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Overexpression of the sweetpotato peroxidase gene swpa4 enhances tolerance to methyl viologen-mediated oxidative stress and dehydration in Arabidopsis thaliana

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Abstract

We previously reported that transgenic Arabidopsis thaliana plants overexpressing the sweet potato peroxidase gene swpa4 under the control of the cauliflower mosaic virus (CaMV) 35 s promoter showed increased levels of reactive oxygen species (ROS) and nitric oxide (NO), and higher expression of ROS and NO related genes than control plants. Here, we investigated the effect of swpa4 overexpression on the abiotic and biotic stress tolerance levels of Arabidopsis plants. Methyl viologen (MV) treatment-induced oxidative stress caused visible damage to the seedlings and rosette leaves of all Arabidopsis plants, although the symptoms were more severe in control plants than in transgenic lines. Additionally, survival rates and ion leakage showed a slight decline in transgenic lines but a more severe decline in control plants after MV treatment. Transgenic plants also showed enhanced tolerance to drought stress. Dehydration treatment, followed by rehydration, resulted in a greater change in the relative water content and lipid peroxidation of control plants than in that of transgenic lines. However, transgenic plants did not show enhanced resistance to biotic stresses such as bacterial and fungal pathogens. These results indicate that transgenic Arabidopsis plants can efficiently regulate defense levels during oxidative stress via the overexpression of swpa4.

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Abbreviations

MV:

Methyl viologen

NO:

Nitric oxide

PR:

Pathogenesis-related

ROS:

Reactive oxygen species

RWC:

Relative water contents

References

  • Amaya I, Botella MA, Calle MD, Medina MI, Heredia A, Bressan RA, Hasegawa PM, Quesada MA, Valpuesta V (1999) Improved germination under osmotic stress of tobacco plants overexpressing a cell wall peroxidase. FEBS Lett 457:80–84

    Article  CAS  Google Scholar 

  • Baxter A, Mittler R, Suzuki N (2014) ROS as key players in plant stress signaling. J Exp Bot 65:1229–1240

    Article  CAS  Google Scholar 

  • Bindschedler LV, Dewdney J, Blee KA, Stone JM, Asai T, Plotnikov J, Denoux C, Hayes T, Gerrish C, Davies DR, Ausubel FM, Bolwell GP (2006) Peroxidase-dependent apoplastic oxidative burst in Arabidopsis required for pathogen resistance. Plant J 47:851–863

    Article  CAS  Google Scholar 

  • Demiral T, Turkan I (2005) Comparative lipid peroxidation, antioxidant defense systems and proline content in roots of two rice cultivars differing in salt tolerance. Environ Exp Bot 53:247–257

    Article  CAS  Google Scholar 

  • Elfstrand M, Sitbon F, Lapierre C, Bottin A, Arnold SV (2002) Altered lignin structure and resistance to pathogens in spi 2-expressing tobacco plants. Planta 214:708–716

    Article  CAS  Google Scholar 

  • Hiraga S, Sasaki K, Ito H, Ohashi Y, Matsui H (2001) A large family of class III plant peroxidases. Plant Cell Physiol 42:462–468

    Article  CAS  Google Scholar 

  • Hu X, Jiang M, Zhang A, Lu J (2005) Abscisic acid-induced apoplastic H2O2 accumulation up-regulates the activities of chloroplastic and cytosolic antioxidant enzymes in maize leaves. Planta 223:57–68

    Article  CAS  Google Scholar 

  • Jang IC, Park SY, Kim KY, Kwon SY, Kim GK, Kwak SS (2004) Differential expression of 10 sweetpotato peroxidase genes in response to bacterial pathogen, Pectobacterium chrysanthemi. Plant Physiol Biochem 42:451–455

    Article  CAS  Google Scholar 

  • Kim YH, Lim S, Han SH, Lee JC, Song WK, Bang JW, Kwon SY, Lee HS, Kwak SS (2007) Differential expression of 10 sweetpotato peroxidases in response to sulfur dioxide, ozone, and ultraviolet radiation. Plant Physiol Biochem 45:908–914

    Article  CAS  Google Scholar 

  • Kim YH, Kim CY, Song WK, Park DS, Kwon SY, Lee HS, Bang JW, Kwak SS (2008) Overexpression of sweetpotato swpa4 peroxidase results in increased hydrogen peroxide production and enhances stress tolerance in tobacco. Planta 227:867–881

    Article  CAS  Google Scholar 

  • Kim YH, Lee HS, Kwak SS (2010) Differential responses of sweetpotato peroxidases to heavy metals. Chemosphere 81:79–85

