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Transcription Analysis of Genes Encoding the Wheat Root Transporter NRT1 and NRT2 Families During Nitrogen Starvation

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Abstract

In the present study, nitrogen (N) starvation for 8 days significantly inhibited the growth of wheat seedlings as manifested by decreased plant height, shoot fresh weight, and shoot dry weight, although it stimulated root growth. The nitrate and protein contents were markedly reduced and the oxidative stress marker, malondialdehyde content, was markedly increased in the leaves and roots of wheat seedlings during N starvation. The genes encoding the NRT1 and NRT2 families in bread wheat (Triticum aestivum L.) were identified, and their transcription levels were measured using quantitative real-time polymerase chain reaction in the roots of N-starved wheat seedlings. N starvation significantly enhanced the transcription levels of TaNRT1.1 at 2 and 4 days; TaNRT1.3 at 2, 4, and 6 days; TaNRT1.4 at 2 days; TaNRT1.7 and TaNRT1.8 at 2 days; TaNRT2.1 and TaNRT2.2 at 2 days; and TaNRT2.3 at 2 and 4 days. However, the TaNRT1.5 and TaNRT2.4 genes were greatly inhibited at all sampling time points after N starvation, whereas the TaNRT1.2 and TaNRT2.5 genes were dramatically induced. The functions of these transporters in N starvation of wheat seedlings based on these expression profiles are herein discussed.

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References

  • Bao S, An L, Su S, Zhou Z, Gan Y (2011) Expression patterns of nitrate, phosphate, and sulfate transporters in Arabidopsis roots exposed to different nutritional regimes. Botany 89(9):647–653

    Article  CAS  Google Scholar 

  • Bates T, Lynch J (1996) Stimulation of root hair elongation in Arabidopsis thaliana by low phosphorus availability. Plant Cell Environ 19(5):529–538

    Article  CAS  Google Scholar 

  • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72(1):248–254

    Article  CAS  PubMed  Google Scholar 

  • Cai H, Lu Y, Xie W, Zhu T, Lian X (2012) Transcriptome response to nitrogen starvation in rice. J Biosci 37(4):731–747

    Article  CAS  PubMed  Google Scholar 

  • Cataldo D, Harron M, Scharader LE, Youngs VL (1975) Rapid colorimetric determination of nitrate in plant tissue by nitration of salicylic acid. Commun Soil Sci Plant Anal 6(1):853–855

    Article  Google Scholar 

  • Criado MV, Roberts IN, Echeverria M, Barneix AJ (2007) Plant growth regulators and induction of leaf senescence in nitrogen-deprived wheat plants. J Plant Growth Regul 26(4):301–307

    Article  CAS  Google Scholar 

  • Dechorgnat J, Nguyen CT, Armengaud P, Jossier M, Diatloff E, Filleur S, Daniel-Vedele F (2011) From the soil to the seeds, the long journey of nitrate in plants. J Exp Bot 62(4):1349–1359

    Article  CAS  PubMed  Google Scholar 

  • Elberse IAM, van Damme JMM, Tienderen PHV (2003) Plasticity of growth characteristics in wild barley (Hordeum spontaneum) in response to nutrient limitation. J Ecol 91(3):371–382

    Article  Google Scholar 

  • Frink CR, Waggoner PE, Ausubel JH (1999) Nitrogen fertilizer: retrospect and prospect. Proc Natl Acad Sci USA 96(4):1175–1180

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Garnett T, Conn V, Plett D, Conn S, Zanghellini J, Mackenzie N, Enju A, Francis K, Holtham L, Roessner U, Boughton B, Bacic A, Shirley N, Rafalski A, Dhugga K, Tester M, Kaiser BN (2013) The response of the maize nitrate transport system to nitrogen demand and supply across the life cycle. New Phytol 198(1):82–94

    Article  CAS  PubMed  Google Scholar 

  • Glass ADM, Brito DT, Kaiser BN, Kronzucker HJ, Kumar A, Okamoto M, Rawat SR, Siddiqi MY, Silim SM, Vidmar JJ, Zhuo D (2001) Nitrogen transporter in plants, with an emphasis on regulation on the regulation of fluxes to match plant demand. J Plant Nutr Soil Sci 164(2):199–207

