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Sugarcane genes differentially expressed during water deficit

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Biologia Plantarum

Abstract

To identify genes that are up and down-regulated by water deficit in sugarcane we used the macroarray methodology and the expression level of 3 575 independent sugarcane cDNAs was measured by hybridization with RNA extracted from plants submitted to mild, moderate and severe water deficit. We identified approximately 1 670 differentially expressed genes from which 62 % were up-regulated by different stress-conditions, whereas many repressed genes were exclusive for each time-point. Analysis of similarity showed that approximately 24 % of the differentially expressed genes shared homology with proteins involved in different processes such as signal transduction, hormone metabolism, photosynthesis, transcription and stress response. Transcripts with no known function accounted for approximately 39 % and those without similarity represented 36 % of the sequences. Five genes analyzed by RT-PCR confirmed the macroarray results.

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Abbreviations

ABA:

abscisic acid

BSA:

bovine serum albumin

bZIP:

basic-leucine zipper

CDPK:

kinase protein calciumdependent

dATG:

deoxyadenosine triphosphate

dCTP:

deoxycytidine triphosphate

dGTP:

deoxyguanosine triphosphate

DTT:

dithiothreitol

dTTP:

deoxythymidine triphosphate

EDTA:

ethylenediaminetetracetic acid

HSP:

heat shock protein

LTP:

lipid transfer proteins

RWC:

relative water content

SAMDC:

s-adenosyl-methionine decarboxylase

SDS:

sodium dodecyl sulfate

SSC:

saline sodium citrate

Tris-HCl:

(hydroxymethyl) aminomethane hydrochloride

ZEP:

zeaxanthin epoxidase

References

  • Agarwal, P.K., Jha, B.: Transcription factors in plants and ABA dependent and independent abiotic stress signalling. — Biol. Plant. 54: 201–212, 2010.

    Article  CAS  Google Scholar 

  • Ahmad, R., Kim, M.D., Back, K., Kim, H., Lee, H., Kwon, S., Murata, N., Chung, W., Kwak, S.: Stress-induced expression of choline oxidase in potato plant chloroplasts confers enhanced tolerance to oxidative, salt, and drought stresses. — Plant Cell Rep. 27: 687–698, 2008.

    Article  CAS  PubMed  Google Scholar 

  • Altschul, S.F., Madden, T., Schaffer, A.A., Zhang, J., Zhang, Z., Miller, W., Lipman, D.J.: Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. — Nucl. Acids Res. 25: 3389–3402, 1997.

    Article  CAS  PubMed  Google Scholar 

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

    Article  CAS  PubMed  Google Scholar 

  • Audran, C., Liotenberg, S., Gonneau, M., North, H., Frey, A., Tap-Waksman, K., Vartanian, N., Marion-Poll, A.: A. Localization and expression of zeaxanthin epoxidase mRNA in Arabidopsis in response to drought stress and during seed development. — Aust. J. Plant Physiol. 28: 1161–1173, 2001.

    CAS  Google Scholar 

  • Benjamini, Y., Hochberg, Y.: Controlling the false discovery rate: a practical and powerful approach to multiple testing. — J. roy. Statistic Soc. B. 57: 289–300, 1995.

    Google Scholar 

  • Bhatt, A., Naidoo, Y., Gairola, S., Nicholas, A.: Ultrastructural responses of the desiccation tolerant plants Xerophyta viscosa and X. retinervis to dehydration and rehydration. — Biol. Plant. 53: 373–377, 2009.

    Article  Google Scholar 

  • Bloch, D., Hoffman, C., Märländer, B.: Impact of water supply on photosynthesis, water use and carbon isotope discrimination of sugar beet genotypes. — Eur. J. Agron. 24: 218–225, 2006.

    Article  CAS  Google Scholar 

  • Bray, E.A., Bailey-Serres, J., Weretilnyk, E.: Responses to abiotic stresses. — In: Buchanan, B.B., Gruissem, W., Jones, R.L. (ed.): Biochemistry and Molecular Biology of Plants. Pp 1158–1203. American Society of Plant Physiologists, Rockville 2000.

