Function Analysis of Wheat (Triticum aestivum) TaWRKY46 Gene in Mediating Salt Stress Tolerance in Transgenic Tobacco (Nicotiana tabacum)
JIANG Ming-Yue1,2, SU Xiao-Shuai1,2, ZHANG Bao-Hua1,2, LI Xiao-Juan1,2,*, XIAO Kai3,*
1 College of life Sciences, Hebei Agricultural University, Baoding 071001, China; 2 Key Laboratory of Plant Physiology and Molecular Pathology, Baoding 071001, China; 3 College of Agronomy, Hebei Agricultural University, Baoding 071001, China
Abstract:The members of the WRKY transcription factor (TF) family play important roles in mediating plant tolerance to salt stress. Previously, TaWRKY46, a member of WRKY gene family, was revealed to obviously respond to salt stress. Thus transgenic tobacco (Nicotiana tabacum) lines overexpressing this wheat gene were generated. The experiment indicated that TaWRKY46 targeted onto nucleus at subcellular level. Using the culture methods of vermiculite-based and Murashige & Skoog (MS) hydroponic solution, the phenotype of wild type (WT) and overexpression lines (OE) under salt stress treatment was investigated. OE1 and OE5, two OE lines overexpression TaWRKY46, displayed increased growth vigor and leaf area of plants, together with enhanced plant fresh weight and contents of soluble sugar and proteins upon salt stress with respect to WT. Assays on the activities of superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT), the enzymes worked as cellular protector, showed the higher activities in OE lines than those in WT plants. Reverse transcription PCR (RT-PCR) analysis indicated the expression levels of some protection enzymes mentioned above from roots were higher in OE1 and OE5 than those in WT under salt stress treatment. Further histochemical staining study via nitroblue tetrazolium (DAB) and diaminobenzidine (NBT) dyeing methods revealed that the accumulative amounts of O2-· and H2O2 were lower in the OE plants than that of WT plants. The expression analysis revealed that the pyrabactin resistance-like abscisic acid receptor gene (PYL8) and a suite of sucrose non-fermenting-1-related protein kinase 2 (SnRK2) family genes were upregulated in expression in the OE plants. Observation on stomata movement showed that the OE plants possessed enlarged stomata aperture and increased closure rate upon salt stress compared with the WT plants. Using yeast-two hybridization assay, TaWRKY46 was identified to be interacted with TaSAP1-1, a stress-related protein in T. aestivum. Therefore, TaWRKY46 played an important role in salt tolerance through enhancing osmotic regulation and protective enzyme system, crossing with ABA signaling pathway, as well as initiating protein interaction. The results enrich the knowledge as to wheat plants coping with salt stress and provide theoretical guidance for breeding stress tolerant cultivars of crops.
[1] 丁长欢, 孙昭华, 李小娟, 等. 2012. 转录因子基因TaWRKY46的克隆与表达分析[J]. 华北农学报, 27(5): 68-74. (Ding C H, Sun Z H, Li X J, et al.2012. Cloning and expression profiles of TaWRKY46, a WRKY type transcription factor gene in wheat (Triticum aestivum L.))[J]. Acta Agriculturae Boreali-Sinica, 27(5): 65-71. [2] 熊庆娥. 2003. 植物生理学实验教程[M]. 成都: 四川科学技术出版社, pp. 81-83. (Xiong Q R.2003. Experimental Course of Plant Physiology[M]. Sichuan Science and Technology Press, Chengdu, China, pp. 81-83) ISBN: 7-5364-5299-3 [3] Berri S, Abbruscato P, Faivre-Rampant O, et al.2009. Characterization of WRKY co-regulatory networks in rice and Arabidopsis[J]. BMC Plant Biology, 9(1): 120-144. [4] Blokhina O, Virolainen E, Fagerstedt K V.2003. Antioxidants, oxidative damage and oxygen deprivation stress: A review[J]. Annals of Botany, 91(2): 179-194. [5] Chen F, Hu Y, Vannozzi A, et al.2018. The WRKY transcription factor family in model plants and crops[J]. Critical Reviews in Plant Sciences, 36(5): 311-315. [6] Choi C, Hwang S H, Fang I R, et al.2015. Molecular characterization of Oryza sativa WRKY6, which binds to W-box-like element 1 of the Oryza sativa pathogenesis-related (PR) 10a