Integration of multiple PCR amplifications and DNA mutation analyses by using oligonucleotide microchip

被引:42
作者
Tillib, SV
Strizhkov, BN
Mirzabekov, AD
机构
[1] Argonne Natl Lab, Biochip Technol Ctr, Argonne, IL 60439 USA
[2] Russian Acad Sci, Engelhardt Inst Mol Biol, Moscow 119991, Russia
关键词
microarray; oligonucleotide microchip; PCR; M; tuberculosis; mutations;
D O I
10.1006/abio.2001.5082
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We have developed a method for parallel independent on-chip amplification and the following sequence variation analysis of multiple DNA regions directly using microchip with an array of nanoliter gel pads containing specific sets of tethered primers. The method has three key features, First, DNA to be amplified is enriched at gel pads by its hybridization with immobilized primers, Second, different sets of specific primers are immobilized within various gel pads, and primers are detached within gel pads just before polymerase chain reaction to enhance the amplification. A gel pad may contain an additional permanently immobilized dormant primer that is activated to carry out the allele-specific primer extension reaction to detect mutations. Third, multiple polymerase chain reactions are confined within nanoliter gel pads covered and separated from each other with mineral oil. The method was applied to simultaneously identify several abundant drug-resistant mutations in three genes of Mycobacterium tuberculosis. (C) 2001 Academic Press.
引用
收藏
页码:155 / 160
页数:6
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