    Google Scholar 

  • Bray, E.A.: Abscisic acid regulation of gene expression during water deficit stress in the era of the Arabidopsis genome. — Plant Cell and Environ. 25: 153–161, 2002.

    Article  CAS  Google Scholar 

  • Bray, E.A.: Genes commonly regulated by water-deficit stress in Arabidopsis thaliana. — J. exp. Bot. 55: 2331–2341, 2004.

    Article  CAS  PubMed  Google Scholar 

  • Brodribb, T.T., Holbrook, N.M.: Stomatal closure during leaf dehydration, correlation with other leaf physiological traits. — Plant Physiol. 132: 2166–2173, 2003.

    Article  CAS  PubMed  Google Scholar 

  • Broner, I., Law, R.A.P.: Evaluation of a modified atmometer for estimating reference ET. — Irrig. Sci. 12: 21–26, 1991.

    Article  Google Scholar 

  • Cameron, K.D., Teece, M.A., Smart, L.B.: Increased accumulation of cuticular wax and expression lipid transfer protein in response to periodic drying events in leaves of tree tobacco. — Plant Physiol. 140: 176–183, 2006.

    Article  CAS  PubMed  Google Scholar 

  • Carson, D.L., Huckett, B.I., Botha, F.C.: Sugarcane ESTs differentially expressed in immature and maturing internodal tissue. — Plant Sci. 162: 289–300, 2002.

    Article  CAS  Google Scholar 

  • Casu, R.E., Grof, C.P.L., Rae, A.L., McIntyre, C.L., Dimmock, C.M., Manners, J.M.: Identification of a novel sugar transporter homologue strongly expressed in maturing stem vascular tissues of sugarcane by expressed sequence tag and microarray analysis. — Plant Mol. Biol. 52: 371–386, 2003.

    Article  CAS  PubMed  Google Scholar 

  • Chinnusamy, V., Schumaker, K., Zhu, J.: Molecular genetics perspectives on cross-talk and specificity in abiotic stress signalling in plants. — J. exp. Bot. 55: 225–236, 2004.

    Article  CAS  PubMed  Google Scholar 

  • Cominelli, E., Galbiati, M., Vavasseur, A., Conti, L., Sala, T., Vuylsteke, M., Leonhardt, N., Dellaporta, S.L., Tonelli, C.: Guard-cell-specific MYB transcription factor regulates stomatal movements and plant drought tolerance. — Curr. Biol. 15: 1196–2000, 2005.

    Article  CAS  PubMed  Google Scholar 

  • Cushman, J.C., Bohnert, H.J.: Genomics approaches to plant stress tolerance. — Plant Biol. 3: 117–124, 2000.

    CAS  Google Scholar 

  • Dai, X., Xu, Y., Ma, Q., Xu, W., Wang, T., Xue, Y., Chong, K.: Overexpression of an R1R2R3 MYB gene, OsMYB3R-2, increases tolerance to freezing, drought, and salt stress in transgenic Arabidopsis. — Plant Physiol. 143: 1739–1751, 2007.

    Article  CAS  PubMed  Google Scholar 

  • Dulai, S., Molnár, I., Prónay, J., Csenák, A., Tarnay, R., Molnár-Láng, M.: Effect of drought on photosynthesis parameters and heat stability of PSII in wheat and in Aegilops species originating from dry habitats. — Acta biol. szeged. 50: 11–17, 2006.

    Google Scholar 

  • Figueira, A., Kido, E.A., Almeida, R.S.: Identifying sugarcane expressed sequences associated with nutrient transporters and peptide metal chelators. — Genet. mol. Biol. 24: 207–220, 2001.

    Article  CAS  Google Scholar 

  • Fujita, Y., Fujita, M., Satoh, R., Maruyama, K., Parvez, M.M., Seki, M., Hiratsu, K., Ohme-Takagi, M., Shinozaki, K., Yamaguchi-Shinozaki, K.: AREB1 Is a transcription activator of novel ABRE-dependent ABA signaling that enhances drought stress tolerance in Arabidopsis. — Plant Cell 17: 3470–3488, 2005.

