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International journal of molecular sciences, v.18 no.7, 2017년, pp.1427 -
Bielach, Agnieszka , Hrtyan, Monika , Tognetti, Vanesa B.
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Plant growth and development are critically influenced by unpredictable abiotic factors. To survive fluctuating changes in their environments, plants have had to develop robust adaptive mechanisms. The dynamic and complementary actions of the auxin and cytokinin pathways regulate a plethora of devel...
1. Skoog F. Miller C.O. Chemical regulation of growth and organ formation in plant tissues cultured in vitro Symp. Soc. Exp. Biol. 1957 54 118 130
2. Benjamins R. Scheres B. Auxin: The Looping Star in Plant Development Annu. Rev. Plant Biol. 2008 59 443 465 10.1146/annurev.arplant.58.032806.103805 18444904
3. Chandler J.W. Werr W. Cytokinin–auxin crosstalk in cell type specification Trends Plant Sci. 2015 20 291 300 10.1016/j.tplants.2015.02.003 25805047
4. Del Bianco M. Giustini L. Sabatini S. Spatiotemporal changes in the role of cytokinin during root development New Phytol. 2013 199 324 338 10.1111/nph.12338 23692218
5. Muller D. Leyser O. Auxin, cytokinin and the control of shoot branching Ann. Bot. 2011 107 1203 1212 10.1093/aob/mcr069 21504914
6. Robert H.S. Crhak Khaitova L. Mroue S. Benková E. The importance of localized auxin production for morphogenesis of reproductive organs and embryos in Arabidopsis J. Exp. Bot. 2015 66 5029 5042 10.1093/jxb/erv256 26019252
7. Saini S. Sharma I. Kaur N. Pati P.K. Auxin: A master regulator in plant root development Plant Cell Rep. 2013 32 741 757 10.1007/s00299-013-1430-5 23553556
8. Schaller G.E. Bishopp A. Kieber J.J. The yin-yang of hormones: Cytokinin and auxin interactions in plant development Plant Cell 2015 27 44 63 10.1105/tpc.114.133595 25604447
9. Skylar A. Wu X. Regulation of Meristem Size by Cytokinin Signaling J. Integr. Plant Biol. 2011 53 446 454 10.1111/j.1744-7909.2011.01045.x 21554538
10. Taylor-Teeples M. Lanctot A. Nemhauser J.L. As above, so below: Auxin’s role in lateral organ development Dev. Biol. 2016 419 156 164 10.1016/j.ydbio.2016.03.020 26994944
11. Werner T. Schmülling T. Cytokinin action in plant development Curr. Opin. Plant Biol. 2009 12 527 538 10.1016/j.pbi.2009.07.002 19740698
12. Adamowski M. Friml J. PIN-Dependent Auxin Transport: Action, Regulation, and Evolution Plant Cell 2015 27 20 32 10.1105/tpc.114.134874 25604445
13. Argueso C.T. Raines T. Kieber J.J. Cytokinin signaling and transcriptional networks Curr. Opin. Plant Biol. 2010 13 533 539 10.1016/j.pbi.2010.08.006 20851038
14. Bennett T. PIN proteins and the evolution of plant development Trends Plant Sci. 2015 20 498 507 10.1016/j.tplants.2015.05.005 26051227
15. Hwang I. Sheen J. Müller B. Cytokinin Signaling Networks Annu. Rev. Plant Biol. 2012 63 353 380 10.1146/annurev-arplant-042811-105503 22554243
16. Kasahara H. Current aspects of auxin biosynthesis in plants Biosci. Biotechnol. Biochem. 2016 80 34 42 10.1080/09168451.2015.1086259 26364770
17. Pan X. Chen J. Yang Z. Auxin regulation of cell polarity in plants Curr. Opin. Plant Biol. 2015 28 144 153 10.1016/j.pbi.2015.10.009 26599954
18. Kieber J.J. Schaller G.E. Cytokinins Arabidopsis Book Am. Soc. Plant Biol. 2014 12 e0168 10.1199/tab.0168 24465173
19. El-Showk S. Ruonala R. Helariutta Y. Crossing paths: Cytokinin signalling and crosstalk Development 2013 140 1373 1383 10.1242/dev.086371 23482484
20. Sehra B. Franks R.G. Auxin and cytokinin act during gynoecial patterning and the development of ovules from the meristematic medial domain Wiley Interdiscip. Rev. Dev. Biol. 2015 4 555 571 10.1002/wdev.193 25951007
21. Su Y.-H. Liu Y.-B. Zhang X.-S. Auxin-cytokinin interaction regulates meristem development Mol. Plant 2011 4 616 625 10.1093/mp/ssr007 21357646
22. Vanstraelen M. Benková E. Hormonal Interactions in the Regulation of Plant Development Annu. Rev. Cell Dev. Biol. 2012 28 463 487 10.1146/annurev-cellbio-101011-155741 22856461
23. Mittler R. Vanderauwera S. Suzuki N. Miller G. Tognetti V.B. Vandepoele K. Gollery M. Shulaev V. Van Breusegem F. ROS signaling: The new wave? Trends Plant Sci. 2011 16 300 309 10.1016/j.tplants.2011.03.007 21482172
24. Tognetti V.B. Mühlenbock P. Van Breusegem F. Stress homeostasis—The redox and auxin perspective Plant Cell Environ. 2012 35 321 333 10.1111/j.1365-3040.2011.02324.x 21443606
25. Kazan K. Auxin and the integration of environmental signals into plant root development Ann. Bot. 2013 112 1655 1665 10.1093/aob/mct229 24136877
26. Krishnamurthy A. Rathinasabapathi B. Auxin and its transport play a role in plant tolerance to arsenite-induced oxidative stress in Arabidopsis thaliana Plant Cell Environ. 2013 36 1838 1849 10.1111/pce.12093 23489261
27. O’Brien J.A. Benkova E. Cytokinin cross-talking during biotic and abiotic stress responses Front. Plant Sci. 2013 4 451 10.3389/fpls.2013.00451 24312105
28. Xia X.-J. Zhou Y.-H. Shi K. Zhou J. Foyer C.H. Yu J.-Q. Interplay between reactive oxygen species and hormones in the control of plant development and stress tolerance J. Exp. Bot. 2015 66 2839 2856 10.1093/jxb/erv089 25788732
29. Zwack P.J. Rashotte A.M. Interactions between cytokinin signalling and abiotic stress responses J. Exp. Bot. 2015 66 4863 4871 10.1093/jxb/erv172 25911740
30. Verma V. Ravindran P. Kumar P.P. Plant hormone-mediated regulation of stress responses BMC Plant Biol. 2016 16 86 10.1186/s12870-016-0771-y 27079791
31. Cerny M. Kuklova A. Hoehenwarter W. Fragner L. Novak O. Rotkova G. Jedelsky P.L. Zakova K. Smehilova M. Strnad M. Proteome and metabolome profiling of cytokinin action in Arabidopsis identifying both distinct and similar responses to cytokinin down- and up-regulation J. Exp. Bot. 2013 64 4193 4206 10.1093/jxb/ert227 24064926
32. Ljung K. Bhalerao R.P. Sandberg G. Sites and homeostatic control of auxin biosynthesis in Arabidopsis during vegetative growth Plant J. 2001 28 465 474 10.1046/j.1365-313X.2001.01173.x 11737783
33. Mühlenbock P. Szechyńska-Hebda M. Płaszczyca M. Baudo M. Mateo A. Mullineaux P.M. Parker J.E. Karpińska B. Karpiński S. Chloroplast Signaling and LESION SIMULATING DISEASE1 Regulate Crosstalk between Light Acclimation and Immunity in Arabidopsis Plant Cell Online 2008 20 2339 2356 10.1105/tpc.108.059618 18790826
34. Kim J.I. Baek D. Park H.C. Chun H.J. Oh D.-H. Lee M.K. Cha J.-Y. Kim W.-Y. Kim M.C. Chung W.S. Overexpression of Arabidopsis YUCCA6 in potato results in high-auxin developmental phenotypes and enhanced resistance to water deficit Mol. Plant 2013 6 337 349 10.1093/mp/sss100 22986790
35. Lee M. Jung J.-H. Han D.-Y. Seo P.J. Park W.J. Park C.-M. Activation of a flavin monooxygenase gene YUCCA7 enhances drought resistance in Arabidopsis Planta 2012 235 923 938 10.1007/s00425-011-1552-3 22109847
36. Park H.C. Cha J.-Y. Yun D.-J. Roles of YUCCAs in auxin biosynthesis and drought stress responses in plants Plant Signal. Behav. 2013 8 e24495 10.4161/psb.24495 23603963
