Вплив посухи на фотосинтетичні показники рослин пшениці

30. Ukozehasi, C. (2020). Proxy-based approach to wheat selection for photosynthetic efficiency. Rwanda J. Agricult. Sci., 2, No. 1, pp. 104-114.

31. Priadkina, G.O. & Makharynska, N.M. (2021). Assimilation apparatus of different leaves tyers in winter wheat varieties under adverse environmental conditions. Fiziol. rast. genet., 53, No. 1, pp. 74-86 [in Ukrainian]. https://doi.org/10.15407/frg2021.01.074.

32. Amanullah, D.R. (2015). Specific leaf area and specific leaf weight in small grain crops wheat, rye, barley, and oats differ at various growth stages and NPK source. J. Plant Nutr., 38, No. 11, pp. 1964-1708.

33. Bhattacharya, A. (2019). Chapter 2 -- Radiation-use efficiency under different climatic conditions. Changing climate and resource use efficiency in plants. London: Elsevier Ltd. Academic Press.

34. Shearman, V.J., Sylvester-Bradley, R., Scott, R.K. & Foulkes, M.J. (2005). Physiological processes associated with wheat yield progress in the UK. Crop Sci., 45, pp. 175-185. https://doi.org/10.2135/cropsci2005.0175.

35. Priadkina, G.A., Stasik, O.O., Polevoy, A.N., Yarmolskaya, E.E. & Kuzmova, K. (2020). Radiation use efficiency of winter wheat canopy during vegetative growth. Fiziol. rast. genet., 52, No. 3, pp. 208-223 [in Ukrainian]. https://doi.org/10.15407/frg2020.03.208.

36. Poorter, H., Niinemets, U., Poorter, L., Wright, I.J. & Villar, R. (2009). Causes and consequences of variation in leaf mass per area (LMA): a meta-analysis. New Phytol., 182, pp. 565-588. https://doi.org/10.11n/j.1469-8137.2009.02830.x.

37. Morgun, V.V., Pryadkina, G.A., Stasik, O.O. & Zborivska, O.V. (2019). Relationships between canopy assimilation surface capacity traits and grain productivity of winter wheat genotypes under drought stress. Agricult. Sci. Pract., 6, No. 2, pp. 18-28. https://doi.org/ 10.15407/agrisp6.02.018.

38. Joudi, M. & Van den Ende, W. (2018). Genotypic variation in pre- and post-anthesis dry matter remobilization in Iranian wheat cultivars: associations with stem characters and grain yield. Czech J. Genet. Plant Breed., 54, pp. 123-134. https://doi.org/10.17221/93/2017 - CJGPB:.

39. Kiriziy, D.A. & Stasik, O.O. (2022). Effects of drought and high temperature on physiological and biochemical processes, and productivity of plants. Fiziol. rast. genet., 54, No. 2, pp. 95-122 [in Ukrainian]. https://doi.org/10.15407/frg2022.02.095.

40. Blum, A., Golan, G., Mayer, J., Sinmena, B. & Burra, J. (1989). The drought response of landraces of wheat from the Northern Negev desert in Israel. Euphytica, 43, pp. 8796.

41. Sallam, A., Mervat, H., El-Sayed, H. & Mohamed, O. (2015). Genetic variation of stem characters in wheat and their relation to kernel weight under drought and heat stresses. J. Crop Sci. Biotechnol., 18, pp. 137-146. https://doi.org/10.1007/s12892-015-0014-z.

42. Morgun, V.V., Priadkina, G.A. & Zborovska, O.V. (2018). Dependence of main shoot ear grain from stem deposited ability of winter wheat varieties. Ukr. J. Ecol., 8, No. 3, pp. 113-118.

43. Ehdaie, B., Alloush, Ghiath, Madore, M.A. & Waines, J. (2006). Genotypic variation for stem reserves and mobilization in wheat: I. Postanthesis changes in internode dry matter. Crop Sci., 46, pp. 735-746. https://doi.org/10.2135/ cropsci2005.04-0033.

44. Morgun, V.V., Tarasiuk, M.W., Priadkina, G^. & Stasik, О.О. (2022). Depositing capacity of winter wheat stem segments under natural drought during grain filling in Ukrainian forest steppe conditions. Biosystems Diversity, 30, No. 2, pp. 29-38. https:// doi.org/110.15421/012217.

