Asymmetric exponential amplification reaction on a toehold/biotin featured template: an ultrasensitive and specific strategy for isothermal microRNAs analysis

被引:72
作者
Chen, Jun [1 ]
Zhou, Xueqing [1 ]
Ma, Yingjun [1 ]
Lin, Xiulian [2 ]
Dai, Zong [1 ]
Zou, Xiaoyong [1 ,3 ]
机构
[1] Sun Yat Sen Univ, Sch Chem & Chem Engn, Guangzhou 510275, Guangdong, Peoples R China
[2] Guangdong Pharmaceut Univ, Coll Pharm, Guangzhou 510006, Guangdong, Peoples R China
[3] SYSU CMU Shunde Int Joint Res Inst, Shunde 528300, Guangdong, Peoples R China
关键词
ROLLING-CIRCLE AMPLIFICATION; SENSITIVE DETECTION; ELECTROCHEMICAL DETECTION; OLIGONUCLEOTIDE PROBES; COLORECTAL-CANCER; DNA AMPLIFICATION; HYBRIDIZATION; ASSAY; PROLIFERATION; METHYLATION;
D O I
10.1093/nar/gkw504
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The sensitive and specific analysis of microRNAs (miRNAs) without using a thermal cycler instrument is significant and would greatly facilitate biological research and disease diagnostics. Although exponential amplification reaction (EXPAR) is the most attractive strategy for the isothermal analysis of miRNAs, its intrinsic limitations of detection efficiency and inevitable non-specific amplification critically restrict its use in analytical sensitivity and specificity. Here, we present a novel asymmetric EXPAR based on a new biotin/toehold featured template. A biotin tag was used to reduce the melting temperature of the primer/template duplex at the 5' terminus of the template, and a toehold exchange structure acted as a filter to suppress the non-specific trigger of EXPAR. The asymmetric EXPAR exhibited great improvements in amplification efficiency and specificity as well as a dramatic extension of dynamic range. The limit of detection for the let-7a analysis was decreased to 6.02 copies (0.01 zmol), and the dynamic range was extended to 10 orders of magnitude. The strategy enabled the sensitive and accurate analysis of let-7a miRNA in human cancer tissues with clearly better precision than both standard EXPAR and RT-qPCR. Asymmetric EXPAR is expected to have an important impact on the development of simple and rapid molecular diagnostic applications for short oligonucleotides.
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页数:9
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共 44 条
[1]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[2]   Miniaturized isothermal nucleic acid amplification, a review [J].
Asiello, Peter J. ;
Baeumner, Antje J. .
LAB ON A CHIP, 2011, 11 (08) :1420-1430
[3]   miRNAs: Micro managers of programmed cell death [J].
Baehrecke, EH .
CURRENT BIOLOGY, 2003, 13 (12) :R473-R475
[4]   MicroRNA binding sites in Arabidopsis class IIIHD-ZIP mRNAs are required for methylation of the template chromosome [J].
Bao, N ;
Lye, KW ;
Barton, MK .
DEVELOPMENTAL CELL, 2004, 7 (05) :653-662
[5]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[6]   bantam encodes a developmentally regulated microRNA that controls cell proliferation and regulates the proapoptotic gene hid in Drosophila [J].
Brennecke, J ;
Hipfner, DR ;
Stark, A ;
Russell, RB ;
Cohen, SM .
CELL, 2003, 113 (01) :25-36
[7]   MicroRNAs modulate hematopoietic lineage differentiation [J].
Chen, CZ ;
Li, L ;
Lodish, HF ;
Bartel, DP .
SCIENCE, 2004, 303 (5654) :83-86
[8]   Highly Sensitive Determination of microRNA Using Target-Primed and Branched Rolling-Circle Amplification [J].
Cheng, Yongqiang ;
Zhang, Xian ;
Li, Zhengping ;
Jiao, Xiaoxia ;
Wang, Yucong ;
Zhang, Yali .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (18) :3268-3272
[9]   Toehold-initiated Rolling Circle Amplification for Visualizing Individual MicroRNAs In Situ in Single Cells [J].
Deng, Ruijie ;
Tang, Longhua ;
Tian, Qianqian ;
Wang, Ying ;
Lin, Lei ;
Li, Jinghong .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2014, 53 (09) :2389-2393
[10]   Circulating micro-RNA expression profiles in early stage nonsmall cell lung cancer [J].
Heegaard, Niels H. H. ;
Schetter, Aaron J. ;
Welsh, Judith A. ;
Yoneda, Mitsuhiro ;
Bowman, Elise D. ;
Harris, Curtis C. .
INTERNATIONAL JOURNAL OF CANCER, 2012, 130 (06) :1378-1386