Physiological and Gene-Expression Variations in Watermelon (Citrullus lanatus L.) Cultivars Exposed to Drought Stress
Abstract
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References
Aebi, H. (1984). Catalase in vitro. In L. Packer (Ed.), Oxygen radicals in biological systems (Vol. 105, pp. 121–126). Academic Press. https://doi.org/10.1016/S0076- 6879(84)05016-3
Arnon, D. I. (1949). Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris. Plant Physiology, 24(1), 1–15. https://doi.org/10.1104/pp.24.1.1
Baillo, E. H., Kimotho, R. N., Zhang, Z., & Xu, P. (2019). Transcription factors associated with abiotic and biotic stress tolerance and their potential for crops improvement. Genes, 10(10), Article 771. https://doi.org/10.3390/genes10100771
Banerjee, A., & Roychoudhury, A. (2016). Group II late embryogenesis abundant (LEA) proteins: Structural and functional aspects in plant abiotic stress. Plant Growth Regulation, 79(1), 1–17. https://doi.org/10.1007/s10725-015-0113-3
Bates, L. S., Waldren, R. P., & Teare, I. (1973). Rapid determination of free proline for water- stress studies. Plant and Soil, 39(1), 205–207. https://doi.org/10.1007/BF00018060
Bota, J., Medrano, H., & Flexas, J. (2004). Is photosynthesis limited by decreased Rubisco activity and RuBP content under progressive water stress? New Phytologist, 162(3), 671–681. https://doi.org/10.1111/j.1469-8137.2004.01056.x
Bourdenx, B., Bernard, A., Domergue, F., Pascal, S., Léger, A., Roby, D., Pervent, M., Vile, D., Haslam, R. P., Napier, J. A., Lessire, R., & Joubès, J. (2011). Overexpression of Arabidopsis ECERIFERUM1 promotes wax very-long-chain alkane biosynthesis and influences plant response to biotic and abiotic stresses. Plant Physiology, 156(1), 29–45. https://doi.org/10.1104/pp.111.172320
Bradford, M. M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry, 72(1–2), 248–254. https://doi.org/10.1016/0003-2697(76)90527-3
Bray, E. A. (2002). Classification of genes differentially expressed during water-deficit stress in Arabidopsis thaliana: An analysis using microarray and differential expression data. Annals of Botany, 89(7), 803–811. https://doi.org/10.1093/aob/mcf104
Christmann, A., Hoffmann, T., Teplova, I., Grill, E., & Müller, A. (2005). Generation of active pools of abscisic acid revealed by in vivo imaging of water-stressed Arabidopsis. Plant Physiology, 137(1), 209–219. https://doi.org/10.1104/pp.104.053082
de Oliveira, T., Cidade, L. C., Gesteira, A. S., Coelho-Filho, M. A., Soares-Filho, W. S., & Costa, M. G. (2011). Analysis of the NAC transcription factor gene family in citrus reveals a novel member involved in multiple abiotic stress responses. Tree Genetics and Genomes, 7(6), 1123–1134. https://doi.org/10.1007/s11295-011-0400-8
Eulgem, T., Rushton, P. J., Robatzek, S., & Somssich, I. E. (2000). The WRKY superfamily of plant transcription factors. Trends in Plant Science, 5(5), 199–206. https://doi.org/10.1016/S1360-1385(00)01600-9
Giannopolitis, C. N., & Ries, S. K. (1977). Superoxide dismutases: I. Occurrence in higher plants. Plant Physiology, 59(2), 309–314. https://doi.org/10.1104/pp.59.2.309
Griffiths, H., & Parry, M. (2002). Plant responses to water stress. Annals of Botany, 89(7), 801–802. https://doi.org/10.1093/aob/mcf159
Haddad, R., & Kamangar, A. (2015). The ameliorative effect of silicon and potassium on drought stressed grape (Vitis vinifera L.) leaves. Iranian Journal of Genetics and Plant Breeding, 4(2), 48–58.
