Author:
Zhang Kewei,Yin Xiaomei,Shi Kaituo,Zhang Shihua,Wang Juan,Zhao Shasha,Deng Huan,Zhang Cheng,Wu Zihui,Li Yuan,Zhou Xiangyu,Deng Wensheng
Abstract
AbstractSite-directed mutagenesis for large plasmids is a difficult task that cannot easily be solved by the conventional methods used in many laboratories. In this study, we developed an effective method for Site-directed Mutagenesis for Large Plasmids (SMLP) based on a PCR technique. The SMLP method combines several effective approaches, including a high-efficiency DNA polymerase for the large DNA amplification, two independent PCR reactions and a fast recombinational ligation. Using this method, we have achieved a variety of mutants for the filamin A gene (7.9 kb) cloned in the pcDNA (5.4 kb) or the pLV-U6-CMV-EGFP (9.4 kb) plasmids, indicating that this method can be applied to site-directed mutagenesis for the plasmids up to 17.3 kb. We show that the SMLP method has a greater advantage than the conventional methods tested in this study, and this method can be applied to substitution, deletion, and insertion mutations for both large and small plasmids as well as the assembly of three fragments from PCR reactions. Altogether, the SMLP method is simple, effective, and beneficial to the laboratories that require completing the mutagenesis of large plasmids.
Funder
National Natural Science Foundation of China
Publisher
Springer Science and Business Media LLC
Reference22 articles.
1. Kato, S. et al. Understanding the function-structure and function-mutation relationships of p53 tumor suppressor protein by high-resolution missense mutation analysis. Proc. Natl. Acad. Sci. USA 100, 8424–8429 (2003).
2. Röder, K., Stirnemann, G., Dock-Bregeon, A. C., Wales, D. J. & Pasquali, S. Structural transitions in the RNA 7SK 5’ hairpin and their effect on HEXIM binding. Nucl. Acids Res. 48, 373–389 (2020).
3. David, J. P. et al. Deletion in mice of X-linked, Brugada syndrome- and atrial fibrillation-associated Kcne5 augments ventricular KV currents and predisposes to ventricular arrhythmia. FASEB J. 33, 2537–2552 (2019).
4. Lõhmussaar, K. et al. Assessing the origin of high-grade serous ovarian cancer using CRISPR-modification of mouse organoids. Nat. Commun. 11, 2660. https://doi.org/10.1038/s41467-020-16432-0 (2020).
5. Liu, H. & Naismith, J. H. An efficient one-step site-directed deletion, insertion, single and multiple-site plasmid mutagenesisprotocol. BMC Biotechnol. 8, 91. https://doi.org/10.1186/1472-6750-8-91 (2008).
Cited by
11 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献