Circadian Network Interactions with Jasmonate Signaling and Defense
Abstract
:1. The Importance of Circadian Rhythms
2. Plant Clock Mechanics: Genes and Proteins
3. Clock Phasing of JA Biosynthesis and Defense
4. JA Gene Suites Are Phased and Gated for Appropriate Time-of-Day Responses
5. Core Clock Transcription Factors Directly Regulate JA Genes
6. The COI1-JAZ-MYC Core JA Signaling Module Is a Target for Gating and Phasing
7. The Clock Gates JA Signaling by TIC-Mediated Changes in MYC2 Protein Abundance
8. The Clock Acts through JAZ Repressors to Control JA Signaling
9. Perspectives
Author Contributions
Funding
Acknowledgments
Conflicts of Interest
References
- Troein, C.; Locke, J.C.W.; Turner, M.S.; Millar, A.J. Weather and Seasons Together Demand Complex Biological Clocks. Curr. Biol. 2009, 19, 1961–1964. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Dodd, A.N.; Salathia, N.; Hall, A.; Kévei, E.; Tóth, R.; Nagy, F.; Hibberd, J.M.; Millar, A.J.; Webb, A.A.R. Plant circadian clocks increase photosynthesis, growth, survival, and competitive advantage. Science 2005, 309, 630–633. [Google Scholar] [CrossRef] [PubMed]
- Covington, M.F.; Harmer, S.L. The Circadian Clock Regulates Auxin Signaling and Responses in Arabidopsis. PLoS Biol. 2007, 5, e222. [Google Scholar] [CrossRef] [PubMed]
- Covington, M.F.; Maloof, J.N.; Straume, M.; Kay, S.A.; Harmer, S.L. Global transcriptome analysis reveals circadian regulation of key pathways in plant growth and development. Genome Biol. 2008, 9, R130. [Google Scholar] [CrossRef] [PubMed]
- Mizuno, T.; Yamashino, T. Comparative Transcriptome of Diurnally Oscillating Genes and Hormone-Responsive Genes in Arabidopsis thaliana: Insight into Circadian Clock-Controlled Daily Responses to Common Ambient Stresses in Plants. Plant Cell Physiol. 2008, 49, 481–487. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Dunlap, J.C. Molecular Bases for Circadian Clocks. Cell 1999, 96, 271–290. [Google Scholar] [CrossRef] [Green Version]
- Harmer, S.L. The circadian system in higher plants. Annu. Rev. Plant Biol. 2009, 60, 357–377. [Google Scholar] [CrossRef] [PubMed]
- Millar, A.J.; Straume, M.; Chory, J.; Chua, N.H.; Kay, S.A. The regulation of circadian period by phototransduction pathways in Arabidopsis. Science 1995, 267, 1163–1166. [Google Scholar] [CrossRef] [PubMed]
- Oakenfull, R.J.; Davis, S.J. Shining a light on the Arabidopsis circadian clock. Plant Cell Environ. 2017, 40, 2571–2585. [Google Scholar] [CrossRef] [Green Version]
- Thines, B.; Harmon, F.G. Ambient temperature response establishes ELF3 as a required component of the core Arabidopsis circadian clock. Proc. Natl. Acad. Sci. USA 2010, 107, 3257–3262. [Google Scholar] [CrossRef]
- Gil, K.E.; Park, C.M. Thermal adaptation and plasticity of the plant circadian clock. New Phytol. 2019, 221, 1215–1229. [Google Scholar] [CrossRef] [PubMed]
