نوع مقاله : علمی - پژوهشی

نویسندگان

1 دانش‌آموخته کارشناسی ارشد گیاهان زینتی، گروه علوم و مهندسی باغبانی، دانشکده کشاورزی و محیط زیست، دانشگاه اراک، اراک، ایران

2 دانشیار، گروه علوم و مهندسی باغبانی، دانشکده کشاورزی و محیط زیست، دانشگاه اراک، اراک، ایران

چکیده

افزایش تنوع ژنتیکی از اهداف اساسی در بهنژادی گیاهان می­باشد. با توجه به مقاومت رز ایرانی در برابر خشکی، این گونه بومی می­تواند منبع ژنتیکی مفیدی جهت برنامه­های اصلاحی به­ویژه اصلاح از طریق جهش می­باشد. هدف از انجام این پژوهش بررسی تأثیر ماده جهش­زای اتیل متان سولفونات (EMS) بر ویژگی­های جوانه­زنی بذر و ویژگی­های دانهال در رُز ایرانی بود که در طی دو آزمایش جداگانه در دانشگاه اراک در سال 1398 اجرا شد. در آزمایش اول تأثیر غلظت­های صفر، 2/0 و 3/0 درصد EMS در زمان­های 4، 8 و 12 ساعت بر ویژگی­های جوانه­زنی بذر و در آزمایش دوم غلظت­های صفر، 2/0 و 3/0 درصد EMS در زمان­های 4 و 8 ساعت بر ویژگی­های جوانه­های زایشی مورد بررسی قرار گرفت. ویژگی­های جوانه­زنی بذر شامل درصد و سرعت جوانه­زنی، شاخص بنیه بذر، شاخص میزان جوانه­زنی، طول گیاه­چه، تعداد و طول برگ، طول ساقه و ریشه و قطر جوانه گل، میزان بازشدگی گل­ها، تعداد جوانه­های نکروز شده و تعداد بذر تشکیل شده در هر هیپ ارزیابی شد. نتایج نشان داد افزایش غلظت EMS و زمان تیمار، سبب کاهش بیشتر شاخص­های جوانه­زنی بذر شد. در تیمار 3/0 درصد EMS به­مدت هشت ساعت بر بذر، درصد و سرعت جوانه‌زنی، شاخص میزان جوانه­زنی و جوانه­زنی روزانه به صفر رسید. نتایج آزمایش دوم نشان داد، در غلظت 2/0 و 3/0 درصد EMS و در زمان چهار ساعت، طول برگ و طول گیاه­چه بلندتر بود. با افزایش غلظت و زمان اعمال EMS، کاهش تعداد بذر در هر هیپ و افزایش تعداد جوانه­های نکروز مشاهده شد. به­منظور موفقیت در یک برنامه بهنژادی به کمک روش‌های جهش­زا باید ابتدا غلظت و زمان مناسب مشخص شود. برای تعیین بهترین غلظت مواد جهش­زا، میزان غلظت نباید به­حدی زیاد باشد که گیاهان را از بین ببرد و غلظت کاربردی باید به میزانی انتخاب شود که فراوانی وقوع جهش به­اندازه کافی رخ دهد. به این دلیل که تیمار بذرها با 3/0 درصد EMS به­مدت چهار ساعت دارای شاخص‌های جوانه­زنی بهتری نسبت به سایر تیمارها نشان داد، از این­رو جهت ایجاد جهش در بذر این تیمار انتخاب شد. همچنین کاربرد غلظت 2/0 درصد EMS به­مدت چهار ساعت بر جوانه­های زایشی دارای اثرات سوء کمتری بر رشد و باز شدن جوانه­های زایشی نسبت به سایر تیمارها داشت و بنابراین جهت القای جهش و ایجاد تنوع در رُز ایرانی این تیمار مناسب می­باشد.

