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Ethylene signaling in rice

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  • Special Topic Phytohormone
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Chinese Science Bulletin

Abstract

Ethylene regulates many aspects of growth, development and responses to environmental stresses in plants. Its signaling pathway has been established in model dicotyledonous plant Arabidopsis. However, its roles and signal transduction in monocotyledous rice plant remain largely unknown. In this review, we summarize the current advances in rice ethylene signaling studies and compare these with the results from Arabidopsis and other plants. Most of the components homologous to those in Arabidopsis ethylene signaling pathway have been found in rice, including five ethylene receptors, OsEIN2, OsEIL1, and OsERFs. Rice ethylene receptors are functionally more divergent than that of Arabidopsis. OsEIN2 and OsEIL1 display limited roles in regulation of rice ethylene responses compared with their Arabidopsis orthologs. ERF-like proteins OsERF1 and OsEBP-89 appear to be involved in rice ethylene signaling. However, whether they are activated through OsEIN2 and OsEIL1-mediated pathway needs further studies. Given that rice uses ethylene to control many processes that do not exist in Arabidopsis, it seems that new components or new mechanisms may exist in rice ethylene signaling pathway.

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References

  1. Abeles F B, Morgan P W, Saltveit M E. Ethylene in Plant Biology. San Diego: Academic Press, 1992

    Google Scholar 

  2. Guo H W, Ecker J R. The ethylene signaling pathway: New insights. Curr Opin Plant Biol, 2004, 7: 40–49

    Article  Google Scholar 

  3. Kendrick M D, Chang C. Ethylene signaling: New levels of complexity and regulation. Curr Opin Plant Biol, 2008, 11: 479–485

    Article  Google Scholar 

  4. Resnick J S, Wen Q K, Shockey J A, et al. REVERSION-TO-ETHYLENE SENSITIVITY1, a conserved gene that regulates ethylene receptor function in Arabidopsis. Proc Natl Acad Sci USA, 2006, 103: 7917–7922

    Article  Google Scholar 

  5. Zhou X, Liu Q, Xie F, et al. RTE1 is a Golgi-associated and ETR1-dependent negative regulator of ethylene responses. Plant Physiol, 2007, 145: 75–86

    Article  Google Scholar 

  6. Qiao H, Chang K N, Yazaki J, et al. Interplay between ethylene, ETP1/ETP2 F-box proteins, and 6 degradation of EIN2 triggers ethylene responses in Arabidopsis. Genes Dev, 2009, 23: 512–521

    Article  Google Scholar 

  7. Guo H, Ecker J. Plant responses to ethylene gas are mediated by SCFEBF1/EBF2-dependent proteolysis of EIN3 transcription factor. Cell, 2003, 115: 667–677

    Article  Google Scholar 

  8. Potuschak T, Lechner E, Parmentier Y, et al. EIN3-dependent regulation of plant ethylene hormone signaling by two Arabidopsis F Box proteins: EBF1 and EBF2. Cell, 2003, 115: 679–689

    Article  Google Scholar 

  9. Gagne J M, Smalle J, Gingerich D J, et al. Arabidopsis EIN3-binding F-box1 and 2 from ubiquitin-protein ligases that repress ethylene action and promote growth by directing EIN3 degradation. Proc Natl Acad Sci USA, 2004, 101: 6803–6808

    Article  Google Scholar 

  10. Yoo S, Cho Y, Tena G, et al. Dual control of nuclear EIN3 by bifurcate MAPK cascades in C2H4 signaling. Nature, 2008, 451: 789–795

    Article  Google Scholar 

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

    Article  Google Scholar 

  12. Itoh J, Nonomura K, Ikeda K. Rice plant development: From zygote to spikelet. Plant Cell Physiol, 2005, 46: 23–47

    Article  Google Scholar 

  13. Fukao T, Bailey-Serres J. Ethylene-A key regulator of submergence responses in rice. Plant Sci, 2008, 175: 43–51

    Article  Google Scholar 

  14. Jackson M B. Ethylene-promoted elongation: An adaptation to submergence stress. Ann Bot, 2008, 101: 229–248

    Article  Google Scholar 

  15. Shiono K, Takahashi H, Colmer T D, et al. Role of ethylene in acclimations to promote oxygen transport in roots of plant in waterlogged soils. Plant Sci, 2008, 175: 52–58