- Strayer, C.; Oyama, T.; Schultz, T.F.; Raman, R.; Somers, D.E.; Más, P.; Panda, S.; Kreps, J.A.; Kay, S.A. Cloning of the Arabidopsis clock gene TOC1, an autoregulatory response regulator homolog. Science 2000, 289, 768–771. [Google Scholar] [CrossRef] [PubMed]
- Wang, Z.Y.; Tobin, E.M. Constitutive Expression of the CIRCADIAN CLOCK ASSOCIATED 1 (CCA1) Gene Disrupts Circadian Rhythms and Suppresses Its Own Expression. Cell 1998, 93, 1207–1217. [Google Scholar] [CrossRef] [Green Version]
- Fujiwara, S.; Wang, L.; Han, L.; Suh, S.-S.; Salomé, P.A.; McClung, C.R.; Somers, D.E. Post-translational Regulation of the Arabidopsis Circadian Clock through Selective Proteolysis and Phosphorylation of Pseudo-response Regulator Proteins. J. Biol. Chem. 2008, 283, 23073–23083. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Más, P.; Kim, W.Y.; Somers, D.E.; Kay, S.A. Targeted degradation of TOC1 by ZTL modulates circadian function in Arabidopsis thaliana. Nature 2003, 426, 567–570. [Google Scholar] [CrossRef] [PubMed]
- Lee, C.M.; Feke, A.; Li, M.W.; Adamchek, C.; Webb, K.; Pruneda-Paz, J.; Bennett, E.J.; Kay, S.A.; Gendron, J.M. Decoys Untangle Complicated Redundancy and Reveal Targets of Circadian Clock F-Box Proteins. Plant Physiol. 2018, 177, 1170–1186. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Lu, S.X.; Knowles, S.M.; Andronis, C.; Ong, M.S.; Tobin, E.M. CIRCADIAN CLOCK ASSOCIATED1 and LATE ELONGATED HYPOCOTYL Function Synergistically in the Circadian Clock of Arabidopsis. Plant Physiol. 2009, 150, 834–843. [Google Scholar] [CrossRef] [Green Version]
- Harmer, S.L.; Hogenesch, J.B.; Straume, M.; Chang, H.S.; Han, B.; Zhu, T.; Wang, X.; Kreps, J.A.; Kay, S.A. Orchestrated transcription of key pathways in Arabidopsis by the circadian clock. Science 2000, 290, 2110–2113. [Google Scholar] [CrossRef]
- Nagel, D.H.; Doherty, C.J.; Pruneda-Paz, J.L.; Schmitz, R.J.; Ecker, J.R.; Kay, S.A. Genome-wide identification of CCA1 targets uncovers an expanded clock network in Arabidopsis. Proc. Natl. Acad. Sci. USA 2015, 112, E4802–E4810. [Google Scholar] [CrossRef]
- Gendron, J.M.; Pruneda-Paz, J.L.; Doherty, C.J.; Gross, A.M.; Kang, S.E.; Kay, S.A. Arabidopsis circadian clock protein, TOC1, is a DNA-binding transcription factor. Proc. Natl. Acad. Sci. USA 2012, 109, 3167–3172. [Google Scholar] [CrossRef]
- Pruneda-Paz, J.L.; Breton, G.; Para, A.; Kay, S.A. A functional genomics approach reveals CHE as a component of the Arabidopsis circadian clock. Science 2009, 323, 1481–1485. [Google Scholar] [CrossRef] [PubMed]
- Nakamichi, N.; Kiba, T.; Henriques, R.; Mizuno, T.; Chua, N.-H.; Sakakibara, H. PSEUDO-RESPONSE REGULATORS 9, 7, and 5 Are Transcriptional Repressors in the Arabidopsis Circadian Clock. Plant Cell 2010, 22, 594–605. [Google Scholar] [CrossRef] [PubMed]
- Adams, S.; Manfield, I.; Stockley, P.; Carré, I.A. Revised Morning Loops of the Arabidopsis Circadian Clock Based on Analyses of Direct Regulatory Interactions. PLoS ONE 2015, 10, e0143943. [Google Scholar] [CrossRef] [PubMed]