37. Cheng Y. Auxin biosynthesis by the YUCCA flavin monooxygenases controls the formation of floral organs and vascular tissues in Arabidopsis Genes Dev. 2006 20 1790 1799 10.1101/gad.1415106 16818609
38. Sakata T. Oshino T. Miura S. Tomabechi M. Tsunaga Y. Higashitani N. Miyazawa Y. Takahashi H. Watanabe M. Higashitani A. Auxins reverse plant male sterility caused by high temperatures Proc. Natl. Acad. Sci. USA 2010 107 8569 8574 10.1073/pnas.1000869107 20421476
39. Cha J.-Y. Kim W.-Y. Kang S.B. Kim J.I. Baek D. Jung I.J. Kim M.R. Li N. Kim H.-J. Nakajima M. A novel thiol-reductase activity of Arabidopsis YUC6 confers drought tolerance independently of auxin biosynthesis Nat. Commun. 2015 6 8041 10.1038/ncomms9041 26314500
40. Ke Q. Wang Z. Ji C.Y. Jeong J.C. Lee H.-S. Li H. Xu B. Deng X. Kwak S.-S. Transgenic poplar expressing Arabidopsis YUCCA6 exhibits auxin-overproduction phenotypes and increased tolerance to abiotic stress Plant Physiol. Biochem. 2015 94 19 27 10.1016/j.plaphy.2015.05.003 25980973
41. Shi H. Chen L. Ye T. Liu X. Ding K. Chan Z. Modulation of auxin content in Arabidopsis confers improved drought stress resistance Plant Physiol. Biochem. 2014 82 209 217 10.1016/j.plaphy.2014.06.008 24992887
42. Woo Y.-M. Park H.-J. Su’udi M. Yang J.-I. Park J.-J. Back K. Park Y.-M. An G. Constitutively wilted 1, a member of the rice YUCCA gene family, is required for maintaining water homeostasis and an appropriate root to shoot ratio Plant Mol. Biol. 2007 65 125 136 10.1007/s11103-007-9203-6 17619151
43. Werner T. Nehnevajova E. Kollmer I. Novak O. Strnad M. Kramer U. Schmulling T. Root-Specific Reduction of Cytokinin Causes Enhanced Root Growth, Drought Tolerance, and Leaf Mineral Enrichment in Arabidopsis and Tobacco Plant Cell 2010 22 3905 3920 10.1105/tpc.109.072694 21148816
44. Mok D.W. Mok M.C. Cytokinin Metabolism and Action Annu. Rev. Plant Physiol. Plant Mol. Biol. 2001 52 89 118 10.1146/annurev.arplant.52.1.89 11337393
45. Sakakibara H. Cytokinins: Activity, biosynthesis, and translocation Annu. Rev. Plant Biol. 2006 57 431 449 10.1146/annurev.arplant.57.032905.105231 16669769
46. Frebort I. Kowalska M. Hluska T. Frebortova J. Galuszka P. Evolution of cytokinin biosynthesis and degradation J. Exp. Bot. 2011 62 2431 2452 10.1093/jxb/err004 21321050
47. Hare P.D. Cress W.A. van Staden J. The involvement of cytokinins in plant responses to environmental stress Plant Growth Regul. 1997 23 79 103 10.1023/A:1005954525087
48. Argueso C.T. Ferreira F.J. Kieber J.J. Environmental perception avenues: The interaction of cytokinin and environmental response pathways Plant Cell Environ. 2009 32 1147 1160 10.1111/j.1365-3040.2009.01940.x 19183294
49. Bano A. Hansen H. Dörffling K. Hahn H. Changes in the contents of free and conjugated abscisic acid, phaseic acid and cytokinins in xylem sap of drought stressed sunflower plants Phytochemistry 1994 37 345 347 10.1016/0031-9422(94)85058-5
50. Shashidhar V.R. Prasad T.G. Sudharshan L. Hormone signals from roots to shoots of sunflower ( Helianthus annuus L.). Moderate soil drying increases delivery of abscisic acid and depresses delivery of cytokinins in xylem sap Ann. Bot. 1996 78 151 155 10.1006/anbo.1996.0107
51. Alvarez S. Marsh E.L. Schroeder S.G. Schachtman D.P. Metabolomic and proteomic changes in the xylem sap of maize under drought Plant Cell Environ. 2008 31 325 340 10.1111/j.1365-3040.2007.01770.x 18088330
52. Davies W.J. Kudoyarova G. Hartung W. Long-distance ABA Signaling and Its Relation to Other Signaling Pathways in the Detection of Soil Drying and the Mediation of the Plant’s Response to Drought J. Plant Growth Regul. 2005 24 285 295 10.1007/s00344-005-0103-1
53. Hansen H. Dörffling K. Root-derived trans-zeatin riboside and abscisic acid in drought-stressed and rewatered sunflower plants: Interaction in the control of leaf diffusive resistance? Funct. Plant Biol. 2003 30 365 375 10.1071/FP02223
54. McDAVID C.R. Sagar G.R. Marshall C. The Effect of Root Pruning and 6-Benzyl-Aminopurine on the Chlorophyll Content, 14 CO 2 Fixation and the Shoot/Root Ratio in Seedlings of Pisvm Sativum L New Phytol. 1973 72 465 470 10.1111/j.1469-8137.1973.tb04395.x
55. Thomas J.C. McElwain E.F. Bohnert H.J. Convergent Induction of Osmotic Stress-Responses 1 Plant Physiol. 1992 100 416 423 10.1104/pp.100.1.416 16652978
56. Lubovská Z. Dobrá J. Štorchová H. Wilhelmová N. Vanková R. Cytokinin oxidase/dehydrogenase overexpression modifies antioxidant defense against heat, drought and their combination in Nicotiana tabacum plants J. Plant Physiol. 2014 171 1625 1633 10.1016/j.jplph.2014.06.021 25171514
57. Mackova H. Hronkova M. Dobra J. Tureckova V. Novak O. Lubovska Z. Motyka V. Haisel D. Hajek T. Prasil I.T. Enhanced drought and heat stress tolerance of tobacco plants with ectopically enhanced cytokinin oxidase/dehydrogenase gene expression J. Exp. Bot. 2013 64 2805 2815 10.1093/jxb/ert131 23669573
58. Nishiyama R. Watanabe Y. Fujita Y. Le D.T. Kojima M. Werner T. Vankova R. Yamaguchi-Shinozaki K. Shinozaki K. Kakimoto T. Analysis of Cytokinin Mutants and Regulation of Cytokinin Metabolic Genes Reveals Important Regulatory Roles of Cytokinins in Drought, Salt and Abscisic Acid Responses, and Abscisic Acid Biosynthesis Plant Cell 2011 23 2169 2183 10.1105/tpc.111.087395 21719693
59. Pospíšilová H. Jiskrová E. Vojta P. Mrízová K. Kokáš F. Čudejková M.M. Bergougnoux V. Plíhal O. Klimešová J. Novák O. Transgenic barley overexpressing a cytokinin dehydrogenase gene shows greater tolerance to drought stress New Biotechnol. 2016 33 692 705 10.1016/j.nbt.2015.12.005 26773738
60. Vojta P. Kokáš F. Husičková A. Grúz J. Bergougnoux V. Marchetti C.F. Jiskrová E. Ježilová E. Mik V. Ikeda Y. Whole transcriptome analysis of transgenic barley with altered cytokinin homeostasis and increased tolerance to drought stress New Biotechnol. 2016 33 676 691 10.1016/j.nbt.2016.01.010 26877151
61. Werner T. Motyka V. Laucou V. Smets R. Van Onckelen H. Schmulling T. Cytokinin-Deficient Transgenic Arabidopsis Plants Show Multiple Developmental Alterations Indicating Opposite Functions of Cytokinins in the Regulation of Shoot and Root Meristem Activity Plant Cell 2003 15 2532 2550 10.1105/tpc.014928 14555694
62. Rivero R.M. Gimeno J. Deynze A.V. Walia H. Blumwald E. Enhanced Cytokinin Synthesis in Tobacco Plants Expressing PSARK::IPT Prevents the Degradation of Photosynthetic Protein Complexes During Drought Plant Cell Physiol. 2010 51 1929 1941 10.1093/pcp/pcq143 20871100
63. Peleg Z. Reguera M. Tumimbang E. Walia H. Blumwald E. Cytokinin-mediated source/sink modifications improve drought tolerance and increase grain yield in rice under water-stress Plant Biotechnol. J. 2011 9 747 758 10.1111/j.1467-7652.2010.00584.x 21284800
64. Qin H. Gu Q. Zhang J. Sun L. Kuppu S. Zhang Y. Burow M. Payton P. Blumwald E. Zhang H. Regulated Expression of an Isopentenyltransferase Gene (IPT) in Peanut Significantly Improves Drought Tolerance and Increases Yield Under Field Conditions Plant Cell Physiol. 2011 52 1904 1914 10.1093/pcp/pcr125 21920877