    Article  Google Scholar 

  16. Magneschi L, Perata P. Rice germination and seedling growth in the absence of oxygen. Ann Bot, 2009, 103: 181–196

    Article  Google Scholar 

  17. Rzewuski G, Sauter M. Ethylene biosynthesis and signaling in rice. Plant Sci, 2008, 175: 32–42

    Article  Google Scholar 

  18. Jackson M B. Ethylene and responses of plants to soil waterlogging and submergence. Annu Rev Plant Physiol, 1985, 36: 145–174

    Article  Google Scholar 

  19. Kende H, Van der Knaap E, Cho H T. Deepwater rice: A model plant to study stem elongation. Plant Physiol, 1998, 118: 1105–1110

    Article  Google Scholar 

  20. Ku H S, Suge H, Rappaport L, et al. Stimulation of rice coleoptile growth by ethylene. Planta, 1970, 90: 333–339

    Article  Google Scholar 

  21. Satler S O, Kende H. Ethylene and the growth of rice seedling. Plant Physiol, 1985, 79: 194–198

    Article  Google Scholar 

  22. Raskin I, Kende H. Regulation of growth in rice seedling. J Plant Growth Regul, 1983, 2: 193–203

    Article  Google Scholar 

  23. Ishizawa K, Esashi Y. Action mechanism of ethylene in the control of sugar translocation in relation to rice coleoptile growth. I. Sucrose metabolism. Plant Cell Environ, 1988, 29: 131–141

    Google Scholar 

  24. Lee T M, Lin Y H. Peroxidase activity in relation to ethylene-induced rice (Oryza sativa L.) coleoptile elongation. Bot Bull Acad Sin, 1996, 37: 239–245

    Google Scholar 

  25. Ismail A M, Ella E S, Vergara G V, et al. Mechanisms associated with tolerance to flooding during germination and early seedling growth in rice (Oryza sativa). Ann Bot, 2009, 103: 197–209

    Article  Google Scholar 

  26. Metraux J P, Kende H. The role of ethylene in the growth response of submerged deep water rice. Plant Physiol, 1983, 72: 441–446

    Article  Google Scholar 

  27. Raskin I, Kende H. Regulation of growth in stem sections of deep-water rice. Planta, 1984, 160: 66–72

    Article  Google Scholar 

  28. van der Straeten, Zhou Z, Prinsen E, et al. A comparative molecular-physiological study of submergence response in lowland and deepwater rice, Plant Physiol, 2001, 125: 955–968

    Article  Google Scholar 

  29. Yang S H, Choi D. Characterization of genes encoding ABA 8′-hydroxylase in ethylene-induced stem growth of deepwater rice (Oryza sativa L.). Biochem Biophys Res Commun, 2006, 350: 685–690

    Article  Google Scholar 

  30. Lorbiecke R, Sauter M. Adventitious root growth and cell-cycle induction in deepwater rice. Plant Physiol, 1999, 119: 21–29

    Article  Google Scholar 

  31. Steffens B, Sauter M. Epidermal cell death in rice (Oryza sativa L.) is regulated by ethylene, gibberellin and abscisic acid. Plant Physiol, 2005, 139: 713–721

    Article  Google Scholar 

  32. Mergemann H, Sauter M. Ethylene induces epidermal cell death at the site of adventitious root emergence in rice. Plant Physiol, 2000, 124: 609–614

    Article  Google Scholar 

  33. Steffens B, Sauter M. Epidermal cell death in rice is confined to cells with a distinct molecular identity and is mediated by ethylene and H2O2 through an autoamplified signal pathway. Plant Cell, 2009, 21: 184–196

    Article  Google Scholar 

  34. Evans D E. Aerenchyma formation. New Phytol, 2003, 161: 35–49

    Article  Google Scholar 

  35. Justin S H F W, Armstrong W. Evidence for the involvement of ethene in aerenchyma formation in adventitious roots of rice (Oryza sativa L.). New Phytol, 1991, 118: 49–62

    Article  Google Scholar 

  36. Colmer T D, Cox M C H, Voesenek L A C J B. Root aeration in rice (Oryza sativa): Evaluation of oxygen, carbon dioxide, and ethylene as possible regulators of root acclimatizations. New Phytol, 2006, 170: 767–778

    Article  Google Scholar 

  37. Kong Y, Wang Z, Gu Y J, et al. Induction of ethephon on aerenchyma formation in rice roots. Rice Sci, 2009, 23: 65–70