- Hicks, K.A.; Albertson, T.M.; Wagner, D.R. EARLY FLOWERING3 Encodes a Novel Protein That Regulates Circadian Clock Function and Flowering in Arabidopsis. Plant Cell 2001, 13, 1281–1292. [Google Scholar] [CrossRef] [PubMed]
- Doyle, M.R.; Davis, S.J.; Bastow, R.M.; McWatters, H.G.; Kozma-Bognár, L.; Nagy, F.; Millar, A.J.; Amasino, R.M. The ELF4 gene controls circadian rhythms and flowering time in Arabidopsis thaliana. Nature 2002, 419, 74. [Google Scholar] [CrossRef]
- Helfer, A.; Nusinow, D.A.; Chow, B.Y.; Gehrke, A.R.; Bulyk, M.L.; Kay, S.A. LUX ARRHYTHMO Encodes a Night Time Repressor of Circadian Gene Expression in the Arabidopsis Core Clock. Curr. Biol. CB 2011, 21, 126–133. [Google Scholar] [CrossRef]
- Nusinow, D.A.; Helfer, A.; Hamilton, E.E.; King, J.J.; Imaizumi, T.; Schultz, T.F.; Farré, E.M.; Kay, S.A. The ELF4-ELF3-LUX Complex Links the Circadian Clock to Diurnal Control of Hypocotyl Growth. Nature 2011, 475, 398–402. [Google Scholar] [CrossRef]
- Zhang, C.; Gao, M.; Seitz, N.C.; Angel, W.; Hallworth, A.; Wiratan, L.; Darwish, O.; Alkharouf, N.; Dawit, T.; Lin, D.; et al. LUX ARRHYTHMO mediates crosstalk between the circadian clock and defense in Arabidopsis. Nat. Commun. 2019, 10, 2543. [Google Scholar] [CrossRef]
- Mizuno, T.; Nomoto, Y.; Oka, H.; Kitayama, M.; Takeuchi, A.; Tsubouchi, M.; Yamashino, T. Ambient Temperature Signal Feeds into the Circadian Clock Transcriptional Circuitry Through the EC Night-Time Repressor in Arabidopsis thaliana. Plant Cell Physiol. 2014, 55, 958–976. [Google Scholar] [CrossRef] [Green Version]
- Dixon, L.E.; Knox, K.; Kozma-Bognar, L.; Southern, M.M.; Pokhilko, A.; Millar, A.J. Temporal repression of core circadian genes is mediated through EARLY FLOWERING 3 in Arabidopsis. Curr. Biol. CB 2011, 21, 120–125. [Google Scholar] [CrossRef]
- Kiba, T.; Henriques, R.; Sakakibara, H.; Chua, N.-H. Targeted degradation of PSEUDO-RESPONSE REGULATOR5 by an SCFZTL complex regulates clock function and photomorphogenesis in Arabidopsis thaliana. Plant Cell 2007, 19, 2516–2530. [Google Scholar] [CrossRef] [PubMed]
- Kim, W.-Y.; Fujiwara, S.; Suh, S.-S.; Kim, J.; Kim, Y.; Han, L.; David, K.; Putterill, J.; Nam, H.G.; Somers, D.E. ZEITLUPE is a circadian photoreceptor stabilized by GIGANTEA in blue light. Nature 2007, 449, 356–360. [Google Scholar] [CrossRef] [PubMed]
- Baudry, A.; Ito, S.; Song, Y.H.; Strait, A.A.; Kiba, T.; Lu, S.; Henriques, R.; Pruneda-Paz, J.L.; Chua, N.-H.; Tobin, E.M.; et al. F-box proteins FKF1 and LKP2 act in concert with ZEITLUPE to control Arabidopsis clock progression. Plant Cell 2010, 22, 606–622. [Google Scholar] [CrossRef] [PubMed]
- Hall, A.; Bastow, R.M.; Davis, S.J.; Hanano, S.; McWatters, H.G.; Hibberd, V.; Doyle, M.R.; Sung, S.; Halliday, K.J.; Amasino, R.M.; et al. The TIME FOR COFFEE Gene Maintains the Amplitude and Timing of Arabidopsis Circadian Clocks. Plant Cell 2003, 15, 2719–2729. [Google Scholar] [CrossRef] [PubMed]
- Ding, Z.; Millar, A.J.; Davis, A.M.; Davis, S.J. TIME FOR COFFEE Encodes a Nuclear Regulator in the Arabidopsis thaliana Circadian Clock. Plant Cell 2007, 19, 1522–1536. [Google Scholar] [CrossRef] [PubMed]