    Article  CAS  PubMed  Google Scholar 

  • Gentleman, R.C., Carey, V.J., Bates, D.M., Bolstad, B., Dettling, M., Dudoit, S., Ellis, B., Gautier, L., Ge, Y., Gentry, J., Hornik, K., Hothorn, T., Huber, W., Iacus, S., Irizarry, R., Leisch, F., Li, C., Maechler, M., Rossini, A.J., Sawitzki, G., Smith, C., Smyth, G., Tierney, L., Yang, J.Y., Zhang, J.: Bioconductor: open software development for computational biology and bioinformatics. — Genome Biol. 5: R80–R80.16, 2004.

    Article  PubMed  Google Scholar 

  • Gorantla, M., Babu, P.R., Reddy Lachagari, V.B., Reddy, A.M.M., Wusirika, R., Bennetzen, J.L., Reddy, A.R.: Identification of stress-responsive genes in an indica rice (Oryza sativa L.) using ESTs generated from drought-stressed seedlings. — J. exp. Bot. 58: 253–265, 2007.

    Article  CAS  PubMed  Google Scholar 

  • Hirschi, K.D.: The calcium conundrum. Both versatile nutrient and specific signal. — Plant Physiol. 136: 2438–2442, 2004.

    Article  CAS  PubMed  Google Scholar 

  • Hsiao, T.C., Xu, L.: Sensitivity of growth of roots versus leaves to water stress: biophysical analysis and relation to water transport. — J. exp. Bot. 51: 1595–1616, 2000.

    Article  CAS  PubMed  Google Scholar 

  • Hoagland, D.R., Arnon, D.I.: The water-culture method for growing for plants without soil. — Agr. Exp. Sta. Circ. 347: 1–32, 1950.

    Google Scholar 

  • Hu, X.J., Zhang, Z.B., Xu, P., Fu, Z.Y., Hu, S.B., Song, W.Y.: Multifunctional genes: the cross-talk among the regulation networks of abiotic stress responses. — Biol. Plant. 54: 213–223, 2010.

    Article  CAS  Google Scholar 

  • Huber, W., Heydebreck, A., Sültmann, H., Poustka, A., Vingron, M.: Variance stabilization applied to microarray data calibration and to the quantification of differential expression. — Bioinformatics 18(Suppl 1): S96–S104, 2002.

    PubMed  Google Scholar 

  • Ihaka, R., Gentleman, R.: R: A language for data analysis and graphics. — J. Comp. Graphic Statistics 5: 229–314, 1996.

    Google Scholar 

  • Ito, Y., Katsura, K., Maruyama, K., Taji, T., Kobayashi, M., Motoaki, S., Shinozaki, K., Yamaguchi-Shinozaki, K.: Functional analysis of rice DREB1/CBF-type transcription factors involved in cold-responsive gene expression in transgenic rice. — Plant Cell Physiol. 47: 141–153, 2006.

    Article  CAS  PubMed  Google Scholar 

  • Jain, M., Nandwal, A.S., Kundu, B.S., Kumar, B., Sheoran, I.S., Kumar, N., Mann, A., Kukreja, S.: Water relations, activities of antioxidants, ethylene evolution and membrane integrity of pigeonpea roots as affected by soil moisture. — Biol. Plant. 50: 303–306, 2006.

    Article  CAS  Google Scholar 

  • Kim, S., Kim, J., Kim, S., An, K., An, G., Kim, S.: Isolation of cold stress-responsive genes in the reproductive organs, and characterization of the OsLti6b gene from rice (Oryza sativa L.). — Plant Cell Rep. 26: 1097–1110, 2007.

    Article  CAS  PubMed  Google Scholar 

  • Lee, Y.P., Yu, G.H., Seo, Y., Han, S., Choi, Y.O., Kim, D., Mok, I.G., Kim, W., Sung, S.K.: Microarray analysis of apple gene expression engaged in early fruit development. — Plant Cell Rep. 26: 917–926, 2007.