    Google Scholar 

  38. Kawai M, Samarajeewa P K, Barrero R A, et al. Cellular dissection of the degradation pattern of cortical cell death during aerenchyma formation of rice roots. Planta, 1998, 204: 277–287

    Article  Google Scholar 

  39. Drew M C, He C J, Morgan P W. Programmed cell death and aerenchyma formation in roots. Trends Plant Sci, 2000, 5: 123–127

    Article  Google Scholar 

  40. Gianinetti A, Laarhoven L J J, Persijn S T, et al. Ethylene production is associated with germination but not seed dormancy in red rice. Ann Bot, 2007, 99: 735–745

    Article  Google Scholar 

  41. Yang J C, Zhang J H, Wang Z Q, et al. Post-anthesis development of inferior and superior spikelets in rice in relation to abscisic acid and ethylene. J Exp Bot, 2006, 57: 149–160

    Article  Google Scholar 

  42. Kao C H, Yang S F. Role of ethylene in the senescence of detached rice leaves. Plant Physiol, 1983, 73: 881–885

    Article  Google Scholar 

  43. Klassen S P, Bugbee B. Sensitivity of wheat and rice to low levels of atmospheric ethylene. Crop Sci, 2000, 42: 746–753

    Article  Google Scholar 

  44. Bleecker A B, Esch J J, Hall A E, et al. The ethylene-receptor family from Arabidopsis: Structure and function. Philos Trans R Soc Lond B Biol Sci, 1998, 353: 1405–1412

    Article  Google Scholar 

  45. Schaller G E, Bleecker A B. Ethylene-binding sites generated in yeast expressing the Arabidopsis ETR1 gene. Science, 1995, 270: 1809–1811

    Article  Google Scholar 

  46. O’Malley R C, Rodriguez F I, Esch J J, et al. Ethylene-binding activity, gene expression levels, and receptor system output for ethylene receptor family members from Arabidopsis and tomato. Plant J, 2005, 41: 651–665

    Article  Google Scholar 

  47. Wang W Y, Esch J J, Shiu S H, et al. Identification of important regions for ethylene binding and signaling in the transmembrane domain of the ETR1 ethylene receptor of Arabidopsis. Plant Cell, 2006, 18: 3429–3442

    Article  Google Scholar 

  48. Gamble R L, Coonfield M L, Schaller G E. Histidine kinase activity of the ETR1 ethylene receptor from Arabidopsis. Proc Natl Acad Sci USA, 1998, 95: 7825–7829

    Article  Google Scholar 

  49. Moussatche P, Klee H J. Autophosphorylation activity of the Arabidopsis ethylene receptor multigene family. J Biol Chem, 2004, 279: 48734–48741

    Article  Google Scholar 

  50. Xie C, Zhang J S, Zhou H L, et al. Serine/threonine kinase activity in the putative histidine kinase-like ethylene receptor NTHK1 from tobacco. Plant J, 2003, 33: 385–393

    Article  Google Scholar 

  51. Zhang Z G, Zhou H L, Chen T, et al. Evidence for serine/threonine and hsitidine kinase activity in the tobacco ethylene receptor protein NTHK2. Plant Physiol, 2004, 136: 2971–2981

    Article  Google Scholar 

  52. Chen Y F, Randlett M D, Findell J L, et al. Localization of the ethylene receptor ETR1 to the endoplasmic reticulum of Arabidopsis. J Biol Chem, 2002, 277: 19861–19866

    Article  Google Scholar 

  53. Ma B, Cui M L, Sun H J, et al. Subcellular localization and membrane topology of the melon ethylene receptor CmERS1. Plant Physiol, 2006, 141: 587–597

    Article  Google Scholar 

  54. Grefen C, Städele K, Ruzicka K, et al. Subcellular localization and in vivo interactions of the Arabidopsis thaliana ethylene receptor family members. Mol Plant, 2007, 1: 308–320

    Article  Google Scholar 

  55. Dong C H, Rivarola M, Resnick J S, et al. Subcellular co-localization of Arabidopsis RTE1 and ETR1 supports a regulatory role for RTE1 in ETR1 ethylene signaling. Plant J, 2008, 53: 275–286

    Article  Google Scholar 

  56. Gao Z Y, We C Q, Binder B M, et al. Heteromeric interactions among ethylene receptors mediate signaling in Arabidopsis. J Biol Chem, 2008, 283: 23801–23810