- Wu, J.F.; Tsai, H.L.; Joanito, I.; Wu, Y.C.; Chang, C.W.; Li, Y.H.; Wang, Y.; Hong, J.C.; Chu, J.W.; Hsu, C.P.; et al. LWD–TCP complex activates the morning gene CCA1 in Arabidopsis. Nat. Commun. 2016, 7, 13181. [Google Scholar] [CrossRef] [PubMed]
- Xie, Q.; Wang, P.; Liu, X.; Yuan, L.; Wang, L.; Zhang, C.; Li, Y.; Xing, H.; Zhi, L.; Yue, Z.; et al. LNK1 and LNK2 Are Transcriptional Coactivators in the Arabidopsis Circadian Oscillator. Plant Cell 2014, 26, 2843–2857. [Google Scholar] [CrossRef]
- Rawat, R.; Takahashi, N.; Hsu, P.Y.; Jones, M.A.; Schwartz, J.; Salemi, M.R.; Phinney, B.S.; Harmer, S.L. REVEILLE8 and PSEUDO-REPONSE REGULATOR5 Form a Negative Feedback Loop within the Arabidopsis Circadian Clock. PLoS Genet. 2011, 7, e1001350. [Google Scholar] [CrossRef]
- Mateos, J.L.; De Leone, M.J.; Torchio, J.; Reichel, M.; Staiger, D. Beyond Transcription: Fine-Tuning of Circadian Timekeeping by Post-Transcriptional Regulation. Genes 2018, 9, 616. [Google Scholar] [CrossRef]
- Seo, P.J.; Mas, P. Multiple layers of posttranslational regulation refine circadian clock activity in Arabidopsis. Plant Cell 2014, 26, 79–87. [Google Scholar] [CrossRef]
- Farmer, E.E.; Ryan, C.A. Octadecanoid Precursors of Jasmonic Acid Activate the Synthesis of Wound-Inducible Proteinase Inhibitors. Plant Cell 1992, 4, 129–134. [Google Scholar] [CrossRef]
- Wasternack, C.; Hause, B. Jasmonates: Biosynthesis, perception, signal transduction and action in plant stress response, growth and development. An update to the 2007 review in Annals of Botany. Ann. Bot. 2013, 111, 1021–1058. [Google Scholar] [CrossRef]
- McConn, M.; Browse, J. The Critical Requirement for Linolenic Acid Is Pollen Development, Not Photosynthesis, in an Arabidopsis Mutant. Plant Cell 1996, 8, 403–416. [Google Scholar] [CrossRef]
- Li, L.; Li, C.; Howe, G.A. Genetic Analysis of Wound Signaling in Tomato. Evidence for a Dual Role of Jasmonic Acid in Defense and Female Fertility. Plant Physiol. 2001, 127, 1414–1417. [Google Scholar] [CrossRef]
- Goodspeed, D.; Chehab, E.W.; Min-Venditti, A.; Braam, J.; Covington, M.F. Arabidopsis synchronizes jasmonate-mediated defense with insect circadian behavior. Proc. Natl. Acad. Sci. USA 2012, 109, 4674–4677. [Google Scholar] [CrossRef]
- Goodspeed, D.; Chehab, E.W.; Covington, M.F.; Braam, J. Circadian control of jasmonates and salicylates. Plant Signal. Behav. 2013, 8, e23123. [Google Scholar] [CrossRef]
- Wang, W.; Barnaby, J.Y.; Tada, Y.; Li, H.; Tör, M.; Caldelari, D.; Lee, D.; Fu, X.D.; Dong, X. Timing of plant immune responses by a central circadian regulator. Nature 2011, 470, 110–114. [Google Scholar] [CrossRef]
- Staswick, P.E.; Tiryaki, I.; Rowe, M.L. Jasmonate Response Locus JAR1 and Several Related Arabidopsis Genes Encode Enzymes of the Firefly Luciferase Superfamily That Show Activity on Jasmonic, Salicylic, and Indole-3-Acetic Acids in an Assay for Adenylation. Plant Cell 2002, 14, 1405–1415. [Google Scholar] [CrossRef]