    Article  CAS  PubMed  Google Scholar 

  • Leung, J., Merlot, S., Giraudat, J.: The Arabidopsis abscisic acid-insensitive2 (ABI2) and ABI1 genes enconde homologous protein phosphatases 2C involved in abscisic acid signal transduction. — Plant Cell 9: 759–771, 1997.

    Article  CAS  PubMed  Google Scholar 

  • Locy, R.D., Hasegawa, P.M., Bressan, R.A.: Stress Physiology. — In: Taiz, L., Zeiger, E. (ed.): Plant Physiology. Pp. 2438–2442. Sinauer Associates, Sunderland 2002.

    Google Scholar 

  • Lokko, Y., Anderson, J.V., Rudd, S., Raji, A., Horvath, D., Mikel, M.A., Kim, R., Liu, L., Hernandez, A., Dixon, A.G.O., Ingelbretch, I.L.: Characterization of an 18,166 EST dataset for cassava (Manihot esculenta Crantz) enriched for drought-responsive genes. — Plant Cell Rep. 26: 1605–1618, 2007.

    Article  CAS  PubMed  Google Scholar 

  • Luu, D.T., Maurel, C.: Aquaporins in a challenging environment: molecular gears for adjusting plant water stress. — Plant Cell Environ. 28: 85–96, 2005.

    Article  CAS  Google Scholar 

  • Marè, C., Mazzucotelli, E., Crosatti, C., Francia, E., Stanca, A.M., Cattivelli, L.: Hv-WRKY38: a new transcription factor involved in cold- and drought-response in barley. — Plant mol. Biol. 55: 399–416, 2004.

    Article  PubMed  Google Scholar 

  • Maskin, L., Frankel, N., Gudesblat, G., Demergasso, M.J., Pietrasanta, L.I.: Dimerization and DNA-binding of ASR1, a small hydrophilic protein abundant in plant tissues suffering from water loss. — Biochem. biophys. Res. Commun. 352: 831–835, 2007.

    Article  CAS  PubMed  Google Scholar 

  • Meadus, W.J.: A semi-quantitative RT-PCR method to measure the in vivo effect of dietary conjugated linolenic acid on procine muscle PPAR gene expression. — Biol. Proceed. Online 5: 20–28, 2003.

    Article  CAS  Google Scholar 

  • Micheletto, S., Rodriguez-Uribe, L., Hernandez, R., Richins, R.D., Curry, J., O’Connell, M.A.: Comparative transcript profiling in roots of Phaseolus acutifolius and P. vulgaris under water deficit stress. — Plant Sci. 173: 510–520, 2007.

    Article  CAS  Google Scholar 

  • Munns, R., Passioura, J.B., Guo, J., Chazen, O., Cramer, G.R.: Water relations and leaf expansion: importance of time scale. — J. exp. Bot. 51: 1495–1504, 2000.

    Article  CAS  PubMed  Google Scholar 

  • Munns, R.: Comparative physiology of salt and water stress. — Plant Cell Environ. 25: 239–250, 2002.

    Article  CAS  PubMed  Google Scholar 

  • Murphy, A.: Auxin: the growth hormone. — In: Taiz, L, Zeiger, E (ed.): Plant Physiology. Pp. 452. Sinauer Associates, Sunderland 2002.

    Google Scholar 

  • Ozturk, Z.N., Talame, V., Deyholos, M., Michalowski, C.B., Galbraith, D.W., Gozukirmizi, N., Tuberosa, R., Bohnert, H.J.: Monitoring large-scale changes in transcript abundance in drought- and salt-stressed barley. — Plant mol. Biol. 48: 551–573, 2002.

    Article  CAS  Google Scholar 

  • Papini-Terzi, F.S., Rocha, F.R., Vêncio, R.Z.N., Oliveira, K.C., Felix, J.M., Vicentini, R., Rocha, C.S., Simões, A.C., Ulian, E.C., Mauro, S.M., Silva, A.M., Pereira, C.A., Menossi, M., Souza, G.M.: Transcription profiling of signal transductionrelated genes in sugarcane tissues. — DNA Res. 12: 27–38, 2005.