45. Semcheddine, N. & Hafsi, M. (2014). Effect of supplementary irrigation on agronomical and physiological traits in durum wheat (Triticum durum Desf.) genotypes. J. Agric. Sci., 6, No. 9, pp. 184-197.

46. Budak, H., Hussain, B., Khan, Z., Ozturk, N.Z. & Ullah, N. (2015). From genetics to functional genomics: improvement in drought signaling and tolerance in wheat. Front. Plant Sci., 6, p. 1012.

47. Krupa, N.M., Kiriziy, D.A. & Rizhikova, P.L. (2011). The effect of soil drought on carbon dioxide gas exchange, assimilates supply and productivity of winter wheat. Fiziol. biokhim. kult. rast., 43, No. 1, pp. 72-80 [in Ukrainian].

48. Yordanov, I., Velikova, V., Georgieva, K., Ivanov, P., Tsenov, N. & Petrova, T. (2001). Change in CO2 assimilation, transpiration and stomatal resistance of different wheat cultivars experiencing drought under field conditions. J. Plant Physiol., 27, No. 3-4, pp. 2033.

49. Zhao, W., Liu, L., Shen, Q., Yang, J., Han, X., Tian, F. & Wu, J. (2020). Effects of water stress on photosynthesis, yield, and water use efficiency in winter wheat. Water, 12, No. 8, p. 2127. https://doi.org/10.3390/w12082127.

50. Morgun, V.V., Stasik, O.O., Kiriziy, D.A., Sokolovska-Sergiienko, O.G. & Makharynska, N.M. (2019). Effects of drought at different periods of wheat development on the leaf photosynthetic apparatus and productivity. Reg. Mech. in Bio., 10, No. 4, pp. 406-414. https://doi.org/10.15421/021961.

51. Pinheiro, C. & Chaves, M.M. (2011). Photosynthesis and drought: can we make metabolic connections from available data? J. Exp. Bot., 62, No. 3, pp. 869-882. https:// doi.org/10.1093/jxb/erq340.

52. Yu, T.F., Xu, Z.S., Guo, J.K., Wang, Y.X., Abernathy, B., Fu, J.D., Chen, X., Zhou, Y.B., Chen, M., Ye, X.G. & Ma, Y.Z. (2017). Improved drought tolerance in wheat plants over expressing a synthetic bacterial cold shock protein gene SeCspA. Sci. Rep., 7, p. 44050. https://doi.org/10.1038/srep44050.

53. Dunn, J., Hunt, L., Afsharinafar, M., Al Meselmani, M., Mitchell, A., Howells, R., Wallington, E., Fleming, A.J. & Gray, J.E. (2019). Reduced stomatal density in bread wheat leads to increased water-use efficiency. J. Exp. Bot., 70, Iss. 18, pp. 4737-4748. https://doi.org/10.1093/jxb/erz248.

54. Mafakheri, A., Siosemardeh, A., Bahramnejad, B., Struik, P. & Sohrabi, E. (2010). Effect of drought stress on yield, proline and chlorophyll contents in three chickpea cul- tivars. Australian J. Crop Sci., 4, pp. 580-585.

55. Ehonen, S., Yarmolinsky, D., Kollist, H. & Kangasjarvi, J. (2019). Reactive oxygen species, photosynthesis, and environment in the regulation of stomata. Antioxid Redox Signal, 30, No. 9, pp. 1220-1237. https://doi.org/10.1089/ars.2017.7455. PMID: 29237281.

56. Sade, B., Soylu, S. & Yetim, E. (2011). Drought and oxidative stress. Afr. J. Biotechnol., 10, No. 54, pp. 11102-11109. https://doi.org/10.5897/AJB11.1564.

57. Kolupaev, E.U. (2016). Plant cell antioxidants, their role in ROS signaling and plant resistance. Uspekhi sovremennoy biologii, 136, No. 2, pp. 181-198 [in Ukrainian].

58. Rumeau, D., Peltier, G. & Cournac, L. (2007). Chlororespiration and cyclic electron flow around PS I during photosynthesis and plant stress response. Plant, Cell and Environ, 30, No. 9, pp. 1041-1051. https://doi.org/10.1111/j.1365-3040.2007.01675.x.

