An insight into drought stress and signal transduction of abscisic acid
DOI:
https://doi.org/10.14719/pst.2018.5.2.388Keywords:
Drought stress, physiological consequences, ABA-dependent signaling, ABA-independent signaling, drought toleranceAbstract
The sustainable crop production is one of the major issue in the era of urbanization, industrialization, and globalization. In the environment, there are number of abiotic and biotic factors which are hampering the sustainable production of crops. The drought is one of the constraints which directly/indirectly affects the crop yield. It has various negative effects on the normal physiology and biochemistry of the plants. Therefore, researchers must have to work in the field of developing drought-tolerant crop plants to meet the food needs of the exponentially growing population of the world. The present study is the outcome of an extensive literature survey on the basic perturbations of drought to the crops, role of abscisic acid (ABA) in stressful conditions and its signal transduction.
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References
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26. Gowda VRP, Henry A, Yamauchi A, Shashidhar HE, Serraj R. Root biology and genetic improvement for drought avoidance in rice. Field Crops Research 2011; 122: 1-13. doi: 10.1016/j.fcr.2011.03.001
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28. Wang H, Yamauchi A. Growth and functions of roots under abiotic stress in soil. In: Huang B (ed) Plant-environment interactions. 3rd edn. CRC Press, New York, 271-320; 2006.
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34. Ahmad P, Alyemeni MN, Ahanger MA, Wijaya L, Alam P, Kumar A, Ashraf M. Upregulation of antioxidant and glyoxalase systems mitigates NaCl stress in Brassica juncea by supplementation of zinc and calcium. Journal of Plant Interactions 2018; 13(1): 151-62. doi: 10.1080/17429145.2018.1441452
35. Kaur, R. Growth biochemical and antimutagenic studies on Chlorophytum borivilianum Sant et Fernand. Ph.D. Thesis, Guru Nanak Dev University, Amritsar; 2013.
36. Yamaguchi-Shinozaki K, Shinozaki K. Transcriptional regulatory networks in cellular responses and tolerance to dehydration and cold stresses. Annual Review of Plant Biology 2006;57:781-03. doi: 10.1146/annurev.arplant.57.032905.105444
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40. Finkelstein RR, Rock CD. Abscisic Acid Biosynthesis and Response. In: The Arabidopsis Book. American Society of Plants 1-52; 2002. doi: 10.1199/tab.0058
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42. Hobo T, Asada M, Kowyama Y. ACGT-containing abscisic acid response element (ABRE) and coupling element 3 (CE3) are functionally equivalent. The Plant Journal 1999; 19(6): 679-89. doi: 10.1046/j.1365-313x.1999.00565.x
43. Yoshida T, Mogami J, Yamaguchi-Shinozaki K. ABA-dependent and ABA-independent signaling in response to osmotic stress in plants. Current Opinion in Plant Biology 2014; 21: 133-39. doi: 10.1016/j.pbi.2014.07.009
44. Hubbard KE, Nishimura N, Hitomi K, Getzoff ED, Schroeder JI. Early abscisic acid signal transduction mechanisms: newly discovered components and newly emerging questions. Genes & Development 2010; 24(16): 1695-08. doi: 10.1101/gad.1953910
45. Lee SC, Lan W, Buchanan BB, Luan S. A protein kinase-phosphatase pair interacts with an ion channel to regulate ABA signaling in plant guard cells. Proceedings of the National Academy of Sciences 2009; 106(50): 21419-24. doi: 10.1073/pnas.0910601106
46. Vahisalu T, Puzorjova I, Brosche M, Valk E, Lepiku M, Moldau H, Pechter P, Wang YS, Lindgren, O, Salojarvi J. et al. Ozone-triggered rapid stomatal response involves the production of reactive oxygen species, and is controlled by SLAC1 and OST1. The Plant Journal 2010; 62: 442-53. doi: 10.1111/j.1365-313X.2010.04159.x
47. Nakashima K, Yamaguchi-Shinozaki K, Shinozaki K. The transcriptional regulatory network in the drought response and its crosstalk in abiotic stress responses including drought, cold, and heat. Frontiers in Plant Science 2014; 57(10): 170. doi: 10.3389/fpls.2014.00170
48. Miyakawa T, Fujita Y, Yamaguchi-Shinozaki K, Tanokura M. Structure and function of abscisic acid receptors. Trends in Plant Science, 2013; 18(5): 259-66. doi: 10.1016/j.tplants.2012.11.002
49. Nakashima K, Yamaguchi-Shinozaki K. ABA signaling in stress-response and seed development. Plant Cell Reports 2013; 32(7): 959-70. doi: 10.1007/s00299-013-1418-1
50. Fujita Y, Nakashima K, Yoshida T, Katagiri T, Kidokoro S, Kanamori N, Kobayashi M. Three SnRK2 protein kinases are the main positive regulators of abscisic acid signaling in response to water stress in Arabidopsis. Plant and Cell Physiology 2009; 50(12): 2123-32. doi: 10.1093/pcp/pcp147
51. Komatsu K, Suzuki N, Kuwamura M, Nishikawa Y, Nakatani M, Ohtawa H, et al. Group A PP2Cs evolved in land plants as key regulators of intrinsic desiccation tolerance. Nature Communications 2013; 4: 2219. doi: 10.1038/ncomms3219
52. Pizzio GA, Rodriguez L, Antoni R, Gonzalez-Guzman M, Yunta C, Merilo E, et al. The PYL4 A194T mutant uncovers a key role of PYR1- LIKE4/PROTEIN PHOSPHATASE 2CA interaction for abscisic acid signaling and plant drought resistance. Plant Physiology 2013; 163: 441-55.
