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Research Articles

Vol. 12 No. sp3 (2025): Advances in Plant Health Improvement for Sustainable Agriculture

Characterization and breeding value of morphological mutants derived from electron beam and gamma rays in rice (Oryza sativa L.)

DOI
https://doi.org/10.14719/pst.10401
Submitted
2 July 2025
Published
02-01-2026

Abstract

Asia dominates global rice production, accounting for around 90 % of the world's total. Rice is considered as one of the model crops for physical irradiation in mutation studies. Among the physical sources of gamma rays, mutagenic studies have been conducted over several years, but nowadays focus on the emerging physical irradiation source of electron beam due to its action towards biomaterial is effective than gamma rays. The seeds of rice variety Anna (R) 4 were subjected to gamma rays and electron beam irradiation with four different doses (200, 250, 300 and 350 Gy). The primary panicles were collected from each plant in M1 generation, forwarded to M2 and M3 generation as panicles-to-progeny row progenies. The identified mutants from irradiated populations were characterised using DUS test guidelines, followed by prepotency assessment for selected mutants. The maximum frequency was recorded in the electron beam (0.057) than in the gamma rays (0.034) irradiated population. Among the irradiation doses, 300 Gy of electron beam showed a higher frequency (0.099). The morphological mutants related to grain mutants, high tillering, early flowering mutants and flower organisation mutants were recorded maximum in the electron beam than in the conventionally used gamma rays. In the M3 generation, the mutants of grassy and extreme dwarf, extra glume type and grain mutant showed true to type. The present study revealed that the electron beam showed a higher frequency of morphological mutants than the gamma rays.

