Fast Construction of dsRNA Prokaryotic Expression Vector of Papaya Ringspot Virus CP Gene
doi: 10.15886/j.cnki.rdswxb.2011.02.006
- Received Date: 2011-06-27
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Key words:
- PRSV-CP /
- dsRNA /
- RNA silencing /
- OZ-LIC method /
- prokaryotic expression vector
Abstract: In the paper,a method for constructing dsRNA prokaryotic expression vector was introduced.The conserved region of PRSV-CP gene,which is 278 bp of 3'-end region,was used as the base,three hairpin structures of different lengths(861 bp,432 bp,279 bp) were cloned and constructed through one-step,zero-background ligation-independent cloning(OZ-LIC) method,and which were successively cloned into pSP73 prokaryotic expression vector after being digested with XhoⅠand ClaⅠ.Finally three recombinants of dsRNA prokaryotic expression plasmid of PRSV-CP gene were obtained.
Citation: | CHEN Yao, SHEN Wentao, YAN Pu, LI Xiaoying, ZHOU Peng. Fast Construction of dsRNA Prokaryotic Expression Vector of Papaya Ringspot Virus CP Gene[J]. Journal of Tropical Biology, 2011, 2(2): 113-116. doi: 10.15886/j.cnki.rdswxb.2011.02.006 |