promoter and confers reduced susceptibility to pathogens[J]. New Phytologist, 208(3): 846-859. [7] Chu X, Wang C, Chen X, et al.2015. The cotton WRKY gene GhWRKY41 positively regulates salt and drought stress tolerance in transgenic Nicotiana benthamiana[J]. PLOS ONE, 10: e143022. [8] Dansana P K, Kothari K S, Vij, et al.2014. OsiSAP1 overexpression improves water-deficit stress tolerance in transgenic rice by affecting expression of endogenous stress-related genes[J]. Plant Cell Reports, 33(9): 1425-1440. [9] Ding W W, Fang W B, Shi S Y, et al.2016. Wheat WRKY type transcription factor gene TaWRKY1 is essential in mediating drought tolerance associated with an ABA-dependent pathway[J]. Plant Molecular Biology Reporter, 34(6): 1111-1126. [10] Ding Z J, Yan J Y, Xu X Y, et al.2014. Transcription factor WRKY46 regulates osmotic stress responses and stomatal movement independently in Arabidopsis[J]. The Plant Journal, 79(1): 13-27. [11] Dou L, Zhang X, Pang C, et al.2014. Genome-wide analysis of the WRKY gene family in cotton[J]. Molecular Genetics & Genomics, 289(6): 1103-1121. [12] Eulgem T, Rushton P J, Robatzek S, et al.2000. The WRKY superfamily of plant transcription factors[J]. Trends in Plant Science, 5(5): 199-206. [13] Fang Y J, Liao K F, Du H, et al.2015. A stress-responsive NAC transcription factor SNAC3 confers heat and drought tolerance through modulation of reactive oxygen species in rice[J]. Journal of Experimental Botany, 66: 6803-6817. [14] Finkelstein R R, Gampala S S, Rock C D.et al.2002. Abscisic acid signaling in seeds and seedlings[J]. The Plant Cell, 14(Supplement): S15-S45. [15] Hassan S, Johanna L, Rasmus B, et al.2019. In silico based screening of WRKY genes for identifying functional genes regulated by WRKY under salt stress[J]. Computational Biology and Chemistry, 83: 107131. [16] Huang X S, Liu J H, Chen X J.2010. Overexpression of PtrABF gene, a bZIP transcription factor isolated from Poncirus trifoliata, enhances dehydration and drought tolerance in tobacco via scavenging ROS and modulating expression of stress responsive genes[J]. BMC Plant Biology, 10(1): 230-248. [17] Ishiguro S, Nakamura K.1994. Characterization of a cDNA encoding a novel DNA-binding protein, SPF1, that recognizes SP8 sequences in the 5' upstream regions of genes coding for sporamin and β-amylase from sweet potato[J]. Molecular and General Genetics, 244(6): 563-571. [18] Khuman A, Arora K, Makkar H, et al.2020. Extensive intragenic divergences amongst ancient WRKY transcription factor gene family is largely associated with their functional diversity in plants[J]. Plant Gene, 22: 100222. [19] Lata C, Prasad M.2011. Role of DREBs in regulation of abiotic stress responses in plants[J]. Journal of Experimental Botany, 62(14): 4731-4748. [20] Lee B H, Lee H, Xiong L, et al.2002. A mitochondrial complex I defect impairs cold regulated nuclear gene expression[J]. The Plant Cell, 14(6): 1235-1251. [21] Liu H, Yang W, Liu D, et al.2011. Ectopic expression of a grapevine transcription factor VvWRKY11 contributes to osmotic stress tolerance in Arabidopsis[J]. Molecular Biology Reports, 38(1): 417-427. [22] Liu Z Q, Yan L, Wu Z, et al.2012. Cooperation of three WRKY domain transcription factors WRKY18, WRKY40, and WRKY60 in repressing two ABA responsive genes ABI4 and ABI5 in Arabidopsis[J]. Journal of Experimental Botany, 63(18): 6371-6392. [23] Lv B, Wu Q, Wang A, et al.2020. A WRKY transcription factor, FtWRKY46, from Tartary Buckwheat improves salt tolerance in transgenic Arabidopsis thaliana[J]. Plant Physiology Biochemistry, 147: 43-53. [24] Ma J H, Gao X L, Liu Q, et al.2017. Overexpression of TaWRKY146 increases drought tolerance through inducing stomatal closure in Arabidopsis thaliana[J]. Frontiers in Plant Science, 8: 2036-2047. [25] Miguel G G, Gaston A P, Regina A, et al.2012. Arabidopsis PYR/PYL/RCAR receptors play a major role in quantitative regulation of stomatal aperture and transcriptional response to abscisic