53. Liu Q, Kasuga M, Sakuma Y, Abe H, Miura S, Yamaguchi-Shinozaki K, Shinozaki K. Two transcription factors, DREB1 and DREB2, with an EREBP/AP2 DNA binding domain separate two cellular signal transduction pathways in drought-and low-temperature-responsive gene expression, respectively, in Arabidopsis. The Plant Cell 1998; 10(8): 1391-06. doi: 10.1105/tpc.10.8.1391
54. Sakuma Y, Maruyama K, Osakabe Y, Qin F, Seki M, Shinozaki K, Yamaguchi-Shinozaki K. Functional analysis of an Arabidopsis transcription factor, DREB2A, involved in drought-responsive gene expression. The Plant Cell 2006; 18(5): 1292-09.
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58. Palusa SG, Ali GS, Reddy ASN. Alternative splicing of pre-mRNAs of Arabidopsis serine/arginine-rich proteins: regulation by hormones and stresses. The Plant Journal 2007; 49: 1091-07. doi: 10.1111/j.1365-313X.2006.03020.x
59. Duque P. A role for SR proteins in plant stress responses. Plant Signaling & Behavior 2011; 6: 49-54. doi: 10.4161/psb.6.1.14063
60. Guerra D, Crosatti C, Khoshro HH, Mastrangelo AM, Mica E, Mazzucotelli E. Post-transcriptional and post-translational regulations of drought and heat response in plants: a spider’s web of mechanisms. Frontier in Plant Science, 2015; 6:57. doi: 10.3389/fpls.2015.00057
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2. Manivannan P, Jaleel CA, Somasundaram R, Panneerselvam R. Osmoregulation and antioxidant metabolism in drought-stressed Helianthus annuus under triadimefon drenching. Comptes Rendus Biologies 2008; 331(6): 418-25. doi: 10.1016/j.crvi.2008.03.003
3. Boyer JS. Plant productivity and environment. Science 1982; 218(4571): 443-48. doi: 10.1126/science.218.4571.443
4. Pennisi E. The blue revolution, drop by drop, gene by gene. Science 2008; 320(5873): 171-73. doi: 10.1126/science.320.5873.171
5. World population projected to reach 9.7 billion by 2050 [Internet].; [cited 6 March 2018]. Available from: http://www.un.org/en/development/desa/ news/population/2015-report.html
6. FAO (Food and Agriculture Organisation), Rome [Internet].; [cited 6 March 2018]. Available from: http://www. fao.org/spfs/about-spfs/mission-spfs/en/
7. Mahajan S, Tuteja N. Cold, salinity andijllh drought stresses: an overview. Archives of Biochemistry and Biophysics 2005;444(2): 139-58. doi: 10.1016/j.abb.2005.10.018
8. Shao HB, Chu LY, Jaleel CA, Manivannan P, Panneerselvam R, Shao MA. Understanding water deficit stress-induced changes in the basic metabolism of higher plants-biotechnologically and sustainably improving agriculture and the ecoenvironment in arid regions of the globe. Critical Reviews in Biotechnology 2009; 29(2): 131-51. doi: 10.1080/07388550902869792
9. Farooq M, Wahid A, Lee DJ, Ito O, Siddique KH. Advances in drought resistance of rice. Critical Reviews in Plant Sciences 2009; 28(4): 199-17. doi: 10.1080/07352680902952173
10. Lawlor DW, Cornic G. Photosynthetic carbon assimilation and associated metabolism in relation to water deficits in higher plants. Plant, Cell & Environment 2002; 25(2): 275-294. doi: 10.1046/j.0016-8025.2001.00814.x
11. Kaya MD, Okçu G, Atak M, C?k?l? Y, Kolsar?c? Ö. Seed treatments to overcome salt and drought stress during germination in sunflower (Helianthus annuus L.). European Journal of Agronomy 2006; 24(4): 291-95. doi: 10.1016/j.eja.2005.08.001
12. Drought [Internet].; [cited 1 June 2017]. Available from: https://wachers.news/category/drought/
13. Drought – Environment – The Guardian [Internet].; [cited 6 March 2018]. Available from: https://www.theguardian.com/environment/drought