- Park, J.H.; Halitschke, R.; Kim, H.B.; Baldwin, I.T.; Feldmann, K.A.; Feyereisen, R. A knock-out mutation in allene oxide synthase results in male sterility and defective wound signal transduction in Arabidopsis due to a block in jasmonic acid biosynthesis. Plant J. 2002, 31, 1–12. [Google Scholar] [CrossRef]
- Suza, W.P.; Staswick, P.E. The role of JAR1 in Jasmonoyl-l-isoleucine production during Arabidopsis wound response. Planta 2008, 227, 1221–1232. [Google Scholar] [CrossRef]
- Zheng, X.Y.; Spivey, N.W.; Zeng, W.; Liu, P.P.; Fu, Z.Q.; Klessig, D.F.; He, S.Y.; Dong, X. Coronatine promotes Pseudomonas syringae virulence in plants by activating a signaling cascade that inhibits salicylic acid accumulation. Cell Host Microbe 2012, 11, 587–596. [Google Scholar] [CrossRef]
- Huang, H.; Liu, B.; Liu, L.; Song, S. Jasmonate action in plant growth and development. J. Exp. Bot. 2017, 68, 1349–1359. [Google Scholar] [CrossRef] [Green Version]
- Havko, N.E.; Major, I.T.; Jewell, J.B.; Attaran, E.; Browse, J.; Howe, G.A. Control of Carbon Assimilation and Partitioning by Jasmonate: An Accounting of Growth–Defense Tradeoffs. Plants 2016, 5, 7. [Google Scholar] [CrossRef]
- Yamashino, T.; Kitayama, M.; Mizuno, T. Transcription of ST2A Encoding A Sulfotransferase Family Protein That Is Involved in Jasmonic Acid Metabolism Is Controlled According to the Circadian Clock- and PIF4/PIF5-Mediated External Coincidence Mechanism in Arabidopsis thaliana. Biosci. Biotechnol. Biochem. 2013, 77, 2454–2460. [Google Scholar] [CrossRef]
- Zheng, X.Y.; Zhou, M.; Yoo, H.; Pruneda-Paz, J.L.; Spivey, N.W.; Kay, S.A.; Dong, X. Spatial and temporal regulation of biosynthesis of the plant immune signal salicylic acid. Proc. Natl. Acad. Sci. USA 2015, 112, 9166–9173. [Google Scholar] [CrossRef] [Green Version]
- Van der Does, D.; Leon-Reyes, A.; Koornneef, A.; Van Verk, M.C.; Rodenburg, N.; Pauwels, L.; Goossens, A.; Körbes, A.P.; Memelink, J.; Ritsema, T.; et al. Salicylic acid suppresses jasmonic acid signaling downstream of SCFCOI1-JAZ by targeting GCC promoter motifs via transcription factor ORA59. Plant Cell 2013, 25, 744–761. [Google Scholar] [CrossRef]
- Fowler, S.G.; Cook, D.; Thomashow, M.F. Low Temperature Induction of Arabidopsis CBF1, 2, and 3 Is Gated by the Circadian Clock. Plant Physiol. 2005, 137, 961–968. [Google Scholar] [CrossRef]
- Ingle, R.A.; Stoker, C.; Stone, W.; Adams, N.; Smith, R.; Grant, M.; Carré, I.; Roden, L.C.; Denby, K.J. Jasmonate signalling drives time-of-day differences in susceptibility of Arabidopsis to the fungal pathogen Botrytis cinerea. Plant J. 2015, 84, 937–948. [Google Scholar] [CrossRef]
- Williamson, B.; Tudzynski, B.; Tudzynski, P.; van Kan, J.A.L. Botrytis cinerea: The cause of grey mould disease. Mol. Plant Pathol. 2007, 8, 561–580. [Google Scholar] [CrossRef]
- Zhang, Y.; Wang, Y.; Wei, H.; Li, N.; Tian, W.; Chong, K.; Wang, L. Circadian Evening Complex Represses Jasmonate-Induced Leaf Senescence in Arabidopsis. Mol. Plant 2018, 11, 326–337. [Google Scholar] [CrossRef] [Green Version]
