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2014 | 36 | 03 |

Tytuł artykułu

Phenotyping shows improved physiological traits and seed yield of transgenic wheat plants expressing the alfalfa aldose reductase under permanent drought stress

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Members of the aldo–keto reductase family including aldose reductases are involved in antioxidant defense by metabolizing a wide range of lipid peroxidation-derived cytotoxic compounds. Therefore, we produced transgenic wheat genotypes over-expressing the cDNA of alfalfa aldose reductase gene. These plants consequently exhibit 1.5–4.3 times higher detoxification activity for the aldehyde substrate. Permanent drought stress was generated in the greenhouse by growing wheat plants in soil with 20 % water capacity. The control and stressed plants were monitored by a semi automatic phenotyping platform providing computer-controlled watering, digital and thermal imaging. Calculation of biomass values was based on the correlation (R²= 0.7556) between fresh weight and green pixel-based shoot surface area. The green biomass production by plants of the three transgenic lines was 12–26–41 % higher than the non-transgenic plants’ grown under water limitation. Thermal imaging of stressed nontransgenic plants indicated an elevation in the leaf temperature. The thermal status of transformants was similar at both normal and suboptimal water regime. In drought, the transgenic plants used more water during the growing season. The described phenotyping platform provided a comprehensive data set demonstrating the improved physiological condition of the drought stressed transgenic wheat plants in the vegetative growth phase. In soil with reduced water capacity two transgenic genotypes showed higher seed weight per plant than the control non-transgenic one. Limitation of greenhouse-based phenotyping in analysis of yield potential is discussed.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

36

Numer

03

Opis fizyczny

p.663-673,fig.,ref.

Twórcy

  • Department of Biotechnology, Cereal Research Non-Profit Ltd., Also kikoto sor 9, Szeged, 6726, Hungary
autor
  • Department of Biotechnology, Cereal Research Non-Profit Ltd., Also kikoto sor 9, Szeged, 6726, Hungary
autor
  • Institute of Plant Biology, Biological Research Center HAS, Temesvari krt 62, Szeged, 6726, Hungary
autor
  • Department of Biotechnology, Cereal Research Non-Profit Ltd., Also kikoto sor 9, Szeged, 6726, Hungary
autor
  • Department of Plant Biology, University of Szeged, Kozep fasor 52, Szeged, 6726, Hungary
autor
  • Institute of Plant Biology, Biological Research Center HAS, Temesvari krt 62, Szeged, 6726, Hungary
autor
  • Department of Biotechnology, Cereal Research Non-Profit Ltd., Also kikoto sor 9, Szeged, 6726, Hungary
autor
  • Institute of Plant Biology, Biological Research Center HAS, Temesvari krt 62, Szeged, 6726, Hungary
  • Department of Plant Biology, University of Szeged, Kozep fasor 52, Szeged, 6726, Hungary
autor
  • Institute of Plant Biology, Biological Research Center HAS, Temesvari krt 62, Szeged, 6726, Hungary
autor
  • Institute of Plant Biology, Biological Research Center HAS, Temesvari krt 62, Szeged, 6726, Hungary
autor
  • Department of Biotechnology, Cereal Research Non-Profit Ltd., Also kikoto sor 9, Szeged, 6726, Hungary