14. Taiz L, Zeiger E. Plant Physiology, 4th Ed. Sinauer Associates Inc. Publishers, Massachusetts; 2006.
15. Farooq M, Hussain M, Wahid A, Siddique KHM. Drought stress in plants: an overview. In Plant Responses to Drought Stress. Springer, Berlin, Heidelberg 1-33; 2012. doi: 10.1007/978-3-642-32653-0_1
16. Desclaux D, Roumet P. Impact of drought stress on the phenology of two soybean (Glycine max L. Merr) cultivars. Field Crops Research 1996; 46(1-3): 61-70. doi: 10.1016/0378-4290(95)00086-0
17. Kirkham MB. 8-Field Capacity, Wilting Point, Available Water, and Nonlimiting Water Range. Principles of Soil and Plant Water Relations, Elsevier Academic Press 101-15; 2005.
18. Siddique MRB, Hamid A, Islam MS. Drought stress effects on water relations of wheat. Botanical Bulletin of Academia Sinica 2000; 41: 35-39.
19. Singh B, Singh G. Influence of soil water regime on nutrient mobility and uptake by Dalbergia sissoo seedlings. Tropical Ecology 2004; 45(2): 337-340.
20. Gutiérrez-Boem FH, Thomas GW. Phosphorus nutrition and water deficits in field-grown soybeans. Plant and Soil 1999; 207(1): 87-96. doi: 10.1023/A:1004469403667
21. Grossman A, Takahashi H. Macronutrient utilization by photosynthetic eukaryotes and the fabric of interactions. Annual Review of Plant Biology 2001; 52(1): 163-10.
22. Baligar VC, Fageria NK, He ZL. Nutrient use efficiency in plants. Communications in Soil Science and Plant Analysis 2001; 32(7-8): 921-50. doi: 10.1081/CSS-100104098
23. Munne-Bosch S, Penuelas J. Photo-and antioxidative protection, and a role for salicylic acid during drought and recovery in field-grown Phillyrea angustifolia plants. Planta 2003; 217(5): 758-66. doi: 10.1007/s00425-003-1037-0
24. Levitt J. Responses of plants to environmental stresses. In: Kozlowski TT (ed) Water, radiation, salt and other stresses. Academic, New York, 2nd edn., 93-186; 1980.
25. Blum A. Drought resistance, water-use efficiency, and yield potential-are they compatible, dissonant, or mutually exclusive? Australian Journal Agricultural Research 2005; 56: 1159-68.
26. Gowda VRP, Henry A, Yamauchi A, Shashidhar HE, Serraj R. Root biology and genetic improvement for drought avoidance in rice. Field Crops Research 2011; 122: 1-13. doi: 10.1016/j.fcr.2011.03.001
27. Yamauchi Y, Pardales JR, Kono Y. Root system structure and its relation to stress tolerance. In: Roots and nitrogen in cropping systems of the semi-arid tropics 211-33; 1996.
28. Wang H, Yamauchi A. Growth and functions of roots under abiotic stress in soil. In: Huang B (ed) Plant-environment interactions. 3rd edn. CRC Press, New York, 271-320; 2006.
29. Kavar T, Maras M, Kidric M, Sustar-Vozlic J, Meglic V. Identification of genes involved in the response of leaves of Phaseolus vulgaris to drought stress. Molecular Breeding 2007; 2: 159-72.
