A maize mitogen-activated protein kinase kinase, ZmMKK1, positively regulated the salt and drought tolerance in transgenic Arabidopsis

Journal of Plant Physiology

Volumn 171, Issue 12, 2014, Pages 1003-1016

  Cai, Guohua ^a   Wang, Guodong ^a   Wang, Li ^a   Liu, Yang ^a   Pan, Jiaowen ^a   Li, Dequan ^a  

^a SHANDONG AGRICULTURAL UNIVERSITY   (China)

Author keywords

Expression analysis; MAPK cascades; Salt and drought stresses; Sensitivity; ZmMKK1

Indexed keywords

ABSCISIC ACID; CATALASE; MITOGEN ACTIVATED PROTEIN KINASE KINASE; PEROXIDASE; PROTEIN BINDING; REACTIVE OXYGEN METABOLITE; SODIUM CHLORIDE; VEGETABLE PROTEIN;

ANATOMY AND HISTOLOGY; ARABIDOPSIS; CELL DEATH; DROUGHT; DRUG EFFECTS; ENZYMOLOGY; GENE EXPRESSION REGULATION; GENETIC TRANSCRIPTION; GENETICS; GERMINATION; GROWTH, DEVELOPMENT AND AGING; MAIZE; METABOLISM; OSMOTIC PRESSURE; PHYSIOLOGICAL STRESS; PHYSIOLOGY; PLANT GENE; PLANT ROOT; PLANT SEED; PLANT STOMA; SACCHAROMYCES CEREVISIAE; SALT TOLERANCE; TRANSGENIC PLANT; TWO HYBRID SYSTEM;

ABSCISIC ACID; ARABIDOPSIS; CATALASE; CELL DEATH; DROUGHTS; GENE EXPRESSION REGULATION, PLANT; GENES, PLANT; GERMINATION; MITOGEN-ACTIVATED PROTEIN KINASE KINASES; OSMOTIC PRESSURE; PEROXIDASE; PLANT PROTEINS; PLANT ROOTS; PLANT STOMATA; PLANTS, GENETICALLY MODIFIED; PROTEIN BINDING; REACTIVE OXYGEN SPECIES; SACCHAROMYCES CEREVISIAE; SALT-TOLERANCE; SEEDS; SODIUM CHLORIDE; STRESS, PHYSIOLOGICAL; TRANSCRIPTION, GENETIC; TWO-HYBRID SYSTEM TECHNIQUES; ZEA MAYS;

EID: 84901981674     PISSN: 01761617     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jplph.2014.02.012     Document Type: Article

References (48)

