PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of bmcbiotBioMed Centralsearchsubmit a manuscriptregisterthis articleBMC Biotechnology
 
BMC Biotechnol. 2012; 12: 39.
Published online Jul 6, 2012. doi:  10.1186/1472-6750-12-39
PMCID: PMC3408372
An asymmetric PCR-based, reliable and rapid single-tube native DNA engineering strategy
Yanzhen Bi,corresponding author1 Xianfeng Qiao,1 Zaidong Hua,1 Liping Zhang,1 Ximei Liu,1 Li Li,1 Wenjun Hua,1 Hongwei Xiao,1 Jingrong Zhou,1 Qingxin Wei,1 and Xinmin Zhengcorresponding author1
1Hubei Key Laboratory of Animal Embryo Engineering and Molecular Breeding, Institute of Animal Science and Veterinary Medicine, Hubei Academy of Agricultural Science, Wuhan, 430064, China
corresponding authorCorresponding author.
Yanzhen Bi: biyanzhen/at/gmail.com; Xianfeng Qiao: qiaoxianfengzi2001/at/163.com; Zaidong Hua: huazaidong123/at/yahoo.com.cn; Liping Zhang: chzlp/at/yahoo.com.cn; Ximei Liu: anbit20/at/hotmail.com; Li Li: lilyzhzlin/at/yahoo.com.cn; Wenjun Hua: huawenjun08/at/yahoo.com.cn; Hongwei Xiao: xiaohongwei2003/at/163.com; Jingrong Zhou: novorigin/at/126.com; Qingxin Wei: weiqingxin/at/sina.com; Xinmin Zheng: anbit20/at/163.com
Received March 16, 2012; Accepted July 6, 2012.
Abstract
Background
Widely used restriction-dependent cloning methods are labour-intensive and time-consuming, while several types of ligase-independent cloning approaches have inherent limitations. A rapid and reliable method of cloning native DNA sequences into desired plasmids are highly desired.
Results
This paper introduces ABI-REC, a novel strategy combining asymmetric bridge PCR with intramolecular homologous recombination in bacteria for native DNA cloning. ABI-REC was developed to precisely clone inserts into defined location in a directional manner within recipient plasmids. It featured an asymmetric 3-primer PCR performed in a single tube that could robustly amplify a chimeric insert-plasmid DNA sequence with homologous arms at both ends. Intramolecular homologous recombination occurred to the chimera when it was transformed into E.coli and produced the desired recombinant plasmids with high efficiency and fidelity. It is rapid, and does not involve any operational nucleotides. We proved the reliability of ABI-REC using a double-resistance reporter assay, and investigated the effects of homology and insert length upon its efficiency. We found that 15 bp homology was sufficient to initiate recombination, while 25 bp homology had the highest cloning efficiency. Inserts up to 4 kb in size could be cloned by this method. The utility and advantages of ABI-REC were demonstrated through a series of pig myostatin (MSTN) promoter and terminator reporter plasmids, whose transcriptional activity was assessed in mammalian cells. We finally used ABI-REC to construct a pig MSTN promoter-terminator cassette reporter and showed that it could work coordinately to express EGFP.
Conclusions
ABI-REC has the following advantages: (i) rapid and highly efficient; (ii) native DNA cloning without introduction of extra bases; (iii) restriction-free; (iv) easy positioning of directional and site-specific recombination owing to formulated primer design. ABI-REC is a novel approach to DNA engineering and gene functional analysis.
Keywords: Asymmetric, Bridge PCR, Intramolecular homologous recombination, Myostatin
Articles from BMC Biotechnology are provided here courtesy of
BioMed Central