    Article  CAS  Google Scholar 

  • Good AG, Shrawat AK, Muench DG (2004) Can less yield more? Is reducing nutrient input into the environment compatible with maintaining crop production? Trends Plant Sci 9(12):597–605

    Article  CAS  PubMed  Google Scholar 

  • Gupta PK, Mir RR, Mohan A, Kumar J (2008) Wheat genomics: present status and future prospects. Int J Plant Genomics 2008:896451

    PubMed Central  CAS  PubMed  Google Scholar 

  • Huang NC, Liu KH, Lo HJ, Tsay YF (1999) Cloning and functional characterization of an Arabidopsis nitrate transporter gene that encodes a constitutive component of low-affinity uptake. Plant Cell 11(8):1381–1392

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Kant S, Bi YM, Rothstein SJ (2011) Understanding plant response to nitrogen limitation for the improvement of crop nitrogen use efficiency. J Exp Bot 62(4):1499–1509

    Article  CAS  PubMed  Google Scholar 

  • Li W, Wang Y, Okamoto M, Crawford NM, Siddiqi MY, Glass AD (2007) Dissection of the AtNRT2.1:AtNRT2.2 inducible high-affinity nitrate transporter gene cluster. Plant Physiol 143(1):425–433

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Li XJ, Yang MF, Chen H, Qu LQ, Chen F, Shen SH (2010) Abscisic acid pretreatment enhances salt tolerance of rice seedlings: proteomic evidence. BBA-Proteins Proteom 1804(4):929–940

    Article  CAS  Google Scholar 

  • Lian X, Wang S, Zhang J, Feng Q, Zhang L, Fan D, Li X, Yuan D, Han B, Zhang Q (2006) Expression profiles of 10,422 genes at early stage of low nitrogen stress in rice assayed using a cDNA microarray. Plant Mol Biol 60(5):617–631

    Article  CAS  PubMed  Google Scholar 

  • Ludewig U, Neuhäuser B, Dynowski M (2007) Molecular mechanisms of ammonium transport and accumulation in plants. FEBS Lett 581(12):2301–2308

    Article  CAS  PubMed  Google Scholar 

  • Migocka M, Warzybok A, Kłobus G (2013) The genomic organization and transcriptional pattern of genes encoding nitrate transporters 1 (NRT1) in cucumber. Plant Soil 364:245–260

    Article  CAS  Google Scholar 

  • Møller AL, Pedas P, Andersen B, Svensson B, Schjoerring JK, Finnie C (2011) Responses of barley root and shoot proteomes to long-term nitrogen deficiency, short-term nitrogen starvation and ammonium. Plant, Cell Environ 34(12):2024–2037

    Article  Google Scholar 

  • Ohdan T, Francisco PB, Sawada JT, Hirose T, Terao T, Satoh H, Nakamura Y (2005) Expression profiling of genes involved in starch synthesis in sink and source organs of rice. J Exp Bot 56(422):3229–3244

    Article  CAS  PubMed  Google Scholar 

  • Okamoto M, Vidmar JJ, Glass ADM (2003) Regulation of NRT1 and NRT2 gene families of Arabidopsis thaliana: responses to nitrate provision. Plant Cell Physiol 44(3):304–317

    Article  CAS  PubMed  Google Scholar 

  • Orsel M, Krapp A, Daniel-Vedele F (2002) Analysis of the NRT2 nitrate transporter family in Arabidopsis. Structure and gene expression. Plant Physiol 129(2):886–896

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Orsel M, Chopin F, Leleu O, Smith SJ, Krapp A, Daniel-Vedele F, Miller AJ (2006) Characterization of a two-component high-affinity nitrate uptake system in Arabidopsis. Physiology and protein–protein interaction. Plant Physiol 142(3):1304–1317

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Pettersson S, Jensen P (1983) Variation among species and varieties in uptake and utilization of potassium. Plant Soil 72:231–237