- Qi, T.; Wang, J.; Huang, H.; Liu, B.; Gao, H.; Liu, Y.; Song, S.; Xie, D. Regulation of Jasmonate-Induced Leaf Senescence by Antagonism between bHLH Subgroup IIIe and IIId Factors in Arabidopsis. Plant Cell 2015, 27, 1634–1649. [Google Scholar] [CrossRef] [Green Version]
- Kim, H.; Kim, Y.; Yeom, M.; Lim, J.; Nam, H.G. Age-associated circadian period changes in Arabidopsis leaves. J. Exp. Bot. 2016, 67, 2665–2673. [Google Scholar] [CrossRef]
- Zentgraf, U.; Doll, J.; Riester, L. Live and Let Die: The Core Circadian Oscillator Coordinates Plant Life History and Pilots Leaf Senescence. Mol. Plant 2018, 11, 351–353. [Google Scholar] [CrossRef]
- Xie, D.X.; Feys, B.F.; James, S.; Nieto-Rostro, M.; Turner, J.G. COI1: An Arabidopsis gene required for jasmonate-regulated defense and fertility. Science 1998, 280, 1091–1094. [Google Scholar] [CrossRef]
- Chini, A.; Fonseca, S.; Fernández, G.; Adie, B.; Chico, J.M.; Lorenzo, O.; García-Casado, G.; López-Vidriero, I.; Lozano, F.M.; Ponce, M.R.; et al. The JAZ family of repressors is the missing link in jasmonate signalling. Nature 2007, 448, 666–671. [Google Scholar] [CrossRef]
- Thines, B.; Katsir, L.; Melotto, M.; Niu, Y.; Mandaokar, A.; Liu, G.; Nomura, K.; He, S.Y.; Howe, G.A.; Browse, J. JAZ repressor proteins are targets of the SCF(COI1) complex during jasmonate signalling. Nature 2007, 448, 661–665. [Google Scholar] [CrossRef]
- Yan, Y.; Stolz, S.; Chételat, A.; Reymond, P.; Pagni, M.; Dubugnon, L.; Farmer, E.E. A Downstream Mediator in the Growth Repression Limb of the Jasmonate Pathway. Plant Cell 2007, 19, 2470–2483. [Google Scholar] [CrossRef] [Green Version]
- Sheard, L.B.; Tan, X.; Mao, H.; Withers, J.; Ben-Nissan, G.; Hinds, T.R.; Kobayashi, Y.; Hsu, F.F.; Sharon, M.; Browse, J.; et al. Jasmonate perception by inositol-phosphate-potentiated COI1-JAZ co-receptor. Nature 2010, 468, 400–405. [Google Scholar] [CrossRef]
- Causier, B.; Ashworth, M.; Guo, W.; Davies, B. The TOPLESS Interactome: A Framework for Gene Repression in Arabidopsis. Plant Physiol. 2012, 158, 423–438. [Google Scholar] [CrossRef]
- Pauwels, L.; Barbero, G.F.; Geerinck, J.; Tilleman, S.; Grunewald, W.; Pérez, A.C.; Chico, J.M.; Bossche, R.V.; Sewell, J.; Gil, E.; et al. NINJA connects the co-repressor TOPLESS to jasmonate signalling. Nature 2010, 464, 788–791. [Google Scholar] [CrossRef] [Green Version]
- Boter, M.; Ruíz-Rivero, O.; Abdeen, A.; Prat, S. Conserved MYC transcription factors play a key role in jasmonate signaling both in tomato and Arabidopsis. Genes Dev. 2004, 18, 1577–1591. [Google Scholar] [CrossRef]
- Fernández-Calvo, P.; Chini, A.; Fernández-Barbero, G.; Chico, J.M.; Gimenez-Ibanez, S.; Geerinck, J.; Eeckhout, D.; Schweizer, F.; Godoy, M.; Franco-Zorrilla, J.M.; et al. The Arabidopsis bHLH Transcription Factors MYC3 and MYC4 Are Targets of JAZ Repressors and Act Additively with MYC2 in the Activation of Jasmonate Responses[C][W]. Plant Cell 2011, 23, 701–715. [Google Scholar] [CrossRef]