59. Zlatev, Z. & Lidon, F.C. (2012). An overview on drought induced changes in plant growth, water relations and photosynthesis. Emir. J. Food Agric., 24, p. 57-72.

60. Shahzad, A.L.I., Yue-Yue, X.U., Xiang-Cheng, M.A., Qian-Min, J.I.A. & Zhi-Kuan, J.I.A. (2022). Improvement in winter wheat productivity through regulating PSII photochemistry, photosynthesis and chlorophyll fluorescence under deficit irrigation conditions. J. Int. Agr., 21, Iss. 3, pp. 654-665. https://doi.org/10.1016/S2095-3119(20)63409-8.

61. Hickey, K., Wood, M., Sexton, T., Sahin, Y., Nazarov, T., Fisher, J., Sanguinet, K.A., Cousins, A., Kirchhoff, H. & Smertenko, A. (2022). Drought tolerance strategies and autophagy in resilient wheat genotypes. Cells, 11, p. 1765. https://doi.org/10.3390/ cells11111765.

62. Chen, Y.E., Cui, J.M. & Su, Y.Q. (2017). Comparison of phosphorylation and assembly of photosystem complexes and redox homeostasis in two wheat cultivars with different drought resistance. Sci. Rep., 7, pp. 12718. https://doi.org/10.1038/s41598-017-13145-1.

63. Makharynska, N.M., Pryadkina, G.O., Sytnyk, S.K. & Stasyk, O.O. (2021, June). The influence of micronutrient treatment of plants on the photosynthetic activity of winter wheat under the influence of drought. Materials of the international scientific conference «Current problems of plant physiology and genetics», dedicated to the 75th anniversary of the Institute of Plant Physiology and Genetics of the National Academy of Sciences of Ukraine (pp. 39-41), Kiev [in Ukrainian].

64. Paknejad, F., Nasri, M., Moghadam, H.R.T, Zahedi, H. & Alahmadi, M.J. (2007). Effects of drought stress on chlorophyll fluorescence parameters, chlorophyll content and grain yield of wheat cultivars. J. Bio. Sci., 7, pp. 841-847. https://doi.org/ 10.3923/jbs.2007.841.847.

65. Todorova, D., Aleksandrov, V., Anev, S. & Sergiev, I. (2022). Photosynthesis alterations in wheat plants induced by herbicide, soil drought or flooding. Agronomy, 12, p. 390. https://doi.org/10.3390/agronomy12020390.

66. Grieco, M., Jain, A., Ebersberger, I. & Teige, M. (2016). An evolutionary view on thylakoid protein phosphorylation uncovers novel phosphorylation hotspots with potential functional implications. J. Exp. Bot., 67, pp. 3883-3896.

67. Kohzuma, K., Cruz, J.A., Akashi, K., Hoshiyasu, S., Munekage, Y.N., Yokota, A. & Kramer, D.M. (2009). The long-term responses of the photosynthetic proton circuit to drought. Plant Cell Environ., 32, No. 3, pp. 209-219. https://doi.org/10.1111/j.1365-3040.2008.01912.x.

68. Goldschmidt-Clermont, M. & Bassi, R. (2015). Sharing light between two photosystems: Mechanism of state transitions. Current Opinion in Plant Biology, 25, pp. 71-78. https:// doi.org/10.1016/j.pbi.2015.04.009.

69. Grieco, M., Roustan, V., Dermendjiev, G., Rantala, S., Jain, A., Leonardelli, M., Neumann, K., Berger, V., Engelmeier, D., Bachmann, G., Ebersberger, I., Aro, E.M., Weckwerth, W. & Teige, M. (2020). Adjustment of photosynthetic activity to drought and fluctuating light in wheat. Plant, Cell and Environment, 43, No. 6, pp. 1484-1500. https://doi.org/10.1111/pce.13756.

70. Terletskaya, N.V., Shcherban, A.B., Nesterov, M.A., Perfil'ev, R.N., Salina, E.A., Altayeva, N.A. & Blavachinskaya, I.V. (2020). Drought stress tolerance and photosynthetic activity of alloplasmic lines T. dicoccum x T. aestivum. Int. J. Mol. Sci., 21, No. 9, p. 3356. https://doi.org/10.3390/ijms21093356.

