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Rice Science ›› 2026, Vol. 33 ›› Issue (4): 411-414.DOI: 10.1016/j.rsci.2026.04.006

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  • 收稿日期:2026-02-04 接受日期:2026-04-10 出版日期:2026-07-28 发布日期:2026-08-06

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. [J]. Rice Science, 2026, 33(4): 411-414.

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链接本文: http://www.ricesci.org/CN/10.1016/j.rsci.2026.04.006

               http://www.ricesci.org/CN/Y2026/V33/I4/411

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Fig. 1. Integrated data workflow of Mutagenesis Directed Breeding Platform (MDBP) toolkit. A‒D, Interfaces of four core modules: Pool Construction generates a standard pooling plan based on field layout (A); Mutation Screening imports the pooling plan to map variants to field plots (B); KASP Primer Design uses mutation results to generate primer design and plate map files (C); and Individual Plant Location uses the design file as a linkage key to trace KASP results back to specific field plants (D). E, Schematic overview of MDBP for rapid screening of target gene mutations in the heavy-ion-mutagenized hybrid rice restorer line R8022. Pooling was performed by combining four experimental plots, each consisting of 96 rice plants (arrayed in 12 rows × 8 plants). DNA was extracted from the mixed pool and subjected to targeted gene sequencing, followed by mutation screening using the Mutation Screening module. For pools where mutations were detected, leaf samples from the corresponding plots were mapped into 96-well plates according to their original field arrangement. Each plate was then genotyped using automatically generated KASP markers, and the results were accurately mapped back to the original field plots and row-plant positions, thereby precisely identifying the individual plants carrying the target gene mutations. KASP, Kompetitive allele-specific PCR; VCF, Variant call format; Mut, Mutant; FAM, 6-Carboxyfluorescein; HEX, Hexachlorofluorescein.

Fig. 1. Integrated data workflow of Mutagenesis Directed Breeding Platform (MDBP) toolkit. A‒D, Interfaces of four core modules: Pool Construction generates a standard pooling plan based on field layout (A); Mutation Screening imports the pooling plan to map variants to field plots (B); KASP Primer Design uses mutation results to generate primer design and plate map files (C); and Individual Plant Location uses the design file as a linkage key to trace KASP results back to specific field plants (D). E, Schematic overview of MDBP for rapid screening of target gene mutations in the heavy-ion-mutagenized hybrid rice restorer line R8022. Pooling was performed by combining four experimental plots, each consisting of 96 rice plants (arrayed in 12 rows × 8 plants). DNA was extracted from the mixed pool and subjected to targeted gene sequencing, followed by mutation screening using the Mutation Screening module. For pools where mutations were detected, leaf samples from the corresponding plots were mapped into 96-well plates according to their original field arrangement. Each plate was then genotyped using automatically generated KASP markers, and the results were accurately mapped back to the original field plots and row-plant positions, thereby precisely identifying the individual plants carrying the target gene mutations. KASP, Kompetitive allele-specific PCR; VCF, Variant call format; Mut, Mutant; FAM, 6-Carboxyfluorescein; HEX, Hexachlorofluorescein.

参考文献 8

[1] Kavuri N, Alavilli H, Manthari R, et al. 2025. Transforming farming: Mutational breeding as a sustainable solution for crop improvement in the 21st century. J Plant Biochem Biotechnol, 34(2): 382-389.
[2] Penna S, Shirani Bidabadi S, Jain S M. 2023. Mutation breeding to promote sustainable agriculture and food security in the era of climate change. In: Mutation Breeding for Sustainable Food Production and Climate Resilience. Singapore: Springer Nature Singapore: 1-23.
[3] Shao Y, Peng Y, Mao B G, et al. 2022. M1TDS technology and creation of low-cadmium accumulation parents for hybrid rice breeding. Hybrid Rice, 37(1): 1-11. (in Chinese with English abstract)
[4] Shao Y, Hu Y Y, Peng Y, et al. 2025. Directed improvement of hybrid rice Zhuoliangyou 1126 by heavy ion beam mutagenesis based on M1TDS targeted screening technology. Chin J Rice Sci, 39(5): 624-634. (in Chinese with English abstract)
[5] Tsai H, Howell T, Nitcher R, et al. 2011. Discovery of rare mutations in populations: TILLING by sequencing. Plant Physiol, 156(3): 1257-1268.
[6] Uauy C, Wulff B B H, Dubcovsky J. 2017. Combining traditional mutagenesis with new high-throughput sequencing and genome editing to reveal hidden variation in polyploid wheat. Annu Rev Genet, 51: 435-454.
[7] Untergasser A, Cutcutache I, Koressaar T, et al. 2012. Primer3: New capabilities and interfaces. Nucleic Acids Res, 40(15): e115.
[8] Zhao H, Yao W, Ouyang Y D, et al. 2015. RiceVarMap: A comprehensive database of rice genomic variations. Nucleic Acids Res, 43(D1): D1018-D1022.

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