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Application and Prospect of Virus-induced Gene Silencing in Crop Gene Function Research
Mengyuan HAO, Qi HANG, Gongyao SHI
Journal of Agricultural Science and Technology    2022, 24 (1): 1-13.   DOI: 10.13304/j.nykjdb.2020.0781
Abstract   (1977 HTML107 PDF(pc) (1362KB)(1102)  

With the completion of crop genome sequencing, a large number of genes' functions affecting important agronomic traits of crops are waiting to be discovered. Due to the lack of genetic transformation methods, the research on gene function of most crops is progressing slowly. Virus-induced gene silencing (VIGS) technology does not rely on genetic transformation. Through virus vector inoculation, efficient silencing of targeted genes can be achieved in contemporary plants. VIGS technology is increasingly used in reverse genetics for analysis of gene functions and metabolic pathways in different crops due to its fast onset time, high silencing efficiency, low operating cost, high-throughput and wide application of plants. This article introduced the technical principles and development process of VIGS, systematically summarized the application of VIGS in different crop research, and then summarized and discussed the limitations of existing VIGS applications and several key factors affecting its silence efficiency, and finally the application in future plant biology research was prospected, which would provide reference for its further application and development.


Fig.1 Mechanism of RNAi and VIGS (taking TRV as an example)
A:RNAi; B:VIGS。A-a: The dsRNA is cleaved into siRNAs; A-b: The formation of RISC; A-c: The RISC is activated; A-d: The RISC binds to complementary mRNA sequences; A-e: Target gene mRNA degradation. B-a: Genomic organization of wild-type TRV RNA 1 and RNA 2; B-b: The structure of pBINTRA6 and PTV00T-DNA after artificial modification; B-c: The process of viral immunity in plant cells. MT—Methyltransferase;H—Helicase; RdRp—RdRp gene; Mp—Movement protein; 16 k—16 kD protein; Cp—Coat protein; 29.4 k—29.4 kD protein; 32.8 k—32.8 kD protein;LB—Left border; 35S—35S promoter;T—Transcription terminator; RB—Right border;MCS—multiple cloning site.
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