Volume 6, Issue 2 ((Autumn & Winter) 2020)                   Iranian J. Seed Res. 2020, 6(2): 61-79 | Back to browse issues page


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Hajiabbasi M, Tavakkol Afshari R, Abbasi A, Kamaei R. (2020). The Effect of ACC and Salicylic Acid on Germination and GAI1 and LOX2 Genes Expression in Deteriorated Soybean Seeds (Glycine max). Iranian J. Seed Res.. 6(2), : 5 doi:10.29252/yujs.6.2.61
URL: http://yujs.yu.ac.ir/jisr/article-1-410-en.html
, Tavakolafshari@um.ac.ir
Abstract:   (6732 Views)


Extended Abstract
Introduction: Soybean (Glycine max (L.) Merrill) is the primary source of vegetable oil. Even in desirable conditions, soybean seeds lose their viability in long term storage. Many factors contribute to seed deterioration, including genetic factors, mechanical damage, relative humidity, storage temperature, seed moisture content, existence of microflora, and seed maturity, which reduce seed quality and make seeds unfit for cultivation purposes.
Materials and Methods: In order to investigate the effects of seed deterioration on seed germination and also the effects of salicylic acid and ethylene on the improvement of deteriorated seeds of G. max., accelerated aging test for 0, 6 and 10 days and natural aging test for 6 months were conducted. After aging conditions, seeds were imbibed with 50 µM salicylic acid and 10 µM ACC (precursor of ethylene) for 6 hours at 25 °C. In addition, after natural and accelerated aging tests, a bunch of seeds was used without any hormonal treatment (i.e., dry seeds) as control seeds. The seeds’ germination percentage, total sugar, fructose, and glucose were investigated. Moreover, the gene expression of GAI1 and LOX1 was measured on dry seeds and under imbibition of water, salicylic acid and ACC at 6, 12 hours using Q-RT-PCR method.
Results: The germination results showed that increasing number of aging days led to a decrease in germination. Total sugar content in seeds aged for 6 days did not have a significant difference, as compared with non-aged seeds. However, total sugar content in seeds aged for 10 days was significantly higher than non-aged seeds. Increasing accelerated aging levels from 0 days to 10 days led to increases in glucose and fructose contents in dry seeds. In addition, genes exhibited different expressions in different days and hours. Increasing aging from 0 days to 10 days led to increases in GAI1 gene expression. Moreover, LOX2 expression increased in accelerated aging from 0 to 6 days. LOX2 gene expression in naturally dried aged seeds also increased and was higher than that in non-aged seeds. SA and ACC had different effects on measured values.
Conclusion: In general, it can be concluded that the deterioration of seed quality and vigor result from numerous degradation processes and disruption in seeds’ physiological activity. This study showed that aging is associated with an increase in total sugar, glucose and fructose levels. In addition, the expression of the genes involved in the germination is also affected. Increases in LOX2 gene expression were observed in both accelerated aging and natural aging pathways. GAI1 gene expression increased in accelerated aging. However, in normal aging, it decreased.
 

Highlights:
  1. Identifying the role of LOX2 and GAL1 genes in soybean seed deterioration.
  2. Investigating seeds’ physiological responses under natural and laboratory aging conditions.
Article number: 5
Full-Text [PDF 676 kb]   (1242 Downloads)    
Type of Study: Research | Subject: Seed Physiology
Received: 2019/03/3 | Revised: 2021/06/27 | Accepted: 2019/09/17 | ePublished: 2020/05/2