- Niu, Y.; Figueroa, P.; Browse, J. Characterization of JAZ-interacting bHLH transcription factors that regulate jasmonate responses in Arabidopsis. J. Exp. Bot. 2011, 62, 2143–2154. [Google Scholar] [CrossRef] [Green Version]
- Figueroa, P.; Browse, J. The Arabidopsis JAZ2 promoter contains a G-Box and thymidine-rich module that are necessary and sufficient for jasmonate-dependent activation by MYC transcription factors and repression by JAZ proteins. Plant Cell Physiol. 2012, 53, 330–343. [Google Scholar] [CrossRef]
- Chico, J.M.; Fernández-Barbero, G.; Chini, A.; Fernández-Calvo, P.; Díez-Díaz, M.; Solano, R. Repression of Jasmonate-Dependent Defenses by Shade Involves Differential Regulation of Protein Stability of MYC Transcription Factors and Their JAZ Repressors in Arabidopsis. Plant Cell 2014, 26, 1967–1980. [Google Scholar] [CrossRef]
- Shin, J.; Heidrich, K.; Sanchez-Villarreal, A.; Parker, J.E.; Davis, S.J. TIME FOR COFFEE Represses Accumulation of the MYC2 Transcription Factor to Provide Time-of-Day Regulation of Jasmonate Signaling in Arabidopsis. Plant Cell 2012, 24, 2470–2482. [Google Scholar] [CrossRef]
- Katsir, L.; Schilmiller, A.L.; Staswick, P.E.; He, S.Y.; Howe, G.A. COI1 is a critical component of a receptor for jasmonate and the bacterial virulence factor coronatine. Proc. Natl. Acad. Sci. USA 2008, 105, 7100–7105. [Google Scholar] [CrossRef] [Green Version]
- Geng, X.; Cheng, J.; Gangadharan, A.; Mackey, D. The Coronatine Toxin of Pseudomonas syringae Is a Multifunctional Suppressor of Arabidopsis Defense. Plant Cell 2012, 24, 4763–4774. [Google Scholar] [CrossRef]
- Bhardwaj, V.; Meier, S.; Petersen, L.N.; Ingle, R.A.; Roden, L.C. Defence Responses of Arabidopsis thaliana to Infection by Pseudomonas syringae Are Regulated by the Circadian Clock. PLoS ONE 2011, 6, e26968. [Google Scholar] [CrossRef]
- Li, R.; Llorca, L.C.; Schuman, M.C.; Wang, Y.; Wang, L.; Joo, Y.; Wang, M.; Vassão, D.G.; Baldwin, I.T. ZEITLUPE in the Roots of Wild Tobacco Regulates Jasmonate-Mediated Nicotine Biosynthesis and Resistance to a Generalist Herbivore. Plant Physiol. 2018, 177, 833–846. [Google Scholar] [CrossRef] [Green Version]
- Li, C.; Teng, W.; Shi, Q.; Zhang, F. Multiple Signals Regulate Nicotine Synthesis in Tobacco Plant. Plant Signal. Behav. 2007, 2, 280–281. [Google Scholar] [CrossRef] [Green Version]
- De Boer, K.; Tilleman, S.; Pauwels, L.; Vanden Bossche, R.; De Sutter, V.; Vanderhaeghen, R.; Hilson, P.; Hamill, J.D.; Goossens, A. APETALA2/ETHYLENE RESPONSE FACTOR and basic helix-loop-helix tobacco transcription factors cooperatively mediate jasmonate-elicited nicotine biosynthesis. Plant J. Cell Mol. Biol. 2011, 66, 1053–1065. [Google Scholar] [CrossRef]
- Yon, F.; Joo, Y.; Cortés Llorca, L.; Rothe, E.; Baldwin, I.T.; Kim, S.G. Silencing Nicotiana attenuata LHY and ZTL alters circadian rhythms in flowers. New Phytol. 2016, 209, 1058–1066. [Google Scholar] [CrossRef]