    Article  CAS  Google Scholar 

  • Plett D, Toubia J, Garnett T, Tester M, Kaiser BN, Baumann U (2010) Dichotomy in the NRT gene families of dicots and grass species. PLoS ONE 5(12):15289

    Article  Google Scholar 

  • Shu Z, Shi Y, Qian H, Tao Y, Tang D (2010) Distinct respiration and physiological changes during flower development and senescence in two Freesia cultivars. HortScience 45(7):1088–1092

    Google Scholar 

  • Socolow RH (1999) Nitrogen management and the future of food: lessons from the management of energy and carbon. Proc Natl Acad Sci USA 96(11):6001–6008

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Sylvester-Bradley R, Kindred DR (2009) Analysing nitrogen responses of cereals to prioritize routes to the improvement of nitrogen use efficiency. J Exp Bot 60(7):1939–1951

    Article  CAS  PubMed  Google Scholar 

  • The International Brachypodium Initiative (2010) Genome sequencing and analysis of the model grass Brachypodium distachyon. Nature 463(7282):763–768

    Article  Google Scholar 

  • Wang X, Bian Y, Cheng K, Zou H, Sun SS, He J (2012) A comprehensive differential proteomic study of nitrate deprivation in Arabidopsis reveals complex regulatory networks of plant nitrogen responses. J Proteome Res 11(4):2301–2315

    Article  CAS  PubMed  Google Scholar 

  • Yan HB, Pan XX, Jiang HW, Wu GJ (2009) Comparison of the starch synthesis genes between maize and rice: copies, chromosome location and expression divergence. Theor Appl Genet 119(5):815–825

    Article  PubMed  Google Scholar 

  • Zheng YH, Jia AJ, Ning TY, Xu JL, Li ZJ, Jiang GM (2008) Potassium nitrate application alleviates sodium chloride stress in winter wheat cultivars differing in salt tolerance. J Plant Physiol 165(14):1455–1465

    Article  CAS  PubMed  Google Scholar 

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Acknowledgments

This study is financially supported by the Twelfth Five-Year National Food Production Technology Project (2011BAD16B07) and the Special Fund for Agro-scientific Research in the Public Interest (201203033).

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The authors declare no competing financial interest.

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Correspondence to Guozhang Kang.

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Supplementary Fig. S1

Transcript levels of TaNRT1 family genes were measured using GAPDH as another internal control during N starvation. Each value is the mean ± standard deviation of at least three independent measurements. Different letters indicate significant differences (P < 0.05). a Transcript levels of TaNRT1.1 in wheat seedling roots. b Transcript levels of TaNRT1.2 in wheat seedling roots. c Transcript levels of TaNRT1.3 in wheat seedling roots. d Transcript levels of TaNRT1.4 in wheat seedling roots. e Transcript levels of TaNRT1.5 in wheat seedling roots. f Transcript levels of TaNRT1.7 in wheat seedling roots. g Transcript levels of TaNRT1.8 in wheat seedling roots. (TIFF 722 kb)

Supplementary Fig. S2

Transcript levels of TaNRT2 family genes were measured using GAPDH as another internal control during N starvation. Each value is the mean ± standard deviation of at least three independent measurements. Different letters indicate significant differences (P < 0.05). a Transcript levels of TaNRT2.1 in wheat seedling roots. b Transcript levels of TaNRT2.2 in wheat seedling roots. c Transcript levels of TaNRT2.3 in wheat seedling roots. d Transcript levels of TaNRT2.4 in wheat seedling roots. e Transcript levels of TaNRT2.5 in wheat seedling roots. (TIFF 1,098 kb)

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Guo, T., Xuan, H., Yang, Y. et al. Transcription Analysis of Genes Encoding the Wheat Root Transporter NRT1 and NRT2 Families During Nitrogen Starvation. J Plant Growth Regul 33, 837–848 (2014). https://doi.org/10.1007/s00344-014-9435-z

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  • DOI: https://doi.org/10.1007/s00344-014-9435-z

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