Bibliografia

  • Abebe T, Guenzi AC, Martin B, Cushman JC (2003) Tolerance of mannitol-accumulating transgenic wheat to water stress and salinity. Plant Physiol 131:1748–1755
  • Áy Z, Mihály R, Cserháti M, Kótai É, Pauk J (2012) The effect of high concentrations of glufosinate ammonium on the yield components of transgenic spring wheat (Triticum aestivum L.) constitutively expressing the bar gene. ScientificWorldJournal. doi:10.1100/2012/657945
  • Bartels D (2001) Targeting detoxification pathways: an efficient approach to obtain plants with multiple stress tolerance? Trends Plant Sci 6:284–286
  • Berger B, Parent B, Tester M (2010) High-throughput shoot imaging to study drought responses. J Exp Bot 61:3519–3528
  • Bhatnagar-Mathur P, Vadez V, Sharma KK (2008) Transgenic approaches for abiotic stress tolerance in plants: retrospect and prospects. Plant Cell Rep 27:411–424
  • Capell T, Bassie L, Christou P (2004) Modulation of the polyamine biosynthetic pathway in transgenic rice confers tolerance to drought stress. P Natl Acad Sci USA 101:9909–9914
  • Castiglioni P, Warner D, Bensen RJ, Anstrom DC, Harrison J, Stoecker M, Abad M, Kumar G, Salvador S, D’Ordine R, Navarro S, Back S, Fernandes MH, Targolli J, Dasgupta S, Bonin C, Luethy MH, Heard JE (2008) Bacterial RNA chaperones confer abiotic stress tolerance in plants and improved grain yield in maize under water-limited conditions. Plant Physiol 147:446–455
  • Chaves MM, Flexas J, Pinheiro C (2008) Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell. Ann Bot 103:551–560
  • Chenu K, Chapman SC, Hammer GL, McLean G, Salah HBH, Tardieu F (2008) Short-term responses of leaf growth rate to water deficit scale up to whole-plant and crop levels: an integrated modelling approach in maize. Plant Cell Environ 31:378–391
  • Chomczynski P, Sacchi N (1987) Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem 162:156–159
  • Christensen AH, Quail PH (1996) Ubiquitin promoter-based vectors for high-level of expression of selectable and/or screenable marker gene in monocotyledone plants. Transgenic Res 5:213–218
  • Collins NC, Tardieu F, Tuberosa R (2008) Quantitative trait loci and crop performance under abiotic stress: where do we stand? Plant Physiol 147:469–486
  • Cseri A, Sass L, Törjék O, Pauk J, Vass I, Dudits D (2013) Monitoring drought responses of barley genotypes with semi-robotic phenotyping platform and association analysis between recorded traits and allelic variants of some stress genes. Aust J Crop Sci 7:1560–1570
  • Deikman J, Petracek M, Heard JE (2012) Drought tolerance through biotechnology: improving translation from the laboratory to farmers’ fields. Curr Opin Biotechnol 2:243–250
  • Fabre J, Dauzat M, Nègre V, Wuyts N, Tireau A, Gennari E, Neveu P, Tisné S, Massonnet C, Hummel I, Granier C (2011) PHENOPSIS DB: an Information System for Arabidopsis thaliana phenotypic data in an environmental context. BMC Plant Biol 11:77–83
  • Felföldi K, Purnhauser L (1992) Induction of regenerating callus from immature embryos of 44 wheat and 3 Triticale cultivars. Cereal Res Commun 20:273–277
  • Golzarian MR, Frick RA, Rajendran K, Berger B, Roy S, Tester M, Lun DS (2011) Accurate inference of shoot biomass from high-throughput images of cereal plants. Plant Methods 7:2–12
  • Granier C, Aguirrezabal L, Chenu K, Cookson SJ, Dauzat M, Hamard P, Thioux JJ, Roland G, Bouchier-Combaud S, Lebaudy A, Muller B, Simonneau T, Tardieu F (2006) FENOPSIS, an automated platform for reproducible phenotyping of plant responses to soils water deficit in Arabidopsis thaliana permitted the identification of an accession with low sensitivity to soil water deficit. New Phytol 169:623–635
  • Hartmann A, Czauderna T, Hoffmann R, Stein N, Schreiber F (2011) HTPheno: an image analysis pipeline for high-throughput plant phenotyping. BMC Bioinform 12:148–156
  • Hideg É, Nagy T, Oberschall A, Dudits D, Vass I (2003) Detoxification function of aldose/aldehyde reductase during drought and ultraviolet-B (280–320 nm) stresses. Plant Cell Environ 26:513–522
  • Houle D, Govindaraju DR, Omholt S (2010) Phenomics: the next challenge. Nat Rev Genet 11:855–866
  • Hsieh TH, Lee JT, Chang YY, Chan MT (2002) Tomato plants ectopically expressing Arabidopsis CBF1 show enhanced resistance to water deficit stress. Plant Physiol 130:618–626
  • Jones HG (2004) Application of thermal imaging and infrared sensing in pant physiology and ecophysiology. Adv Bot Res 41:107–163