65. Kuppu S. Mishra N. Hu R. Sun L. Zhu X. Shen G. Blumwald E. Payton P. Zhang H. Water-Deficit Inducible Expression of a Cytokinin Biosynthetic Gene IPT Improves Drought Tolerance in Cotton PLoS ONE 2013 8 e64190 10.1371/journal.pone.0064190 23675526
66. Décima Oneto C. Otegui M.E. Baroli I. Beznec A. Faccio P. Bossio E. Blumwald E. Lewi D. Water deficit stress tolerance in maize conferred by expression of an isopentenyltransferase (IPT) gene driven by a stress- and maturation-induced promoter J. Biotechnol. 2016 220 66 77 10.1016/j.jbiotec.2016.01.014 26784988
67. Rivero R. M. Kojima M. Gepstein A. Sakakibara H. Mittler R. Gepstein S. Blumwald E. Delayed leaf senescence induces extreme drought tolerance in a flowering plant Proc. Natl. Acad. Sci. USA 2007 104 19631 19636 10.1073/pnas.0709453104 18048328
68. Merewitz E.B. Gianfagna T. Huang B. Photosynthesis, water use, and root viability under water stress as affected by expression of SAG12-ipt controlling cytokinin synthesis in Agrostis stolonifera J. Exp. Bot. 2011 62 383 395 10.1093/jxb/erq285 20841349
69. Xu Y. Burgess P. Zhang X. Huang B. Enhancing cytokinin synthesis by overexpressing ipt alleviated drought inhibition of root growth through activating ROS-scavenging systems in Agrostis stolonifera J. Exp. Bot. 2016 67 1979 1992 10.1093/jxb/erw019 26889010
70. Wang Y. Shen W. Chan Z. Wu Y. Endogenous Cytokinin Overproduction Modulates ROS Homeostasis and Decreases Salt Stress Resistance in Arabidopsis Thaliana Front. Plant Sci. 2015 6 1004 10.3389/fpls.2015.01004 26635831
71. Žižková E. Dobrev P.I. Muhovski Y. Hošek P. Hoyerová K. Haisel D. Procházková D. Lutts S. Motyka V. Hichri I. Tomato ( Solanum lycopersicum L.) SlIPT3 and SlIPT4 isopentenyltransferases mediate salt stress response in tomato BMC Plant Biol. 2015 10.1186/s12870-015-0415-7
72. Tognetti V.B. Van Aken O. Morreel K. Vandenbroucke K. van de Cotte B. De Clercq I. Chiwocha S. Fenske R. Prinsen E. Boerjan W. Perturbation of indole-3-butyric acid homeostasis by the UDP-glucosyltransferase UGT74E2 modulates Arabidopsis architecture and water stress tolerance Plant Cell 2010 22 2660 2679 10.1105/tpc.109.071316 20798329
73. Maruyama K. Urano K. Yoshiwara K. Morishita Y. Sakurai N. Suzuki H. Kojima M. Sakakibara H. Shibata D. Saito K. Integrated analysis of the effects of cold and dehydration on rice metabolites, phytohormones, and gene transcripts Plant Physiol. 2014 164 1759 1771 10.1104/pp.113.231720 24515831
74. Tripathi A.K. Pareek A. Sopory S.K. Singla-Pareek S.L. Narrowing down the targets for yield improvement in rice under normal and abiotic stress conditions via expression profiling of yield-related genes Rice N. Y. 2012 5 37 10.1186/1939-8433-5-37 24280046
75. Wu C. Cui K. Wang W. Li Q. Fahad S. Hu Q. Huang J. Nie L. Mohapatra P.K. Peng S. Heat-Induced Cytokinin Transportation and Degradation Are Associated with Reduced Panicle Cytokinin Expression and Fewer Spikelets per Panicle in Rice Front. Plant Sci. 2017 8 371 10.3389/fpls.2017.00371 28367158
76. Joshi R. Sahoo K.K. Tripathi A.K. Kumar R. Gupta B.K. Pareek A. Singla-Pareek S.L. TKnockdown of an inflorescence meristem-specific cytokinin oxidase—OsCKX2 in rice reduces yield penalty under salinity stress condition Plant Cell Environ. 2017 10.1111/pce.12947 28337744
77. Chang Z. Liu Y. Dong H. Teng K. Han L. Zhang X. Effects of Cytokinin and Nitrogen on Drought Tolerance of Creeping Bentgrass PLoS ONE 2016 11 e0154005 10.1371/journal.pone.0154005 27099963
78. Liu X. Huang B. Cytokinin Effects on Creeping Bentgrass Response to Heat Stress Crop Sci. 2002 42 466 472 10.2135/cropsci2002.0466
79. Mýtinová Z. Motyka V. Haisel D. Gaudinová A. Lubovská Z. Wilhelmová N. Effect of abiotic stresses on the activity of antioxidative enzymes and contents of phytohormones in wild type and AtCKX2 transgenic tobacco plants Biol. Plant. 2010 54 461 470 10.1007/s10535-010-0082-3
80. Skalák J. Černý M. Jedelský P. Dobrá J. Ge E. Novák J. Hronková M. Dobrev P. Vanková R. Brzobohatý B. Stimulation of ipt overexpression as a tool to elucidate the role of cytokinins in high temperature responses of Arabidopsis thaliana J. Exp. Bot. 2016 67 2861 2873 10.1093/jxb/erw129 27049021
81. Zavaleta-Mancera H.A. López-Delgado H. Loza-Tavera H. Mora-Herrera M. Trevilla-García C. Vargas-Suárez M. Ougham H. Cytokinin promotes catalase and ascorbate peroxidase activities and preserves the chloroplast integrity during dark-senescence J. Plant Physiol. 2007 164 1572 1582 10.1016/j.jplph.2007.02.003 17485137
82. Kawano T. Roles of the reactive oxygen species-generating peroxidase reactions in plant defense and growth induction Plant Cell Rep. 2003 21 829 837 12789499
83. Jansen M.A.K. van den Noort R.E. Tan M.Y.A. Prinsen E. Lagrimini L.M. Thorneley R.N.F. Phenol-Oxidizing Peroxidases Contribute to the Protection of Plants from Ultraviolet Radiation Stress Plant Physiol. 2001 126 1012 1023 10.1104/pp.126.3.1012 11457952
84. Vatulescu A.D. Fortunato A.S. Sá M.C. Amâncio S. Ricardo C.P.P. Jackson P.A. Cloning and characterisation of a basic IAA oxidase associated with root induction in Vitis vinifera Plant Physiol. Biochem. 2004 42 609 615 10.1016/j.plaphy.2004.06.009 15331089
85. Cosio C. Vuillemin L. Meyer M.D. Kevers C. Penel C. Dunand C. An anionic class III peroxidase from zucchini may regulate hypocotyl elongation through its auxin oxidase activity Planta 2009 229 823 836 10.1007/s00425-008-0876-0 19116728
86. Potters G. Pasternak T.P. Guisez Y. Jansen M.A.K. Different stresses, similar morphogenic responses: integrating a plethora of pathways Plant Cell Environ. 2009 32 158 169 10.1111/j.1365-3040.2008.01908.x 19021890
87. Vanderauwera S. Zimmermann P. Rombauts S. Vandenabeele S. Langebartels C. Gruissem W. Inze D. Van Breusegem F. Genome-Wide Analysis of Hydrogen Peroxide-Regulated Gene Expression in Arabidopsis Reveals a High Light-Induced Transcriptional Cluster Involved in Anthocyanin Biosynthesis Plant Physiol. 2005 139 806 821 10.1104/pp.105.065896 16183842
88. Ahrazem O. Rubio-Moraga A. Trapero-Mozos A. Climent M.F.L. Gómez-Cadenas A. Gómez-Gómez L. Ectopic expression of a stress-inducible glycosyltransferase from saffron enhances salt and oxidative stress tolerance in Arabidopsis while alters anchor root formation Plant Sci. 2015 234 60 73 10.1016/j.plantsci.2015.02.004 25804810
89. Ludwig-Müller J. Auxin conjugates: Their role for plant development and in the evolution of land plants J. Exp. Bot. 2011 62 1757 1773 10.1093/jxb/erq412 21307383
90. Du H. Wu N. Fu J. Wang S. Li X. Xiao J. Xiong L. A GH3 family member, OsGH3-2, modulates auxin and abscisic acid levels and differentially affects drought and cold tolerance in rice J. Exp. Bot. 2012 63 6467 6480 10.1093/jxb/ers300 23112280
91. Park J.-E. Park J.-Y. Kim Y.-S. Staswick P.E. Jeon J. Yun J. Kim S.-Y. Kim J. Lee Y.-H. Park C.-M. GH3-mediated Auxin Homeostasis Links Growth Regulation with Stress Adaptation Response in Arabidopsis J. Biol. Chem. 2007 282 10036 10046 10.1074/jbc.M610524200 17276977