References
1. Achard, P., Cheng, H., De Grauwe, L., Decat, J., Schoutteten, H., Moritz, T., Van Der Straeten, D., Peng, J. and Harberd, N.P. 2006. Integration of plant responses to environmentally activated phytohormonal signals. Science, 311: 91-94. [DOI:10.1126/science.1118642] [PMID]
2. Achard, P., Liao, L., Jiang, C., Desnos, T., Bartlett, J., Fu, X. and Harberd, N.P. 2007. DELLAs contribute to plant photomorphogenesis. Plant Physiology, 143: 1163-1172. [DOI:10.1104/pp.106.092254] [PMID] [PMCID]
3. AOAC.1995. Official method of analysis (16th Ed.). Arlington, VA., USA: AOAC.
4. Beaudoin, N., Serizet, C., Gosti, F. and Giraudat, J. 2000. Interactions between bscisic acid and ethylene signaling cascades. The Plant Cell, 12(7): 1103- 1115. [DOI:10.1105/tpc.12.7.1103] [PMID] [PMCID]
5. Bernal-Lugo, I. and Leopold, A.C. 1995. Seed stability during storage: raffinose content and seed glassy state. Seed Science Research, 5: 75-80. [DOI:10.1017/S0960258500002646]
6. Bleecker, A.B. and Kende, H. 2000. Ethylene: a gaseous signal molecule in plants. Annual Review of Cell and Developmental Biology, 16(1): 1-18. [DOI:10.1146/annurev.cellbio.16.1.1] [PMID]
7. Bolle, C. 2004. The role of GRAS proteins in plant signal transduction and development. Planta, 218(5): 683-692. https://doi.10.1007/s00425-004-1203-z [DOI:10.1007/s00425-004-1203-z] [PMID]
8. Chang, S., Puryear, J. and Cairney, K. 1993. A simple and efficient method for isolating RNA from pine trees. Plant Molecular Biology Reporter, 11(2): 113-116. [DOI:10.1007/BF02670468]
9. Feussner, I., Kiihn, H. and Wasternack, C. 2001. Lipoxygenase-dependent degradation of storage lipids. Trends in Plant Science, 6(6): 268-273. [DOI:10.1016/S1360-1385(01)01950-1]
10. Forcella, F., Benech Arnold, R.L., Sanchez, R. and Ghersa, C.M. 2000. Modeling seedling emergence. Field Crop Research, 67(2): 123-139. [DOI:10.1016/S0378-4290(00)00088-5]
11. Fu, X., Sudhakar, D., Peng, J., Richards, D.E., Christou, P. and Harberd, N.P. 2001. Expression of Arabidopsis GAI in transgenic rice represses multiple gibberellin responses. The Plant Cell, 13(8): 1791-1802. [DOI:10.1105/TPC.010020] [PMID] [PMCID]
12. Hampton, J.G. and Tekrony, D.M. 2005. Handbook of vigour test methods (3rd.ed). The International Seed Testing Association, 70-72.
13. Ievinsh, G. 1992. Soluble lipoxygenase activity in rye seedlings as related to endogenous and exogenous ethylene and wounding. Plant Science, 82(2): 155-159. [DOI:10.1016/0168-9452(92)90217-A]
14. International Seed Testing Association (ISTA). 2009. International rules for seed testing. Seed Science and Technology, 24: 155-202.
15. Kolomiets, M.V., Hannapel, D.J., Chen, H., Tymenson, M. and Gladon, R.J. 2001. Lipoxygenase is involved in the control of potato tuber development. The Plant Cell, 13(3): 613-626. [DOI:10.1105/tpc.13.3.613] [PMID] [PMCID]
16. Kozarewa, I., Cantliffe, D.J., Nagata, R.T. and Stoffella, P.J. 2006. High maturation temperature of lettuce seeds during development increased ethylene production and germination at elevated temperatures. American Horticulture Science, 131: 564-570. [DOI:10.21273/JASHS.131.4.564]
17. Lee, G.J., Wu, X., Shannon, J.G. Sleper, D.A. and Nguyen, H.T. 2007. Genome mapping and molecular breeding in plants. In Oilseeds, Volume II, ed. Kole, C. (Springer-Verlag Berlin Heidelberg, 2007). pp. 21-53.
18. Lima, W.A.A., Borem, A., Dias, D.C.F.S., Moreira, M.A. and Dias, L.A.S. 2010. Lipoxygenase and physiological quality of soybean seeds during storage. Seed Science and Technology, 38(3): 767-771. [DOI:10.15258/sst.2010.38.3.23]
19. Marshal, A.H. and Lewis, D.N. 2004. Influence of seed storage conditions on seedling emergence, seedling growth and dry matter production of temperature forage grasses. Seed Science and Technology, 32(2): 493-501. [DOI:10.15258/sst.2004.32.2.19]
