Skip to main content
Log in

Effect of selenium and silicon on transcription factors NAC5 and DREB2A involved in drought-responsive gene expression in rice

  • Original Papers
  • Published:
Biologia Plantarum

Abstract

Drought is one of the main environmental stresses and many investigators identified beneficial effects of both silicon and selenium on plant growth and development. To examine the effects of Si and Se on rice (Oryza sativa L.) responses to drought, two cultivars Giza 177 and IET 1444 pretreated with 1.5 mM Si or 0.03 mM Se were then exposed to a water stress until leaf rolling was observed. The enhanced growth of Se or Si pre-treated plants was associated with a significant increase in the content of proline and glycine betaine in both shoots and roots. Furthermore, the transcription factors (TFs), dehydration responsive element-binding protein DREB2A, and NAC5 [no apical meristem (NAM), Arabidopsis thaliana activating factor (ATAF), and cup-shaped cotyledon (CUC)] were over-expressed in the drought stressed rice shoots. Notably, a pretreatment with either Se or Si significantly enhanced the expression of both TFs, DREB2A, NAC5, as well as the expression of the ring domain containing OsRDCP1 gene and some drought specific genes, such as OsCMO coding rice choline monooxygenase and dehydrin OsRAB16b. Expression of TFs and the studied genes was markedly enhanced in the Si-stressed shoots of cv. IET 1444 which favors its drought tolerance.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

ABA:

abscisic acid

ATAF:

Arabidopsis thaliana activating factor

CMO:

choline monooxygenase

CUC:

cupshaped cotyledon

DREB:

dehydration responsive element-binding protein

GB:

glycine betaine

NAC:

acronym derived from the genes NAM/ATAF/CUC

Pro:

proline

RDCP:

ring domain containing protein

ROS:

reactive oxygen species

TFs:

transcription factors

Ub:

ubiquitin

References

  • Agarie, S., Uchida, H., Qgata, W., Kubota, F., Kaufman, P.B.: Effects of silicon on transpiration and leaf conductance in rice plants (Oryza sativa L.). — Plant Prod. Sci. 1: 89–95, 1998.

    Article  Google Scholar 

  • Andjelkovic, V., Thompson, R.: Changes in gene expression in maize kernel in response to water and salt stress. — Plant Cell Rep. 25: 71–79, 2006.

    Article  PubMed  CAS  Google Scholar 

  • Armengaud, P., Thierry, L., Buhot, N., Grenier-de March, G., Savouré, A.: Transcriptional regulation of proline biosynthesis in Medicago truncatula reveals developmental and environmental specific features. — Physiol. Plant. 120: 442–450, 2004.

    Article  PubMed  CAS  Google Scholar 

  • Ashraf, M.: Inducing drought tolerance in plants: some recent advances. — Biotechnol. Adv. 28: 169–183, 2010.

    Article  PubMed  CAS  Google Scholar 

  • Ashraf, M., Foolad, M.R.: Roles of glycine betaine and proline in improving plant abiotic stress resistance. — Environ. exp. Bot. 59: 206–216, 2007.

    Article  CAS  Google Scholar 

  • Bae, H., Kim, S.K., Cho, S.K., Kang, B.G., Kim, W.T.: Over expression of OsRDCP1, a rice RING domain-containing E3 ubiquitin ligase, increased tolerance to drought stress in rice (Oryza sativa L.). — Plant. Sci. 180: 775–782, 2011.

    Article  PubMed  CAS  Google Scholar 

  • Bartels, D., Sunkar, R.: Drought and salt tolerance in plants. — Crit. Rev. Plant. Sci. 24: 23–58, 2005.

    Article  CAS  Google Scholar 

  • Bates, I.S., Waldren, R.P., Teare, I.D.: Rapid determination of free proline for water stress studies. — Plant. Soil 39: 205–207, 1973.

    Article  CAS  Google Scholar 

  • Bies-Ethève, N., Gaubier-Comella, P., Debures, A., Lasserre, E., Jobet, E., Raynal, M., Cooke, R., Delseny, M.: Inventory, evolution and expression profiling diversity of the LEA (late embryogenesis abundant) protein gene family in Arabidopsis thaliana. — Plant mol. Biol. 67: 107–724, 2008.