92. Teichmann T. Bolu-Arianto W.H. Olbrich A. Langenfeld-Heyser R. Göbel C. Grzeganek P. Feussner I. Hänsch R. Polle A. GH3::GUS reflects cell-specific developmental patterns and stress-induced changes in wood anatomy in the poplar stem Tree Physiol. 2008 28 1305 1315 10.1093/treephys/28.9.1305 18595842
93. Zhang S.-W. Li C.-H. Cao J. Zhang Y.-C. Zhang S.-Q. Xia Y.-F. Sun D.-Y. Sun Y. Altered Architecture and Enhanced Drought Tolerance in Rice via the Down-Regulation of Indole-3-Acetic Acid by TLD1/OsGH3.13 Activation Plant Physiol. 2009 151 1889 1901 10.1104/pp.109.146803 19776160
94. Junghans U. Polle A. Düchting P. Weiler E. Kuhlman B. Gruber F. Teichmann T. Adaptation to high salinity in poplar involves changes in xylem anatomy and auxin physiology Plant Cell Environ. 2006 29 1519 1531 10.1111/j.1365-3040.2006.01529.x 16898015
95. Singh V.K. Jain M. Garg R. Genome-wide analysis and expression profiling suggest diverse roles of GH3 genes during development and abiotic stress responses in legumes Front. Plant Sci. 2015 10.3389/fpls.2014.00789 25642236
96. Feng S. Yue R. Tao S. Yang Y. Zhang L. Xu M. Wang H. Shen C. Genome-wide identification, expression analysis of auxin-responsive GH3 family genes in maize ( Zea mays L.) under abiotic stresses J. Integr. Plant Biol. 2015 57 783 795 10.1111/jipb.12327 25557253
97. Kinoshita N. Wang H. Kasahara H. Liu J. MacPherson C. Machida Y. Kamiya Y. Hannah M.A. Chua N.-H. IAA-Ala Resistant3, an Evolutionarily Conserved Target of miR167, Mediates Arabidopsis Root Architecture Changes during High Osmotic Stress Plant Cell 2012 24 3590 3602 10.1105/tpc.112.097006 22960911
98. Ostrowski M. Ciarkowska A. Jakubowska A. The auxin conjugate indole-3-acetyl-aspartate affects responses to cadmium and salt stress in Pisum sativum L. J. Plant Physiol. 2016 191 63 72 10.1016/j.jplph.2015.11.012 26717013
99. Li Y. Wang B. Dong R. Hou B. AtUGT76C2, an Arabidopsis cytokinin glycosyltransferase is involved in drought stress adaptation Plant Sci. 2015 236 157 167 10.1016/j.plantsci.2015.04.002 26025529
100. Gidrol X. Lin W.S. Dégousée N. Yip S.F. Kush A. Accumulation of Reactive Oxygen Species and Oxidation of Cytokinin in Germinating Soybean Seeds Eur. J. Biochem. 1994 224 21 28 10.1111/j.1432-1033.1994.tb19990.x 7521301
101. Peer W.A. Cheng Y. Murphy A.S. Evidence of oxidative attenuation of auxin signalling J. Exp. Bot. 2013 64 2629 2639 10.1093/jxb/ert152 23709674
102. Peer W.A. Murphy A.S. Flavonoids and auxin transport: Modulators or regulators? Trends Plant Sci. 2007 12 556 563 10.1016/j.tplants.2007.10.003 18198522
103. Santelia D. Henrichs S. Vincenzetti V. Sauer M. Bigler L. Klein M. Bailly A. Lee Y. Friml J. Geisler M. Flavonoids Redirect PIN-mediated Polar Auxin Fluxes during Root Gravitropic Responses J. Biol. Chem. 2008 283 31218 31226 10.1074/jbc.M710122200 18718912
104. Kuhn B.M. Geisler M. Bigler L. Ringli C. Flavonols Accumulate Asymmetrically and Affect Auxin Transport in Arabidopsis Plant Physiol. 2011 156 585 595 10.1104/pp.111.175976 21502189
105. Agati G. Brunetti C. Di Ferdinando M. Ferrini F. Pollastri S. Tattini M. Functional roles of flavonoids in photoprotection: New evidence, lessons from the past Plant Physiol. Biochem. 2013 72 35 45 10.1016/j.plaphy.2013.03.014 23583204
106. Brown D.E. Rashotte A.M. Murphy A.S. Normanly J. Tague B.W. Peer W.A. Taiz L. Muday G.K. Flavonoids act as negative regulators of auxin transport in vivo in arabidopsis Plant Physiol. 2001 126 524 535 10.1104/pp.126.2.524 11402184
107. Buer C.S. Muday G.K. The transparent testa4 mutation prevents flavonoid synthesis and alters auxin transport and the response of Arabidopsis roots to gravity and light Plant Cell 2004 16 1191 1205 10.1105/tpc.020313 15100399
108. Peer W.A. Bandyopadhyay A. Blakeslee J.J. Makam S.N. Chen R.J. Masson P.H. Murphy A.S. Variation in Expression and Protein Localization of the PIN Family of Auxin Efflux Facilitator Proteins in Flavonoid Mutants with Altered Auxin Transport in Arabidopsis thaliana Plant Cell 2004 16 1898 1911 10.1105/tpc.021501 15208397
109. Kuhn B.M. Nodzyński T. Errafi S. Bucher R. Gupta S. Aryal B. Dobrev P. Bigler L. Geisler M. Zažímalová E. Flavonol-induced changes in PIN2 polarity and auxin transport in the Arabidopsis thaliana rol1-2 mutant require phosphatase activity Sci. Rep. 2017 10.1038/srep41906 28165500
110. Buer C.S. Kordbacheh F. Truong T.T. Hocart C.H. Djordjevic M.A. Alteration of flavonoid accumulation patterns in transparent testa mutants disturbs auxin transport, gravity responses, and imparts long-term effects on root and shoot architecture Planta 2013 238 171 189 10.1007/s00425-013-1883-3 23624937
111. Rushton P.J. Somssich I.E. Ringler P. Shen Q.J. WRKY transcription factors Trends Plant Sci. 2010 15 247 258 10.1016/j.tplants.2010.02.006 20304701
112. Grunewald W. De Smet I. Lewis D.R. Löfke C. Jansen L. Goeminne G. Vanden Bossche R. Karimi M. De Rybel B. Vanholme B. Transcription factor WRKY23 assists auxin distribution patterns during Arabidopsis root development through local control on flavonol biosynthesis Proc. Natl. Acad. Sci. USA 2012 109 1554 1559 10.1073/pnas.1121134109 22307611
113. Smith A.P. Nourizadeh S.D. Peer W.A. Xu J. Bandyopadhyay A. Murphy A.S. Goldsbrough P.B. Arabidopsis AtGSTF2 is regulated by ethylene and auxin, and encodes a glutathione S -transferase that interacts with flavonoids Plant J. 2003 36 433 442 10.1046/j.1365-313X.2003.01890.x 14617075
114. Kokubo T. Ambe-Ono Y. Nakamura M. Ishida H. Yamakawa T. Kodama T. Promotive effect of auxins on UDP-glucose: Flavonol glucosyltransferase activity in Vitis sp. cell cultures J. Biosci. Bioeng. 2001 91 564 569 10.1016/S1389-1723(01)80174-2 16233040
115. Silva-Navas J. Moreno-Risueno M.A. Manzano C. Téllez-Robledo B. Navarro-Neila S. Carrasco V. Pollmann S. Gallego F.J. del Pozo J.C. Flavonols Mediate Root Phototropism and Growth through Regulation of Proliferation-to-Differentiation Transition Plant Cell 2016 28 1372 1387 10.1105/tpc.15.00857 26628743
116. Pasternak T. Rudas V. Potters G. Jansen M.A.K. Morphogenic effects of abiotic stress: Reorientation of growth in Arabidopsis thaliana seedlings Environ. Exp. Bot. 2005 53 299 314 10.1016/j.envexpbot.2004.04.009
117. Jiang Y. Deyholos M.K. Comprehensive transcriptional profiling of NaCl-stressed Arabidopsis roots reveals novel classes of responsive genes BMC Plant Biol. 2006 6 25 10.1186/1471-2229-6-25 17038189
118. Liu W. Li R.-J. Han T.-T. Cai W. Fu Z.-W. Lu Y.-T. Salt Stress Reduces Root Meristem Size by Nitric Oxide-Mediated Modulation of Auxin Accumulation and Signaling in Arabidopsis Plant Physiol. 2015 168 343 356 10.1104/pp.15.00030 25818700
119. Sun F. Zhang W. Hu H. Li B. Wang Y. Zhao Y. Li K. Liu M. Li X. Salt Modulates Gravity Signaling Pathway to Regulate Growth Direction of Primary Roots in Arabidopsis Plant Physiol. 2008 146 178 188 10.1104/pp.107.109413 18024552
