Multiplex polymerase chain reaction for simultaneous quantitation of human nuclear, mitochondrial, and male Y-chromosome DNA: application in human identification

被引:64
作者
Walker, JA
Hedges, DJ
Perodeau, BP
Landry, KE
Stoilova, N
Laborde, ME
Shewale, J
Sinha, SK
Batzer, MA
机构
[1] Louisiana State Univ, Ctr Biomodular Microsyst, Dept Biol Sci, Biol Computat & Visualizat Ctr, Baton Rouge, LA 70803 USA
[2] ReliaGene Technol Inc, New Orleans, LA 70123 USA
关键词
forensic genomics; triplex;
D O I
10.1016/j.ab.2004.09.036
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Human forensic casework requires sensitive quantitation of human nuclear (nDNA), mitochondrial (mtDNA), and male Y-chromosome DNA from complex biomaterials. Although many such systems are commercially available, no system is capable of simultaneously quantifying all three targets in a single reaction. Most available methods either are not multiplex compatible or lack human specificity. Here, we report the development of a comprehensive set of human-specific, target-specific multiplex polymerase chain reaction (PCR) assays for DNA quantitation. Using TaqMan-MGB probes, our duplex qPCR for nDNA/mtDNA had a linear quantitation range of 100 ng to 1 pg, and our triplex qPCR assay for nDNA/mtDNA/male Y DNA had a linear range of 100-0.1 ng. Human specificity was demonstrated by the accurate detection of 0.05 and 5% human DNA from a complex source of starting templates. Target specificity was confirmed by the lack of cross-amplification among targets. A high-throughput alternative for human gender determination was also developed by multiplexing the male Y primer/probe set with an X-chromosome-based system. Background cross-amplification with DNA templates derived from 14 other species was negligible aside from the male Y assay which produced spurious amplifications from other nonhuman primate templates. Mainstream application of these assays will undoubtedly benefit forensic genomics. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:89 / 97
页数:9
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