کلیدواژه‌ها

موضوعات

عنوان مقاله [English]

Effect of EMS Ethyl Methane Sulfonate (EMS) mutagen on Iranian rose (Rosa persica Michx) to generate morphological variation

نویسندگان [English]

  • Mohammad Mahdi Mehrabi 1
  • Mina Taghizadeh 2
  • Mousa Solgi 2

1 M.Sc. Graduate of Horticultural science, Faculty of agricultural and environmental science, Arak University, Arak, Iran, Iran

2 Associate Professor, Department of Horticultural science, Faculty of agricultural and environmental science, Arak University, Arak, Iran

چکیده [English]

Introduction
Genetic diversity is one of the major goals of plant breeding. Mutation induction is a method to increase genetic variety that is used in plant breeding along with selection, recombination or a combination of the both. Rosa persica Michx can serve as a valuable genetic resource for breeding programs, especially due to the market demand for variety in rose cultivars as well as its drought resistance.  In two independent experiments, this study examined the effect of ethyl methane sulfonate (EMS) as a chemical mutagen on seed germination and seedling characteristics of Rosa persica.
 
Materials and Methods
 The seeds of Rosa persica Mich.seeds were collected from an adult shrub on the Arak University campus, Karbala St., Sardasht (34° N, 49.6° E) and an altitude of 1872 m above sea level during mid-summer. The seeds were separated from the hips by a sharp scalpel and the damaged and abnormal seeds were removed. Before applying the cold stratification, the seeds were washed for several hours and then placed in layers of wet sand at 4 ° C for 60 days.
First, the effects of 0, 0.2, and 0.3% EMS at 4, 8 and 12 hours on seed germination characteristics were examined. Second, 0, 0.2, and 0.3 concentrations of EMS at 4 and 8 hours were studied on reproductive buds. Seed germination characteristics such as final germination percentage, germination rate index, coefficient velocity germination, germination rate, mean daily germination, daily germination speed, mean germination rate, germination index, seed vigor, seed dormancy and seedling vegetative traits such as stem lengths, root lengths, and leaf number are evaluated at first experiment. In second experiment, flower diameter, flower opening rate, number of necrotic buds and the number of seeds in each hip were measured.
 
Results and Discussion
The results showed that increasing the concentration of EMS and the time of seed treatment caused a further decrease in germination indices. In 0.3% EMS treatment for 8 hours on seeds, traits such as germination percentage, germination rate index and daily germination were reduced to zero. According to the results of the second experiment, leaf and seedling lengths were longer at 0.2 and 0.3% EMS concentrations and at 4 h incubation. There was a decline in the number of seeds per hip and an increase in necrotic buds with increasing concentration and time of EMS application. In order to succeed in a breeding program using mutagenic methods, the appropriate concentration and time must first be optimized. To determine the best concentration of mutagens, there are two important factors to consider: first, that the concentration should not be so high as to destroy plants, and second, that the applied concentration should be selected moderately. Although, that the frequency of mutations occurs sufficiently.
 
Conclusion
In order to induce a positive mutation and diversity in Iranian roses for the purpose of introducing a new cultivar, seed treatment with a concentration of 0.3% EMS and an incubation time of 4 h is recommended. It is also recommended to apply a concentration of 0.2% EMS on the reproductive buds for 4 h to induce mutations.
 
Keywords: Seed, breeding, germination, mutation, ornamental plant

کلیدواژه‌ها [English]