120. Yue R. Tie S. Sun T. Zhang L. Yang Y. Qi J. Yan S. Han X. Wang H. Shen C. Genome-Wide Identification and Expression Profiling Analysis of ZmPIN, ZmPILS, ZmLAX and ZmABCB Auxin Transporter Gene Families in Maize ( Zea mays L.) under Various Abiotic Stresses PLoS ONE 2015 10 e0118751 10.1371/journal.pone.0118751 25742625
121. Geldner N. Anders N. Wolters H. Keicher J. Kornberger W. Muller P. Delbarre A. Ueda T. Nakano A. Jürgens G. The Arabidopsis GNOM ARF-GEF mediates endosomal recycling, auxin transport, and auxin-dependent plant growth Cell 2003 112 219 230 10.1016/S0092-8674(03)00003-5 12553910
122. Kleine-Vehn J. Łangowski Ł. Wiśniewska J. Dhonukshe P. Brewer P.B. Friml J. Cellular and Molecular Requirements for Polar PIN Targeting and Transcytosis in Plants Mol. Plant 2008 1 1056 1066 10.1093/mp/ssn062 19825603
123. Benková E. Michniewicz M. Sauer M. Teichmann T. Seifertová D. Jürgens G. Friml J. Local, efflux-dependent auxin gradients as a common module for plant organ formation Cell 2003 115 591 602 10.1016/S0092-8674(03)00924-3 14651850
124. Friml J. Wiśniewska J. Benková E. Mendgen K. Palme K. Lateral relocation of auxin efflux regulator PIN3 mediates tropism in Arabidopsis Nature 2002 415 806 809 10.1038/415806a 11845211
125. Friml J. Vieten A. Sauer M. Weijers D. Schwarz H. Hamann T. Offringa R. Jürgens G. Efflux-dependent auxin gradients establish the apical-basal axis of Arabidopsis Nature 2003 426 147 153 10.1038/nature02085 14614497
126. Reinhardt D. Pesce E.-R. Stieger P. Mandel T. Baltensperger K. Bennett M. Traas J. Friml J. Kuhlemeier C. Regulation of phyllotaxis by polar auxin transport Nature 2003 426 255 260 10.1038/nature02081 14628043
127. Heisler M.G. Ohno C. Das P. Sieber P. Reddy G.V. Long J.A. Meyerowitz E.M. Patterns of Auxin Transport and Gene Expression during Primordium Development Revealed by Live Imaging of the Arabidopsis Inflorescence Meristem Curr. Biol. 2005 15 1899 1911 10.1016/j.cub.2005.09.052 16271866
128. Shibasaki K. Uemura M. Tsurumi S. Rahman A. Auxin Response in Arabidopsis under Cold Stress: Underlying Molecular Mechanisms Plant Cell 2009 21 3823 3838 10.1105/tpc.109.069906 20040541
129. Zwiewka M. Nodzyński T. Robert S. Vanneste S. Friml J. Osmotic Stress Modulates the Balance between Exocytosis and Clathrin-Mediated Endocytosis in Arabidopsis thaliana Mol. Plant 2015 8 1175 1187 10.1016/j.molp.2015.03.007 25795554
130. Galvan-Ampudia C.S. Julkowska M.M. Darwish E. Gandullo J. Korver R.A. Brunoud G. Haring M.A. Munnik T. Vernoux T. Testerink C. Halotropism Is a Response of Plant Roots to Avoid a Saline Environment Curr. Biol. 2013 23 2044 2050 10.1016/j.cub.2013.08.042 24094855
131. Bishopp A. Help H. El-Showk S. Weijers D. Scheres B. Friml J. Benková E. Mähönen A.P. Helariutta Y. A Mutually Inhibitory Interaction between Auxin and Cytokinin Specifies Vascular Pattern in Roots Curr. Biol. 2011 21 917 926 10.1016/j.cub.2011.04.017 21620702
132. Gillissen B. Bürkle L. André B. Kühn C. Rentsch D. Brandl B. Frommer W.B. A New Family of High-Affinity Transporters for Adenine, Cytosine, and Purine Derivatives in Arabidopsis Plant Cell 2000 12 291 300 10.1105/tpc.12.2.291 10662864
133. Kudo T. Kiba T. Sakakibara H. Metabolism and Long-distance Translocation of Cytokinins J. Integr. Plant Biol. 2010 52 53 60 10.1111/j.1744-7909.2010.00898.x 20074140
134. Bürkle L. Cedzich A. Döpke C. Stransky H. Okumoto S. Gillissen B. Kühn C. Frommer W.B. Transport of cytokinins mediated by purine transporters of the PUP family expressed in phloem, hydathodes, and pollen of Arabidopsis Plant J. 2003 34 13 26 10.1046/j.1365-313X.2003.01700.x 12662305
135. Hirose N. Takei K. Kuroha T. Kamada-Nobusada T. Hayashi H. Sakakibara H. Regulation of cytokinin biosynthesis, compartmentalization and translocation J. Exp. Bot. 2007 59 75 83 10.1093/jxb/erm157 17872922
136. Bishopp A. Lehesranta S. Vatén A. Help H. El-Showk S. Scheres B. Helariutta K. Mähönen A.P. Sakakibara H. Helariutta Y. Phloem-Transported Cytokinin Regulates Polar Auxin Transport and Maintains Vascular Pattern in the Root Meristem Curr. Biol. 2011 21 927 932 10.1016/j.cub.2011.04.049 21620705
137. Ko D. Kang J. Kiba T. Park J. Kojima M. Do J. Kim K.Y. Kwon M. Endler A. Song W.-Y. Arabidopsis ABCG14 is essential for the root-to-shoot translocation of cytokinin Proc. Natl. Acad. Sci. USA 2014 111 7150 7155 10.1073/pnas.1321519111 24778257
138. Zhang K. Novak O. Wei Z. Gou M. Zhang X. Yu Y. Yang H. Cai Y. Strnad M. Liu C.-J. Arabidopsis ABCG14 protein controls the acropetal translocation of root-synthesized cytokinins Nat. Commun. 2014 5 3274 10.1038/ncomms4274 24513716
139. Ulmasov T. Murfett J. Hagen G. Guilfoyle T.J. Aux/IAA proteins repress expression of reporter genes containing natural and highly active synthetic auxin response elements Plant Cell Online 1997 9 1963 1971 10.1105/tpc.9.11.1963 9401121
140. Shu W. Liu Y. Guo Y. Zhou H. Zhang J. Zhao S. Lu M. A Populus TIR1 gene family survey reveals differential expression patterns and responses to 1-naphthaleneacetic acid and stress treatments Front. Plant Sci. 2015 6 719 26442033
141. Blomster T. Salojarvi J. Sipari N. Brosche M. Ahlfors R. Keinanen M. Overmyer K. Kangasjarvi J. Apoplastic Reactive Oxygen Species Transiently Decrease Auxin Signaling and Cause Stress-Induced Morphogenic Response in Arabidopsis Plant Physiol. 2011 157 1866 1883 10.1104/pp.111.181883 22007024
142. Farcot E. Lavedrine C. Vernoux T. A modular analysis of the auxin signalling network PLoS ONE 2015 10 e0122231 10.1371/journal.pone.0122231 25807071
143. Iglesias M.J. Terrile M.C. Bartoli C.G. D’Ippólito S. Casalongué C.A. Auxin signaling participates in the adaptative response against oxidative stress and salinity by interacting with redox metabolism in Arabidopsis Plant Mol. Biol. 2010 74 215 222 10.1007/s11103-010-9667-7 20661628
144. Ha C.V. Le D.T. Nishiyama R. Watanabe Y. Sulieman S. Tran U.T. Mochida K. Dong N.V. Yamaguchi-Shinozaki K. Shinozaki K. The auxin response factor transcription factor family in soybean: Genome-wide identification and expression analyses during development and water stress DNA Res. Int. J. Rapid Publ. Rep. Genes Genomes 2013 20 511 524
145. Jain M. Khurana J.P. Transcript profiling reveals diverse roles of auxin-responsive genes during reproductive development and abiotic stress in rice FEBS J. 2009 276 3148 3162 10.1111/j.1742-4658.2009.07033.x 19490115
146. Wang S. Bai Y. Shen C. Wu Y. Zhang S. Jiang D. Guilfoyle T.J. Chen M. Qi Y. Auxin-related gene families in abiotic stress response in Sorghum bicolor Funct. Integr. Genom. 2010 10 533 546 10.1007/s10142-010-0174-3 20499123
147. Jung H. Lee D.-K. Choi Y.D. Kim J.-K. OsIAA6, a member of the rice Aux/IAA gene family, is involved in drought tolerance and tiller outgrowth Plant Sci. 2015 236 304 312 10.1016/j.plantsci.2015.04.018 26025543
148. Matsui A. Ishida J. Morosawa T. Mochizuki Y. Kaminuma E. Endo T.A. Okamoto M. Nambara E. Nakajima M. Kawashima M. Arabidopsis Transcriptome Analysis under Drought, Cold, High-Salinity and ABA Treatment Conditions using a Tiling Array Plant Cell Physiol. 2008 49 1135 1149 10.1093/pcp/pcn101 18625610