    Article  Google Scholar 

  57. Cao W H, Dong Y, Zhang J S, et al. Characterization of an ethylene receptor homolog gene from rice. Sci China Ser C: Life Sci, 2003, 46: 370–378

    Article  Google Scholar 

  58. Watanabe H, Saigusa M, Hase S, et al. Cloning of a cDNA encoding an ETR2-like protein (Os-ERL1) from deep water rice (Oryza sativa L.) and increase in its mRNA level by submergence, ethylene, and gibberellin treatments. J Exp Bot, 2004, 55: 1145–1148

    Article  Google Scholar 

  59. Yau C P, Wang L, Yu M, et al. Differential expression of three genes encoding an ethylene receptor in rice during development, and in response to indole-3-acetic acid and silver ions. J Exp Bot, 2004, 55: 547–556

    Article  Google Scholar 

  60. Ma Q H, Wang X M. Characterization of an ethylene receptor homologue from wheat and its expression during leaf senescence. J Exp Bot, 2003, 54: 1489–1490

    Article  Google Scholar 

  61. Gallie D R, Young T E. The ethylene biosynthetic and perception machinery is differentially expressed during endosperm and embryo development in maize. Mol Genet Genomics, 2004, 271: 267–281

    Article  Google Scholar 

  62. Wuriyanghan H, Zhang B, Cao W H, et al. The Ethylene receptor ETR2 delays floral transition and affects starch accumulation in rice. Plant Cell, 2009, 21: 1473–1494

    Article  Google Scholar 

  63. Chen T, Liu J, Lei G, et al. Effects of tobacco ethylene receptor mutations on receptor kinase activity, plant growth and stress responses. Plant Cell Physiol, 2009, 50: 1636–1650

    Article  Google Scholar 

  64. Cancel J D, Larsen P B. Loss-of-function mutations in the ethylene receptor ETR1 cause enhanced sensitivity and exaggerated response to ethylene in Arabidopsis. Plant Physiol, 2002, 129: 1557–1567

    Article  Google Scholar 

  65. Kieber J J, Rothenberg M, Roman G, et al. CTR1, a negative regulator of the ethylene response pathway in Arabidopsis, encodes a member of the Raf family of protein kinases. Cell, 1993, 72: 427–441

    Article  Google Scholar 

  66. Clark K L, Larsen P B, Wang X, et al. Association of the Arabidopsis CTR1 Raf-like kinase with the ETR1 and ERS1 ethylene receptors. Proc Natl Acad Sci USA, 1998, 95: 5401–5406

    Article  Google Scholar 

  67. Gao Z Y, Chen Y F, Randlett M D, et al. Localization of the Raf-like kinase CTR1 to the endoplasmic reticulum of Arabidopsis through participation in ethylene receptor signaling complex. J Biol Chem, 2003, 278: 34725–34732

    Article  Google Scholar 

  68. Zhong S L, Lin Z F, Grierson D. Tomato ethylene receptor-CTR interactions: Visualization of NEVER-RIPE interactions with multiple CTRs at the endoplasmic reticulum. J Exp Bot, 2008, 59: 965–972

    Article  Google Scholar 

  69. Huang Y F, Li H, Hutchison C E, et al. Biochemical and functional analysis of CTR1, a protein kinase that negatively regulates ethylene signaling in Arabidopsis. Plant J, 2003, 33: 221–233

    Article  Google Scholar 

  70. Adams-Phillips L, Barry C, Kannan P, et al. Evidence that CTR1-mediated ethylene signal transduction in tomato is encoded by a multigene family whose members display distinct regulatory features. Plant Mol Biol, 2004, 54: 387–404

    Article  Google Scholar 

  71. Alonso J M, Hirayama T, Roman G, et al. EIN2, a bifunctional transducer of ethylene and stress responses in Arabidopsis. Science, 1999, 284: 2148–2152

    Article  Google Scholar 

  72. Thomine S, Wang R, Ward J M, et al. Cadmium and iron transport by members of a plant metal transporter family in Arabidopsis with homology to Nramp genes. Proc Natl Acad Sci USA, 2000, 97: 4991–4996

    Article  Google Scholar 

  73. Shibuya K, Barry K G, Ciardi J A, et al. The central role of PhEIN2 in ethylene responses throughout plant development in Petunia1. Plant Physiol, 2004, 136: 2900–2912

