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2014 | 36 | 08 |

Tytuł artykułu

Exogenous ABA induces drought tolerance in upland rice: the role of chloroplast and ABA biosynthesis-related gene expression on photosystem II during PEG stress

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Abscisic acid (ABA) plays an important role in regulating photosynthesis under stress. To understand the differential function of exogenous ABA in the regulation of drought tolerance between two rice (Oryza sativa L.) genotypes, upland rice (UR, resistant to drought stress) and lowland rice (LR, susceptible to drought stress), photosynthetic parameters, chlorophyll fluorescence parameters, and the expression of chloroplast and ABA biosynthesisrelated genes were investigated under 15 % polyethylene glycol (PEG) and exogenous ABA (60 µM) treatments. In both rice lines, most of the photosynthetic parameters, chlorophyll fluorescence parameters, and chloroplast and ABA biosynthesis-related gene transcript levels were rapidly reduced by PEG stress, with the exception of up-regulated levels of OsPsbA, OsNCED3, OsNCED4, and OsZEP in LR and OsNCED3, OsNCED4, and OsZEP in UR. Moreover, a rapid stress-responsive regulation mechanism was found in UR according to the more rapid and strong up-regulation of three ABA biosynthesis-related genes in UR than in LR. Under PEG stress, exogenous ABA application significantly enhanced the recovery of the net photosynthetic rate (Pₙ), stomatal conductance (Gₛ), and transpiration rate (Tᵣ) in UR, with increased expression of OsPsbD1, OsPsbD2, OsNCED2, OsNCED3, OsNCED4, and OsNCED5. These data suggest a role for chloroplast and ABA biosynthesis-related genes in photosystem II (PSII) induction by exogenous ABA in the UR genetic background.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

36

Numer

08

Opis fizyczny

p.2219-2227,fig.,ref.

Twórcy

autor
  • Collaborative Innovation Center of Henan Grain Crops, Rice Engineering Center and Key Laboratory of Physiology, Ecology and Genetic Improvement of Food Crop in Henan Province, Henan Agricultural University, 450002 Zhengzhou, China
autor
  • Collaborative Innovation Center of Henan Grain Crops, Rice Engineering Center and Key Laboratory of Physiology, Ecology and Genetic Improvement of Food Crop in Henan Province, Henan Agricultural University, 450002 Zhengzhou, China
autor
  • Collaborative Innovation Center of Henan Grain Crops, Rice Engineering Center and Key Laboratory of Physiology, Ecology and Genetic Improvement of Food Crop in Henan Province, Henan Agricultural University, 450002 Zhengzhou, China
autor
  • Collaborative Innovation Center of Henan Grain Crops, Rice Engineering Center and Key Laboratory of Physiology, Ecology and Genetic Improvement of Food Crop in Henan Province, Henan Agricultural University, 450002 Zhengzhou, China
autor
  • Collaborative Innovation Center of Henan Grain Crops, Rice Engineering Center and Key Laboratory of Physiology, Ecology and Genetic Improvement of Food Crop in Henan Province, Henan Agricultural University, 450002 Zhengzhou, China
autor
  • Collaborative Innovation Center of Henan Grain Crops, Rice Engineering Center and Key Laboratory of Physiology, Ecology and Genetic Improvement of Food Crop in Henan Province, Henan Agricultural University, 450002 Zhengzhou, China
autor
  • Collaborative Innovation Center of Henan Grain Crops, Rice Engineering Center and Key Laboratory of Physiology, Ecology and Genetic Improvement of Food Crop in Henan Province, Henan Agricultural University, 450002 Zhengzhou, China
autor
  • Collaborative Innovation Center of Henan Grain Crops, Rice Engineering Center and Key Laboratory of Physiology, Ecology and Genetic Improvement of Food Crop in Henan Province, Henan Agricultural University, 450002 Zhengzhou, China

