Degenerate oligonucleotide primed polymerase chain reaction and capillary electrophoretic analysis of human DNA on microchip-based devices

被引:97
作者
Cheng, J
Waters, LC
Fortina, P
Hvichia, G
Jacobson, SC
Ramsey, JM
Kricka, LJ
Wilding, P
机构
[1] Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Childrens Hosp Philadelphia, Dept Pediat, Philadelphia, PA 19104 USA
[3] Oak Ridge Natl Lab, Div Chem & Analyt Sci, Oak Ridge, TN 37831 USA
[4] Univ Penn, Dept Pathol, Philadelphia, PA 19104 USA
[5] Univ Penn, Dept Lab Med, Philadelphia, PA 19104 USA
关键词
whole human genome amplification; degenerate oligonucleotide primer; dystrophin gene; chip PCR; microchip electrophoresis;
D O I
10.1006/abio.1997.2531
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Random amplification of the human genome using the degenerate oligonucleotide primed-polymerase chain reaction (DOP-PCR) was performed in a silicon-glass chip. An aliquot of the DOP-PCR amplified genomic DNA was then introduced into another silicon-glass chip for a locus-specific, multiplex PCR of the dystrophin gene exons in order to detect deletions causing Duchenne/Becker muscular dystrophy, Amplicons were analyzed by both conventional capillary electrophoresis and microchip electrophoresis and results were compared to those obtained using standard non-chip-based PCR assays, Results from microchip electrophoresis were consistent with those from conventional capillary electrophoresis. Whole genome amplification products obtained by DOP-PCR proved to be a suitable template for multiplex PCR as long as amplicon size was <250 bp. Successful detection and resolution of all PCR products from the multiplex PCR clearly shows the feasibility of performing complex PCR assays using microfabricated devices. (C) 81998 Academic Press.
引用
收藏
页码:101 / 106
页数:6
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