Constructing recombinant herpesvirus BAC vectors with mating-assisted genetically integrated clone method
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Updated: Jun 14, 2026

The MultiBac Protein Complex Production Platform at the EMBL
Published on: July 11, 2013
Sijing Jiang1, Xing Zhong, Chao Zhai
1National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, 430070, Hubei, People's Republic of China. jiangsijing@hubu.edu.cn
Abstract:
The large capacity of pseudorabies virus (PRV) for foreign DNA and broad host range make it a prospective tool for the preparation of vaccines and agents of gene and tumour therapy. Here we introduced a cloning strategy that facilitates construction of recombinant PRV-BAC vectors based on mating-assisted genetically integrated clone (MAGIC). The target gene was cloned into a small conditionally replicating donor plasmid, followed by shuffling to a recipient PRV-BAC plasmid in vivo of Escherichia coli through MAGIC. The average efficiency of successful clones was 89%. Moreover, permanent integration of unwanted sequences was avoided.