    Article  PubMed  CAS  Google Scholar 

  • Blumwald, E., Grover, A., Good, A.G.: Breeding for abiotic stress resistance: challenges and opportunities. — In: Fischer, R.A. (ed.): New Directions for a Diverse Planet (Proceeding of the 4th International Crop Science Congress). Brisbane 2004.

  • Buchanan, C.D., Lim, S.Y., Salzman, R.A.: Sorghum bicolor transcriptome response to dehydration, high salinity and ABA. — Plant. mol. Biol. 58: 699–720, 2005.

    Article  PubMed  CAS  Google Scholar 

  • Burnet, M., Lafontaine, P.J., Hanson, A.D.: Assay, purification, and partial characterization of choline monooxygenase from spinach. — Plant Physiol. 108: 581–588, 1995.

    PubMed Central  PubMed  CAS  Google Scholar 

  • Chaitanya, K.V., Rasineni, G.K., Reddy, A.R.: Biochemical responses to drought stress in mulberry (Morus alba L.): evaluation of proline, glycine betaine and abscisic acid accumulation in five cultivars. — Acta Physiol. Plant. 31: 437–443, 2010.

    Article  CAS  Google Scholar 

  • Chaves, M.M., Oliveira, M.M.: Mechanisms underlying plant resilience to water deficits: prospects for water-saving agriculture. — J. exp. Bot. 55: 2365–2384, 2004.

    Article  PubMed  CAS  Google Scholar 

  • Chazen, O., Neumann, P.M.: Hydraulic signals from the roots and rapid cell-wall hardening in growing maize (Zea mays L.) leaves are primary responses to polyethylene glycolinduced water deficits. — Plant Physiol. 104: 1385–1392, 1994.

    PubMed Central  PubMed  CAS  Google Scholar 

  • Chen, J.Q., Meng, Q.P., Zhang, Y., Xia M., Wang, X.P.: Over expression of OsDREB genes lead to enhanced drought tolerance in rice. — Biotechnol. Lett. 30: 2191–2198, 2008.

    Article  PubMed  CAS  Google Scholar 

  • Chomczynski, P., Mackey, K., Modification of the TRI Reagent procedure for isolation of RNA from polysaccharide- and proteoglycan-rich sources. — BioTechniques 19: 924–945, 1995.

    Google Scholar 

  • De Lacerda, C.F., Cambraia, J., Oliva, M.A., Ruiz, H.A., Prisco, J.T.: Solute accumulation and distribution during shoot and leaf development in two sorghum genotypes under salt stress. — Environ. exp. Bot. 47: 107–120, 2003.

    Article  CAS  Google Scholar 

  • Djibril, S., Mohamed, O.K., Diaga, D., Diégane, D., Abaye, B.F., Maurice, S., Alain, B.: Growth and development of date palm (Phoenix dactylifera L.) seedlings under drought and salinity stresses. — Afr. J. Biotechnol. 4: 968–972, 2005.

    Google Scholar 

  • Du, H., Wang, N., Cui, F., Li, X., Xiao, J., Xiong, L.: Characterization of a β-carotene hydroxylase gene DSM2 conferring drought and oxidative stress resistance by increasing xanthophylls and ABA synthesis in rice. — Plant Physiol. 154: 1304–1318, 2010.

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Dubouzet, J.G., Sakuma, Y., Ito, Y., Kasuga, M., Dubouzet, E.G., Miura, S., Seki, M., Shinozaki, K., Yamaguchi-Shinozaki, K.: OsDREB genes in rice, Oryza sativa L., encode transcription activators that function in drought-, high-salt- and cold-responsive gene expression. — Plant J. 33: 751–763, 2003.

    Article  PubMed  CAS  Google Scholar 

  • Epstein, E.: Silicon. — Annu. Rev. Plant Physiol. Plant mol. Biol. 50: 641–664, 1999.

    Article  PubMed  CAS  Google Scholar 

  • Fang, Y., You, J., Xie, K., Xie, W., Xiong, L.: Systematic sequence analysis and identification of tissue-specific or stress-responsive genes of NAC transcription factor family in rice. — Mol. Genet. Genomics 280: 547–563, 2008.

    Article  PubMed  CAS  Google Scholar 

  • Fujita, Y., Fujita, M., Shinozaki, K., Yamaguchi-Shinozaki, K.: ABA-mediated transcriptional regulation in response to osmotic stress in plants. — J. Plant Res. 124: 509–525, 2011.

