تعداد نشریات | 19 |
تعداد شمارهها | 380 |
تعداد مقالات | 3,121 |
تعداد مشاهده مقاله | 4,251,473 |
تعداد دریافت فایل اصل مقاله | 2,845,929 |
Characterization of pollen tube growth and induced molecular changes in Berasicca napus L. by UV-B treatment | ||
Iranian Journal of Genetics and Plant Breeding | ||
دوره 10، شماره 1 - شماره پیاپی 19، تیر 2021، صفحه 1-9 اصل مقاله (735.28 K) | ||
نوع مقاله: Research paper | ||
شناسه دیجیتال (DOI): 10.30479/ijgpb.2021.15126.1290 | ||
نویسندگان | ||
Saeid Navabpour* ؛ Dariush Ebadi Almas؛ Maryam Pakdel | ||
Department of Plant Breeding and Biotechnology, Gorgan University of Agricultural Sciences and Natural Resources, Gorgan, Iran. | ||
تاریخ دریافت: 21 اسفند 1399، تاریخ بازنگری: 08 خرداد 1401، تاریخ پذیرش: 02 آذر 1400 | ||
چکیده | ||
During the past few decades, the problems caused by the stratospheric ozone reduction has stimulated remarkable research on higher plant responses to UV-B radiation. Depletion of the stratospheric ozone layer is leading to an increase in ultraviolet-B (UV-B: 280–320 nm) radiation reaching the earth’s surface. This has raised interest in the possible consequences of increased UV-B levels on plant growth and development and the mechanisms underlying these responses. Although the effects of UV-B are now well characterized at the physiological level, little is known about the involved cellular and molecular mechanisms. Recent studies have shown that UV-B affects a number of important physiological processes, such as photosynthesis, through effects on gene expression. However, little research has addressed the reproductive biology of plants. The purpose of this study was to investigate the effects of UV-B radiation on reactive oxygen species (ROS) accumulation and antioxidant defense system in relation to germination and pollen tube growth of canola (Brassica napus L.). Our results illustrated that increased UV-B radiation decreased the pollen germination rate and tube length in vitro. Production of superoxide anion radical (O2•−) and hydrogen peroxide (H2O2) increased by UV-B radiation treatment, and their accumulation resulted in lipid peroxidation. The activities and gene expression of superoxide dismutase (SOD), catalase (CAT) and peroxidase (POD) were decreased by enhanced UV-B radiation. The increased ROS and lipid peroxidation, as well as decreased antioxidant activities may be attributed to the effects of UV-B radiation on pollen germination and tube growth. | ||
کلیدواژهها | ||
Brassica napus L؛ Pollen germination؛ Reactive oxygen species؛ UV-B radiation | ||
عنوان مقاله [English] | ||
نقش گونه های اکسیژن واکنشی در جوانه زنی گرده و رشد لوله کلزا (Brassica napus L.) مهار شده توسط UV-B | ||
نویسندگان [English] | ||
سعید نواب پور؛ داریوش عبادی الماس؛ مریم پاکدل | ||
گروه اصلاح نباتات و بیوتکنولوژی، دانشگاه علوم کشاورزی و منابع طبیعی گرگان، گرگان، ایران. | ||
چکیده [English] | ||
در چند دهه اخیر معضل آسیب لایه اوزون منجر به انجام مطالعات در واکنش گیاهان عالی به پرتو فرابنفش شده است. خلائ لایه اوزون درناحیه استراتوسفیک جو زمین منجر به افزایش نفوذ پرتو فرابنفش در محدوده طول موج 280 تا 320 نانومتر میگردد. این امر ضرورت و اهمیت مطالعه اثر پرتو فرابنفش بر گیاهان و سازوکار واکنش گیاه را افزون می نماید. اگر چه تاثیر پرتو فرابنفش بر گیاهان از نظر فیزیولوژیک بخوبی شناخته شده است، با این حال اطلاعات محدودی در سطح سلولی و مولکولی در این خصوص وجود دارد. تحقیقات اخیر از اثر پرتو فرابنفش بر فرایندهای مهم فیزولوژیک نظیر فتوسنتز و بیان برخی ژن ها گزارش می نماید. به هر حال تعداد محدودی ازاین تحقیقات در زمینه واکنش اندام زایشی به پرتو فرابنفش بوده است. هدف از این پژوهش ارزیابی اثر پرتو فرابنفش بر تولید رادیکال های فعال اکسیژن و تاثیر آن بر سیستم واکنش دفاعی در زمان جوانه زنی لوله گرده در گیاه کلزا است. نتایج نشان داد که با افزایش شدت پرتو فرابنفش سرعت جوانه زنی لوله گرده کاهش یافت. در این راستا غلظت یون سوپراکسید و پراکسید هیدروژن افزایش یافت، که منجر به بالا رفتن میزان پراکسیداسیون چربی ها شد. همچنین میزان فعالیت آنزیم های سوپراکسید دیسموتاز، کاتالاز و پراکسیداز با افزایش شدت پرتوتابی، کاهش یافت. افزایش غلظت رادیکال های فعال اکسیژن و پراکسیداسیون چربی ها همراه با کاهش فعالیت آنزیم های دفاعی میتواند دلیل موجهی بر روند کاهش سرعت جوانه زنی لوله گرده باشد. - - - - - - - - - - | ||