Hamurcu, M., Demiral, T., Hakki, E. E., Turkmen, Ö., Gezgin, S., & Bell, R. W. (2015). Oxidative stress responses in watermelon (Citrullus lanatus) as influenced by boron toxicity and drought. Zemdirbyste-Agriculture, 102(2), 209–216. https://doi.org/10.13080/z-a.2015.102.027
Heath, R. L., & Packer, L. (1968). Photoperoxidation in isolated chloroplasts: I. Kinetics and stoichiometry of fatty acid peroxidation. Archives of Biochemistry and Biophysics, 125(1), 189–198. https://doi.org/10.1016/0003-9861(68)90654-1
Hu, C., Delauney, A. J., & Verma, D. (1992). A bifunctional enzyme (delta 1-pyrroline-5- carboxylate synthetase) catalyzes the first two steps in proline biosynthesis in plants. Proceedings of the National Academy of Sciences of the United States of America, 89(19), 9354–9358. https://doi.org/10.1073/pnas.89.19.9354
Ishizaki, T., Maruyama, K., Obara, M., Fukutani, A., Yamaguchi-Shinozaki, K., Ito, Y., & Kumashiro, T. (2013). Expression of Arabidopsis DREB1C improves survival, growth, and yield of upland New Rice for Africa (NERICA) under drought. Molecular Breeding, 31(2), 255–264. https://doi.org/10.1007/s11032-012-9785-9
Lee, S. B., Jung, S. J., Go, Y. S., Kim, H. U., Kim, J. K., Cho, H. J., Park, O. K., & Suh, M. C. (2009). Two Arabidopsis 3-ketoacyl CoA synthase genes, KCS20 and KCS2/DAISY, are functionally redundant in cuticular wax and root suberin biosynthesis, but differentially controlled by osmotic stress. The Plant Journal, 60(3), 462–475. https://doi.org/10.1111/j.1365-313X.2009.03973.x
Leng, P., & Zhao, J. (2019). Transcription factors as molecular switches to regulate drought adaptation in maize. Theoretical and Applied Genetics, 133, 1455–1465. https://doi.org/10.1007/s00122-019-03494-y
Liu, H., Sultan, M. A. R. F., Liu, X. I., Zhang, J., Yu, F., & Zhao, H. X. (2015). Physiological and comparative proteomic analysis reveals different drought responses in roots and leaves of drought-tolerant wild wheat (Triticum boeoticum). PLoS One, 10(4), Article e0121852. https://doi.org/10.1371/journal.pone.0121852
Matallana-Ramirez, L. P., Rauf, M., Farage-Barhom, S., Dortay, H., Xue, G. P., Dröge- Laser, W., Lers, A., Balazadeh, S., & Mueller-Roeber, B. (2013). NAC transcription factor ORE1 and senescence-induced BIFUNCTIONAL NUCLEASE1 (BFN1) constitute a regulatory cascade in Arabidopsis. Molecular Plant, 6(5), 1438–1452. https://doi.org/10.1093/mp/sst012
Nakano, Y., & Asada, K. (1981). Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant and Cell Physiology, 22(5), 867–880.