149. Sun X. Xu L. Wang Y. Yu R. Zhu X. Luo X. Gong Y. Wang R. Limera C. Zhang K. Identification of novel and salt-responsive miRNAs to explore miRNA-mediated regulatory network of salt stress response in radish ( Raphanus sativus L.) BMC Genom. 2015 16 197 10.1186/s12864-015-1416-5 25888374
150. Liu H.-H. Tian X. Li Y.-J. Wu C.-A. Zheng C.-C. Microarray-based analysis of stress-regulated microRNAs in Arabidopsis thaliana RNA 2008 14 836 843 10.1261/rna.895308 18356539
151. Zürcher E. Müller B. Cytokinin Synthesis, Signaling, and Function—Advances and New Insights Int. Rev. Cell Mol. Biol. 2016 324 1 38 27017005
152. Argyros R.D. Mathews D.E. Chiang Y.-H. Palmer C.M. Thibault D.M. Etheridge N. Argyros D.A. Mason M.G. Kieber J.J. Schaller G.E. Type B Response Regulators of Arabidopsis Play Key Roles in Cytokinin Signaling and Plant Development Plant Cell Online 2008 20 2102 2116 10.1105/tpc.108.059584 18723577
153. Sakai H. Aoyama T. Bono H. Oka A. Two-Component Response Regulators from Arabidopsis thaliana Contain a Putative DNA-Binding Motif Plant Cell Physiol. 1998 39 1232 1239 10.1093/oxfordjournals.pcp.a029325 9891419
154. Sakai H. Aoyama T. Oka A. Arabidopsis ARR1 and ARR2 response regulators operate as transcriptional activators Plant J. Cell Mol. Biol. 2000 24 703 711 10.1046/j.1365-313x.2000.00909.x
155. Sakai H. Honma T. Aoyama T. Sato S. Kato T. Tabata S. Oka A. ARR1, a transcription factor for genes immediately responsive to cytokinins Science 2001 294 1519 1521 10.1126/science.1065201 11691951
156. Brandstatter I. Kieber J.J. Two genes with similarity to bacterial response regulators are rapidly and specifically induced by cytokinin in Arabidopsis Plant Cell 1998 10 1009 1019 10.1105/tpc.10.6.1009 9634588
157. D’Agostino I.B. Deruère J. Kieber J.J. Characterization of the response of the Arabidopsis response regulator gene family to cytokinin Plant Physiol. 2000 124 1706 1717 10.1104/pp.124.4.1706 11115887
158. Hwang I. Sheen J. Two-component circuitry in Arabidopsis cytokinin signal transduction Nature 2001 413 383 389 10.1038/35096500 11574878
159. Tran L.-S.P. Urao T. Qin F. Maruyama K. Kakimoto T. Shinozaki K. Yamaguchi-Shinozaki K. Functional analysis of AHK1/ATHK1 and cytokinin receptor histidine kinases in response to abscisic acid, drought, and salt stress in Arabidopsis Proc. Natl. Acad. Sci. USA 2007 104 20623 20628 10.1073/pnas.0706547105 18077346
160. Kumar M.N. Verslues P.E. Stress physiology functions of the Arabidopsis histidine kinase cytokinin receptors Physiol. Plant. 2015 154 369 380 10.1111/ppl.12290 25263537
161. Jeon J. Kim N.Y. Kim S. Kang N.Y. Novak O. Ku S.-J. Cho C. Lee D.J. Lee E.-J. Strnad M. A Subset of Cytokinin Two-component Signaling System Plays a Role in Cold Temperature Stress Response in Arabidopsis J. Biol. Chem. 2010 285 23371 23386 10.1074/jbc.M109.096644 20463025
162. Jeon J. Kim J. Arabidopsis Response Regulator1 and Arabidopsis Histidine Phosphotransfer Protein2 (AHP2), AHP3, and AHP5 Function in Cold Signaling Plant Physiol. 2013 161 408 424 10.1104/pp.112.207621 23124324
163. Kang N.Y. Cho C. Kim J. Inducible Expression of Arabidopsis Response Regulator 22 (ARR22), a Type-C ARR, in Transgenic Arabidopsis Enhances Drought and Freezing Tolerance PLoS ONE 2013 10.1371/journal.pone.0079248 24244460
164. Bhargava A. Clabaugh I. To J.P. Maxwell B.B. Chiang Y.-H. Schaller G.E. Loraine A. Kieber J.J. Identification of Cytokinin-Responsive Genes Using Microarray Meta-Analysis and RNA-Seq in Arabidopsis Plant Physiol. 2013 162 272 294 10.1104/pp.113.217026 23524861
165. Brenner W.G. Schmulling T. Transcript profiling of cytokinin action in Arabidopsis roots and shoots discovers largely similar but also organ-specific responses BMC Plant Biol. 2012 12 112 10.1186/1471-2229-12-112 22824128
166. Kocsy G. Tari I. Vanková R. Zechmann B. Gulyás Z. Poór P. Galiba G. Redox control of plant growth and development Plant Sci. 2013 211 77 91 10.1016/j.plantsci.2013.07.004 23987814
167. Reguera M. Peleg Z. Abdel-Tawab Y.M. Tumimbang E.B. Delatorre C.A. Blumwald E. Stress-Induced Cytokinin Synthesis Increases Drought Tolerance through the Coordinated Regulation of Carbon and Nitrogen Assimilation in Rice Plant Physiol. 2013 163 1609 1622 10.1104/pp.113.227702 24101772
168. Kang N.Y. Cho C. Kim N.Y. Kim J. Cytokinin receptor-dependent and receptor-independent pathways in the dehydration response of Arabidopsis thaliana J. Plant Physiol. 2012 169 1382 1391 10.1016/j.jplph.2012.05.007 22704545
169. Dello Ioio R. Linhares F.S. Scacchi E. Casamitjana-Martinez E. Heidstra R. Costantino P. Sabatini S. Cytokinins Determine Arabidopsis Root-Meristem Size by Controlling Cell Differentiation Curr. Biol. 2007 17 678 682 10.1016/j.cub.2007.02.047 17363254
170. Nishiyama R. Watanabe Y. Leyva-Gonzalez M.A. Van Ha C. Fujita Y. Tanaka M. Seki M. Yamaguchi-Shinozaki K. Shinozaki K. Herrera-Estrella L. Arabidopsis AHP2, AHP3, and AHP5 histidine phosphotransfer proteins function as redundant negative regulators of drought stress response Proc. Natl. Acad. Sci. USA 2013 110 4840 4845 10.1073/pnas.1302265110 23487796
171. Sun L. Zhang Q. Wu J. Zhang L. Jiao X. Zhang S. Zhang Z. Sun D. Lu T. Sun Y. Two Rice Authentic Histidine Phosphotransfer Proteins, OsAHP1 and OsAHP2, Mediate Cytokinin Signaling and Stress Responses in Rice Plant Physiol. 2014 165 335 345 10.1104/pp.113.232629 24578505
172. Mason M.G. Jha D. Salt D.E. Tester M. Hill K. Kieber J.J. Eric Schaller G. Type-B response regulators ARR1 and ARR12 regulate expression of AtHKT1;1 and accumulation of sodium in Arabidopsis shoots Plant J. 2010 64 753 763 10.1111/j.1365-313X.2010.04366.x 21105923
173. Rashotte A.M. Mason M.G. Hutchison C.E. Ferreira F.J. Schaller G.E. Kieber J.J. A subset of Arabidopsis AP2 transcription factors mediates cytokinin responses in concert with a two-component pathway Proc. Natl. Acad. Sci. USA 2006 103 11081 11085 10.1073/pnas.0602038103 16832061
174. Shi X. Gupta S. Rashotte A.M. Characterization of two tomato AP2/ERF genes, SlCRF1 and SlCRF2 in hormone and stress responses Plant Cell Rep. 2014 33 35 45 10.1007/s00299-013-1510-6 24081612
175. Inzé A. Vanderauwera S. Hoeberichts F.A. Vandorpe M. van Gaever T. Van Breusegem F. A subcellular localization compendium of hydrogen peroxide-induced proteins Plant Cell Environ. 2012 35 308 320 10.1111/j.1365-3040.2011.02323.x 21443605
176. Zwack P.J. Robinson B.R. Risley M.G. Rashotte A.M. Cytokinin Response Factor 6 Negatively Regulates Leaf Senescence and is Induced in Response to Cytokinin and Numerous Abiotic Stresses Plant Cell Physiol. 2013 54 971 981 10.1093/pcp/pct049 23539244
177. Zwack P.J. De Clercq I. Howton T.C. Hallmark H.T. Hurny A. Keshishian E.A. Parish A.M. Benkova E. Mukhtar M.S. Van Breusegem F. Cytokinin Response Factor 6 Represses Cytokinin-Associated Genes during Oxidative Stress Plant Physiol. 2016 172 1249 1258 10.1104/pp.16.00415 27550996
178. Gupta S. Rashotte A.M. Expression patterns and regulation of SlCRF3 and SlCRF5 in response to cytokinin and abiotic stresses in tomato ( Solanum lycopersicum ) J. Plant Physiol. 2014 171 349 358 10.1016/j.jplph.2013.09.003 24120534