71. Reddy, A.R., Chaitanya, M. & Vivekanandan, M. (2004). Drought-induced responses of photosynthesis and antioxidant metabolism in higher plants. J. Plant Physiol., 161, pp. 189202. https://doi.org/10.1016/jjplph.2004.01.013.

72. Rehman, S., Bilal, M., Rana, R., Tahir, N., Shah, M., Ayalew, H. & Yan, G. (2016). Cell membrane stability and chlorophyll content variation in wheat (Triticum aestivum L.) genotypes under heat and drought conditions. Crop and Pasture Sci., 67, pp. 225-302. https://doi.org 10.1071/CP15385.

73. Sharifi, P. & Mohammadkhani, N. (2016). Effect of drought stress on photosynthesis factors in wheat genotypes during grain anthesis. Cer. Res. Comm., 44, No. 2, pp. 229239. https://doi.org/10.1556/0806.43.2015.054.

74. Yasir, T.A., Wasaya, A., Hussain, M., Ijaz, M., Farooq, M., Farooq, O., Nawaz, A. & Hu, Y.G. (2019). Evaluation of physiological markers for assessing drought tolerance and yield potential in bread wheat. Int. J. Funct. Plant Biol., 25, No. 5, pp. 1163-1174. https://doi.org/10.1007/s12298-019-00694-0.

75. Morgun, V.V., Stasik, O.O., Kiriziy, D.A. & Pryadkina, G.O. (2016). Relations between reactions of photosynthetic traits and grain productivity on soil drought in winter wheat varieties contrasting in their tolerance. Fiziol. rast. genet., 48, No. 5, pp. 371-381 [in Ukrainian]. https://doi.org/10.15407/frg2016.05.371.

76. Zhang, K., Zhang, Y., Chen, G. & Tian, J. (2009). Genetic analysis of grain yield and leaf chlorophyll content in common wheat. Cereal Res. Communicat., 37, No. 4, pp. 499511. http://www.jstor.org/stable/23789994.

77. El Basyoni, I., Saadalla, M., Baenziger, S., Bockelman, H. & Morsy, S. (2017). Cell membrane stability and association mapping for drought and heat tolerance in a worldwide wheat collection. Sustainability, 9, pp. 1-16.

78. Singh, M., Srivastava, Jai & Kumar, A. (2008). Cell membrane stability in relation to drought tolerance in wheat genotypes. J. Agr. Crop Sci., 168, pp. 186-190. https:// doi.org/10.1111/j. 1439-037X.1992.tb00997.x.

79. Bilal, M., Iqbal, I., Rana, R.M., Shoaib, U.R., Rehman, Haidery, Q.A., Ahmad, F., Ijaz, A. & Umar, H.M.I. (2015). A comprehensive review of effects of water stress and tolerance in wheat (Triticuma estivum L.). Tropical Plant Research., 2, No. 3, pp. 271275.

80. Dulai, S., Molnar, I., Pronay, J., Csernak, A., Tarnai, R. & Molnar-Lang, M. (2006). Effects of drought on photosynthetic parameters and heat stability of PSII in wheat and in Aegilops species originating from dry habitats. Acta Biol. Szegediensis, 50, pp. 11-17.

81. Qayyum, A., Al Ayoubi, S., Sher, A., Bibi, Y., Ahmad, S., Shen, Z. & Jenks, M.A. (2021). Improvement in drought tolerance in bread wheat is related to an improvement in osmolyte production, antioxidant enzyme activities, and gaseous exchange. Saudi J. Biol. Sci., 28, No. 9, pp. 5238-5249. https://doi.org/10.1016/j.sjbs.2021.05.040.

82. Li-Hong, Li, Hui-Lan, Yi, Xiu-Pingk, Liu & Hong-Xue, Qi (2021). Sulfur dioxide enhance drought tolerance of wheat seedlings through H2S signaling. Ecotoxicology and Environmental Safety, 207, p. 111248. https://doi.org/10.1016/j.ecoenv.2020.111248.

