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Abstract
Plant viral vectors may provide a rapid, transgene-free alternative for genetic intervention in crops.
- Advanced designs of viral vectors, such as deconstructed genomes and synthetic regulatory circuits, enhance cargo capacity and specificity.
- The combination of viral delivery with CRISPR-Cas systems enables new genome editing techniques like virus-induced genome editing (VIGE) and base editing.
- Heritable trait modifications can be achieved without tissue culture using these advanced viral vectors.
- Key challenges include expanding the host range, ensuring environmental containment, and developing scalable delivery methods.
- Emerging synergies with nanobiotechnology could lead to more targeted and efficient applications.
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