  • breeding
  • germination
  • mutation
  • ornamental plant
  • Seed
Ahloowalia, B.S., Maluszynski, M. and Nichterlein, N. (2004). Global impact of mutation-derived varieties. Euphytica, 135(2), 187-204.
Amiri, A. and Taghizade, M. (2013). In vitro polyploidization induced of African violet (Saintpaulia ionantha Wendl.) in using Colchicine. 8th national biotechnology congress of I.R.  Iran & 4th National Conference on biosecurity Proceeding, Tehran. [In Persian]
Ashraf, M. and Orooj, A. (2006). alt stress effects on growth, ion accumulation and seed oil concentration in an arid zone traditional medicinal plant ajwain (Trachyspermum ammi [L.] Sprague). Journal of Arid Environments, 64(2), 209-220.
Babaei, A., Nematzadeh, Gh. and Hashemi, H. (2011). An evaluation of genetic differentiation in rice mutants using semi-random markers and morphological characteristics. Australian Journal of Crop Science, 5 (13), 1715-1722.
Bagheri, N., Babaeian Jelodar, N. and Hasan Nataj, E. (2008). Genetic diversity if Iranian rice germplasm based on morphological traits. Iran Journal Agriculture Research, 6(2), 235-243. [In Persian]
Biradar, K.S., Salimath, P.M. and Ravikumar, R.L. (2010). Genetic variability for seedling vigour, yield and yield Components in local germplasm collections of Greengram (Vigna radiata (L.) wilczek). Kamataka Journal of Agricultural Sciences, 20(3): 608-609.
Borovsky, Y., Tadmor, Y., Bar, E., Meir, A., Lewinsohn, E. and Paran, I. (2013). Induced mutation in β-carotene hydroxylase results in accumulation of β-carotene and conversion of red to orange color in pepper fruit. Theoretical and applied genetics, 126 (3), 557-565.
Dehkhodaei, P., Reezi, S. and Ghasemi Ghehsareh, M. (2021). Effect of Artificial (LEDs) and Natural Lighting on Quantitative and Qualitative Traits of Petunia, Geranium and Solenostemon Transplants. Journal of Plant Productions, 44(3), 369-381. [In Persian]
Devi, A.S. and Mullainathan, L. (2011). Physical and chemical mutagenesis for improvement of chilli (Capsicum annuum L.). World Applied Sciences Journal, 15, 108-113.
Dhakshanamoorthy, D., Selvaraj, R. and Chidambaram, A. (2010). Physical and chemical mutagenesis in Jatropha curcas l. to induce variability in seed germination, growth and yield traits. Romanian Journal of Biology, 55 2, 113–125.
Ellis, R.H. and Roberts, E.H. (1981). The quantification of aging and survival in orthodox seeds. Seed Science and Technology, 9, 377-409.
Fang, J.Y. (2011). In Vitro Mutation Induction of Saintpaulia Using Ethyl Methanesulfonate. Hort Science, 46, 981-984.
Fotookian, M.H. and Esfahani, M. (2001). Induction of short culm mutant in Domsiah rice (Oryza sativa L.) variety. ranian Journal of Crop Sciences, 3(3), 31-41. [In Persian]
Ganji, M., Taghizadeh, M., Khadivi, A. and Ghorbanpour, M. (2019). The potential of EMS mutagen on increasing tolerability and remediation Cd of Spartium junceum callus as an ornamental shrub.  Plant Process and Function, 8 (32), 419-432. [In Persian]
Harkness, J. (1977). Breeding with Hulthemia persica (Rosa persica). American Rose Annual. American Rose Society.
He, H., Ueda, Y., Kurosawa, T., Ogawa, S., Nishino, E., Wang, B. and Liao, K. (2001). Morphological character and germination in achenes of Rosa persica Michx. Acta Horticulturae, 547, 129-140.
Heyun Wan, G., Chen, S., Zonglai, X.U., Jin Tang, G. and Zhou, W. (2007). Effects of mutagenic treatments of isolated microspores and microspore –derived embryos on embryogenesis and plant regeneration in oilseed rape. International Rapeseed Congress. 326-330.
Hohmann, U., Jacobs, G. and Jung, C. (2005). An EMS mutagenesis protocol for sugar beet and isolation of non‐bolting mutants. Plant Breeding, 124 (4), 317-321.