    Article  CAS  PubMed  Google Scholar 

  • Patharkar, O.R., Cushman, J.C.: A novel coiled-coli protein colocalizes and interact with a calcium-dependet protein kinase in the common ice plant during low-humidity stress. — Planta 225: 57–73, 2006.

    Article  CAS  PubMed  Google Scholar 

  • Quirino, B.F., Noh, Y., Himelblau, E., Amasino, R.M.: Molecular aspects of leaf senescence. — Trends Plant Sci. 5: 278–282, 2000.

    Article  CAS  PubMed  Google Scholar 

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

    Article  CAS  PubMed  Google Scholar 

  • Rae, A. L., Grof, C. P. L., Casu, R. E., Bonnett, G. D.: Sucrose accumulation in the sugarcane stem: pathways and control point for transport and compartmentation. — Field Crops Res. 92: 159–168, 2005.

    Article  Google Scholar 

  • Riera, M., Valon, C., Fenzi, F., Giraudat, J., Leung, J.: The genetics of adaptive responses to drought stress: abscisic acid-dependent and abscisic acid-independent signaling components. — Physiol. Plant. 123: 111–119, 2005.

    Article  CAS  Google Scholar 

  • Rizhsky, L., Liang, H., Shuman, J., Shulaev, V., Davletova, S., Mittler, R.: When defense pathways collide. The response of Arabidopsis to a combination of drought and heat stress. — Plant Physiol. 134: 1683–1696, 2004.

    Article  CAS  PubMed  Google Scholar 

  • Rocha, F.R., Papini-Terzi, F.S., Nishiayama, M.Y., et al.: Signal transduction-related responses to phytohormones and environmental challenges in sugarcane. — BMC Genomics 8: 71–92, 2007.

    Article  PubMed  Google Scholar 

  • Roche, J., Hewezi, T., Bouniols, A., Gentzbittel, L.: Transcriptional profiles of primary metabolism and signal transduction-related genes in response to water stress in field-grown sunflower genotypes using a thematic cDNA microarray. — Planta 226: 601–617 2007.

    Article  CAS  PubMed  Google Scholar 

  • Rom, S., Gilad, A., Kalifa, Y., Konrad, Z., Karpasas, M.M., Yehuda, G., Goldgur, Y, Bar-Zvi, D.: Mapping the DNA- and zinc-binding domains of ASR1 (abscisic acid stress ripening), an abiotic-stress regulated plant specific protein. — Biochimie 88: 621–628, 2006.

    Article  CAS  PubMed  Google Scholar 

  • Sambrook, J., Fritsch, E.F., Maniatis, T. (ed.): Molecular Cloning: a Laboratory Manual. — Cold Spring Harbour Laboratory Press, Cold Spring Harbour — New York 1989.

    Google Scholar 

  • Santos, M.G., Ribeiro, R.V., Machado, E.C., Pimentel, C.: Photosynthetic parameters and leaf water potential of five common bean genotypes under mild water deficit. — Biol. Plant. 53: 229–236, 2009.

    Article  CAS  Google Scholar 

  • Scippa, G.S., Michele, M., Onelliz, E., Patrignani, G., Chiatante, D., Bray, E.A.: The histone-like protein H1-S and the response of tomato leaves to water deficit. — J. exp. Bot. 55: 99–109, 2004.

    Article  CAS  PubMed  Google Scholar 

  • Schor-Fumbarov, T., Goldsbrought, P.B., Adam, Z., Tel-Or, E.: Characterization and expression of a metallothionein gene of aquatic fern Azolla filiculoids under heavy metal stress. — Planta 223: 69–76, 2005.

    Article  CAS  PubMed  Google Scholar 

  • Schummer, M., Wailap, V.N.G., Bumgarner, R.E., Nelson, P.S., Schummer, B., Bednarski, D.W., Hassell, L., Baldwin, R.L., Karlan, B.Y., Hood, L.: Comparative hybridization of an array of 21500 ovarian cDNAs for the discovery of genes over expressed in ovarian carcinomas. — Gene 238: 375–385, 1999.