    Article  CAS  Google Scholar 

  • Kim YH, Jeong JC, Lee HS, Kwak SS (2013) Comparative characterization of sweetpotato antioxidant genes from expressed sequence tags of dehydration-treated fibrous roots under different abiotic stress conditions. Mol Biol Rep 40:2887–2896

    Article  CAS  Google Scholar 

  • Kim YH, Park SC, Yun BW, Kwak SS (2017) Overexpressing sweetpotato peroxidase gene swpa4 affects nitric oxide production by activating the expression of reactive oxygen species- and nitric oxide-related genes in tobacco. Plant Physiol Biochem 120:52–60

    Article  CAS  Google Scholar 

  • Kim YH, Yun BW, Kwak SS (2019) Expression of the sweet potato peroxidase gene swpa4 in Arabidopsis activates defense genes mediated by reactive oxygen species and nitric oxide. Plant Biotechnol Rep 13:329–336

    Article  Google Scholar 

  • Lee YH, Kim SH, Yun BW, Hong JK (2014) Altered cultivar resistance of kimchi cabbage seedlings mediated by salicylic acid, jasmonic acid and ethylene. Plant Pathol J 30:323–329

    Article  Google Scholar 

  • Lee YH, Hong JK (2015) Differential defence responses of susceptible and resistant kimchi cabbage cultivars to anthracnose, black spot and black rot diseases. Plant Pathol 64:406–415

    Article  CAS  Google Scholar 

  • Liang Y, Chen Q, Liu Q, Zhang W et al (2003) Exogenous silicon (Si) increases antioxidant enzyme activity and reduces lipid peroxidation in roots of salt-stressed barley (Hordeum vulgare L.). J Plant Physiol 160:1157–1164

    Article  CAS  Google Scholar 

  • Mittova V, Guy M, Tal M, Volokita M (2004) Salinity up-regulates the antioxidative system in root mitochondria and peroxisomes of the wild salt-tolerant tomato species Lycopersicon pennellii. J Exp Bot 55:1105–1113

    Article  CAS  Google Scholar 

  • Murashige T, Skoog F (1962) A revised medium for rapid growth and bioassay with tobacco tissue cultures. Physiol Plant 15:473–497

    Article  CAS  Google Scholar 

  • Oliveira HC, Saviani EE, Oliveira JFP, Salgado I (2010) Nitrate reductase-dependent nitric oxide synthesis in the defense response of Arabidopsis thaliana against Pseudomonas syringae. Trop Plant Pathol 35:104–107

    Article  Google Scholar 

  • Shi H, Chen Y, Tan D-X, Reiter RJ, Chan Z, He C (2015) Melatonin induces nitric oxide and the potential mechanisms relate to innate immunity against bacterial pathogen infection in Arabidopsis. J Pineal Res 59:102–108

    Article  CAS  Google Scholar 

  • Shinozaki K, Yamaguchi-Shinozaki K, Seki M (2003) Regulatory network of gene expression in the drought and cold stress responses. Curr Opin Plant Biol 6:410–417

    Article  CAS  Google Scholar 

  • Vitor SC, Duarte GT, Saviani EE, Vincentz MGA, Oliveira HC, Salgodo I (2013) Nitrate reductase is required for the transcriptional modulation and bactericidal activity of nitric oxide during the defense response of Arabidopsis thaliana against. Pseudomonas syringae Planta 238:475–186

    CAS  PubMed  Google Scholar 

  • Xiong L, Schumaker KS, Zhu JK (2002) Cell signaling during cold, drought, and salt stress. Plant Cell 14:S165–S183

    Article  CAS  Google Scholar 

  • Yun BW, Huh GH, Lee HS, Kwon SY, Jo JK, Kim JS, Cho KY, Kwak SS (2000) Differential resistance to methyl viologen in transgenic tobacco plants that express sweetpotato peroxidases. J Plant Physiol 156:504–509

    Article  CAS  Google Scholar 

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Acknowledgements

This research was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT and Future Planning (NRF-2018R1A1A1A05018446), and the Systems & Synthetic Agrobiotech Center (PJ01318401), the Biogreen 21 Project for the Next Generation, Rural Development Administration, Korea.

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Correspondence to Yun-Hee Kim or Sang-Soo Kwak.

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Kim, YH., Hong, J.K., Kim, H.S. et al. Overexpression of the sweetpotato peroxidase gene swpa4 enhances tolerance to methyl viologen-mediated oxidative stress and dehydration in Arabidopsis thaliana. J. Plant Biochem. Biotechnol. 30, 215–220 (2021). https://doi.org/10.1007/s13562-020-00588-3

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  • DOI: https://doi.org/10.1007/s13562-020-00588-3

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