US 12,391,952 B2
Method for simply constructing two-component viral vector and related applications thereof
Guoli Song, Anyang (CN); Yunfei Hao, Anyang (CN); Dongyun Zuo, Anyang (CN); Hailiang Cheng, Anyang (CN); Ji Liu, Anyang (CN); Qiaolian Wang, Anyang (CN); and Zhenhui Guan, Anyang (CN)
Assigned to INSTITUTE OF COTTON RESEARCH OF THE CHINESE ACADEMY OF AGRICULTURAL SCIENCES, Anyang (CN); and NATIONAL NANFAN RESEARCH INSTITUTE (SANYA), CHINESE ACADEMY OF AGRICULTURAL SCIENCES, Sanya (CN)
Filed by Institute of Cotton Research of the Chinese Academy of Agricultural Sciences, Anyang (CN); and National Nanfan Research Institute (Sanya), Chinese Academy of Agricultural Sciences, Sanya (CN)
Filed on Jun. 24, 2024, as Appl. No. 18/752,372.
Claims priority of application No. 202311569075.7 (CN), filed on Nov. 23, 2023.
Prior Publication US 2025/0171793 A1, May 29, 2025
Int. Cl. C12N 15/82 (2006.01); C12N 7/00 (2006.01); C12N 15/66 (2006.01)
CPC C12N 15/8218 (2013.01) [C12N 7/00 (2013.01); C12N 15/66 (2013.01); C12N 15/8203 (2013.01); C12N 2750/12021 (2013.01); C12N 2750/12043 (2013.01); C12N 2770/00021 (2013.01); C12N 2770/00043 (2013.01)] 1 Claim
 
1. A method for simply constructing a two-component viral vector comprising a first genomic component and a second genomic component, the method comprising:
modifying a restriction site within the multiple cloning site of the first genomic component into a new restriction site, modifying the flanking sites of the new restriction site into the adapter sequences set forth by SEQ ID NO: 31 and SEQ ID NO: 32, and concatenating the first genomic component via the adapter sequences through PCR and homologous recombination;
ligating the concatenated first genomic component and the second genomic component into a plasmid to obtain a single plasmid encoding the two-component viral vector;
wherein the two-component viral vector is a two-component DNA or a two-component RNA viral vector;
when the two-component DNA viral vector is the cotton leaf crumple virus (CLCrV), the two genomic components are flanked by respective common regions (CRs), the plasmid is the Agrobacterium Ti plasmid, the CRs can be linked via a restriction site sequence, and the two genomic components are inserted between the T-DNA borders of the Agrobacterium Ti plasmid;
when the two-component RNA viral vector is the tobacco rattle virus (TRV), the two genomic components are placed in two separate expression cassettes for independent expression from the 35S promoter, wherein each expression cassette comprises the NOS terminator.