Bibliografia

  • Audran C, Borel C, Frey A, Sotta B, Meyer C, Simonneau T, Marion-Poll A (1998) Expression studies of the zeaxanthin epoxidase gene in Nicotiana plumbaginifolia. Plant Physiol 118(3):1021–1028
  • Desikan R, Cheung MK, Bright J, Henson D, Hancock JT, Neill SJ (2004) ABA, hydrogen peroxide and nitric oxide signalling in stomatal guard cells. J Exp Bot 55(395):205–212
  • Duan HG, Yuan S, Liu WJ, Xi DH, Qing DH, Liang HG, Lin HH (2006) Effects of exogenous spermidine on photosystem II of wheat seedlings under water stress. J Integr Plant Biol 48(8):920–927
  • Flexas J, Bota J, Loreto F, Cornic G, Sharkey TD (2004) Diffusive and metabolic limitations to photosynthesis under drought and salinity in C3 plants. Plant Biol 6(3):269–279
  • Flexas J, Diaz-Espejo A, Galmes J, Kaldenhoff R, Medrano H, Ribas-Carbo M (2007) Rapid variations of mesophyll conductance in response to changes in CO₂ concentration around leaves. Plant, Cell Environ 30(10):1284–1298
  • Gao FH, Zhang HL, Wang HG, Gao H, Li ZC (2009) Comparative transcriptional profiling under drought stress between upland and lowland rice (Oryza sativa L.) using cDNA-AFLP. Chin Sci Bull 54(19):3555–3571
  • Guo DL, Liang JH, Li L (2009) Abscisic acid (ABA) inhibition of lateral root formation involves endogenous ABA biosynthesis in Arachis hypogaea L. Plant Growth Regul 58(2):173–179
  • Hao LM, Liang HG, Wang ZL, Liu XM (1999) Effects of water stress and rewatering on turnover and gene expression of photosystem II reaction center polypeptide D1 in Zea mays. Funct Plant Biol 26(4):375–378
  • Iuchi S, Kobayashi M, Yamaguchi-Shinozaki K, Shinozaki K (2000) A stress-inducible gene for 9-cis-epoxycarotenoid dioxygenase involved in abscisic acid biosynthesis under water stress in drought-tolerant cowpea. Plant Physiol 123(2):553–562
  • Kilian J, Whitehead D, Horak J, Wanke D, Weinl S, Batistic O, D’Angelo C, Bornberg-Bauer E, Kudla J, Harter K (2007) The AtGenExpress global stress expression data set: protocols, evaluation and model data analysis of UV-B light, drought and cold stress responses. Plant J 50(2):347–363
  • Kramer DM, Johnson G, Kiirats O, Edwards GE (2004) New fluorescence parameters for the determination of QA redox state and excitation energy fluxes. Photosynth Res 79(2): 209–218
  • Lawlor DW, Cornic G (2002) Photosynthetic carbon assimilation and associated metabolism in relation to water deficits in higher plants. Plant, Cell Environ 25(2):275–294
  • Li JZ, Wang DP, Xie Y, Zhang HL, Hu GL, Li JJ, Dai AY, Liu LF, Li ZC (2011) Development of upland rice introgression lines and identification of QTLs for basal root thickness under different water regimes. J Genet Genomics 38(11):547–556
  • Lian HL, Yu X, Lane D, Sun WN, Tang ZC, Su WA (2006) Upland rice and lowland rice exhibited different PIP expression under water deficit and ABA treatment. Cell Res 16(7):651–660
  • Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method. Methods 25(4):402–408
  • Moumeni A, Satoh K, Kondoh H, Asano T, Hosaka A, Venuprasad R, Serraj R, Kumar A, Leung H, Kikuchi S (2011) Comparative analysis of root transcriptome profiles of two pairs of droughttolerant and susceptible rice near-isogenic lines under different drought stress. BMC Plant Biol 11(1):174–191
  • Mu P, Li ZC, Li CP, Zhang HL, Wang XK (2003) QTL mapping of the root traits and their correlation analysis with drought resistance using DH lines from paddy and upland rice cross. Chin Sci Bull 34(2):198–206
  • Park H, Kreunen SS, Cuttriss AJ, DellaPenna D, Pogson BJ (2002) Identification of the carotenoid isomerase provides insight into carotenoid biosynthesis, prolamellar body formation, and photomorphogenesis. Plant Cell 14(2):321–332