83. Abid, M., Ali, S., Qi, L.K., Zahoor, R., Tian, Z., Jiang, D., Snider, J.L. & Dai, T. (2018). Physiological and biochemical changes during drought and recovery periods at tillering and jointing stages in wheat (Triticum aestivum L.). Scientific Reports, 8, No. 1, p. 4615. https://doi.org/10.1038/s41598-018-21441-7.

84. Chorfil, A. & Taibi1, K. (2011). Biochemical screening for osmotic adjustment of wheat genotypes under drought stress. Tropicultura, 29, No. 2, pp. 82-87.

85. El Sabagh, A., Hossain, A., Barutcular, C., Gormus, O., Ahmad, Z., Hussain, S., Islam, M., Alharby, H., Bamagoos, A. & Kumar, N. (2019). Effects of drought stress on the quality of major oilseed crops: Implications and possible mitigation strategies. Appl. Ecol. Environ. Res., 17, No. 2, pp. 4019-4043. https://doi.org/10.15666/aeer/1702_40194043.

86. Guo, X., Xin, Z., Yang, T., Ma, X., Zhang, Y., Wang, Z., Ren, Y. & Lin, T. (2020). Metabolomics response for drought stress tolerance in chinese wheat genotypes (Triticum aestivum). Plants (Basel), 9, No. 4, p. 520. https://doi.org/10.3390/plants9040520.

87. Smirnov, O., Karpets, L.-А., Zinchenko, A., Kovalenko, M., Belava, V. & Taran, N. (2020). Changes of morphofunctional traits of Triticum aestivum and Triticum dicoccum seedlings caused by polyethylene glycol-modeling drought. J. Central European Agricult., 21, No. 2, pp. 268-274. https://doi.org/10.5513/JCEA01/2L2.2341.

88. Ibrahim, H.A. & Abdellafit, Y.M.R. (2016). Effect of maltose and tregalose on growth, yield and some biochemival components of wheat plant under water stress. Ann. Agric. Sci., 61, pp. 267-274. https://doi.org/10.1016/j.aoas.2016.05.002.

89. Khamssi, N.N. (2014). Leaf proline content and yield performance of wheat genotypes under irrigated and rainfedconditions. Ind. J. Fund. Appl. LifeSci., 4 (2), pp. 295-299.

90. Zadehbagheri, M., Azarpanah, A. & Javanmardi, S. (2014). Proline metabolite transport an efficient approach in corn yield improvement as response to drought conditions. American-Eurasian J. Agric. & Environ. Sci., 14, No. 5, pp. 476-485. https://doi.org/10.5829/idosi.aejaes.2014.14.05.12328.

91. Hayat, S., Hayat, Q., Alyemeni, M.N., Wani, A.S., Pichtel, J. & Ahmad, A. (2012). Role of proline under changing environments: a review. Plant Signal. Behav., 7, No. 11, pp. 1456-1466. https://doi.org/10.4161/psb.21949.

92. Jayant, K.S. & Saranji, S.K. (2014). Effect of drought stress on praline accumulation in peanut genotypes. J. Adv. Res., 2, pp. 301-309.

93. de Carvalho, K., de Campos, M.K.F., Domingues, D.S., Pereira, L.F. & Vieira, L.G.E. (2013). The accumulation of endogenous proline induces changes in gene expression of several antioxidant enzymes in leaves of transgenic Swinglecitrumelo. Mol. Biol. Rep., 40, pp. 3269-3279. https://doi.org/10.1007/s11033-012-2402-5.

94. Kadam, S., Shukla, Y., Subhash, N., Singh, C. & Suthar, K. (2017). Screening of wheat genotypes (Triticum durum L.) in response to drought stress by some physiological and biochemical indices. J. Pure App. Biosci., 5, No. 3, pp. 969-977. https:// doi.org/10.18782/2320-7051.2795.

95. Shunde, S., Villamor, J.G., Lin, W., Sharma, S. & Verslues, P.E. (2016). Proline coordination with fatty acid synthesis and redox metabolism of chloroplasts and mitochondria. Plant Physiol., 172, pp. 1074-1088. https://doi.org/10.1104/pp.16.01097.

96. Monirul, I., Begum, M.C., Kabir, A.H. & Alam, M.F. (2015). Molecular and biochemical mechanisms associated with differential responses to drought tolerance in wheat (Triticum aestivum L.). J. Plant Int., 10, No. 1, pp. 195-201. https:// doi.org/10.1080/17429145.2015.1064174.

