American Journal of Biomedical Research. 2016, 4(1), 1-4
DOI: 10.12691/ajbr-4-1-1
Open AccessCommentary
Gang Zhang1, 2, and Yi Zhang3
1Department of Medicine, Centre for Research in Neurodegenerative Diseases, University of Toronto, 6 Queen’s Park Crescent West, Toronto, ON, M5S 3H2, Canada
2Department of Cell & Systems Biology, University of Toronto, 25 Harbord Street, Toronto, ON, M5S 3G5, Canada
3Program in Life Science, New College, University of Toronto, 40 Willcocks St, Toronto, ON, M5S 1C6, Canada
Pub. Date: January 09, 2016
Cite this paper:
Gang Zhang and Yi Zhang. On the “All or Half” Law of Recombinant DNA. American Journal of Biomedical Research. 2016; 4(1):1-4. doi: 10.12691/ajbr-4-1-1
Abstract
Plasmid vectors are one of the most important tools for the investigation of the functions of genes of interest. Efficient cloning of various vectors, according to different purposes, is critical for biomedical research. Previously, we reported a new method, designated as “Combinatorial Strategy”, for cloning different vectors with various clone sites. We demonstrated that it is a quantitative law for recombinant DNA with our method, which is when two different clone sites are used, almost 100% transformants are positive clones, on the other hand, when one over-hang clone site, or different blunt clone sites are used, about 50% of the transformants are positive clones. We named this quantitative law as the "All or Half" law of recombinant DNA. Here, we summarized the mechanisms of recombinant DNA, provided a general protocol and suggested the predicted results for plasmid vector cloning. This is a revolutionary breakthrough of recombinant DNA technology.Keywords:
recombinant DNA Combinatorial Strategy "All or Half" law Calf Intestinal Phosphatase site-directed mutagenesis Top10 clone sites
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References:
| [1] | Jackson, D.A., Symons, R.H. and Berg, P., Biochemical method for inserting new genetic information into DNA of Simian Virus 40: Circular SV40 DNA molecules containing Lambda phage genes and the galactose operon of Escherichia Coli, Proc Nat Acad Sci USA, 69: 2904-2909, 1972. |
| |
| [2] | Cohen, S. N., Chang, A. C. Y., Boyer, H. W. and Helling, R. B., Construction of biologically functional bacteria plasmids in vitro, Proc. Nat. Acad. Sci. USA., 70: 3240-3244, 1973. |
| |
| [3] | Sambrook, J. and Russell, D. W., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press: Plainview, NY, 2001. |
| |
| [4] | Zhang, G. and Tandon, A., Quantitative assessment on the cloning efficiencies of lentiviral transfer vectors with a unique clone site, Sci Rep, 2: 415, 2012. |
| |
| [5] | Zhang, G. and Tandon, A., “Combinatorial Strategy”: A highly efficient method for cloning different plasmid vectors with various clone site, American Journal of Biomedical Research, 1: 112-119, 2013. |
| |
| [6] | Zhang, G., A new overview on the old topic: The theoretical analysis of “Combinatorial Strategy” for DNA recombination, American Journal of Biomedical Research, 1: 108-111, 2013. |
| |
| [7] | Wu, D.Y. and Wallace, R.B., Specificity of the nick-closing activity of bacteriophage T4 DNA ligase, Gene, 76: 245-254, 1989. |
| |
| [8] | Harada, K. and Orgel, L., Unexpected substrate specificity of T4 DNA ligase revealed by in vitro selection, Nucl Acids Res, 21: 2287-2291, 1993. |
| |
| [9] | Landegren, U., Kaiser, R., Sanders, J. and Hood, L., A ligase-mediated gene detection technique, Science, 241: 1077-1080, 1988. |
| |