Please wait a minute...
Journal of Integrative Agriculture  2017, Vol. 16 Issue (01): 27-35    DOI: 10.1016/S2095-3119(16)61367-9
Crop Genetics · Breeding · Germplasm Resources Advanced Online Publication | Current Issue | Archive | Adv Search |
Expression and functional analyses of the mitogen-activated protein kinase (MPK) cascade genes in response to phytohormones in wheat (Triticum aestivum L.)
YAO Su-fei2*, WANG Yan-xia3*, YANG Tong-ren2, HAO Lin1, 2, LU Wen-jing2, XIAO Kai1
College of Agronomy, Agricultural University of Hebei, Baoding 071001, P.R.China
2 College of Life Sciences, Agricultural University of Hebei, Baoding 071001, P.R.China
3 Shijiazhuang Academy of Agriculture and Forestry Sciences, Shijiazhuang 050041, P.R.China
Download:  PDF in ScienceDirect  
Export:  BibTeX | EndNote (RIS)      
Abstract  Mitogen-activated protein kinase (MPK) cascades consist of a set of kinase types (MPKKKs, MPKKs, MPKs) to establish
conserved signal-transducing modules mediating plant growth, development as well as responses to internal and external
cues. In this study, the expression patterns of six MPKKK, two MPKK, and 11 MPK genes in wheat in responses to external
treatments of phytohormones, including naphthylacetic acid (NAA), abscisic acid (ABA), 6-benzyladenine (6-BA), gibberellin
(GA3), salisylic acid (SA), jasmonic acid (JA), and ethylene (ETH), were investigated. Expression analysis revealed
that several of the MPK cascade genes are responses to the external phytohormone signaling. Of which, TaMPKKKA;3
is induced by 6-BA and NAA while TaMPK4 repressed by ETH, GA3, SA, and JA; TaMPKKKA, TaMPKKKA;3 and TaMPK1
are down-regulated by ETH and GA3 whereas TaMPK9 and TaMPK12 repressed by ETH and JA in addition that TaMPK12
also repressed by GA3; TaMPK12;1 is down-regulated by ABA, GA3 and SA while TaMPK17 repressed by all exogenous
phytonormones examined. TaMPK4, a MPK type gene previously characterized to mediate tolerance to phosphate (Pi)
deprivation, was functionally evaluated for its role in mediation of responses of plants to exogenous GA3, ETH, SA, and JA.
Results indicated that overexpression and antisense expression of TaMPK4 in tobacco dramatically modify the growth of
seedlings upon treatments of GA3, SA and JA, in which the overexpressors behaved deteriorated growth feature whereas
the seedlings with antisense expression of TaMPK4 exhibited improved seedling phenotype. The growth behaviors in
lines overexpressing or antisensely expressing TaMPK4 are closely associated with the biomass and the corresponding
hormone-associated parameters. These results demonstrated that TaMPK4 acts as a critical player in mediating the phytohormone
signaling. Our findings have identified the phytohormone-responsive MPK cascade genes in wheat and provided
a connection between the phytohormone-mediated responses and the MPK cascade pathways.
Keywords:  wheat (Triticum aestivum L.)      phytohormone      mitogen-activated protein kinase (MPK) cascade      expression, transgene analysis  
Received: 28 December 2015   Accepted:
Fund: 

This work was financially supported by the National Natural Science Foundation of China (31371618, 31201674), the National Transgenic Major Program of China (2011ZX08008) and the Key Laboratory of Crop Growth Regulation of Hebei Province, China.

Corresponding Authors:  XIAO Kai, Tel: +86-312-7528115, Fax: +86-312-7528400, E-mail: xiaokai@hebau.edu.cn; LU Wen-jing, Tel: +86-312-7528246, Fax: +86-312-7528200, E-mail: luwenjing@sohu.com    

Cite this article: 

YAO Su-fei, WANG Yan-xia, YANG Tong-ren, HAO Lin, LU Wen-jing, XIAO Kai. 2017. Expression and functional analyses of the mitogen-activated protein kinase (MPK) cascade genes in response to phytohormones in wheat (Triticum aestivum L.). Journal of Integrative Agriculture, 16(01): 27-35.

Asai S, Yoshioka H. 2008. The role of radical burst via MAPK signaling in plant immunity. Plant Signal & Behavior, 3, 920–922.

Bhattacharya A, Kourmpetli S, Ward DA, Thomas S G, Gong F, Powers S J, Carrera E, Taylor B, Gonzalez F N D, Tudzynski B, Phillips A L, Davey M R, Hedden P. 2012. Characterization of the fungal gibberellin desaturase as a 2-oxoglutarate-dependent dioxygenase and its utilization for enhancing plant growth. Plant Physiology, 160, 837–845.

Cardinale F, Meskiene I, Ouaked F, Hirt H. 2002. Convergence and divergence of stress-induced mitogen-activated protein kinase signaling pathways at the level of two distinct mitogen-activated protein kinase kinases. The Plant Cell, 14, 703–711.