    Article  Google Scholar 

  74. Varma Penmetsa R, Uribe P, Anderson J, et al. The Medicago truncatula ortholog of Arabidopsis EIN2, sickle, is a negative regulator of symbiotic and pathogenic microbial associations. Plant J, 2008, 55: 580–595

    Article  Google Scholar 

  75. Jun S H, Han M J, Lee S, et al. OsEIN2 is a positive component in ethylene signaling in rice. Plant Cell Physiol, 2004, 45: 281–285

    Article  Google Scholar 

  76. Guzman P, Ecker J R. Exploiting the triple response of Arabidopsis to identify ethylene-related mutants. Plant Cell, 1990, 2: 513–523

    Article  Google Scholar 

  77. Chao Q, Rothenberg M, Solano R, et al. Activation of the ethylene gas response pathway in Arabidopsis by the nuclear protein ETHYLENE-INSENSITIVE3 and related proteins. Cell, 1997, 89: 1133–1144

    Article  Google Scholar 

  78. Solano R, Stepanova A, Chao Q, et al. Nuclear events in ethylene signaling: A transcriptional cascade mediated by ETHYLENE-INSENSITIVE3 and ETHYLENERESPONSE-FACTOR1. Genes Dev, 1998, 12: 3703–3714

    Article  Google Scholar 

  79. Mao C, Wang S, Jia Q, et al. OsEIL1, a rice homolog of the Arabidopsis EIN3 regulates the ethylene response as a positive component. Plant Mol Biol, 2006, 61: 141–152

    Article  Google Scholar 

  80. Yang H J, Shen H, Chen L, et al. The OsEBP-89 gene of rice encodes a putative EREBP transcription factor and is temporally expressed in developing endosperm and intercalary meristem. Plant Mol Biol, 2002, 50: 379–391

    Article  Google Scholar 

  81. Hu Y B, Zhao L F, Chong K, et al. Overexpression of OsERF1, a novel rice ERF gene, up-regulates ethylene-responsive genes expression besides affects growth and development in Arabidopsis. J Plant Physiol, 2008, 165: 1717–1725

    Article  Google Scholar 

  82. Hattori Y, Miura K, Asano K, et al. A major QTL confers rapid internode elongation in response to water rise in deepwater rice. Breeding Sci, 2007, 57: 305–314

    Article  Google Scholar 

  83. Hattori Y, Nagai K, Mori H, et al. Mapping of three QTLs that regulate internode elongation in deepwater rice. Breeding Sci, 2008, 58: 38–44

    Article  Google Scholar 

  84. Hattori Y, Nagai K, Furukawa S, et al. The ethylene response factors Snorkel1 and Snorkel2 allow rice to adapt to deep water. Nature, 2009, 460: 1025–1030

    Article  Google Scholar 

  85. Xu K, Xu X, Fukao T, et al. Sub1A is an ethylene-response-factor-like gene that confers submergence tolerance to rice. Nature, 2006, 442: 705–708

    Article  Google Scholar 

  86. Fukao T, Xu K, Ronald P C, et al. A variable cluster of ethylene response factor-like genes regulates metabolic and developmental acclimation responses to submergence in rice. Plant Cell, 2006, 18: 2021–2034

    Article  Google Scholar 

  87. Dong H, Rivarola M, Resnick J S, et al. Subcellular co-localization of Arabidopsis RTE1 and ETR1 supports a regulatory role of RTE1 in ETR1 ethylene signaling. Plant J, 2008, 53: 275–286

    Article  Google Scholar 

  88. Olmedo G, Guo H, Gregory B, et al. ETHYLENE-INSENSITIVE5 encodes a 5′→3′ exoribonuclease required for regulation of the EIN3-targeting F-box proteins EBF1/2. Proc Natl Acad Sci USA, 2006, 103: 13286–13293

    Article  Google Scholar 

  89. Potuschak T, Vansiri A, Binder B, et al. The exoribonuclease XRN4 is a component of the ethylene response pathway in Arabidopsis. Plant Cell, 2006, 18: 3047–3057

    Article  Google Scholar 

  90. Schoof H, Karlowski W M. Comparison of rice and Arabidopsis annotation. Curr Opin Plant Biol, 2003, 3: 106–112

    Article  Google Scholar 

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Correspondence to JinSong Zhang.

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Ma, B., Chen, S. & Zhang, J. Ethylene signaling in rice. Chin. Sci. Bull. 55, 2204–2210 (2010). https://doi.org/10.1007/s11434-010-3192-2

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