Transcriptomics: Open Access

Transcriptomics: Open Access
Open Access

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Opinion Article - (2015) Volume 3, Issue 2

Plant Stress Tolerance: Engineering ABA: A Potent Phytohormone

Shabir H Wani1* and Vinay Kumar2
1Division of Genetics and Plant Breeding, SKUAST-K, Shalimar, Srinagar, Jammu and Kashmir, India
2Department of Biotechnology, Modern College, S. P. Pune University, Ganeshkhind, India
*Corresponding Author: Shabir H Wani, Division of Genetics and Plant Breeding, SKUAST-K, Shalimar, Srinagar 190025, Jammu And Kashmir, India, Tel: 91-0194- 2461258 Email:

Abstract

Abiotic stresses, primarily drought, salinity, heat, cold, flooding and ultra-violet rays are causing widespread crop losses worldwide. Because of the complexity of the stress-tolerance traits, conventional breeding techniques have met with little success in fulfilling the world fooddemands . Therefore, to face the abiotic stresses, novel and potent approaches should be devised and engineering of phytohormones could be a method of choice to increase the crop productivity

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Opinion

Abiotic stresses, primarily drought, salinity, heat, cold, flooding and ultra-violet rays are causing widespread crop losses worldwide. Because of the complexity of the stress-tolerance traits, conventional breeding techniques have met with little success in fulfilling the world fooddemands [1-3]. Therefore, to face the abiotic stresses, novel and potent approaches should be devised and engineering of phytohormones could be a method of choice to increase the crop productivity. Recent research has shown that phytohormones including the classical well-known auxins, cytokinins, ethylene, gibberellins and newer members including brassinosteroids, jasmonates and strigolactones may prove to be potent targets for their engineering for producing abiotic stress tolerance crop plants. Considering phytohormones being key-regulators of plant growth and development as well as mediators of the environmental stress-responses [4], hormone metabolism and signaling process are the potential targets for manipulation to obtain enhanced abiotic stress tolerance. Amongst various phytohormones, Abscisic Acid (ABA) is perhaps the most sought-after hormone for engineering abiotic stress tolerance in crop plants owing to its identity as stress-hormone and vast array of functions it carry out under environmental stress conditions, particularly drought. It is credited as an essential messenger involved in stress adaptive response of plants and regulates the expression of stressresponsive genes involved in accumulation of compatible osmolytes, synthesis of Late Embryogenesis Abundant (LEA) proteins, dehydrins and other protective proteins beside antioxidant enzymes [5,6].

As a result, many of the key ABA biosynthetic pathway enzymes have been manipulated for conferring improved abiotic stress tolerance in resultant transgenics [7]. Transgenic Arabidopsis constitutively overexpressing the zeaxanthin epoxidase gene involved in ABA synthesis from isopentenyl pyrophosphate (IPP) and β-carotene exhibited enhanced drought and salinity tolerance [8]. Similarly, Park et al. [9] reported enhanced osmotic stress tolerance by overexpressing an ABA-responsive stress-related gene in Arabidopsis. C-Repeat Binding Factor (CBF) and/or dehydration-responsive element-binding (DREB) genes have been manipulated to confer improved drought tolerance. For example, overexpression of CBF1/DREB1B from Arabidopsis was able to improve tolerance to water-deficit stress in tomato [10]. Furthermore, when driven by three copies of an ABAresponsive complex (ABRC1) from barley HAV22 gene, the resultant transgenic tomato expressing CBF1 showed enhanced tolerance to chilling, water deficit, and salt stress, while maintaining the normal growth and yield under non-stressed conditions as compared to their control counterparts [10]. However, on some occasions, though over-expression of gene(s) involved in ABA biosynthesis/catabolism pathways resulted in increased drought tolerance, but with undesired growth penalties due to pleiotropic effects even with the use of inducible promoters [11]. To offset this, Zhang et al. [12] overexpressed CRK45, a stress-inducible kinase involved in ABA signaling, and the resultant transgenics showed enhanced drought tolerance but with a more tight control of ABA levels and signaling, indicating the role of CRK45 in fine-tuning of ABA levels. Recently, transgenic poplars were produced via overexpressing Arabidopsis YUCCA6 gene (a member of the YUCCA family of flavin monooxygenase-like proteins), which is involved in tryptophan-dependent IAA biosynthesis pathway and known to respond to environmental cues, under the control of stressinducible SWPA2 promoter [13]. The transgenic lines displayed auxin overproducing phenotypes and exhibited tolerance to drought stress, associated with reduced levels of reactive oxygen species. However, as biosynthetic pathways and convergence points for cross-talk are still not clear with great understandings, there is a further scope to increase our understandings in this regard and identify novel genes encoding phytohormone metabolisms to be targeted for engineering abiotic stress tolerance in crop plants. Nevertheless, the recent findings have opened various avenues in transgenic breeding via targeting ABA for conferring abiotic stress tolerance in important crop species.