کلیدواژهها [English] | ||
کلزا, جوانهزنی لوله گرده, رادیکالهای فعال اکسیژن, پرتوفرابنفش | ||
مراجع | ||
Agarwal R. (2007). Increased antioxidant activity in Cassia seedling under UV-B radiation. Biologia Plantarum, 51: 157-160. DOI: https://doi.org/10.1007/s10535-007-0030-z. Agrawal S. B., and Rathore D. (2007). Changes in oxidative stress defense system in wheat (Triticum aestivum L.) and mung bean (Vigna radiata L.) cultivars grown with and without mineral nutrients and irradiated by supplemental ultraviolet-B. Environmental and Experimental Botany, 59: 21-33. Ahmad P., Sarwat M., and Sharma S. (2008). Reactive oxygen species, antioxidants and signaling in plants. Journal of Plant Biology, 51: 167-173. Ayala A. F., Muñoz M., and Argüelles S. (2014). Lipid peroxidation: production, metabolism, and signaling mechanisms of malondialdehyde and 4-hydroxy-2-nonena. Oxidative Medicine and Cellular Longevity, 360438: 1-31. DOI: 10.1155/2014/360438. Bais A. F., Bernhard G., McKenize R. L., Aucamp P. J., Young P. J., Ilyas M., Jockel P., and Deushi M. (2019). Ozone–climate interactions and effects on solar ultraviolet radiation. Photochemical & Photobiological Sciences, 18: 602-640. Beauchamp C., and Fridovich I. (1971). Superoxide dismutase, improved assays and assay applicable to acrylamide gels. Analytical Biochemistry, 44: 276-287. Benca J. P., Duijnstee I. A. P., and Looy C. V. (2018). UV-B-induced forest sterility: Implications of ozone shield failure in Earth’s largest extinction. Science Advances, 4: 1-10. Bornman J. F., Barnes P. W., Robson T. M., Robinson S. A., Jansen M. A. K., Ballare C. L., and Flint S. D. (2019). Linkages between stratospheric ozone, UV radiation and climate change and their implications for terrestrial ecosystems. Photochemical & Photobiological Sciences, 18: 681-716. Bradford M. M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry, 72: 248-254. Chance B., Sies H., and Boveris A. (1979). Hydroperoxide metabolism in mammalian organs. Physiological Reviews, 59: 527-605. De Jager T. L., Cockrell A. E., and Du Plessis S. S. (2017). Ultraviolet light induced generation of reactive oxygen species. Advances in Experimental Medicine and Biology-Springer, 996: 15-23. DOI: 10.1007/978-3-319-56017-5_2. Feng H., An L., Tan L., Hou Z., and Wang X. (2000). Effect of enhanced ultraviolet-B radiation on pollen germination and tube growth of 19 taxa in vitro. Environmental and Experimental Botany, 43: 45-53. Halliwell B., and Gutteridge J. M. C. (1989). Free radicals in biology and medicine. Oxford, UK: Clarendon Press, pp. 543. Hasanuzzaman M., Bhuyan M. H. M. B., Anee T. I., Parvin K., Nahar K., Mahmud J. A., and Fujita M. (2019). Regulation of Ascorbate-Glutathione pathway in mitigating oxidative damage in plants under abiotic stress. Antioxidants Journal, 8: 1-50. Hasanuzzaman M., Bhuyan M. H. M. B., Zulfiqar F., Raza A., Mohsin S. M., Mahmud J. A., Fujita M., and Fotopoulos V. (2020). Reactive oxygen species and antioxidant defense in plants under abiotic stress: revisiting the crucial role of a universal defense regulator. Antioxidants Journal, 9: 1-52. He J. M., Liu Z. H., Xu H., She X. P., and Huang C. (2006). The involvement of hydrogen peroxide in UV-B-inhibited pollen germination and tube growth of Paeonia suffruticosa and Paulownia tomentosa in vitro. Plant Growth Regulation, 49: 199-208. Heath R. L., and Packer L. (1968). Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of fatty acid peroxidation. Archives of Biochemistry and Biophysics, 125: 189-198. Holdaway-Clarke T. L., Feijò J. A., Hackett G. R., Kunkel J. G., and Hepler P. K. (1997). Pollen tube growth and the intracellular cytosolic calcium gradient oscillate in phase while extracellular calcium influx is delayed. Plant Cell, 9: 1999-2010. Kataria S., Baroniya S. S., Baghel L., and Kanungo M. (2014). Effect of exclusion of solar UV radiation on plants. Plant Science Today, 1: 224-232. Kerr J. B., and McElroy C. T. (1993). Evidence for large upward trends of ultraviolet-B radiation linked to ozone depletion. Science, 262: 1032-1034. Kumari R., Singh S., and Agrawal S. B. (2010). Response of ultraviolet-B induced antioxidant defense system in a medicinal plant, Acorus calamus. Journal of Environmental Biology, 31: 907-911. Liu L., and Wang T. (2021). Male gametophyte development in flowering plants: A story of quarantine and sacrifice. Journal of Plant Physiology, 2021: 258-259. Mittler R. (2002). Oxidative stress, antioxidants and stress tolerance. Trends in Plant Science, 7: 405-410. Obermeyer G., and Weisenseel M. H. (1991). Calcium-channel blocker and calmodulin antagonists affect the gradient of free calcium ions in lily pollen tubes. European Journal of Cell Biology, 56: 319-327. Patterson B. D., Macrae E. A., and Ferguson I. B. (1984) Estimation of hydrogen peroxide in plant extracts using titanium (IV). Analytical Biochemistry, 139: 487-492. Rao G. U., Jain A., and Shivanna K. R. (1992). Effects of high temperature stress on Brassica pollen: viability, germination and ability to set fruits and seeds. Annals of Botany, 69: 193-198. Reyes T. H., Scartazza A., Pompeiano A., and Guglielminetti L. (2019). Physiological responses of Lepidium meyenii plants to ultraviolet-B radiation challenge. BMC Plant Biology, 19: 1-12. Shivanna K. R., and Sawhney V. K. (1997). Pollen biology and pollen biotechnology: an introduction. In: Pollen biotechnology for crop production and improvement. UK: Cambridge University Press, Cambridge, pp. 448. Stadler L. J., and Uber F. M. (1942). Genetic effects of ultraviolet radiation in maize. IV. Comparison of monochromatic radiation. Genetics, 27: 84-118. Tewari R. K., Kumar P., and Sharma N. P. N. (2005). Signs of oxidative stress in the chlorotic leaves of iron starved plants. Plant Sciences, 169: 1037-1045. Torabinejad J., Caldwell M. M., Flint S. D., Durham S. (1998). Susceptibility of pollen to UV-B radiation: an assay of 34 taxa. American Journal of Botany, 85: 360-369. UNEP (2002). Executive summary. Final of UNEP/WMO scientific assessment panel of the montreal protocol on substances that deplete the ozone layer, Nairobi, UNEP. UNEP (2008). Environmental effects of ozone depletion and its interactions with climate change. Photochemical & Photobiological Sciences, 7: 15-27. Wang S., Xie B., Yin L., Duan L., Li Z., Eneji A. E., Tsuji W., and Tsunekawa A. (2010). Increased UV-B radiation affects the viability, reactive oxygen species accumulation and antioxidant enzyme activities in maize (Zea mays L.) pollen. Photochemical & Photobiological Sciences, 86: 110-116. Wang Y., Feng H., Qu Y., Cheng J., Zhao Z., Zhang M., Wang X., and An L. (2006). The relationship between reactive oxygen species and nitric oxide in ultraviolet-B-induced ethylene production in leaves of maize seedlings. Environmental and Experimental Botany, 57: 51-56. Williamson C. E., Neale P. J., Hylander S., Rose K. C., Figueroa F. L., Robinson S. A., Hader D. P., Wangberg S. A., and Worrest R. C. (2019). The interactive effects of stratospheric ozone depletion, UV radiation, and climate change on aquatic ecosystems. Photochemical & Photobiological Sciences, 18: 717-746. Wu J., Jin C., Qu H., Jiang X., Wu J., Xu G., and Zhang S. (2012). The activity of plasma membrane hyperpolarization-activated Ca2+ channels during pollen development of Pyrus pyrifolia. Acta Physiologiae Plantarum, 34: 969-975. Wu J., Qu H., Jin C., Shang Z., Xu G., Gao Y., and Zhang S. (2011). cAMP activates hyperpolarization-activated Ca2+ channels in the pollen of Pyrus pyrifolia. Plant Cell Reports, 30: 1193-1200. | ||
آمار تعداد مشاهده مقاله: 186 تعداد دریافت فایل اصل مقاله: 239 |