Delivery of Marker‐Free DNA to Plant Genome by the Transgenic Selection‐Associated Fragment Elimination (T‐SAFE) System
The presence of a selection marker in transgenic plants has raised public concerns regarding health safety. We have developed a CRISPR/Cas9-based DNA delivery system termed transgenic selection-associated fragment elimination (T-SAFE). The T-SAFE system comprises four cassettes: the selection marker, CRISPR/Cas9, spacer-plus-protospacer adjacent motif (SP), and the cargo. The first two cassettes, the selection marker and CRISPR/Cas9, are collectively referred to as SCC. The SCC is flanked by two identical SPs derived from the fruit fly <i>Ebony</i> gene, which efficiently facilitate the SCC cleavage and subsequently lead to self-elimination of the selection marker upon integration of exogenous DNA into the plant genome. To inhibit the production of a functional Cas9 protein in bacteria, the IV2 intron of the potato ST-LS1 gene has been incorporated into the Cas9 gene. Additionally, the Cas9 gene is driven by a reproductive cell-specific or inducible promoter to avoid SCC cleavage in nonreproductive plant cells. These innovative features allow the T-SAFE system to achieve an elimination efficiency of the selection marker ranging from 10%-30% in <i>Arabidopsis</i> and 5%-8% in rice, with a DNA delivery capacity of approximately 10 kb. This approach offers a safe means for genetically modifying plants.
Authors
- Leiwen Pan
- Shun Peng (ORCID: https://orcid.org/0000-0002-5048-0773)
- Dongbei Guo (ORCID: https://orcid.org/0000-0002-8246-0232)
- Huan Chang (ORCID: https://orcid.org/0000-0002-8055-223X)
- Ting Mao (ORCID: https://orcid.org/0000-0003-3720-3410)
- Shui Wang (ORCID: https://orcid.org/0000-0002-5687-8715)
- Yuehui Zhang (ORCID: https://orcid.org/0000-0001-5257-1671)
- Yi Yang (ORCID: https://orcid.org/0000-0003-2360-634X)
Institutions
- Shanghai Normal University (CN)
Publication Details
- Journal
- Plant Direct
- Published
- 2025-02-01
- DOI
- https://doi.org/10.1002/pld3.70046
- Citations
- 2
- Primary Topic
- CRISPR and Genetic Engineering
- Type
- article
- Field-Weighted Citation Impact
- 1.61
Funders
- National Natural Science Foundation of China