    Article  PubMed  CAS  Google Scholar 

  • Gao, J.P., Chao, D.Y., Lin, H.X.: Understanding abiotic stress tolerance mechanisms: recent studies on stress response in rice. — J. Integr. Plant Biol. 49: 742–750, 2007.

    Article  CAS  Google Scholar 

  • Germ, M., Kreft, I., Stibilj, V., Urbanc-Berčič, O.: Combined effects of selenium and drought on photosynthesis and mitochondrial respiration in potato. — Plant Physiol. Biochem. 162: 145–167, 2007.

    Google Scholar 

  • Grieve, C.M., Grattan, S.R.: Rapid assay for determination of water-soluble quaternary-amino compounds. — Plant Soil 70: 303–307, 1983.

    Article  CAS  Google Scholar 

  • Hu, H., You, J., Fang, Y., Zhu, X., Qi, Z., Xiong, L.: Characterization of transcription factor gene SNAC2 conferring cold and salt tolerance in rice. — Plant mol. Biol. 67: 169–181, 2008.

    Article  PubMed  CAS  Google Scholar 

  • Hussain, S.S., Kayani, M.A., Amjad, M.: Transcription factors as tools to engineer enhanced drought tolerance in plants. — Biotechnol. Progr. 27: 297–306, 2011.

    Article  CAS  Google Scholar 

  • Jaleel, C.A., Manivannan, P., Sankar, B., Kishorekumar, A., Gopi, R., Somasundaram, R., Panneerselvam, R.: Water deficit stress mitigation by calcium chloride in Catharanthus roseus; effects on oxidative stress, proline metabolism and indole alkaloid accumulation. — Colloids Surf. B 60: 110–116, 2007.

    Article  CAS  Google Scholar 

  • James, D.J., Uratsu, S., Cheng, J., Negri, P., Viss, P., Dandekar, A.M.: Acetosyringone and osmoprotectants like betaine or proline synergistically enhance Agrobacterium-mediated transformation of apple. — Plant Cell Rep. 45: 437–448, 1993.

    Google Scholar 

  • Khattab, H.: Metabolic and oxidative responses associated with exposure of Eruca sativa (rocket) plants to different levels of selenium. — Int. J. agr. Biol. 6: 1101–1106, 2004.

    CAS  Google Scholar 

  • Kraft, E., Stone, S.L., Ma, L., Su, N., Gao, Y., Lau, O.S., Deng, X.W., Callis, J.: Genome analysis and functional characterization of the E2 and RING-type E3 ligase ubiquitination enzymes of Arabidopsis. — Plant Physiol. 139: 1597–1611, 2005.

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Kuznetsov, V.V., Kholodova, V.P., Kuznetsov, V.V., Yagodin, B.A.: Selenium regulates the water status of plants exposed to drought. — Dokl. Akad. Nauk. Biol. 266: 268–390, 2003.

    Google Scholar 

  • Lenka, S.K., Katiyar, A., Chinnusamy, V., Bansal, K.C.: Comparative analysis of drought-responsive transcriptome in Indica rice genotypes with contrasting drought tolerance. — Plant Biotechnol J. 9: 315–327, 2011.

    Article  PubMed  CAS  Google Scholar 

  • Liang, Y., Sun, W., Zhu, Y-G., Christie, P.: Mechanism of silicon-mediated alleviation of abiotic stresses in higher plants. — Environ. Pollut. 147: 422–428, 2007.

    Article  PubMed  CAS  Google Scholar 

  • Liu, W., He, Y., Xiang, J., Fu, C., Yu, L., Zhang, J., Li, M.: The physiological response of suspension cell of Capparis spinosa L. to drought stress. — J. med. Plants Res. 5: 5899–5906, 2011.

    CAS  Google Scholar 

  • Lucas, S., Durmaz, E., Akpinar, B.A., Budak, H.: The drought response displayed by a DRE-binding protein from Triticum dicoccoides. — Plant Physiol. Biochem. 49: 346–351, 2011.