  • Pinheiro C, Chaves M (2011) Photosynthesis and drought: can we make metabolic connections from available data? J Exp Bot 62(3):869–882
  • Qin XQ, Zeevaart JAD (2002) Overexpression of a 9-cis-epoxycarotenoid dioxygenase gene in Nicotiana plumbaginifolia increases abscisic acid and phaseic acid levels and enhances drought tolerance. Plant Physiol 128(2):544–551
  • Qu YY, Mu P, Li XQ, Tian YX, Wen F, Zhang HL, Li ZC (2008) QTL mapping and correlations between leaf water potential and drought resistance in rice under upland and lowland environments. Acta Agron Sin 34(2):198–206
  • Schreiber U (2004) Pulse-amplitude-modulation (PAM) fluorometry and saturation pulse method: an overview. In: Chlorophyll a fluorescence. Springer, Berlin, pp 279–319
  • Shangguan ZP, Shao MG, Dyckmans J (1999) Interaction of osmotic adjustment and photosynthesis in winter wheat under soil drought. J Plant Physiol 154(5):753–758
  • Tan BC, Joseph LM, Deng WT, Liu LJ, Li QB, Cline K, McCarty DR (2003) Molecular characterization of the Arabidopsis 9-cis epoxycarotenoid dioxygenase gene family. Plant J 35(1):44–56
  • Thompson AJ, Jackson AC, Parker RA, Morpeth DR, Burbidge A, Taylor IB (2000) Abscisic acid biosynthesis in tomato: regulation of zeaxanthin epoxidase and 9-cis-epoxycarotenoid dioxygenase mRNAs by light/dark cycles, water stress and abscisic acid. Plant Mol Biol 42(6):833–845
  • Tian L, DellaPenna D, Zeevaart JA (2004) Effect of hydroxylated carotenoid deficiency on ABA accumulation in Arabidopsis. Physiol Plant 122(3):314–320
  • 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(4):523–539
  • Wang N, Fang W, Han H, Sui N, Li B, Meng QW (2008) Overexpression of zeaxanthin epoxidase gene enhances the sensitivity of tomato PSII photoinhibition to high light and chilling stress. Physiol Plant 132(3):384–396
  • Wang YX, Suo B, Zhao PF, Qu XF, Yuan LG, Zhao XJ, Zhao HJ (2011) Effect of Exogenous abscisic acid on psbA gene expression in two wheat cultivars during grain filling stage under drought stress. Acta Agron Sin 37(8):1372–1377
  • Wong CE, Li Y, Labbe A, Guevara D, Nuin P, Whitty B, Diaz C, Golding GB, Gray GR, Weretilnyk EA (2006) Transcriptional profiling implicates novel interactions between abiotic stress and hormonal responses in Thellungiella, a close relative of Arabidopsis. Plant Physiol 140(4):1437–1450
  • Xiong LM, Zhu JK (2003) Regulation of abscisic acid biosynthesis. Plant Physiol 133(1):29–36
  • Xiong LM, Schumaker KS, Zhu JK (2002) Cell signaling during cold, drought, and salt stress. Plant Cell 14:S165–S183
  • Ye NH, Zhu GH, Liu YG, Li YX, Zhang JH (2011) ABA controls H₂O₂ accumulation through the induction of OsCATB in rice leaves under water stress. Plant Cell Physiol 52(4):689–698
  • Yuan S, Liu WJ, Zhang NH, Wang MB, Liang HG, Lin H (2005) Effects of water stress on major photosystem II gene expression and protein metabolism in barley leaves. Physiol Plant 125(4):464–473
  • Zhang AY, Jiang MY, Zhang JH, Ding HD, Xu SC, Hu XL, Tan MP (2007) Nitric oxide induced by hydrogen peroxide mediates abscisic acid-induced activation of the mitogen-activated protein kinase cascade involved in antioxidant defense in maize leaves. New Phytol 175(1):36–50
  • Zhou JL, Wang XF, Jiao YL, Qin YH, Liu XG, He K, Chen C, Ma LG, Wang J, Xiong LZ (2007) Global genome expression analysis of rice in response to drought and high-salinity stresses in shoot, flag leaf, and panicle. Plant Mol Biol 63(5):591–608
  • Zhu GH, Ye NH, Zhang JH (2009) Glucose-induced delay of seed germination in rice is mediated by the suppression of ABA catabolism rather than an enhancement of ABA biosynthesis. Plant Cell Physiol 50(3):644–651

Typ dokumentu

Bibliografia

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Identyfikator YADDA

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