97. Dubrovna, O.V., Stasik, O.O., Priadkina, G.O., Zborivska, O.V. & Sokolovska- Sergienko, O.G. (2020). Resistance of genetically modified wheat plants, containing a double-stranded RNA suppressor of the proline dehydrogenase gene, to soil moisture deficiency. Agricult. Sci. Pract., 7, No. 2, pp. 24-34. https://doi.org/10.15407/ agrisp7.02.024.

98. Lawson, T. & Matthews, J. (2020). Guard cell metabolism and stomatal function. Annu. Rev. Plant Biol., 71, pp. 273-302. https://doi.org/10.1146/annurev-arplant-050718- 100251.

99. Wani, S.H., Kumar, V., Shriram, V. & Sah, S.K. (2016). Phytohormones and their metabolic engineering for abiotic stress tolerance in crop plants. Crop J., 4, No. 3, pp. 162-176. https://doi.org/10.1016/j.cj.2016.01.010.

100. Geiger, D., Maierhofer, T., Al-Rasheid, K.A., Scherzer, S., Mumm, P., Liese, A., Ache, P., Wellmann, C., Marten, I., Grill, E., Romeis, T. & Hedrich, R. (2011). Stomatal closure by fast abscisic acid signaling is mediated by the guard cell anion channel SLAH3 and the receptor RCAR1. Sci. Signal., 4, p. 32. https://doi.org/ 10.1126/scisignal.200134614.

101. Kim, T.H., Bohmer, M., Hu, H., Nishimura, N. & Schroeder, J.I. (2010). Guard cell signal transduction network: advances in understanding abscisic acid, CO2 and Ca2+ signaling. Annu. Rev. Plant Biol., 61, pp. 561-591. https://doi.org/10.1146/annurev-arplant-042809-112226.

102. Wilkinson, S. & Davies, W.J. (2009). Drought, ozone, ABA and ethylene: New insights from cell to plant to community. Plant, Cell and Environment. 33, No. 4, pp. 510-525. https://doi.org/10.1111/j.1365-3040.2009.02052.x.

103. Ji, X., Dong, B., Shiran, B., Talbot, M.J., Edlington, J.E. & Hughes, T. (2011). Control of abscisic acid catabolism and abscisic acid homeostasis is important for reproductive stage stress tolerance in cereals. Plant Physiol., 156, pp. 647-662. https://doi.org/ 10.1104/pp.m.176164.

104. Alam, M.M., Nahar, K., Hasanuzzaman, M. & Fujita, M. (2014). Exogenous jasmonic acid modulates the physiology, antioxidant defense and glyoxalase systems in imparting drought stress tolerance in different Brassica species. Plant Biotechnol., 8, pp. 279293. https://doi.org/10.1007/s11816-014-0321-8.

105. Xie, Z.J., Jiang, D., Cao, W.X., Dai, T.B. & Jing, Q. (2003). Relationships of endogenous plant hormones to accumulation of grain protein and starch in winter wheat under different post-anthesis soil water statuses. Plant Growth Regul., 41, pp. 117-127. https://doi.org/10.1023/A:1027371906349.

106. Kagale, S., Divi, U.K., Krochko, J.E., Keller, W.A. & Krishna, P. (2007). Brassinosteroid confers tolerance in Arabidopsisthaliana and Brassica napusto a range of abiotic stresses. Planta, 225, pp. 353-364.

107. Sairam, S.K. (1994). Effects of homobrassinolide application on plant metabolism and grain yield under irrigated and moisture-stress conditions of two wheat varieties. Plant Growth Regul., 14, pp. 173-181. https://doi.org/10.1111/j.1439-037X.1994.tb00568.x.

108. Ulfat, A., Majid, S.A. & Hameed, A. (2017). Hormonal seed priming improves wheat (Triticum aestivum L.) field performance under drought and non-stress conditions. Pak. J. Bot., 49, No. 4, pp. 1239-1253.