    Article  PubMed  CAS  Google Scholar 

  • Luo, D., Niu, X., Yu, J., Yan, J., Gou, X., Lu, B.R., Liu, Y.: Rice choline monooxygenase (OsCMO) protein functions in enhancing glycine betaine biosynthesis in transgenic tobacco but does not accumulate in rice (Oryza sativa L. ssp. japonica). — Plant Cell Rep. 31: 1625–1635, 2012.

    Article  PubMed  CAS  Google Scholar 

  • Luo, M., Liu, J., Lee, R.D., Scully, B.T., Guo, B.: Monitoring the expression of maize genes in developing kernels under drought stress using oligo-microarray. — J. Integr. Plant Biol. 52: 1059–1074, 2010.

    Article  PubMed  CAS  Google Scholar 

  • Ma, J.F., Yamaji, N.: Silicon uptake and accumulation in higher plants. — Trends Plant Sci. 11: 392–397, 2006.

    Article  PubMed  CAS  Google Scholar 

  • Mafakheri, A., Siosemardeh, A., Bahramnejad, B., Struik, P.C, Sohrabi, Y.: Effect of drought stress on yield, proline and chlorophyll contents in three chickpea cultivars. — Aust. J. Crop Sci. 4: 580–585, 2010.

    CAS  Google Scholar 

  • Mahajan, S., Tuteja, N.: Cold, salinity and drought stresses: an overview. — Arch. Biochem. Biophys. 444: 139–158, 2005.

    Article  PubMed  CAS  Google Scholar 

  • Mansour, M.M.: Protection of plasma membrane of onion epidermal cells by glycinebetaine and proline against NaCl stress. — Plant Physiol. Biochem. 35: 767–772, 1998.

    Article  Google Scholar 

  • Matsukura, S., Mizoi, J., Yoshida, T., Todaka, D., Ito, Y., Maruyama, K., Shinozaki, K., Yamaguchi-Shinozaki, K.: Comprehensive analysis of rice DREB2-type genes that encode transcription factors involved in the expression of abiotic stress responsive genes. — Mol. Genet. Genomics 283: 185–196, 2010.

    Article  PubMed  CAS  Google Scholar 

  • Mingo, D.M., Theobald, J.C., Bacon, M.A., Davies, W.J., Dodd, I.C.: Biomass allocation in tomato (Lycopersicon esculentum) plants grown under partial root zone drying: enhancement of root growth. — Funct. Plant Biol. 31: 971–978, 2004.

    Article  Google Scholar 

  • Mitani, N., Ma, J.F.: Uptake system of silicon in different plant species. — J. exp. Bot. 56: 1255–1261, 2005.

    Article  PubMed  CAS  Google Scholar 

  • Mizoi, J., Shinozaki, K., Yamaguchi-Shinozaki, K.: AP2/ERF family transcription factors in plant abiotic stress responses. — Biochim. biophys. Acta 1819: 86–96, 2011.

    Article  PubMed  CAS  Google Scholar 

  • Nakashima, K., Ito, Y., Yamaguchi-Shinozaki, K.: Transcriptional regulatory networks in response to abiotic stresses in Arabidopsis and grasses. — Plant Physiol. 149: 88–95, 2009.

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Nayyar, H., Walia, D.P.: Water stress induced proline accumulation in contrasting wheat genotypes as affected by calcium and abscisic acid. — Biol. Plant. 46: 275–279, 2003.

    Article  CAS  Google Scholar 

  • Ning, Y., Jantasuriyarat, C., Zhao, Q., Zhang, H., Chen, S., Liu, J., Liu, L., Tang, S., Park, C.H., Wang, X.: The SINA E3 ligase OsDIS1 negatively regulates drought response in rice. — Plant Physiol. 157: 242–255, 2011.

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Nonami, H., Boyer, J.S.: Primary events regulating stem growth at low water potentials. — Plant Physiol. 94: 1601–1609, 1990.

    Article  Google Scholar 

  • Papageorgiou, G.C., Murata, N.: The unusually strong stabilizing effect of glycine betaine on the structure and function of the oxygen-evolving photosystem II complex. — Photosynth. Res. 44: 243–252, 1995.

    Article  PubMed  CAS  Google Scholar 

  • Park, J.J., Yi, J., Yoon, J., Cho, L.H., Ping, J., Jeong, H.J., Cho, S.K., Kim, W.T.: OsPUB15, an E3 ubiquitin ligase, functions to reduce cellular oxidative stress during seedling establishment. — Plant J. 65: 194–205, 2011.