1. Acharya B.R., Assmann S.M. Hormone interactions in stomatal function. Plant Mol Biol 2009, 69:451-462.
2. Cai G.H., Wang G.D., Wang L., Pan J.W., Liu Y., Li D.Q. ZmMKK1, a novel group A mitogen-activated protein kinase kinase gene in maize, conferred chilling stress tolerance and was involved in pathogen defense in transgenic tobacco. Plant Sci 2014, 214:57-73.
3. Clough S.J., Bent A.F. Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabdopsis thaliana. Plant J 1998, 16:735-743.
4. 2 activates a MAP kinase-like enzyme in Arabidopsis thaliana suspension cultures. J Exp Bot 1999, 50:1863-1866.
5. Desikan R., Hancock J.T., Ichimura K., Shinozaki K., Neill S.J. Harpin induces activation of the Arabidopsis MAP kinases AtMPK4 and AtMPK6. Plant Physiol 2001, 126:1579-1587.
6. Finkelstein R.R., Gamplal S.S., Rock C.D. Abscisic acid signaling in seeds and seedlings. Plant Cell 2002, 14:S15-S45.
7. Gadjev I., Vanderauwera S., Gechev T., Laloi C., Minkov I.N., Shulaev V., et al. Transcriptomic footprints disclose specificity of reactive oxygen species signaling in Arabidopsis. Plant Physiol 2006, 141:436-445.
8. Gill S.S., Tuteja N. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol Biochem 2010, 48:909-930.
9. Hadiarto T., Nanmori T., Matsuoka D., Iwasaki T., Sato K., Fukami Y., et al. Activation of Arabidopsis MAPK kinase kinase (AtMEKK1) and induction of AtMEKK1-AtMEK1 pathway by wounding. Planta 2006, 223:708-713.
10. Herskowitz I. MAP kinase pathways in yeast: for mating and more. Cell 1995, 80:187-197.
11. Hetherington A.M. Guard cell signaling. Cell 2001, 107:711-714.
12. Hua Z.M., Yang X., Fromm M.E. Activation of the NaCl-and drought-induced RD29A and RD29B promoters by constitutively active Arabidopsis MAPKK or MAPK proteins. Plant Cell Environ 2006, 29:1761-1770.
13. Ichimura K., Mizoguchi T., Irie K., Morris P., Giraudat J., Matsumoto K., et al. Isolation of AtMEKK1 (a MAP kinase kinase kinase)-interacting proteins and analysis of a MAP kinase cascade in Arabidopsis. Biochem Biophys Res Commun 1998, 253:532-543.
14. Kumar D., Klessig D.F. Differential induction of tobacco MAP kinases by the defense signals nitric oxide, salicylic acid, ethylene, and jasmonic acid. Mol Plant Microbe Interact 2000, 13:347-351.
15. Kim S.H., Woo D.H., Kim J.M., Lee S.Y., Chung W.S., Moon Y.H. Arabidopsis MKK4 mediates osmotic-stress response via its regulation of MPK3 activity. Biochem Biophys Res Commun 2011, 412:150-154.
16. Kong Q., Qu N., Gao M., Zhang Z., Ding X., Yang F., et al. The MEKK1-MKK1/MKK2-MPK4 kinase cascade negatively regulates immunity mediated by a mitogen-activated protein kinase kinase kinase in Arabidopsis. Plant Cell 2012, 24:2225-2236.
17. Kong X.P., Pan J.W., Zhang D., Jiang S.S., Cai G.H., Wang L., et al. Identification of mitogen-activated protein kinase kinase gene family and MKK-MAPK interaction network in maize. Biochem Biophys Res Commun 2013, 441:964-969.
18. Kong X.P., Pan J.W., Zhang M.Y., Xing X., Zhou Y., Liu Y., et al. ZmMKK4, a novel group C mitogen-activated protein kinase kinase in maize (Zea mays), confers salt and cold tolerance in transgenic Arabidopsis. Plant Cell Environ 2011, 34:1291-1303.
19. Kong X.P., Sun L.P., Zhou Y., Zhang M.Y., Liu Y., Pan J.W., et al. ZmMKK4 regulates osmotic stress through reactive oxygen species scavenging in transgenic tobacco. Plant Cell Rep 2011, 30:2097-2104.
20. Lee J.H., Van Montagu M., Verbruggen N.A. highly conserved kinase is an essential component for stress tolerance in yeast and plant cells. Plant Biol 1999, 96:5873-5877.
21. Liu L., Hu X., Song J., Zong X., Li D., Li D. Over-expression of a Zea mays L. protein phosphatase 2C gene (ZmPP2C) in Arabidopsis thaliana decreases tolerance to salt and drought. J Plant Physiol 2009, 166:531-542.
22. Liu Y., Wang L., Xing X., Sun L.P., Pan J.W., Kong X.P., et al. ZmLEA3, a multifunctional group 3 LEA protein from maize (Zea mays L.), is involved in biotic and abiotic stresses. Plant Cell Physiol 2013, 54:944-959.
23. Mafakheril A., Siosemardeh A., Bahramnejadl B., Struik P.C., Sohrabi Y. Effect of drought stress on yield, proline and chlorophyll contents in three chickpea cultivars. Aust J Crop Sci 2010, 4:580-585.
24. Mizoguchi T., Ichimura K., Irie K., Morris P., Giraudat J., Matsumoto K., et al. Identification of a possible MAP kinase cascade in Arabidopsis thaliana based on pairwise yeast two-hybrid analysis and functional complementation tests of yeast mutants. FEBS Lett 1998, 437:56-60.