30. Serraj R, Sinclair TR Osmolyte accumulation: can it really help increase crop yield under drought conditions? Plant, Cell Environment 2002; 25: 333-41. doi: 10.1046/j.1365-3040.2002.00754.x
31. Chimenti CA, Marcantonio M, Hall AJ. Divergent selection for osmotic adjustment results in improved drought tolerance in maize (Zea mays L.) in both early growth and flowering phases. Field Crops Research 2006; 95: 305-15. doi: 10.1016/j.fcr.2005.04.003
32. Kiani SP, Talia P, Maury P, Grieu P, Heinz R, Perrault A, Nishinakamasu V, Hopp E, Gentzbittel L, Paniego N, Sarrafi A. Genetic analysis of plant water status and osmotic adjustment in recombinant inbred lines of sunflower under two water treatments. Plant Science 2007; 172: 773-87. doi: 10.1016/j.plantsci.2006.12.007
33. Taiz L, Zeiger E. Plant Physiology. 5th edn. Sinauer Associates Inc. Publishers, Massachusetts; 2010.
34. Ahmad P, Alyemeni MN, Ahanger MA, Wijaya L, Alam P, Kumar A, Ashraf M. Upregulation of antioxidant and glyoxalase systems mitigates NaCl stress in Brassica juncea by supplementation of zinc and calcium. Journal of Plant Interactions 2018; 13(1): 151-62. doi: 10.1080/17429145.2018.1441452
35. Kaur, R. Growth biochemical and antimutagenic studies on Chlorophytum borivilianum Sant et Fernand. Ph.D. Thesis, Guru Nanak Dev University, Amritsar; 2013.
36. Yamaguchi-Shinozaki K, Shinozaki K. Transcriptional regulatory networks in cellular responses and tolerance to dehydration and cold stresses. Annual Review of Plant Biology 2006;57:781-03. doi: 10.1146/annurev.arplant.57.032905.105444
37. Buchanan BB, Gruissem W, Jones, RL. Biochemistry & Molecular Biology of Plants. Rockville, MD: American Society of Plant Physiologists; 2015.
38. Abscisic acid – Wikipedia [Internet].; [cited 6 March 2018]. Available from: https://en.wikipedia.org/wiki/Abscisic_acid
39. Tuteja N. Abscisic acid and abiotic stress signaling. Plant Signaling & Behavior 2007; 2(3): 135-38. doi: 10.4161/psb.2.3.4156
40. Finkelstein RR, Rock CD. Abscisic Acid Biosynthesis and Response. In: The Arabidopsis Book. American Society of Plants 1-52; 2002. doi: 10.1199/tab.0058
41. Zandkarimi H, Ebadi A, Salami SA, Alizade H. Analyzing the expression profile of AREB / ABF and DREB / CBF genes under drought and salinity stresses in grape (Vitis vinifera L.). PloS One 2015; 1-16. doi: 10.1371/journal.pone.0134288
42. Hobo T, Asada M, Kowyama Y. ACGT-containing abscisic acid response element (ABRE) and coupling element 3 (CE3) are functionally equivalent. The Plant Journal 1999; 19(6): 679-89. doi: 10.1046/j.1365-313x.1999.00565.x
43. Yoshida T, Mogami J, Yamaguchi-Shinozaki K. ABA-dependent and ABA-independent signaling in response to osmotic stress in plants. Current Opinion in Plant Biology 2014; 21: 133-39. doi: 10.1016/j.pbi.2014.07.009
44. Hubbard KE, Nishimura N, Hitomi K, Getzoff ED, Schroeder JI. Early abscisic acid signal transduction mechanisms: newly discovered components and newly emerging questions. Genes & Development 2010; 24(16): 1695-08. doi: 10.1101/gad.1953910
45. Lee SC, Lan W, Buchanan BB, Luan S. A protein kinase-phosphatase pair interacts with an ion channel to regulate ABA signaling in plant guard cells. Proceedings of the National Academy of Sciences 2009; 106(50): 21419-24. doi: 10.1073/pnas.0910601106
46. Vahisalu T, Puzorjova I, Brosche M, Valk E, Lepiku M, Moldau H, Pechter P, Wang YS, Lindgren, O, Salojarvi J. et al. Ozone-triggered rapid stomatal response involves the production of reactive oxygen species, and is controlled by SLAC1 and OST1. The Plant Journal 2010; 62: 442-53. doi: 10.1111/j.1365-313X.2010.04159.x