    Article  PubMed  CAS  Google Scholar 

  • Qin, F., Sakuma, Y., Li, J., Liu, Q., Li, Y.Q., Shinozaki, K., Yamaguchi-Shinozaki, K.: Cloning and functional analysis of a novel DREB1/CBF transcription factor involved in cold-responsive gene expression in Zea mays L. Plant Cell Physiol. 45: 1042–1052, 2004.

    Article  PubMed  CAS  Google Scholar 

  • Qin, F., Sakuma, Y., Tran, L.S., Maruyama, K., Kidokoro, S., Fujita, Y., Fujita, M., Umezawa, T., Sawano, Y., Miyazono, K.: Arabidopsis DREB2A interacting proteins function as RING E3 ligases and negatively regulate plant drought stress-responsive gene expression. — Plant Cell 20: 1693–1707, 2008.

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Qin, F., Shinozaki, K., Yamaguchi-Shinozaki, K.: Achievements and challenges in understanding plant abiotic stress responses and tolerance. — Plant Cell Physiol. 52: 1569–1582, 2011.

    Article  PubMed  CAS  Google Scholar 

  • Rabbani, M.A., Abe, H., Maruyama, K., Khan, M.A., Katsura, K., Ito, Y., Yoshiwara, K., Seki, M., Shinozaki, K., Yamaguchi-Shinozaki, K.: Monitoring expression profiles of rice (Oryza sativa L.) genes under cold, drought and high-salinity stresses, and ABA application using both cDNA microarray and RNA gel blot analyses. — Plant Physiol. 133: 1755–1767, 2003.

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Rahman, M.S., Miyake, H., Takeoka, Y.: Effects of exogenous glycine betaine on growth and ultrastructure of salt-stressed rice seedlings (Oryza sativa L.). — Plant Prod. Sci. 5: 33–44, 2002.

    Article  CAS  Google Scholar 

  • Rathinasabapathi, B., Gage, D.A., Mackill, D.J., Hanson, A.D.: Cultivated and wild rices do not accumulate glycine betaine due to deficiencies in two biosynthetic steps. — Crop Sci. 33: 534–538, 1993.

    Article  CAS  Google Scholar 

  • Rauf, S., Sadaqat, H.A.: Effect of osmotic adjustment on root length and dry matter partitioning in sunflower (Helianthus annuus L.) under drought stress. — Acta agr. scand. Sect. B Soil Plant Sci. 58: 252–260, 2008.

    CAS  Google Scholar 

  • Savant, N.K., Snyder, G.H., Datnoff, L.E.: Silicon management and sustainable rice production. — Adv.Agron. 58: 151–199. 1997.

    Article  CAS  Google Scholar 

  • Shinozaki, K., Yamaguchi-Shinozaki, K.: Molecular responses to dehydration and low temperature: differences and crosstalk between two stress signaling pathways. — Curr. Opin. Plant Biol. 3: 217–223, 2000.

    Article  PubMed  CAS  Google Scholar 

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

    Article  PubMed  CAS  Google Scholar 

  • Shirasawa, K., Takabe, T., Takabe, T., Kishitani, K.: Accumulation of glycinebetaine in rice plants that overexpress choline monooxygenase from spinach and evaluation of their tolerance to abiotic stress. — Ann. Bot. 98: 565–571, 2006.

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Snedecor, G.W., Cochran, W.G.: Statistical Methods. 7th Ed. — Iowa State University Press, Ames 1980.

    Google Scholar 

  • Song, S.Y., Chen, Y., Chen, J., Dai, X.Y., Zhang, W.H.: Physiological mechanisms underlying OsNAC5-dependent tolerance of rice plants to abiotic stress. — Planta 234: 331–345, 2011.

    Article  PubMed  CAS  Google Scholar 

  • Spollen, W.G., Sharp, R.E., Saab, I.N., Wu, Y.: Regulation of cell expansion in roots and shoots at low water potentials. — In: Smith, J.A.C., Griffiths, H. (ed.): Water Deficits: Plant Responses from Cell to Community. Pp. 37–52. BIOS Scientific Publishers, Oxford 1993.

    Google Scholar 

  • Steel, R.G.D., Torrie, J.H.: Principles and Procedures of Statistics. 2nd Ed. — McGraw Hill, New York 1980.