25. Pan J., Zhang M., Kong X., Xing X., Liu Y., Zhou Y., et al. ZmMPK17, a novel maize group D MAP kinase gene, is involved in multiple stress responses. Planta 2012, 235:661-676.
26. Pastori G.M., Foyer C.H. Common components, networks, and pathways of cross-tolerance to stress. The central role of "redox" and abscisic acid-mediated controls. Plant Physiol 2002, 129:460-468.
27. Pitzschke A., Hirt H. Disentangling the complexity of mitogen-activated protein kinases and reactive oxygen species signaling. Plant Physiol 2009, 149:606-615.
28. Pitzschke A., Djamei A., Bitton F., Hirt H. A major role of the MEKK1-MKK1/2-MPK4 pathway in ROS signaling. Mol Plant 2009, 2:120-137.
29. Qiu J.L., Zhou L., Yun B.W., Nielsen H.B., Fiil B.K., Petersen K., et al. Arabidopsis mitogen-activated protein kinase kinases MKK1 and MKK2 have overlapping functions in defense signaling mediated by MEKK1, MPK4, and MKS1. Plant Physiol 2008, 148:212-222.
30. Rasmussen M.W., Roux M., Petersen M., Mundy J. MAP kinase cascades in Arabidopsis innate immunity. Front Plant Sci 2012, 3:169. (doi: 10.3389).
31. Saito H. Regulation of cross-talk in yeast MAPK signaling pathways. Curr Opin Microbiol 2010, 13:677-683.
32. Schaeffer H.J., Weber M.J. Mitogen-activated protein kinases: specific messages from ubiquitous messengers. Mol Cell Biol 1999, 19:2435-2444.
33. Schroeder J.I., Allen G.J., Hugouvieux V., Kwak J.M., Waner D. Guard cell signal transduction. Annu Rev Plant Physiol and Plant Mol Biol 2001, 52:627-658.
34. Sirichandra C., Wasilewska A., Vlad F., Valon C., Leung J. The guard cell as a single-cell model towards understanding drought tolerance and abscisic acid action. J Exp Bot 2009, 60:1439-1463.
35. Soderlund C., Descour A., Kudrna D., Bomhoff M., Boyd L., Currie J., et al. Sequencing, mapping, and analysis of 27, 455 maize full-length cDNAs. PLoS Genet 2009, 5(11):e1000740.
36. Tena G., Asai T., Chiu W.L., Sheen J. Plant mitogen-activated protein kinase signaling cascades. Curr Opin Plant Biol 2001, 4:392-401.
37. Teige M., Scheikl E., Eulgem T., Doczi R., Ichimura K., Shinozaki K., et al. The MKK2 pathway mediates cold and salt stress signaling in Arabidopsis. Mol Cell 2004, 15:141-152.
38. Tuteja N. Mechanisms of high salinity tolerance in plants. Method Enzymol 2007, 428:419-438.
39. Ueda A., Shi W., Shimada T., Miyake H., Takabe T. Altered expression of barley proline transporter causes different growth responses in Arabidopsis. Planta 2008, 227:277-286.
40. Umezawa T., Okamoto M., Kushiro T., Nambara E., Oono Y., Seki M., et al. CYP707A3, a major ABA 80-hydroxylase involved in dehydration and rehydration response in Arabidopsis thaliana. Plant J 2006, 46:171-182.
41. Xiong L., Schumaker K.S., Zhu J.K. Cell signaling during cold, drought, and salt stress. Plant Cell 2002, 14(suppl):S165-S183.
42. Ying S., Zhang D.F., Fu J., Shi Y.S., Song Y.C., Wang T.Y., et al. Cloning and characterization of a maize bZIP transcription factor, ZmbZIP72, confers drought and salt tolerance in transgenic Arabidopsis. Planta 2012, 235:253-266.
43. Zhang A.Y., Jiang M.Y., Zhang J.H., Tan M.P., Hu X.L. Mitogen-activated protein kinase is involved in abscisic acid-induced antioxidant defense and acts downstream of reactive oxygen species production in leaves of maize plants. Plant Physiol 2006, 141:475-487.
44. Zhang A.Y., Jiang M.Y., Zhang J.H., Ding H., Xu S.C., Hu X.L., et al. Nitric oxide induced by hydrogen peroxide mediates abscisic acid-induced activation of the mitogen-activated protein kinase cascade involved in antioxidant defense in maize leaves. New Phytol 2007, 175:36-50.
45. Zhang M.Y., Pan J.W., Kong X.P., Zhou Y., Liu Y., Sun L.P., et al. ZmMKK3, a novel maize group B mitogen-activated protein kinase kinase gene, mediates osmotic stress and ABA signal responses. J Plant Physiol 2012, 169:1501-1510.
46. Zhang X., Wang L., Meng H., Wen H., Fan Y., Zhao J. Maize ABP9 enhances tolerance to multiple stresses in transgenic Arabidopsis by modulating ABA signaling and cellular levels of reactive oxygen species. Plant Mol Biol 2011, 75:365-378.
47. Zhu J.K. Salt and drought stress signal transduction in plants. Annu Rev Plant Biol 2002, 53:247-273.
48. Zong X.J., Li D.P., Gu L.K., Li D.Q., Liu L.X., Hu X.L. Abscisic acid and hydrogen peroxide induce a novel maize group C MAP kinase gene, ZmMPK7, which is responsible for the removal of reactive oxygen species. Planta 2009, 229:485-495.