Rare target enrichment for ultrasensitive PCR detection using cot-rehybridization and duplex-specific nuclease

详细信息    查看全文

• 作者：Charul Gijavanekar^a ; ¹ ; Ulrich Strych^a ; Yuriy Fofanov^a ; ^b ; ^c ; George E. Fox^a ; ^d ; Richard C. Willson^a ; ^c ; ^d ; ^{willson@uh.edu}
• 关键词：Cot&ndash ; rehybridization ; Cot analysis ; Target enrichment ; Duplex-specific nuclease ; PCR sensitivity ; PCR diagnostics
• 刊名：Analytical Biochemistry
• 出版年：2012
• 出版时间：1 February 2012
• 年：2012
• 卷：421
• 期：1
• 页码：81-85
• 全文大小：328 K

文摘

Nucleic acid detection by polymerase chain reaction (PCR) is invaluable for the detection of dilute and rare sequences, including pathogens and infrequent species in complex clinical and environmental backgrounds. The presence of excess complex background nucleic acid can reduce sensitivity and specificity. This is because mispriming can cause failure of the amplification reaction. Here we describe a new approach to ultrasensitive PCR detection, using enrichment of rare target nucleic acid from abundant background by combining the classic technique of cot-rehybridization to convert the abundant background to double-stranded form, with the use of a newly described, highly processive duplex-specific crab nuclease. We show that trace sequences in a vast excess of background DNA can be undetectable by PCR, independent of the amount of the mixture added to the PCR, and that these sequences can be made detectable by background suppression using this method.