Ecker J R. 2004. Reentry of the ethylene MPK6 module. The Plant Cell, 16, 3169–3173.

Guo C, Zhao X, Liu X, Zhang L, Gu J, Li X, Lu W, Xiao K. 2013. Function of wheat phosphate transporter gene TaPHT2;1 in Pi translocation and plant growth regulation under replete and limited Pi supply conditions. Planta, 237, 1163–1178.

Hahn A, Harter K. 2009. Mitogen-activated protein kinase cascades and ethylene: signaling, biosynthesis, or both? Plant Physiology, 149, 1207–1210.

Hao L, Wen Y, Zhao Y, Lu W, Xiao K. 2015. Wheat mitogen-activated protein kinase gene TaMPK4 improves plant tolerance to multiple stresses through modifying root growth, ROS metabolism, and nutrient acquisitions. Plant Cell Reports, 34, 2081–2097.

Ichimura K, Casais C, Peck S C, Shinozaki K, Shirasu K. 2006. MEKK1 is required for MPK4 activation and regulates tissue-specific and temperature-dependent cell death in Arabidopsis. Journal of Biological Chemistry, 281, 36969–36976.

Kim C Y, Liu Y, Thorne E T, Yang H, Fukushige H, Gassmann W. 2003. Activation of a stress-responsive mitogen-activated protein kinase cascade induces the biosynthesis of ethylene in plants. The Plant Cell, 15, 2707–2718.

Kovtun Y, Chiu W L, Zeng W, Sheen J. 1998. Suppression of auxin signal transduction by a MAPK cascade in higher plants. Nature, 395, 716–720.

Liu Y, Zhang S. 2004. Phosphorylation of 1-aminocyclopropane-1-carboxylic acid synthase by MPK6, a stress-responsive mitogen-activated protein kinase, induces ethylene biosynthesis in Arabidopsis. The Plant Cell, 16, 3386–3399.

Livak K J, Schmittgen T D. 2001. Analysis of relative gene expression data using real-time quantitative PCR and the 2–ΔΔCT method. Methods, 25, 402–408.

Moustafa K, AbuQamar S, Jarrar M, Al-Rajab A J, Tremouillaux-Guiller J. 2014. MAPK cascades and major abiotic stresses. Plant Cell Reports, 33, 1217–1225.

Mundy J, Nielsen H B, Brodersen P. 2006. Crosstalk. Trends in Plant Science, 11, 63–64.

Nakagami H, Soukupová H, Schikora A, Zárský V, Hirt H. 2006. A Mitogen-activated protein kinase kinase kinase mediates reactive oxygen species homeostasis in Arabidopsis. Journal of Biological Chemistry, 281, 38697–38704.

Peat T S, Böttcher C, Newman J, Lucent D, Cowieson N, Davies C. 2012. Crystal structure of an indole-3-acetic acid amido synthetase from grapevine involved in auxin homeostasis. The Plant Cell, 24, 4525–4538.

Pitzschke A, Schikora A, Hirt H. 2009. MAPK cascade signalling networks in plant defence. Current Opinion in Plant Biology, 12, 421–426.

Qin G, Gu H, Zhao Y, Ma Z, Shi G, Yang Y, Pichersky E, Chen H, Liu M, Chen Z, Qu L J. 2005. An indole-3-acetic acid carboxyl methyltransferase regulates Arabidopsis leaf development. The Plant Cell, 17, 2693–2704.

Rodriguez M C, Petersen M, Mundy J. 2010. Mitogen-activated protein kinase signaling in plants. Annual Review of Plant Biology, 6, 621–649.

Sun Z, Ding C, Li X, Xiao K. 2012. Molecular characterization and expression analysis of TaZFP15, a C2H2-type zinc finger transcription factor gene in wheat (Triticum aestivum L.). Journal of Integrative Agriculture, 11, 31–42.

Takahashi F, Yoshida R, Ichimura K, Mizoguchi T, Seo S, Yonezawa M. 2007. The mitogen-activated protein kinase cascade MKK3-MPK6 is an important part of the jasmonate signal transduction pathway in Arabidopsis. The Plant Cell, 19, 805–818.

Vert G, Walcher C L, Chory J, Nemhauser J L. 2008. Integration of auxin and brassinosteroid pathways by Auxin Response Factor 2. Proceedings of the National Academy of Sciences of the United States of America, 105, 9829–9834.

Wasternack C, Hause B. 2013. Jasmonates: Biosynthesis, perception, signal transduction and action in plant stress response, growth and development. An update to the 2007 review in Annals of Botany. Annals of Botany, 111, 1021–1058.