References

  1. 1. International Atomic Energy Agency IAEA mutant variety search. 2021. https://mvd.iaea.org/#search
  2. 2. Kharkwal MC, Shu QY. The role of induced mutations in world food security. In: Induced Plant Mutations in the Genomics Era. Rome: FAO; 2009. p. 33–38.
  3. 3. Forster BP, Shu QY. Plant mutagenesis in crop improvement: basic terms and applications. In: Plant Mutation Breeding and Biotechnology. Wallingford (UK): CABI; 2012. p. 9–20. https://doi.org/10.1079/9781780640853.0009
  4. 4. Jankowicz-Cieslak J, Mba C, Till BJ. Mutagenesis for crop breeding and functional genomics. In: Biotechnologies for Plant Mutation Breeding: Protocols. 2017. p. 3–18. https://doi.org/10.1007/978-3-319-45021-6_1
  5. 5. Gowthami R, Vanniarajan C, Souframanien J, Pillai MA. Comparison of radiosensitivity of two rice (Oryza sativa L.) varieties to gamma rays and electron beam in M1 generation. Electron J Plant Breed. 2017;8(3):732-41. https://doi.org/10.5958/0975-928X.2017.00111.9
  6. 6. Sao R, Sahu PK, Sharma D, Vishwakarma G, Nair JP, Petwal VC, et al. Comparative study of radio-sensitivity and relative biological effectiveness of gamma rays, X-rays, electron beam and proton beam in short grain aromatic rice. Indian J Genet. 2020;80(04):384-94. https://doi.org/10.31742/IJGPB.80.4.3
  7. 7. Mondal S, Petwal VC, Badigannavar AM, Bhad PG, Verma VP, Goswami SG, et al. Electron beam irradiation revealed genetic differences in radio-sensitivity and generated mutants in groundnut (Arachis hypogaea L.). Appl Radiat Isot. 2017;122:78-83. https://doi.org/10.1016/j.apradiso.2017.01.016
  8. 8. Zhu H, Xu J, Li S, Sun X, Yao S, Wang S. Effects of high-energy-pulse-electron beam radiation on biomacromolecules. Sci China Ser B Chem. 2008;51(1):86-91. https://doi.org/10.1007/s11426-008-0017-4
  9. 9. Lalitha R, Arunachalam P, Mothilal A, Senthil N, Hemalatha G, Vanniarajan C, et al. Radiation effect on germination and seedling traits in rice (Oryza sativa L.). Electron J Plant Breed. 2019;10(3):1038-48. https://doi.org/10.5958/0975-928X.2019.00133.9
  10. 10. Gowthami R, Vanniarajan C, Souframanien J, Veni K, Renganathan VG. Efficiency of electron beam over gamma rays to induce desirable grain-type mutation in rice (Oryza sativa L.). Int J Radiat Biol. 2021;97(5):727-36. https://doi.org/10.1080/09553002.2021.1889702
  11. 11. Gautam V, Swaminathan M, Akilan M, Gurusamy A, Suresh M, Kaithamalai B, et al. Early flowering, good grain quality mutants through gamma rays and EMS for enhancing per day productivity in rice (Oryza sativa L.). Int J Radiat Biol. 2021;97(12):1716-30. https://doi.org/10.1080/09553002.2021.1987563
  12. 12. Chowdhury N, Islam S, Mim MH, Akter S, Naim J, Nowicka B, et al. Characterization and genetic analysis of the selected rice mutant populations. SABRAO J Breed Genet. 2023;55(1):25–37. https://doi.org/10.54910/sabrao2023.55.1.3
  13. 13. Mori M, Nomura T, Ooka H, Ishizaka M, Yokota T, Sugimoto K, et al. Isolation and characterization of a rice dwarf mutant with a defect in brassinosteroid biosynthesis. Plant Physiol. 2002;130(3):1152–61. https://doi.org/10.1104/pp.007179
  14. 14. Hong Z, Ueguchi-Tanaka M, Umemura K, Uozu S, Fujioka S, Takatsuto S, et al. A rice brassinosteroid-deficient mutant, ebisu dwarf (d2), is caused by a loss of function of a new member of cytochrome P450. Plant Cell. 2003;15(12):2900–10. https://doi.org/10.1105/tpc.014712
  15. 15. Itoh H, Tatsumi T, Sakamoto T, Otomo K, Toyomasu T, Kitano H, et al. A rice semi-dwarf gene, Tan-Ginbozu (D35), encodes the gibberellin biosynthesis enzyme ent-kaurene oxidase. Plant Mol Biol. 2004;54:533–47. https://doi.org/10.1023/B:PLAN.0000038261.21060.47
  16. 16. Li X, Qian Q, Fu Z, Wang Y, Xiong G, Zeng D, et al. Control of tillering in rice. Nature. 2003;422(6932):618–21. https://doi.org/10.1038/nature01518
  17. 17. Coen ES, Meyerowitz EM. The war of the whorls: genetic interactions controlling flower development. Nature. 1991;353(6339):31–7. https://doi.org/10.1038/353031a0
  18. 18. Robles P, Pelaz S. Flower and fruit development in Arabidopsis thaliana. Int J Dev Biol. 2005;49(5–6):633–43. https://doi.org/10.1387/ijdb.052020pr
  19. 19. Rijpkema AS, Vandenbussche M, Koes R, Heijmans K, Gerats T. Variations on a theme: changes in the floral ABCs in angiosperms. Semin Cell Dev Biol. 2010;21(1):100–7. https://doi.org/10.1016/j.semcdb.2009.11.002
  20. 20. Agrawal GK, Abe K, Yamazaki M, Miyao A, Hirochika H. Conservation of the E-function for floral organ identity in rice revealed by the analysis of tissue culture-induced loss-of-function mutants of the OsMADS1 gene. Plant Mol Biol. 2005;59:125–35. https://doi.org/10.1007/s11103-005-2161-y
  21. 21. Luo J, Liu H, Zhou T, Gu B, Huang X, Shangguan Y, et al. An-1 encodes a basic helix-loop-helix protein that regulates awn development, grain size and grain number in rice. Plant Cell. 2013;25(9):3360–76. https://doi.org/10.1105/tpc.113.113589
  22. 22. Hua L, Wang DR, Tan L, Fu Y, Liu F, Xiao L, et al. LABA1, a domestication gene associated with long, barbed awns in wild rice. Plant Cell. 2015;27(7):1875–88. https://doi.org/10.1105/tpc.15.00260
  23. 23. Tan YF, Xing YZ, Li JX, Yu SB, Xu CG, Zhang Q. Genetic bases of appearance quality of rice grains in Shanyou 63, an elite rice hybrid. Theor Appl Genet. 2000;101:823–9. https://doi.org/10.1007/s001220051549
  24. 24. Takeda K. Inheritance of grain size and its implications for rice breeding. In: Khush GS, editor. Rice Genetics II. Manila: International Rice Research Institute. 1991. p. 181–189. https://doi.org/10.1142/9789812814272_0018
  25. 25. Manikandan V, Vanniarajan C. Induced macromutational spectrum and frequency of viable mutants in M2 generation of rice (Oryza sativa L.). Int J Curr Microbiol Appl Sci. 2017;6:1825–34. https://doi.org/10.20546/ijcmas.2017.607.220
  26. 26. Dhole VJ, Souframanien J, Reddy KS, Petwal VC. Comparison of effectiveness and efficiency of electron beam over gamma rays to induce novel mutations in mungbean (Vigna radiata L. Wilczek). Appl Radiat Isot. 2023;194:110719. https://doi.org/10.1016/j.apradiso.2023.110719
  27. 27. Ariharasutharsan G, Karthikeyan A, Geetha S, Raveendran M, Lalitha R, Ananda-Lekshmi L, et al. Prioritization of candidate genes regulating the dwarfness in rice by integration of whole-genome and transcriptome analyses. Funct Integr Genomics. 2025;25(1):19. https://doi.org/10.1007/s10142-025-01532-1

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