179. De Clercq I. Vermeirssen V. van Aken O. Vandepoele K. Murcha M.W. Law S.R. Inzé A. Ng S. Ivanova A. Rombaut D. The membrane-bound NAC transcription factor ANAC013 functions in mitochondrial retrograde regulation of the oxidative stress response in Arabidopsis Plant Cell 2013 25 3472 3490 10.1105/tpc.113.117168 24045019
180. Ng S. Ivanova A. Duncan O. Law S.R. Van Aken O. de Clercq I. Wang Y. Carrie C. Xu L. Kmiec B. A membrane-bound NAC transcription factor, ANAC017, mediates mitochondrial retrograde signaling in Arabidopsis Plant Cell 2013 25 3450 3471 10.1105/tpc.113.113985 24045017
181. Zwack P.J. Compton M.A. Adams C.I. Rashotte A.M. Cytokinin response factor 4 (CRF4) is induced by cold and involved in freezing tolerance Plant Cell Rep. 2015 1 12 10.1007/s00299-015-1904-8 26650835
182. Feng J. Wang C. Chen Q. Chen H. Ren B. Li X. Zuo J. S -nitrosylation of phosphotransfer proteins represses cytokinin signaling Nat. Commun. 2013 4 1529 10.1038/ncomms2541 23443557
183. Terrile M.C. París R. Calderón-Villalobos L.I.A. Iglesias M.J. Lamattina L. Estelle M. Casalongué C.A. Nitric Oxide Influences Auxin Signaling through S-nitrosylation of the Arabidopsis Transport Inhibitor Response1 Auxin Receptor Plant J. 2012 70 492 500 10.1111/j.1365-313X.2011.04885.x 22171938
184. Jones B. Ljung K. Auxin and cytokinin regulate each other’s levels via a metabolic feedback loop Plant Signal. Behav. 2011 6 901 904 10.4161/psb.6.6.15323 21543904
185. Birnbaum K.D. How many ways are there to make a root? Curr. Opin. Plant Biol. 2016 34 61 67 10.1016/j.pbi.2016.10.001 27780106
186. De Rybel B. Mähönen A.P. Helariutta Y. Weijers D. Plant vascular development: From early specification to differentiation Nat. Rev. Mol. Cell Biol. 2016 17 30 40 10.1038/nrm.2015.6 26580717
187. Naseem M. Kaltdorf M. Dandekar T. The nexus between growth and defence signalling: Auxin and cytokinin modulate plant immune response pathways J. Exp. Bot. 2015 66 4885 4896 10.1093/jxb/erv297 26109575
188. Miyawaki K. Matsumoto-Kitano M. Kakimoto T. Expression of cytokinin biosynthetic isopentenyltransferase genes in Arabidopsis: Tissue specificity and regulation by auxin, cytokinin, and nitrate Plant J. Cell Mol. Biol. 2004 37 128 138 10.1046/j.1365-313X.2003.01945.x
189. Dello Ioio R. Nakamura K. Moubayidin L. Perilli S. Taniguchi M. Morita M.T. Aoyama T. Costantino P. Sabatini S. A genetic framework for the control of cell division and differentiation in the root meristem Science 2008 322 1380 1384 10.1126/science.1164147 19039136
190. Tanaka M. Takei K. Kojima M. Sakakibara H. Mori H. Auxin controls local cytokinin biosynthesis in the nodal stem in apical dominance Plant J. 2006 45 1028 1036 10.1111/j.1365-313X.2006.02656.x 16507092
191. Nordström A. Tarkowski P. Tarkowska D. Norbaek R. Astot C. Dolezal K. Sandberg G. Auxin regulation of cytokinin biosynthesis in Arabidopsis thaliana : A factor of potential importance for auxin-cytokinin-regulated development Proc. Natl. Acad. Sci. USA 2004 101 8039 8044 10.1073/pnas.0402504101 15146070
192. Werner T. Köllmer I. Bartrina I. Holst K. Schmülling T. New Insights into the Biology of Cytokinin Degradation Plant Biol. 2006 8 371 381 10.1055/s-2006-923928 16807830
193. Carabelli M. Possenti M. Sessa G. Ciolfi A. Sassi M. Morelli G. Ruberti I. Canopy shade causes a rapid and transient arrest in leaf development through auxin-induced cytokinin oxidase activity Genes Dev. 2007 21 1863 1868 10.1101/gad.432607 17671088
194. Jones B. Gunnerås S.A. Petersson S.V. Tarkowski P. Graham N. May S. Dolezal K. Sandberg G. Ljung K. Cytokinin regulation of auxin synthesis in Arabidopsis involves a homeostatic feedback loop regulated via auxin and cytokinin signal transduction Plant Cell 2010 22 2956 2969 10.1105/tpc.110.074856 20823193
195. Polanská L. Vicánková A. Nováková M. Malbeck J. Dobrev P.I. Brzobohaty B. Vanková R. Machácková I. Altered cytokinin metabolism affects cytokinin, auxin, and abscisic acid contents in leaves and chloroplasts, and chloroplast ultrastructure in transgenic tobacco J. Exp. Bot. 2007 58 637 649 10.1093/jxb/erl235 17175552
196. Müller B. Sheen J. Cytokinin and auxin interaction in root stem-cell specification during early embryogenesis Nature 2008 453 1094 1097 10.1038/nature06943 18463635
197. Zhao Z. Andersen S.U. Ljung K. Dolezal K. Miotk A. Schultheiss S.J. Lohmann J.U. Hormonal control of the shoot stem-cell niche Nature 2010 465 1089 1092 10.1038/nature09126 20577215
198. Moubayidin L. Perilli S. Dello Ioio R. Di Mambro R. Costantino P. Sabatini S. The rate of cell differentiation controls the Arabidopsis root meristem growth phase Curr. Biol. 2010 20 1138 1143 10.1016/j.cub.2010.05.035 20605455
199. Pernisová M. Klíma P. Horák J. Válková M. Malbeck J. Souček P. Reichman P. Hoyerová K. Dubová J. Friml J. Cytokinins modulate auxin-induced organogenesis in plants via regulation of the auxin efflux Proc. Natl. Acad. Sci. USA 2009 106 3609 3614 10.1073/pnas.0811539106 19211794
200. Marhavý P. Bielach A. Abas L. Abuzeineh A. Duclercq J. Tanaka H. Pařezová M. Petrášek J. Friml J. Kleine-Vehn J. Cytokinin Modulates Endocytic Trafficking of PIN1 Auxin Efflux Carrier to Control Plant Organogenesis Dev. Cell 2011 21 796 804 10.1016/j.devcel.2011.08.014 21962902
201. Rŭžička K. Šimášková M. Duclercq J. Petrášek J. Zažímalová E. Simon S. Friml J. Van Montagu M.C. Benková E. Cytokinin regulates root meristem activity via modulation of the polar auxin transport Proc. Natl. Acad. Sci. USA 2009 106 4284 4289 10.1073/pnas.0900060106 19246387
202. Moreira S. Bishopp A. Carvalho H. Campilho A. AHP6 Inhibits Cytokinin Signaling to Regulate the Orientation of Pericycle Cell Division during Lateral Root Initiation PLoS ONE 2013 10.1371/journal.pone.0056370 23457561
203. Kuppusamy K.T. Walcher C.L. Nemhauser J.L. Cross-regulatory mechanisms in hormone signaling Plant Mol. Biol. 2009 69 375 381 10.1007/s11103-008-9389-2 18726558
204. Ramireddy E. Chang L. Schmülling T. Cytokinin as a mediator for regulating root system architecture in response to environmental cues Plant Signal. Behav. 2014 10.4161/psb.27771
205. Hruz T. Laule O. Szabo G. Wessendorp F. Bleuler S. Oertle L. Widmayer P. Gruissem W. Zimmermann P. Genevestigator V3: A Reference Expression Database for the Meta-Analysis of Transcriptomes Adv. Bioinform. 2008 2008 e420747 10.1155/2008/420747 19956698
206. Bennett T. Hines G. van Rongen M. Waldie T. Sawchuk M.G. Scarpella E. Ljung K. Leyser O. Connective Auxin Transport in the Shoot Facilitates Communication between Shoot Apices PLoS Biol. 2016 14 e1002446 10.1371/journal.pbio.1002446 27119525
207. Bainbridge K. Guyomarc’h S. Bayer E. Swarup R. Bennett M. Mandel T. Kuhlemeier C. Auxin influx carriers stabilize phyllotactic patterning Genes Dev. 2008 22 810 823 10.1101/gad.462608 18347099
