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Tissue Culture Optimization and Construction of a Suitable Vector for Engineering Very Long-Chain Fatty Acids in Camelina sativa L. | ||
| Agrotechniques in Industrial Crops | ||
| دوره 6، شماره 1، خرداد 2026، صفحه 112-121 اصل مقاله (841.45 K) | ||
| نوع مقاله: Original Article | ||
| شناسه دیجیتال (DOI): 10.22126/atic.2026.11724.1193 | ||
| نویسندگان | ||
| Hamideh Baghi1؛ Alireza Tarinejad* 1؛ Maghsoud Pazhouhandeh2؛ Nasser Mahna3 | ||
| 1Agricultural Biotechnology Department, Faculty of Agriculture, Azarbaijan Shahid Madani University, Tabriz, Iran | ||
| 2Department of Plant, Cell and Molecular Biology, Faculty of Natural Science, University of Tabriz, Tabriz, Iran | ||
| 3Department of Horticultural Sciences, University of Tabriz, Tabriz, Iran | ||
| چکیده | ||
| Oil quality from oilseeds is determined by the fatty acid (FA) content. Fatty Acid Elongase 1 (FAE1) is an essential FA gene that has been genetically modified to change the constitution of fatty acids in oilseed plants. In this study, recombinant vector construction for genome editing of the CsFAE1B, CsFAE1A, and CsFAE1C genes using CRISPR/Cas9 was used to improve the quality of Camelina Sativa oil (which contains about 50% oil and 4% erucic acid). Additionally, camelina tissue culture optimization for recombinant vector transfer was performed concurrently. Finally, gRNA was designed to target three copies of the CsFAE1 genes, and after transfer to the pFGC-pcoCas9 vector, the recombinant vector was confirmed by PCR and enzymatic digestion. The tissue culture optimization results indicated that hormone ratios of 0.5 mg L-1 NAA and 3 mg L-1 BAP for cotyledon and hypocotyl in the Gamborg medium induced embryogenic calluses three weeks after cultivation. Additionally, hormone ratios of 0.5 NAA, 2 BAP, and 1 (mg L-1) Kin led to direct regeneration in cotyledon explants. In future studies, tissue culture optimization and recombinant vector construction for genome editing of FAEs genes could improve oil quality with the genetic transformation of camelina. | ||
| کلیدواژهها | ||
| CRISPR-Cas9؛ CsFAE1؛ gRNA؛ Recombinant vector | ||
| اصل مقاله | ||
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