    Article  CAS  PubMed  Google Scholar 

  • Schützendübel, A., Polle, A.: Plant responses to abiotic stresses: heavy metal-induced and oxidative stress and protection by micorrhization. — J. exp. Bot. 53: 1351–1365, 2002.

    Article  PubMed  Google Scholar 

  • Schwartz, S.H., Qin, X., Zeevaart, J.A.D.: Elucidation of the indirect pathway of abscisic acid biosynthesis by mutants, genes and enzymes. — Plant Physiol. 131: 1591–1601, 2003.

    Article  CAS  PubMed  Google Scholar 

  • Seki, M., Kamel, A., Yamaguchi-Shinozaki, K., Shinozaki, K.: Molecular responses to drought, salinity and frost: common and different paths for plant protection. — Curr. Opin. Biotechnol. 14: 194–199, 2003.

    Article  CAS  PubMed  Google Scholar 

  • Seki, M., Umezawa, T., Urano, K., Shinozaki, K.: Regulatory metabolic networks in drought stress responses. — Curr. Opin. Plant Biol. 10: 296–302, 2007.

    Article  CAS  PubMed  Google Scholar 

  • Shinozaki, K., Yamaguchi-Shinozaki, K.: Gene networks involved in drought stress response and tolerance. — J. exp. Bot. 58: 221–227, 2007.

    Article  CAS  PubMed  Google Scholar 

  • Shou, H., Bordallo, P., Wang, K.: Expression of the Nicotiana protein kinase (NPK1) enhanced drought tolerance in transgenic maize. — J. exp. Bot. 55: 1013–1019, 2004.

    Article  CAS  PubMed  Google Scholar 

  • Silva, M.A., Jifon, J.L., Silva, J.A.G., Sharma, V.: Use as physiological parameters as fast tools to screen for drought tolerance in sugarcane. — Braz. J. Plant Physiol. 19: 193–201, 2007.

    Article  Google Scholar 

  • Smyth, G.K., Yang, Y.H., Speed, T.P.: Statistical issues in microarray data analysis. — In: Brownstein, M.J., Khodursky, A.B. (ed.): Functional Genomics: Methods and Protocols. Pp. 111–136. Humana Press, Totowa 2003.

    Chapter  Google Scholar 

  • Smyth, G.K.: Linear models and empirical Bayes methods for assessing differential expression in microarray experiments. — Statist. Appl. Genet. mol. Biol. 3: 1–26, 2004.

    Google Scholar 

  • Sperotto, R.A., Boff, T., Duarte, G.L., Fett, J.P.: Increased senescence-associated gene expression and lipid peroxidation induced by iron deficiency in rice root. — Plant Cell Rep. 27: 183–195, 2008.

    Article  CAS  PubMed  Google Scholar 

  • Steudle, E.: Water uptake by roots: effects of water deficit. — J. exp. Bot. 51: 1531–1542, 2000.

    Article  CAS  PubMed  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  CAS  PubMed  Google Scholar 

  • Tardieu, F., Reymond, M., Hamard, P., Granier, C., Muller, B.: Spatial distribution of expansion rate, cell division rate and cell size in maize leaves: a synthesis of the effects of soil water status, evaporative demands and temperature. — J. exp. Bot. 51: 1505–1514, 2000.

    Article  CAS  PubMed  Google Scholar 

  • Trewavas, A.: Signal perception and transductions. — In: Buchanan, B.B., Gruissem, W., Jones, R.L. (ed.): Biochemistry and Molecular Biology of Plants. Pp. 975–977. American Society of Plant Physiologists, Rockville 2000.

