A novel strategy for the expression of foreign genes from plant virus vectors

• Published in: FEBS letters 2001-02, Vol.489 (2), p.215-219
• Main Authors: Toth, Rachel L, Chapman, Sean, Carr, Fiona, Santa Cruz, Simon
• Format: Article
• Language: English
• Subjects: Binding Sites - genetics; Capsid - genetics; DNA, Recombinant; Gene Expression Regulation; Genetic Vectors - genetics; Green Fluorescent Proteins; Internal initiation; Internal ribosome entry site; Luminescent Proteins - genetics; Luminescent Proteins - metabolism; Microscopy, Confocal; Nicotiana - genetics; Plant Leaves - genetics; Plant Viruses - genetics; Plants, Genetically Modified; Plants, Toxic; Potato virus X; Potexvirus - genetics; Recombinant Fusion Proteins - genetics; Recombinant Fusion Proteins - metabolism; Ribosomes - metabolism; Tobacco Mosaic Virus - genetics; Transfection - methods; Virus vector
• ISSN: 0014-5793; 1873-3468
• DOI: 10.1016/S0014-5793(01)02091-9

Potato virus X (PVX)-based vector constructs were generated to investigate the use of an internal ribosome entry site (IRES) sequence to direct translation of a viral gene. The 148-nucleotide IREScp sequence from a crucifer-infecting strain of tobacco mosaic virus was used to direct expression of the PVX coat protein (CP). The IRES was inserted downstream of the gene encoding green fluorescent protein (GFP) and upstream of the PVX CP, in either sense or antisense orientation, such that CP expression depended on ribosome recruitment to the IRES. Stem–loop structures were inserted at either the 3′- or 5′-end of the IRES sequence to investigate its mode of action. In vitro RNA transcripts were inoculated to Nicotiana benthamiana plants and protoplasts: levels of GFP and CP expression were analysed by enzyme-linked immunosorbent assay and the rate of virus cell-to-cell movement was determined by confocal laser scanning microscope imaging of GFP expression. PVX CP was expressed, allowing cell-to-cell movement of virus, from constructs containing the IRES sequence in either orientation, and from the construct containing a stem–loop structure at the 5′-end of the IRES sequence. No CP was expressed from a construct containing a stem–loop at the 3′-end of the IRES sequence. Our results suggest that the IRES sequence is acting in vivo to direct expression of the 3′-proximal open reading frame in a bicistronic mRNA thereby demonstrating the potential of employing IRES sequences for the expression of foreign proteins from plant virus-based vectors.