  • Karaba A, Dixit S, Greco R, Aharoni A, Trijatmiko KR, Marsch-Martinez N, Krishnan A, Nataraja KN, Udayakumar M, Pereira A (2007) Improvement of water use efficiency in rice by expression of HARDY, on Arabidopsis drought and salt tolerance gene. P Natl Acad Sci USA 104:15270–15275
  • Lendvai A, Pettkó-Szandtner A, Csordás-Tóth É, Miskolczi P, Horváth GV, Györgyey J, Dudits D (2007) Dicot and monocot plants differ in retinoblastoma-related protein subfamilies. J Exp Bot 58:1663–1675
  • Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2T-Δ ΔCT method. Methods 25:402–408
  • Majer P, Sass L, Lelley T, Cseuz L, Vass I, Dudits D, Pauk J (2008) Testing drought tolerance of wheat by complex stress diagnostic system installed in greenhouse. Acta Biol Szeged 52:97–100
  • Merlot S, Mustilli AC, Genty B, North H, Lefebvre V, Sotta B, Vavasseur A, Giraudat J (2002) Use of infrared thermal imaging to isolate Arabidopsis mutants defective in stomatal regulation. Plant J 30:601–609
  • Moran JF, Becana M, Iturbe-Ormaetxe I, Frechilla S, Klucas RV, Aparicio-Tejo P (1994) Drought induces oxidative stress in pea plants. Planta 194:346–352
  • Munns R, James RA, Sirault XR, Furbank RT, Jones HG (2010) New phenotyping methods for screening wheat and barley for beneficial responses to water deficit. J Exp Bot 61:3499–3507
  • Nelson DE, Repetti PP, Adams TR, Creelman RA, Wu J, Warner DC, Anstrom DC, Bensen RJ, Castiglioni PP, Donnarummo MG et al (2007) Plant nuclear factor Y (NF-Y) B subunits confer drought tolerance and lead to improved corn yields on water-limited acres. P Natl Acad Sci USA 104:16450–16455
  • Oberschall A, Deák M, Török K, Sass L, Vass I, Kovács I, Fehér A, Dudits D, Horváth VG (2000) A novel aldose/aldehyde reductase protects transgenic plants against lipid peroxidation under chemical and drought stresses. Plant J 24(4):434–446
  • Passioura J (2007) The drought environment: physical, biological and agricultural perspectives. J Exp Bot 58:113–117
  • Pellegrineschi A, Reynolds M, Pacheco M, Brito RM, Almeraya R, Yamaguchi-Shinozaki K, Hoisington D (2004) Stress-induced expression in wheat of the Arabidopsis thaliana DREB1A gene delays water stress symptoms under greenhouse conditions. Genome 47:493–500
  • Rohila JS, Jain RK, Wu R (2002) Genetic improvement of Basmati rice for salt and drought tolerance by regulated expression of a barley Hva1 cDNA. Plant Sci 163:525–532
  • Salekdeh GH, Reynolds M, Bennett J, Boyer J (2009) Conceptual framework for drought phenotyping during molecular breeding. Trends in Plant Sci 14:488–496
  • Sivamani E, Bahieldin A, Wraith JM, Al-Niemi T, Dyer WE, Ho T-HD, Qu R (2000) Improved biomass productivity and water use efficiency under water deficit conditions in transgenic wheat constitutively expressing the barley HVA1 gene. Plant Sci 155:1–9
  • Skirycz A, Vandenbroucke K, Clauw P, Maleux K, De Meyer B, Dhondt S, Pucci A, Gonzalez N, Hoeberichts F, Tognetti VB, Galbiati M, Tonelli C, van Breusegem F, Vuylsteke M, Inzé D (2011) Survival and growth of Arabidopsis plants given limited water are not equal. Nature Biotechnol 29:212–214
  • Smirnoff N (1993) The role of active oxygen in the response of plants to water deficit and desiccation. New Phytol 125:27–58
  • Takeda S, Matsuoka M (2008) Genetic approaches to crop improvement: responding to environmental and population changes. Nat Rev Genet 9:444–457
  • Tamás-Nyitrai C, Jones HD, Tamás L (2012) Biolistic- and Agrobacterium-mediated transformation protocols for wheat. Methods Mol Biol 877:357–384
  • Tuberosa R, Salvi S (2006) Genomics-based approaches to improve drought tolerance of crops. Trends Plant Sci 11:405–412
  • Valliyodan B, Nguyen HT (2006) Understanding regulatory networks and engineering for enhanced drought tolerance in plants. Curr Opin Plant Biol 9:189–195
  • Vander Jagt DL, Kolb NS, Vander Jagt TJ, Chino J, Martinez FJ, Hunsaker LA, Royer RE (1995) Substrate specificity of human aldose reductase. Identification of 4-hydroxynonenal as an endogenous substrate. Biochem Biophys Acta 1249:117–126
  • Xu C, Jing R, Mao X, Jia X, Chang X (2007) A wheat (Triticum aestivum) protein phosphatase 2A catalytic subunit gene provides enhanced drought tolerance in tobacco. Ann Bot-Lond 99:434–450
  • Yu L, Setter TL (2003) Comparative transcriptional filing of placenta and endosperm in developing maize kernels in response to water deficit. Plant Physiol 131:568–582
  • Zhao C-X, Guo L-Y, Cheruth JA, Shao H-B, Yang H-B (2008) Prospectives for applying molecular and genetic methodology to improve wheat cultivars in drought environments. C R Biol 331:579–586

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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