208. Revalska M. Vassileva V. Zechirov G. Iantcheva A. Is the auxin influx carrier LAX3 essential for plant growth and development in the model plants Medicago truncatula, Lotus japonicus and Arabidopsis thaliana ? Biotechnol. Biotechnol. Equip. 2015 29 786 797 10.1080/13102818.2015.1031698
209. Wolters H. Anders N. Geldner N. Gavidia R. Jürgens G. Coordination of apical and basal embryo development revealed by tissue-specific GNOM functions Development 2011 138 117 126 10.1242/dev.059147 21138974
210. Ren H. Gray W.M. SAUR Proteins as Effectors of Hormonal and Environmental Signals in Plant Growth Mol. Plant 2015 8 1153 10.1016/j.molp.2015.05.003 25983207
211. Chae K. Isaacs C.G. Reeves P.H. Maloney G.S. Muday G.K. Nagpal P. Reed J.W. Arabidopsis SMALL AUXIN UP RNA63 promotes hypocotyl and stamen filament elongation Plant J. 2012 71 684 697 10.1111/j.1365-313X.2012.05024.x 22507274
212. Spartz A.K. Ren H. Park M.Y. Grandt K.N. Lee S.H. Murphy A.S. Sussman M.R. Overvoorde P.J. Gray W.M. SAUR Inhibition of PP2C-D Phosphatases Activates Plasma Membrane H+-ATPases to Promote Cell Expansion in Arabidopsis Plant Cell 2014 26 2129 2142 10.1105/tpc.114.126037 24858935
213. Chen D. Richardson T. Chai S. McIntyre C.L. Rae A.L. Xue G.-P. Drought-Up-Regulated TaNAC69-1 is a Transcriptional Repressor of TaSHY2 and TaIAA7, and Enhances Root Length and Biomass in Wheat Plant Cell Physiol. 2016 57 2076 2090 10.1093/pcp/pcw126 27440550
214. Fan M. Bai M.-Y. Kim J.-G. Wang T. Oh E. Chen L. Park C.H. Son S.-H. Kim S.-K. Mudgett M.B. The bHLH transcription factor HBI1 mediates the trade-off between growth and pathogen-associated molecular pattern-triggered immunity in Arabidopsis Plant Cell 2014 26 828 841 10.1105/tpc.113.121111 24550223
215. Benekos K. Kissoudis C. Nianiou-Obeidat I. Labrou N. Madesis P. Kalamaki M. Makris A. Tsaftaris A. Overexpression of a specific soybean GmGSTU4 isoenzyme improves diphenyl ether and chloroacetanilide herbicide tolerance of transgenic tobacco plants J. Biotechnol. 2010 150 195 201 10.1016/j.jbiotec.2010.07.011 20638428
216. Jha Y. Subramanian R.B. Patel S. Combination of endophytic and rhizospheric plant growth promoting rhizobacteria in Oryza sativa shows higher accumulation of osmoprotectant against saline stress Acta Physiol. Plant. 2011 33 797 802 10.1007/s11738-010-0604-9
217. Roxas V.P. Smith R.K. Allen E.R. Allen R.D. Overexpression of glutathione S-transferase/glutathioneperoxidase enhances the growth of transgenic tobacco seedlings during stress Nat. Biotechnol. 1997 15 988 991 10.1038/nbt1097-988 9335051
218. Sharma R. Sahoo A. Devendran R. Jain M. Over-Expression of a Rice Tau Class Glutathione S-Transferase Gene Improves Tolerance to Salinity and Oxidative Stresses in Arabidopsis PLoS ONE 2014 10.1371/journal.pone.0092900 24663444
219. Tiwari V. Patel M.K. Chaturvedi A.K. Mishra A. Jha B. Functional Characterization of the Tau Class Glutathione- S -Transferases Gene (SbGSTU) Promoter of Salicornia brachiata under Salinity and Osmotic Stress PLoS ONE 2016 10.1371/journal.pone.0148494 26885663
220. Diaz-Vivancos P. de Simone A. Kiddle G. Foyer C.H. Glutathione—Linking cell proliferation to oxidative stress Free Radic. Biol. Med. 2015 89 1154 1164 10.1016/j.freeradbiomed.2015.09.023 26546102
221. Foyer C.H. Noctor G. Ascorbate and Glutathione: The Heart of the Redox Hub Plant Physiol. 2011 155 2 18 10.1104/pp.110.167569 21205630
222. Noctor G. Mhamdi A. Chaouch S. Han Y. Neukermans J. Marquez-Garcia B. Queval G. Foyer C.H. Glutathione in plants: An integrated overview Plant Cell Environ. 2012 35 454 484 10.1111/j.1365-3040.2011.02400.x 21777251
223. Passaia G. Queval G. Bai J. Margis-Pinheiro M. Foyer C.H. The effects of redox controls mediated by glutathione peroxidases on root architecture in Arabidopsis thaliana J. Exp. Bot. 2014 65 1403 1413 10.1093/jxb/ert486 24470466
224. Remy E. Cabrito T.R. Baster P. Batista R.A. Teixeira M.C. Friml J. Sa-Correia I. Duque P. A Major Facilitator Superfamily Transporter Plays a Dual Role in Polar Auxin Transport and Drought Stress Tolerance in Arabidopsis Plant Cell 2013 25 901 926 10.1105/tpc.113.110353 23524662
225. Kamimoto Y. Terasaka K. Hamamoto M. Takanashi K. Fukuda S. Shitan N. Sugiyama A. Suzuki H. Shibata D. Wang B. Arabidopsis ABCB21 is a Facultative Auxin Importer/Exporter Regulated by Cytoplasmic Auxin Concentration Plant Cell Physiol. 2012 53 2090 2100 10.1093/pcp/pcs149 23147222
226. Terasaka K. Blakeslee J.J. Titapiwatanakun B. Peer W.A. Bandyopadhyay A. Makam S.N. Lee O.R. Richards E.L. Murphy A.S. Sato F. PGP4, an ATP Binding Cassette P-Glycoprotein, Catalyzes Auxin Transport in Arabidopsis thaliana Roots Plant Cell 2005 17 2922 2939 10.1105/tpc.105.035816 16243904
227. Barbez E. Kubeš M. Rolčík J. Béziat C. Pěnčík A. Wang B. Rosquete M.R. Zhu J. Dobrev P.I. Lee Y. A novel putative auxin carrier family regulates intracellular auxin homeostasis in plants Nature 2012 485 119 122 10.1038/nature11001 22504182
228. Sugawara S. Hishiyama S. Jikumaru Y. Hanada A. Nishimura T. Koshiba T. Zhao Y. Kamiya Y. Kasahara H. Biochemical analyses of indole-3-acetaldoxime-dependent auxin biosynthesis in Arabidopsis Proc. Natl. Acad. Sci. USA 2009 106 5430 5435 10.1073/pnas.0811226106 19279202
229. Zhao Y. Auxin Biosynthesis Arabidopsis Book Am. Soc. Plant Biol. 2014 10.1199/tab.0173 24955076
230. Mellor N. Band L.R. Pěnčík A. Novák O. Rashed A. Holman T. Wilson M.H. Voß U. Bishopp A. King J.R. Dynamic regulation of auxin oxidase and conjugating enzymes AtDAO1 and GH3 modulates auxin homeostasis Proc. Natl. Acad. Sci. USA 2016 113 11022 11027 10.1073/pnas.1604458113 27651495
231. Bou-Torrent J. Salla-Martret M. Brandt R. Musielak T. Palauqui J.-C. Martínez-García J.F. Wenkel S. ATHB4 and HAT3, two class II HD-ZIP transcription factors, control leaf development in Arabidopsis Plant Signal. Behav. 2012 7 1382 1387 10.4161/psb.21824 22918502
232. Hu Y. Xie Q. Chua N.-H. The Arabidopsis Auxin-Inducible Gene ARGOS Controls Lateral Organ Size Plant Cell 2003 15 1951 10.1105/tpc.013557 12953103
233. Shi J. Habben J.E. Archibald R.L. Drummond B.J. Chamberlin M.A. Williams R.W. Lafitte H.R. Weers B.P. Overexpression of ARGOS Genes Modifies Plant Sensitivity to Ethylene, Leading to Improved Drought Tolerance in Both Arabidopsis and Maize Plant Physiol. 2015 169 266 282 10.1104/pp.15.00780 26220950
234. Rawat R. Schwartz J. Jones M.A. Sairanen I. Cheng Y. Andersson C.R. Zhao Y. Ljung K. Harmer S.L. REVEILLE1, a Myb-like transcription factor, integrates the circadian clock and auxin pathways Proc. Natl. Acad. Sci. USA 2009 106 16883 16888 10.1073/pnas.0813035106 19805390
235. Kim H.J. Chiang Y.-H. Kieber J.J. Schaller G.E. SCFKMD controls cytokinin signaling by regulating the degradation of type-B response regulators Proc. Natl. Acad. Sci. USA 2013 110 10028 10.1073/pnas.1300403110 23720308
236. Zhang X. Gou M. Guo C. Yang H. Liu C.-J. Down-Regulation of Kelch Domain-Containing F-Box Protein in Arabidopsis Enhances the Production of (Poly) phenols and Tolerance to Ultraviolet Radiation Plant Physiol. 2015 167 337 10.1104/pp.114.249136 25502410
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