47. Nakashima K, Yamaguchi-Shinozaki K, Shinozaki K. The transcriptional regulatory network in the drought response and its crosstalk in abiotic stress responses including drought, cold, and heat. Frontiers in Plant Science 2014; 57(10): 170. doi: 10.3389/fpls.2014.00170
48. Miyakawa T, Fujita Y, Yamaguchi-Shinozaki K, Tanokura M. Structure and function of abscisic acid receptors. Trends in Plant Science, 2013; 18(5): 259-66. doi: 10.1016/j.tplants.2012.11.002
49. Nakashima K, Yamaguchi-Shinozaki K. ABA signaling in stress-response and seed development. Plant Cell Reports 2013; 32(7): 959-70. doi: 10.1007/s00299-013-1418-1
50. Fujita Y, Nakashima K, Yoshida T, Katagiri T, Kidokoro S, Kanamori N, Kobayashi M. Three SnRK2 protein kinases are the main positive regulators of abscisic acid signaling in response to water stress in Arabidopsis. Plant and Cell Physiology 2009; 50(12): 2123-32. doi: 10.1093/pcp/pcp147
51. Komatsu K, Suzuki N, Kuwamura M, Nishikawa Y, Nakatani M, Ohtawa H, et al. Group A PP2Cs evolved in land plants as key regulators of intrinsic desiccation tolerance. Nature Communications 2013; 4: 2219. doi: 10.1038/ncomms3219
52. Pizzio GA, Rodriguez L, Antoni R, Gonzalez-Guzman M, Yunta C, Merilo E, et al. The PYL4 A194T mutant uncovers a key role of PYR1- LIKE4/PROTEIN PHOSPHATASE 2CA interaction for abscisic acid signaling and plant drought resistance. Plant Physiology 2013; 163: 441-55.
53. Liu Q, Kasuga M, Sakuma Y, Abe H, Miura S, Yamaguchi-Shinozaki K, Shinozaki K. Two transcription factors, DREB1 and DREB2, with an EREBP/AP2 DNA binding domain separate two cellular signal transduction pathways in drought-and low-temperature-responsive gene expression, respectively, in Arabidopsis. The Plant Cell 1998; 10(8): 1391-06. doi: 10.1105/tpc.10.8.1391
54. Sakuma Y, Maruyama K, Osakabe Y, Qin F, Seki M, Shinozaki K, Yamaguchi-Shinozaki K. Functional analysis of an Arabidopsis transcription factor, DREB2A, involved in drought-responsive gene expression. The Plant Cell 2006; 18(5): 1292-09.
55. Mastrangelo AM, Marone D, Laidò G, De Leonardis AM, De Vita P. Plant Science 2012; 185-186: 40-49. doi: 10.1016/j.plantsci.2011.09.006
56. Kruszka K, Pieczynski M, Windels D, Bielewicz D, Jarmolowski A, Szweykowska-Kulinska Z. et al. Role
of microRNAs and others RNAs of plants in their changing environments. Journal of Plant Physiology 2012; 169: 1664-72. doi: 10.1016/j.jplph.2012.03.009
57. Reddy, ASN. Alternative splicing of pre-messenger RNAs in plants in the genomic era. Annual Review of Plant Biology 2007; 58: 267-94.
58. Palusa SG, Ali GS, Reddy ASN. Alternative splicing of pre-mRNAs of Arabidopsis serine/arginine-rich proteins: regulation by hormones and stresses. The Plant Journal 2007; 49: 1091-07. doi: 10.1111/j.1365-313X.2006.03020.x
59. Duque P. A role for SR proteins in plant stress responses. Plant Signaling & Behavior 2011; 6: 49-54. doi: 10.4161/psb.6.1.14063
60. Guerra D, Crosatti C, Khoshro HH, Mastrangelo AM, Mica E, Mazzucotelli E. Post-transcriptional and post-translational regulations of drought and heat response in plants: a spider’s web of mechanisms. Frontier in Plant Science, 2015; 6:57. doi: 10.3389/fpls.2015.00057
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24-04-2018
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Kumari A, Kaur R, Kaur R. An insight into drought stress and signal transduction of abscisic acid. Plant Sci. Today [Internet]. 2018 Apr. 24 [cited 2024 Nov. 24];5(2):72-80. Available from: https://horizonepublishing.com/journals/index.php/PST/article/view/388
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