References

  1. Wani SH, Singh NB, Haribhushan A, Mir JI (2013) Compatible solute engineering in plants for abiotic stress tolerance - role of glycine betaine. Curr Genomics 14: 157-165.
  2. Wani SH, Saroj SK (2014) Biotechnology and Abiotic Stress Tolerance in Rice. J Rice Res 2 e105.
  3. Pathak MR,Teixeira da Silva JA,Wani SH3 (2014) Polyamines in response to abiotic stress tolerance through transgenic approaches. GM Crops Food 5: 87-96.
  4. Sreenivasulu N,Harshavardhan VT, Govind G, Seiler C, Kohli A (2012) Contrapuntal role of ABA: does it mediate stress tolerance or plant growth retardation under long-term drought stress?. Gene 506: 265-273.
  5. Chaves MM, Maroco JP, Pereira JS (2003) Understanding plant responses to drought: from genes to the whole plant. Funct Plant Biol 30: 239-264.
  6. Verslues PE,Agarwal M, Katiyar-Agarwal S, Zhu J, Zhu JK (2006) Methods and concepts in quantifying resistance to drought, salt and freezing, abiotic stresses that affect plant water status. Plant J 45: 523-539.
  7. Jewell MC, Campbell BC, Godwin ID (2010) Transgenic plants for abiotic stress resistance. In: Kole C, Michler C, Abbott AG, Hall TC (Eds), Transgenic crop plants. Vol. 2: Utilization and biosafety, Springer-Verlag, Berlin, pp 67-131.
  8. Schwartz SH, Qin X, Zeevaart JA (2003) Elucidation of the indirect pathway of abscisic acid biosynthesis by mutants, genes, and enzymes. Plant Physiol 131: 1591-1601.
  9. Park HY,Seok HY, Park BK, Kim SH, Goh CH, et al. (2008) Overexpression of Arabidopsis ZEP enhances tolerance to osmotic stress. BiochemBiophys Res Commun 375: 80-85.
  10. Lee JT, Prasad V, Yang PT, Wu JF, David Ho TH, et al. (2003) Expression of Arabidopsis CBF1 regulated by an ABA/stress inducible promoter in transgenic tomato confers stress tolerance without affecting yield. Plant Cell Environ 26: 1181-1190.
  11. Hwang SG, Chen HC, Huang WY, Chu YC, Shi CT et al. (2010) Ectopic expression of rice OsNCED3 in Arabidopsis increases ABA level and alters leaf morphology. Plant Sci 178: 12-22.
  12. Zhang X, Yang G, Shi R, Han X, Qi L, et al. (2013) Arabidopsis cysteine-rich receptor-like kinase 45 functions in the responses to abscisic acid and abiotic stresses. Plant PhysiolBiochem 67: 189-198.
  13. Ke Q, Wang Z, Ji CY, Jeong JC, Lee HS et al. (2015) Transgenic poplar expressing Arabidopsis YUCCA6 exhibits auxin-overproduction phenotypes and increased tolerance to abiotic stress. Plant PhysiolBiochem 94: 19-27.
Citation: Wani SH, Kumar V (2015) Plant Stress Tolerance: Engineering ABA: A Potent Phytohormone.Transcriptomics 3:113.

Copyright: © 2015 Wani SH, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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