20. Matilla, A.J. 2000. Ethylene in seed formation and germination. Seed Science Research. 10(2): 111-126. [DOI:10.1017/S096025850000012X]
21. Mc Donald, M.B. 1999. Seed deterioration: Physiology, repair and assessment. Seed Science and Technology, 27(1): 177-237.
22. McDonald, M.B. 2004. Orthodx seed deterioration and its repair. 2004. In Handbook of seed physiology applications to agriculture. Food Products Press. Volum II, ed. Benech, R.L. and Sanchez, R.A. (Food Products Press, 2004), pp.273-304. [DOI:10.1017/S0021859605235347]
23. Mishra, A. and Choudhuri, M.A. 1999. Effect of salicylic acid on heavy metal-induced membrane deterioration mediated by lipoxgenase in rice. Biologial Plantrum, 42(3): 409-415. [DOI:10.1023/A:1002469303670]
24. Narayana Murthy, U.M. and Sun, W.Q. 2000. Protein modification by amadori and maillard reactions during seed storage: roles of sugar hydrolysis and lipid peroxidation. Journal of Experimental Botany, 51: 1221-1228. [DOI:10.1093/jexbot/51.348.1221] [PMID]
25. Olszewski, N., Sun, T.P. and Gubler, F. 2002. Gibberellin signaling: biosynthesis, catabolism, and response pathways. The Plant Cell, 61-80. [DOI:10.1105/tpc.010476] [PMID] [PMCID]
26. Park, T.K., Holland, M.A., Laskey, J.M. and Palacco, J.C. 1994. Germination-associated lipoxygenase transcripts persist in maturing soybean plants and are induced by jasmonate. Plant Science, 96: 109-117. [DOI:10.1016/0168-9452(94)90227-5]
27. Raskin, L. 1992. Role of salicylic in plant. Plant Molecular Biology, 43: 439-463. [DOI:10.1146/annurev.pp.43.060192.002255 10.1146/annurev.pp.43.060192.002255]
28. Rivas-San Vicente, M. and Javier Plasencia, J. 2011. Salicylic acid beyond defence: its role in plant growth and Development. Journal of Experimental Botany, 62(10): 3321-3338. [DOI:10.1093/jxb/err031] [PMID]
29. Royo, J., Vancanneyt, G., Perez, A.G., Sanz, C., Siormann, K., Rosahl, S. and Sanchez Serrano, J.J. 1996. Characterization of three potato lipoxyenases with distinct enzymatic activities and different organ-specific and wound-regulated expression patterns. Journal of Biological Chemistry, 271: 21012-21019. [DOI:10.1074/jbc.271.35.21012] [PMID]
30. Sharma, S., Virdi. P., Gambhir, S. and Munshi, S.K. 2005. Changes in soluble sugar content and antioxidant enzymes in soybean seeds stored under different storage conditions. Agricultural Biochemistry, 18: 9-12. [DOI:10.15258/sst.2007.35.2.14]
31. Shelar, V.R., Shaikh, R.S. and Nikam, A.S. 2008. Soybean seed quality during storage: A review. Agricultural Reviews, 29(2): 125-131. [DOI:10.1590/1807-1929/agriambi.v20n11p1025-1030]
32. Shoresh, M., Yedidia, I. and Chet, I. 2005. Involvement of jasmonic acid/ethylene signaling pathway in the systemic resistance induced in cucumber by Trichoderma asperellum T203. Phytopathology, 95(1): 76-84. [DOI:10.1094/PHYTO-95-0076] [PMID]
33. Sun, T. and Gubler, F. 2004. Molecular mechanism of gibberellin signalling plants. Annual Review of Plant Biology, 55: 197-223. [DOI:10.1146/annurev.arplant.55.031903.141753] [PMID]
34. Sun, W.Q. and Leopold, A.C. 1995. The Maillard reaction and oxidative stress during aging of soybean seeds. Physiologia Plantarum, 94(1): 94-105. https://doi.org/10.1034/j.1399-3054.1995.940114.x [DOI:10.1111/j.1399-3054.1995.tb00789.x]
35. Wettlaufer, S. and Leopold, A.C. 1991. Relevance of amadori and maillard products to seed deterioration. Plant Physiology, 97: 165-1 69. [DOI:10.1104/pp.97.1.165] [PMID] [PMCID]
36. Yamaguchi, S. 2008. Gibberellin metabolism and its regulation. Annual Review of Plant Biology, 59: 225-251. [DOI:10.1146/annurev.arplant.59.032607.092804] [PMID]

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