Nakashima, K., Takasaki, H., Mizoi, J., Shinozaki, K., & Yamaguchi-Shinozaki, K. (2012). NAC transcription factors in plant abiotic stress responses. Biochimica et Biophysica Acta (BBA) – Gene Regulatory Mechanisms, 1819(2), 97–103. https://doi.org/10.1016/j.bbagrm.2011.10.005
Ni, F. T., Chu, L. Y., Shao, H. B., & Liu, Z. H. (2009). Gene expression and regulation of higher plants under soil water stress. Current Genomics, 10(4), 269–280. https://doi.org/10.2174/138920209788488535
Pan, Y., Wu, L. J., & Yu, Z. L. (2006). Effect of salt and drought stress on antioxidant enzymes activities and SOD isoenzymes of liquorice (Glycyrrhiza uralensis Fisch). Plant Growth Regulation, 49(2-3), 157–165. https://doi.org/10.1007/s10725-006-9101-y
Qin, F., Sakuma, Y., Li, J., Liu, Q., Li, Y. Q., Shinozaki, K., & Yamaguchi-Shinozaki, K. (2004). Cloning and functional analysis of a novel DREB1/CBF transcription factor involved in cold-responsive gene expression in Zea mays L. Plant and Cell Physiology, 45(8), 1042–1052. https://doi.org/10.1093/pcp/pch118
Raghavendra, A. S., Gonugunta, V. K., Christmann, A., & Grill, E. (2010). ABA perception and signalling. Trends in Plant Science, 15(7), 395–401. https://doi.org/10.1016/j.tplants.2010.04.006
Reddy, A. R., Chaitanya, K. V., & Vivekanandan, M. (2004). Drought-induced responses of photosynthesis and antioxidant metabolism in higher plants. Journal of Plant Physiology, 161(11), 1189–1202. https://doi.org/10.1016/j.jplph.2004.01.013
Sakuraba, Y., Jeong, J., Kang, M. Y., Kim, J., Paek, N. C., & Choi, G. (2014). Phytochrome- interacting transcription factors PIF4 and PIF5 induce leaf senescence in Arabidopsis. Nature Communications, 5(1), Article 4636. https://doi.org/10.1038/ncomms5636
Shakirova, F. M., Sakhabutdinova, A. R., Bezrukova, M. V., Fatkhutdinova, R. A., & Fatkhutdinova, D. R. (2003). Changes in the hormonal status of wheat seedlings induced by salicylic acid and salinity. Plant Science, 164(3), 317–322. https://doi.org/10.1016/S0168-9452(02)00415-6
Sharma, S., Villamor, J. G., & Verslues, P. E. (2011). Essential role of tissue-specific proline synthesis and catabolism in growth and redox balance at low water potential. Plant Physiology, 157(1), 292–304. https://doi.org/10.1104/pp.111.183210
Si, Y., Zhang, C., Meng, S., & Dane, F. (2009). Gene expression changes in response to drought stress in Citrullus colocynthis. Plant Cell Reports, 28(6), 997–1009. https://doi.org/10.1007/s00299-009-0703-5
Siddiqui, M. H., Al-Khaishany, M. Y., Al-Qutami, M. A., Al-Whaibi, M. H., Grover, A., Ali, H. M., Al-Wahibi, M. S., & Bukhari, N. A. (2015). Response of different genotypes of faba bean plant to drought stress. International Journal of Molecular Sciences, 16(5), 10214–10227. https://doi.org/10.3390/ijms160510214
Yokota, A., Kawasaki, S., Iwano, M., Nakamura, C., Miyake, C., & Akashi, K. (2002). Citrulline and DRIP-1 protein (ArgE homologue) in drought tolerance of wild watermelon. Annals of Botany, 89(7), 825–832. https://doi.org/10.1093/aob/mcf074
Zeevaart, J., & Creelman, R. (1988). Metabolism and physiology of abscisic acid. Annual Review of Plant Physiology and Plant Molecular Biology, 39(1), 439–473. https://doi.org/10.1146/annurev.pp.39.060188.002255
Zhao, Y., Chan, Z., Gao, J., Xing, L., Cao, M., Yu, C., Hu, Y., You, J., Shi, H., Zhu, Y., Gong, Y., Mu, Z., Wang, H., Deng, X., Wang, P., Bressan, R. A., & Zhu, J. K. (2016). ABA receptor PYL9 promotes drought resistance and leaf senescence. Proceedings of the National Academy of Sciences of the Unites States of America, 113(7), 1949–1954. https://doi.org/10.1073/pnas.1522840113
DOI: https://doi.org/10.5586/asbp.8921
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