G. ;
Kumaresan, Palani ;
Mathies, Richard A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (19) :7240-7245
[4]   Robust allele-specific polymerase chain reaction markers developed for single nucleotide polymorphisms in expressed barley sequences [J].
Bundock, PC ;
Cross, MJ ;
Shapter, FM ;
Henry, RJ .
THEORETICAL AND APPLIED GENETICS, 2006, 112 (02) :358-365
[5]  
Butler JM, 2005, Forensic DNA Typing. Biology, Technology, and Genetics of STR Markers, V2nd
[6]   Oligonucleotide ligation assay-based DNA chip for multiplex detection of single nucleotide polymorphism [J].
Deng, HY ;
Zhang, XE ;
Mang, Y ;
Zhang, ZP ;
Zhou, YF ;
Liu, Q ;
Lu, HB ;
Fu, ZJ .
BIOSENSORS & BIOELECTRONICS, 2004, 19 (10) :1277-1283
[7]   Whole genome sequencing of a single Bos taurus animal for single nucleotide polymorphism discovery [J].
Eck, Sebastian H. ;
Benet-Pages, Anna ;
Flisikowski, Krzysztof ;
Meitinger, Thomas ;
Fries, Ruedi ;
Strom, Tim M. .
GENOME BIOLOGY, 2009, 10 (08) :R82
[8]   Electrokinetically based approach for single-nucleotide polymorphism discrimination using a microfluidic device [J].
Erickson, D ;
Liu, XZ ;
Venditti, R ;
Li, DQ ;
Krull, UJ .
ANALYTICAL CHEMISTRY, 2005, 77 (13) :4000-4007
[9]   Pharmacogenomics: Translating functional genomics into rational therapeutics [J].
Evans, WE ;
Relling, MV .
SCIENCE, 1999, 286 (5439) :487-491
[10]  
Hagan KA, 2011, LAB CHIP, V11, P957, DOI [10.1039/c0lc00136h, 10.1039/c01c00136h]