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Updated: Mar 7, 2026

Author Spotlight: Streamlining Rice Breeding with CRISPR/Cas for Obtaining Optimal Phenotypic and Agronomic Traits
Published on: January 3, 2025
Accelerated development of rice near-isogenic lines based on rapid generation advance (RGA) and target capture
Seung-Kyo Jeong1, So-Myeong Lee1, Jin-Kyung Cha1
1Field crop research division, National Institute of Crop and Food Science, RDA, Miryang, 50424 Republic of Korea.
None:
Developing new crop cultivars with enhanced disease resistance, stress tolerance, and superior quality is urgently needed to address climate change and evolving agricultural demands. However, conventional breeding methods, particularly the development of near-isogenic lines (NILs), are notoriously time-consuming and labor-intensive. This study presents an innovative, integrated strategy to accelerate rice NIL development by combining a Rapid Generation Advance (RGA) system, Target Capture Sequencing (TCS), and a bulk DNA-based background selection approach applied at an advanced generation (BC2F6). Our strategy successfully established a NIL population within four years, a process traditionally requiring nearly a decade. The developed NILs exhibited a high recurrent parent genome (RPG) recovery rate, averaging 90.8% and reaching up to 97.2%. We validated the successful introgression of target genes, including x a5 (bacterial blight resistance) and Pita-2 (blast resistance), through both phenotypic and genotypic analyses. Notably, our RGA system utilized natural short-day conditions, effectively overcoming photoperiod sensitivity constraints in late-maturing cultivars and enabling two generations per year. This integrated strategy provides a scalable and efficient framework that dramatically reduces the time, labor, and costs associated with conventional NIL development while ensuring high precision, offering significant potential to accelerate functional genomics and marker-assisted breeding programs in rice and other major crop species.
Supplementary Information:
The online version contains supplementary material available at 10.1007/s11032-026-01647-8.
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