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CRISPR-enhanced iron accumulation in TBR225 rice via OsNRAMP7 overexpression
Wednesday, 2025/04/09 | 08:21:11

Phuong Duy Nguyen, Van Thi Pham, Diep Hong Le, Yen Hai Hoang, Xuan Hoi Pham, Mai Quynh Le

 

Plant Biotechnology; Published online March 26, 2025

https://doi.org/10.5010/JPB.2025.52.006.051

Abstract

Rice is a staple food for over half of the world’s population; hence, its nutritional quality is crucial for global health. Iron deficiency anemia affects billions of people worldwide and is particularly prevalent in rice-consuming regions. Accordingly, the biofortification of rice through genetic enhancement offers a sustainable solution to this widespread nutritional challenge. Suitably, the elite Vietnamese rice cultivar TBR225, known for its high yield and superior quality, presents an ideal candidate for iron biofortification. Therefore, this study builds upon previous research that used CRISPR/Cas9 technology to overexpress a key iron transporter gene (OsNRAMP7) in TBR225. The genotype and phenotype of these previously developed OsNRAMP7- overexpressing TBR225 lines were evaluated. Molecular analysis confirmed the successful insertion of the 35S promoter upstream of OsNRAMP7 and the resulting increase in OsNRAMP7 expression. Under greenhouse conditions, the edited lines exhibited substantially higher iron accumulation in the roots, shoots, and grains than in wild-type plants, with grain iron content increasing by 18-72%. Importantly, OsNRAMP7 overexpression did not affect the accumulation of other metals, such as zinc and cadmium, thereby demonstrating its specificity for iron transport. Moreover, key agronomic traits, including growth duration, plant height, yield, and grain quality, remained unaffected in the edited lines. Overall, these findings validate the promising potential of OsNRAMP7 overexpression as a strategy to develop ironbiofortified rice varieties without compromising essential agronomic qualities. This approach will effectively address iron deficiency in rice-consuming populations while maintaining agricultural productivity.

 

See https://www.kspbtjpb.org/journal/view.html?uid=2457&vmd=Full

 

Figure 1:

Genotyping analysis of OsNRAMP7-edited TBR225 line. (A) Schematic diagram of OsNRAMP7 gene structure showing the insertion site of the 35S promoter. Black rectangles: exons; lines: introns and untranslated regions (UTR); arrows: positions of polymerase chain reaction (PCR) primers; (35Sx2): two repeating sequences of the 35S promoter. (B) PCR analysis of transgene presence. Top: OsEF1α (endogenous control, 191 bp); Middle: HPT (selectable marker gene, 260 bp); Bottom: Ubi::Cas9 cassette (361 bp); C: positive control (DNA from T0 TBR225 edited line); V: positive control (CRISPR/Cas9 transformation vector) (Sup. ). (C) 35S promoter insertion detection. PCR analysis using two specific primer pairs to confirm 35S promoter integration (expected band sizes: 1198 bp and 302 bp). (D) OsNRAMP7 expression analysis using reverse transcription (RT)-PCR; OsEF1α: internal control (191 bp). M: DNA ladder (1.0 kb), WT: wild-type TBR225 plant; MU: edited TBR225 plants. Images are representative of three independent experiments

 

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