Westfall C S, Zubieta C, Herrmann J, Kapp U, Nanao M H, Jez J M. 2012. Structural basis for prereceptor modulation of plant hormones by GH3 proteins. Science, 336, 1708–1711.
[1] Asad RIAZ, Ahmad M. ALQUDAH, Farah KANWAL, Klaus PILLEN, YE Ling-zhen, DAI Fei, ZHANG Guo-ping. Advances in studies on the physiological and molecular regulation of barley tillering[J]. >Journal of Integrative Agriculture, 2023, 22(1): 1-13.
[2] TANG Zi-kai, SUN Man-yi, LI Jia-ming, SONG Bo-bo, LIU Yue-yuan, TIAN Yi-ke, WANG Cai-hong, WU Jun. Comparative transcriptome analysis provides insights into the mechanism of pear dwarfing[J]. >Journal of Integrative Agriculture, 2022, 21(7): 1952-1967.
[3] LI Hui-juan, JIAO Zhi-xin, NI Yong-jing, JIANG Yu-mei, LI Jun-chang, PAN Chao, ZHANG Jing, SUN Yu-long, AN Jun-hang, LIU Hong-jie, LI Qiao-yun, NIU Ji-shan. Heredity and gene mapping of a novel white stripe leaf mutant in wheat[J]. >Journal of Integrative Agriculture, 2021, 20(7): 1743-1752.
[4] WANG Hai-xia, WANG Ming-lun, WANG Xiu-zhong, DING Yu-long . Detection of seven phytohormones in peanut tissues by ultra-high-performance liquid chromatography-triple quadrupole tandem mass spectrometry[J]. >Journal of Integrative Agriculture, 2020, 19(3): 700-708.
[5] ZHOU Su-mei, ZHANG Man, ZHANG Ke-ke, YANG Xi-wen, HE De-xian, YIN Jun, WANG Chen-yang. Effects of reduced nitrogen and suitable soil moisture on wheat (Triticum aestivum L.) rhizosphere soil microbiological, biochemical properties and yield in the Huanghuai Plain, China[J]. >Journal of Integrative Agriculture, 2020, 19(1): 234-250.
[6] LI Cheng-yang, ZHANG Nan, GUAN Bin, ZHOU Zhu-qing, MEI Fang-zhu . Reactive oxygen species are involved in cell death in wheat roots against powdery mildew[J]. >Journal of Integrative Agriculture, 2019, 18(9): 1961-1970.
[7] YANG Meng-ya, CHEN Jia-qi, TIAN He-yang, NI Chen-yang, XIAO Kai. TaARR1, a cytokinin response regulator gene in Triticum aestivum, is essential in plant N starvation tolerance via regulating the N acquisition and N assimilation[J]. >Journal of Integrative Agriculture, 2019, 18(12): 2691-2702.
[8] SHI Gui-qing, FU Jing-ying, RONG Ling-jie, ZHANG Pei-yue, GUO Cheng-jin, XIAO Kai. TaMIR1119, a miRNA family member of wheat (Triticum aestivum), is essential in the regulation of plant drought tolerance[J]. >Journal of Integrative Agriculture, 2018, 17(11): 2369-2378.
[9] WANG Zhi-qin, ZHANG Wei-yang, YANG Jian-chang. Physiological mechanism underlying spikelet degeneration in rice[J]. >Journal of Integrative Agriculture, 2018, 17(07): 1475-1481.
[10] LIU Tong-tong, LIU Kai, WANG Fang-fang, ZHANG Ying, LI Qing-fang, ZHANG Kai-ran, XIE Chu-peng, TIAN Ji-chun, CHEN Jian-sheng. Conditional and unconditional QTLs mapping of gluten strength in common wheat (Triticum aestivum L.)[J]. >Journal of Integrative Agriculture, 2017, 16(10): 2145-2155.
[11] DOU Jun-ling, YUAN Ping-li, ZHAO Sheng-jie, HE Nan, ZHU Hong-ju, GAO Lei, JI Wan-li, LU Xuqiang, LIU Wen-ge. Effect of ploidy level on expression of lycopene biosynthesis genes and accumulation of phytohormones during watermelon (Citrullus lanatus) fruit development and ripening[J]. >Journal of Integrative Agriculture, 2017, 16(09): 1956-1967.
[12] LI Wen-jing, DENG Zhi-ying, CHEN Guang-feng, CHEN Fang, LI Xing-feng, TIAN Ji-chun. Genetic dissection of the sensory and textural properties of Chinese white noodles using a specific RIL population[J]. >Journal of Integrative Agriculture, 2017, 16(02): 454-463.
[13] WANG Shu-guang, JIA Shou-shan, SUN Dai-zhen, FAN Hua, CHANG Xiao-ping, JING Rui-lian. Mapping QTLs for stomatal density and size under drought stress in wheat (Triticum aestivum L.)[J]. >Journal of Integrative Agriculture, 2016, 15(9): 1955-1967.
[14] SHI Shu-ya, ZHANG Fei-fei, GAO Si, XIAO Kai. Expression pattern and function analyses of the MADS thranscription factor genes in wheat (Triticum aestivum L.) under phosphorusstarvation condition[J]. >Journal of Integrative Agriculture, 2016, 15(8): 1703-1715.
[15] ZHAO Lei, ZHANG Ya-qing. Effects of phosphate solubilization and phytohormone production of Trichoderma asperellum Q1 on promoting cucumber growth under salt stress[J]. >Journal of Integrative Agriculture, 2015, 14(8): 1588-1597.
No Suggested Reading articles found!