Jankowicz-Cieslak, J. and Till, B.J. (2016). Chemical mutagenesis of seed and vegetatively propagated plants using EMS. Current Protocols in Plant Biology, 1(1), 617-635.
Khan, S. and Goyal, S. (2009). Improvement of mungbean varieties through induced mutations. African Journal of Plant Science, 3 (8), 174-180.
Khosh-Khui, M. and Teixeira da Silva., A. (2006). In Vitro Culture of the Rosa Species, Floriculture Ornamental and Plant Biotechnology, 66 (1), 514-526.
Lee, S.Y., Cheong, J.I. and Kim, T.S. (2003). Production of doubled haploids through another culture of M1 rice plants derived from mutagenized fertilized egg cells. Plant Cell Reports, 22, 218-223.
Maguire, J. D. (1962). Speed of germination, aid in selection and evaluation for seedling emergence and vigour. Crop Science, 2, 176-177.
Micke, A. (1999). Mutation and in vitro mutation breeding. Bahar Samiullah Khan, Kalani Publishers, Ludhiana, India. Pp: 1-19.
Misra, P., Datta, S. K. and Chakrabarty, D. (2003). Mutation in flower colour and shape of Chrysanthemum morifolium induced by γ-radiation. Biologia Plantarum, 47(1), 153-156.
Panwar, P. and Bhardwaj, S.D. (2005). Handbook of practical forestry, Agro biosystem (India), 191 p.
Patrick Greer, S. and Rinehart, T.A. (2009). In Vitro Germination and Dormancy Responses of Hydrangea macrophylla and Hydrangea paniculata Seeds to Ethyl Methane Sulfonate and Cold Treatment. Horticulture science, 44(3),769.
Rajabi, A., Gharib Block, S., Kazemi Tabar, S. and Sinki, J. (2016). Evaluation of traits of peppermint mutant plant using EMS mutagenesis method. Journal of Cellular-Molecular Biotechnology, 6 (24), 87-96. [In Persian]
Roychowdhury, R. and Tah, J. (2011). Germination behaviors in M2 generation of Dianthus after chemical mutagenesis. International Journal of Advanced Scientific and Technical Research, 1, 448-154.
Saeiahagh, H., Mousavi, M. and Pathirana, R. (2019). Determination of the Optimal Dosage of Physical and Chemical Mutagenesis Agents in Callus Tissue of Kiwifruit Leaf. Plant Productions. 42(4), 523-534. [In Persian]
Sangram Ramdas, B. (2015). Mutation Breeding in Rose (Rose indica L.). M.Sc. Thesis of Floriculture and Landscaping, Mahatma Phule Krishi Vidyapeeth, Rahuri.
Scotte, S.J, Jones, R.A. and Williams, W.A. (1984). Review of data analysis methods for seed germination. Crop Science, 24: 1192-1199.
Shah, S.N.M., Gong, Z.H., Arisha, M.H., Khan, A. and Tian, S.L. (2015). Effect of ethyl methyl sulfonate concentration and different treatment conditions on germination and seedling growth of the Cucumber cultivar Chinese long (9930). Genetics and Molecular Research, 14(1), 2440-2449.
Singh, R. and Kole, C. (2005). Effect of mutagenic treatment with EMS on germination and some seedling parameters in mungbean. Crops Research, 30, 236-240.
Taghizadeh, M., Kafi, M., Ftahi Moghadam, M. R. and Savaghebi, G. R. (2012). Assessment of turfgrass potential for lead phytoremediation, in vitrocally inducing and molecular tracing. Ph.D. Thesis of Horticultural science, Tehran University, Tehran. [In Persian]
Tejklova, E. (2002). Curly Stem- an Induced Mutation in Fliax (Linnum usitatissimum). Czech Journal of Genetics and Plant Breeding, 38 (3-4), 125-128.
Van harten, A.M. (1998). Mutation breeding: Theory and practical applications. Cambridge University Press, London, U.K. 22 pp.
Yadav, R.D.S. (1987). Effect of mutagens on mitotic index, seedling vigour and chlorophyll mutations in mung beam [Vigna radiata (L.) Wilczek]. Journal of Nuclear Agriculture and Biology, 16, 13-17.
Yusuf K.K. and Nair, P.M. (1974). Effect of gamma irradiation on the indole acetic acid synthesizing system and its significance in sprout inhibition of potatoes. Radiation Botany, 14, 251-256.
Zhu, B., Gu, A., Deng, X., Geng, Y. and Lu, Z. (1995). Effects of caffeine or EDTA post-treatment on EMS mutagenesis in soybean. Mutation Research, 334: 157-159.