    Google Scholar 

  • Vettore, A.L., Silva, F.R., Kemper, E.L., Souza, G.M., Silva, A.M., Ferro, M.I.T., Silva, F.H., Giglioti, E.A., Lemos, M.V.F., Coutinho, L.L., Nobrega, M.P., Carrer, H., França, S.C., Bacci, M., Goldman, M.H.S., Gomes, S.L., Nunes, L.R., Camargo, L.E.A., Siqueira, W.J., Sluys, M.A.V., Thimann, O.H., Kuramae, E.E., Santelli, R.V., Marino, C.L., Targon, M.L.P.N., Ferro, J.A., Silveira, H.C.S., Marini, D.C., Lemos, E.G.M., Monteiro-Vitorello, C.B., Tambor, J.H.M., Carraro, D. C., Roberto, P.G., Martins, V.G., Goldman, G.H., Oliveira, R.C., Truffi, D., Colombo, C.A., Rossi, M., Araujo, P.G., Sculaccio, S.A., Angella, A., Lima, M.M.A., Rosa, V.E., Jr., Siviero, F., Coscrato, V.E., Machado, M.A., Grivet, L., Di Mauro, S.M.Z., Nobrega, F.G., Menck, C.F.M., Braga, M.D.V., Telles, G.P., Cara, F.A.A., Pedrosa, G., Meidanis, J., Arruda, P.: Analysis and functional annotation of an expressed sequence tag collection for tropical crop sugarcane. — Genome Res. 13: 2725–2735, 2003.

    Article  PubMed  Google Scholar 

  • Walia, H., Wilson, C., Condamine, P., Liu, X., Ismail, A.M., Zeng, L., Wanamaker, S.I., Mandal, J., Xu, J., Cui, X., Close, T.J.: Comparative transcriptional profiling of two contrasting rice genotypes under salinity stress during the vegetative growth stage. — Plant Physiol. 139: 822–835, 2005.

    Article  CAS  PubMed  Google Scholar 

  • Wang, J.P., Bughrara, S.S.: Monitoring of gene expression profiles and identification of candidate genes involved in drought responses in Festuca mairei. — Mol. Genet. Genomics 277: 551–587, 2007.

    Google Scholar 

  • Yu, Y., Wang, H., Liu, L., Chen, Z., Xia, G.: Functional identification of cytokinesis-related genes from tobacco BY-2 cells. — Plant Cell Rep. 26: 889–894, 2007.

    Article  CAS  PubMed  Google Scholar 

  • Zheng, J., Zhao, J., Tao, Y., Wang, J.H., Liu, Y.J., Fu, J.J., Jin, Y., Peng Gao, P., Zhang, J.P., Bai, Y.F., Wang, G.Y.: Isolation and analysis of water stress induced genes in maize seedlings by subtractive PCR and cDNA macroarray. — Plant mol. Biol. 55: 807–823, 2004.

    CAS  PubMed  Google Scholar 

  • Zheng, J., Zhao, J., Zhang, J., Fu, J., Gou, M., Dong, Z., Hou, W., Huang, Q., Wang, G.: Comparative expression profiles of maize genes from a water stress-specific cDNA macroarray in response to high-salinity, cold or abscisic acid. — Plant Sci. 170: 1125–1132, 2006.

    Article  CAS  Google Scholar 

  • Zhou, M., Guan, Y., Ren, H., Zhang, F., Chen, F.: A bZIP transcription factor, OsABI5, is involved in rice fertility and stress tolerance. — Plant mol. Biol. 66: 675–683, 2008.

    Article  Google Scholar 

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Acknowledgments

This work was supported by Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP project # 2002/04600-8). F.A. Rodrigues received scholarships from Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) and Coordenação de Aperfeiçoamento de Pessoal de NÍvel Superior (CAPES). We thank MSc. R. de Assis Sordi (Sugarcane Technology Center, Piracicaba-Brazil) for the sugarcane plantlets and Dr. M.C. Roque Barreira (Department of Cellular and Molecular Biology — FMRP-USP) for the use of Phosphorimager FLA3000-G.

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Rodrigues, F.A., Da Graça, J.P., De Laia, M.L. et al. Sugarcane genes differentially expressed during water deficit. Biol Plant 55, 43–53 (2011). https://doi.org/10.1007/s10535-011-0006-x

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