    Google Scholar 

  • Stone, S.L., Hauksdottir, H., Troy, A., Herschleb, J., Kraft, E., Callis, J.: Functional analysis of the RING-type ubiquitin ligase family of Arabidopsis. — Plant Physiol. 137: 13–30, 2005.

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Szabados, L., Savoure, A.: Proline: a multifunctional amino acid. — Trends Plant Sci. 15: 89–97, 2010.

    Article  PubMed  CAS  Google Scholar 

  • Takasaki, H., Maruyama, K., Kidokoro, S., Ito, Y., Fujita, Y., Shinozaki, K.: The abiotic stress-responsive NAC-type transcription factor OsNAC5 regulates stress-inducible genes and stress tolerance in rice. — Mol. Genet. Genomics 284: 173–183, 2010.

    Article  PubMed  CAS  Google Scholar 

  • Talame, V., Ozturk, N.Z., Bohnert, H.J., Tuberosa, R.: Barley transcript profiles under dehydration shock and drought stress treatments: a comparative analysis. — J. exp. Bot. 58: 229–240, 2007.

    Article  PubMed  CAS  Google Scholar 

  • Terry, N., Zayed, A.M., De Souza, M.P., Tarun, A.S.: Selenium in higher plants. — Annu. Rev. Plant Physiol. Plant mol. Biol. 51: 401–432, 2000.

    Article  PubMed  CAS  Google Scholar 

  • Tran, L.S.P., Nishiyama, R., Yamaguchi-Shinozaki, K., Shinozaki, K.: Potential utilization of NAC transcription factors to enhance abiotic stress tolerance in plants by biotechnological approach. — GM Crops 1: 32–39, 2010.

    Article  PubMed  Google Scholar 

  • Trovato, M., Matioli, R., Costantino, P.: Multipe roles of proline in plant stress tolerance and development. — Rendiconti Lincei 19: 325–346, 2008.

    Article  Google Scholar 

  • Tunnacliffe, A., Wise, M.J.: The continuing conundrum of the LEA proteins. — Naturwissenschaften 94: 791–812, 2007.

    Article  PubMed  CAS  Google Scholar 

  • Umezawa, T., Fujita, M., Fujita, Y., Yamaguchi-Shinozaki, K., Shinozaki, K.: Engineering drought tolerance in plants: discovering and tailoring genes unlock the future. — Curr. Opin. Biotechnol. 17: 113–122, 2006.

    Article  PubMed  CAS  Google Scholar 

  • Wang, C., Zhang, I., Yuan, M., Ge, Y., Liu, Y., Fan, J., Cui, Z., Tong, S., Zhang, S.: The microfilament cytoskeleton plays a vital role in salt and osmotic stress tolerance in Arabidopsis. — Plant Biol. 12: 70–78, 2010.

    Article  PubMed  CAS  Google Scholar 

  • Wang, Q., Guan, Y., Yu, Y., Chen, H., Chen, F., Chu, C.: Overexpression of a rice OsDREB1F gene increases salt, drought, and low temperature tolerance in both Arabidopsis and rice. — Plant mol. Biol. 67: 589–602, 2008.

    Article  PubMed  CAS  Google Scholar 

  • Xiong, L., Schumaker, K.S., Zhu, J.K.: Cell signaling during cold, drought, and salt stress. — Plant Cell 14: S165–S183, 2002.

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Xoconostle-Cázares, B., Ramírez-Ortega, F.A., Flores-Elenes, L., Ruiz-Medrano, R.: Drought tolerance in crop plants. — Amer. J. Plant Physiol. 5: 241–256, 2010.

    Article  Google Scholar 

  • Yamaguchi-Shinozaki, K., Shinozaki, K.: Organization of cisacting regulatory elements in osmotic and cold-stressresponsive promoters. — Trends. Plant Sci. 10: 88–94, 2005.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to H. I. Khattab.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Khattab, H.I., Emam, M.A., Emam, M.M. et al. Effect of selenium and silicon on transcription factors NAC5 and DREB2A involved in drought-responsive gene expression in rice. Biol Plant 58, 265–273 (2014). https://doi.org/10.1007/s10535-014-0391-z

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10535-014-0391-z

Additional key words

Navigation