acid[J]. The Plant Cell, 24(6): 2483-2496. [26] Mukhopadhyay A, Vij S, Tyagi A K, et al.2004. Overexpression of a zinc finger protein gene from rice confers tolerance to cold, dehydration, and salt stress in transgenic tobacco[J]. Proceedings of the National Academy of Sciences of the USA, 101(16): 6309-6314. [27] Niu C F, Wei W, Zhou Q Y, et al.2012. Wheat WRKY genes TaWRKY2 and TaWRKY19 regulate abiotic stress tolerance in transgenic Arabidopsis plants[J]. Plant Cell & Environment, 35(6): 1156-1170. [28] Ouyang S Q, Liu Y F, Liu P, et al.2010. Receptor-like kinase OsSIK1 improves drought and salt stress tolerance in rice (Oryza sativa L.) plants[J]. The Plant Journal, 62(2): 316-329. [29] Özge Ç, Sina M, Ayan A, et al.2018. Epigenetic analysis of WRKY transcription factor genes in salt stressed rice (Oryza sativa L.) plants[J]. Environmental & Experimental Botany, 159: 121-131. [30] Rengasamy P.2006. World salinization with emphasis on Australia[J]. Journal of Experimental Botany, 57(5): 1017-1023. [31] Rushton P J, Somssich I E, Ringler P, et al.2010. WRKY transcription factors[J]. Trends in Plant Science, 15(5): 0-258. [32] Shi G C, Fu J Y, Rong L J, et al.2018. TaMIR1119, a miRNA family member of wheat (Triticum aestivum), is essential in the regulation of plant drought tolerance[J]. Journal of Integrative Agriculture, 17(11): 5-4. [33] Sun X, Wang Y, Sui N.2018. Transcriptional regulation of bHLH during plant response to stress[J]. Biochemical & Biophysical Research Communications, 503(2): 397-401. [34] Takahashi Y, Zhang J B, Hsu Po-Kai, et al.2020. MAP3 kinase-dependent SnRK2-kinase activation is required for abscisic acid signal transduction and rapid osmotic stress response[J]. Nature Communications, 11(1): 1-12. [35] Wang C, Deng P, Wang X, et al.2013. A wheat WRKY transcription factor TaWRKY10 confers tolerance to multiple abiotic stresses in transgenic tobacco[J]. PLOS ONE, 8(6): 20-31. [36] Wang X T, Zeng J, Li Y, et al.2015. Expression of TaWRKY44, a wheat WRKY gene, in transgenic tobacco confers multiple abiotic stress tolerances[J]. Frontiers in Plant Science, 6: 615-629. [37] Wei W, Cui M Y, Hu Y, et al.2018. Ectopic expression of FvWRKY42, a WRKY transcription factor from the diploid woodland strawberry (Fragaria vesca), enhances resistance to powdery mildew, improves osmotic stress resistance, and increases abscisic acid sensitivity in Arabidopsis[J]. Plant Science, 275: 60-74. [38] Xu Z, Raza Q, Xu L, et al.2018. GmWRKY49, a salt-responsive nuclear protein, improved root length and governed better aalinity tolerance in transgenic Arabidopsis[J]. Frontiers in Plant Science, 9: 809-820. [39] Yamaguchi-Shinozaki K, Shinozaki K.2006. Transcriptional regulatory networks in cellular responses and tolerance to dehydration and cold stresses[J]. Annual Review of Plant Biology, 57(1): 781-803. [40] Yang Y, Guo Y.2018. Elucidating the molecular mechanisms mediating plant salt-stress responses[J]. New Phytologist, 217(2): 523-539. [41] Yin G, Xu H, Xiao S, et al.2013. The large soybean (Glycine max) WRKY TF family expanded by segmental duplication events and subsequent divergent selection among subgroups[J]. BMC Plant Biology, 13(1):148-167. [42] Zhang J, Shi H.2013. Physiological and molecular mechanisms of plant salt tolerance[J]. Photosynthesis Research, 115(1): 1-22. [43] Zhou S, Zheng W J, Liu B H, et al.2019. Characterizing the role of TaWRKY13 in salt tolerance[J]. International Journal of Molecular Sciences, 20(22): 5712. [44] Zhu D, Hou L, Xiao P, et al.2018. VvWRKY30, a grape WRKY transcription factor, plays a positive regulatory role under salinity stress[J]. Plant Science, 280: 132-142. [45] Zhu H, Zhou Y, Zhai H, et al.2020. A novel sweetpotato WRKY transcription factor, IbWRKY2, positively regulates drought and salt tolerance in transgenic Arabidopsis[J]. Biomolecules, 10(4): 506. [46] Zhu J K.2002. Salt and drought stress signal transduction in plants[J]. Annual Review of Plant Biology, 53(1): 247-273.