109. Tomas, M., Medrano, H., Brugnoli, E., Escalona, J., Martorell, S., Pou, A., Ribas-Cabro, M. & Flexas, J. (2014). Variability of mesohyll conductance in grapevine cultivars under water stress conditions in relation to leaf anatomy and water use efficiency. Aus. J. Grape Wina Res., 20, No. 2, pp. 272-280. https://doi.org/10.1111/ajgw.12069.

110. Afzal, Z., Howton, T.C., Sun, Y. & Mukhtar, M.S. (2016). The roles of aquaporins in plant stress responses. J. Dev. Biol., 9, pp. 1-22. https://doi.org/10.3390/jdb4010009.

111. Bhargava, S. & Sawant, K. (2013). Drought stress adaptation: Metabolic adjustment and regulation of gene expression. Plant Breeding, 132, pp. 21-32. https:// doi.org/10.1111/pbr.12004.

112. Kaur, G. & Asthir, B. (2017). Molecular responses to drought stress in plants. Biol. Plant., 61, pp. 201-209. https://doi.org/10.1007/s10535-016-0700-9.

113. Yang, S., Vanderbeld, B., Wan, J. & Huang, Y. (2010). Narrowing down the targets: Towards successful genetic engineering of drought-tolerant crops. Molecular. Plant., 3, pp. 469-490. https://doi.org/10.1093/mp/ssq016.

114. Xu, K., Chen, S., Li, T., Ma, X., Liang, X., Ding, X., Liu, H. & Luo, L. (2015). OsGRAS23, a rice GRAS transcription factor gene, is involved in drought stress response through regulating expression of stress-responsive genes. BMC Plant Biol., 15, p. 141.

115. Huang, Q., Wang, Y., Li, B., Chang, J., Chen, M., Li, K., Yang, G. & He, G. (2015). TaNAC29, a NAC transcription factor from wheat, enhances salt and drought tolerance in transgenic. Arabidopsis. BMC Plant Biol., 15, p. 268. https://doi.org/10.1186/s12870- 015-0644-9.

116. Iuchi, S., Kobayashi, M, Taji, T., Naramoto, M., Seki, M., Kato, T., Tabata, S., Kakubari, Y, Yamaguchi-Shinozaki, K. & Shinozaki, K. (2001). Regulation of drought tolerance by gene manipulation of 9-cis-epoxycarotenoid dioxygenase, a key enzyme in abscisic acid biosynthesis in Arabidopsis. Plant J., 27, No. 4, pp. 325-333. https:// doi.org/10.1046/j.1365-313x.2001.01096.x.

117. Gahlaut, V., Jaiswal, V., Tyagi, B.S., Singh, G., Sareen, S. & Balyan, H.S. (2017). QTL mapping for nine drought-responsive agronomic traits in bread wheat under irrigated and rain-fed environments. PLoS One, 12, p. e0182857. https://doi.org/10.1371/ journal.pone.0182857.

118. Ballesta, P., Mora, F. & DelPozo, A. (2020). Association mapping of drought tolerance indices in wheat: QTL-rich regions on chromosome 4A. Sci. Agricola, 77, No. 2, p. e20180153. https://dx.doi.org/10.1590/1678-992x-2018-0153.

119. Kulkarni, M., Soolanayakanahally, R., Ogawa, S., Uga, Y., Selvaraj, M.G. & Kagale, S. (2017). Drought response in wheat: key genes and stimilatory mechanisms controlling root system architecture and transpiration efficiency. Frontiers in Chem., 5, p. 106. https://doi.org/10.3389/fchem.2017.00106.

120. Dhakal, A. (2021). Effect of drought stress and management in wheat -- a rewiev. Food and Agribusiness Managmenet, 2, No. 2, pp. 62-66. https://doi.org/10.26480/ fabm.02.2021.62.66.

121. Abebe, T., Guenzi, A.C., Martin, B. & Cushman, J.C. (2003). Tolerance of mannitol-accumulating transgenic wheat to water stress and salinity. Plant Physiol., 131, No. 4, pp. 1748-1755. https://doi.org/10.1104/pp.102.003616.

122. Khan, S., Anwar, S., Yu, S., Sun, M. Yang, Z. & Gao, Z-q. (2019). Development of drought-tolerant transgenic wheat: achievements and limitations. Int. J. Mol. Sci., 20, No. 13, p. 3350. https://doi.org/10.3390/ijms20133350.

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