- Schuman, M.C.; Meldau, S.; Gaquerel, E.; Diezel, C.; McGale, E.; Greenfield, S.; Baldwin, I.T. The Active Jasmonate JA-Ile Regulates a Specific Subset of Plant Jasmonate-Mediated Resistance to Herbivores in Nature. Front. Plant Sci. 2018, 9, 787. [Google Scholar] [CrossRef] [Green Version]
- Bosch, M.; Wright, L.P.; Gershenzon, J.; Wasternack, C.; Hause, B.; Schaller, A.; Stintzi, A. Jasmonic Acid and Its Precursor 12-Oxophytodienoic Acid Control Different Aspects of Constitutive and Induced Herbivore Defenses in Tomato. Plant Physiol. 2014, 166, 396–410. [Google Scholar] [CrossRef] [Green Version]
- Gonzalez, L.E.; Keller, K.; Chan, K.X.; Gessel, M.M.; Thines, B.C. Transcriptome analysis uncovers Arabidopsis F-BOX STRESS INDUCED 1 as a regulator of jasmonic acid and abscisic acid stress gene expression. BMC Genom. 2017, 18, 533. [Google Scholar] [CrossRef]
- Hu, Y.; Jiang, L.; Wang, F.; Yu, D. Jasmonate Regulates the INDUCER OF CBF EXPRESSION–C-REPEAT BINDING FACTOR/DRE BINDING FACTOR1 Cascade and Freezing Tolerance in Arabidopsis. Plant Cell 2013, 25, 2907–2924. [Google Scholar] [CrossRef]
- Nitschke, S.; Cortleven, A.; Iven, T.; Feussner, I.; Havaux, M.; Riefler, M.; Schmülling, T. Circadian Stress Regimes Affect the Circadian Clock and Cause Jasmonic Acid-Dependent Cell Death in Cytokinin-Deficient Arabidopsis Plants. Plant Cell 2016, 28, 1616–1639. [Google Scholar] [CrossRef] [Green Version]
- Sharma, M.; Laxmi, A. Jasmonates: Emerging Players in Controlling Temperature Stress Tolerance. Front. Plant Sci. 2016, 6, 1129. [Google Scholar] [CrossRef]
- Guo, Q.; Yoshida, Y.; Major, I.T.; Wang, K.; Sugimoto, K.; Kapali, G.; Havko, N.E.; Benning, C.; Howe, G.A. JAZ repressors of metabolic defense promote growth and reproductive fitness in Arabidopsis. Proc. Natl. Acad. Sci. USA 2018, 115, E10768–E10777. [Google Scholar] [CrossRef]
- Endo, M.; Shimizu, H.; Nohales, M.A.; Araki, T.; Kay, S.A. Tissue-specific clocks in Arabidopsis show asymmetric coupling. Nature 2014, 515, 419–422. [Google Scholar] [CrossRef] [Green Version]
- Bendix, C.; Marshall, C.M.; Harmon, F.G. Circadian Clock Genes Universally Control Key Agricultural Traits. Mol. Plant 2015, 8, 1135–1152. [Google Scholar] [CrossRef] [Green Version]
- Evans, N.; Baierl, A.; Semenov, M.A.; Gladders, P.; Fitt, B.D.L. Range and severity of a plant disease increased by global warming. J. R. Soc. Interface 2008, 5, 525–531. [Google Scholar] [CrossRef]
- Baker, R.H.A.; Sansford, C.E.; Jarvis, C.H.; Cannon, R.J.C.; MacLeod, A.; Walters, K.F.A. The role of climatic mapping in predicting the potential geographical distribution of non-indigenous pests under current and future climates. Agric. Ecosyst. Environ. 2000, 82, 57–71. [Google Scholar] [CrossRef]
© 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Share and Cite
Thines, B.; Parlan, E.V.; Fulton, E.C. Circadian Network Interactions with Jasmonate Signaling and Defense. Plants 2019, 8, 252. https://doi.org/10.3390/plants8080252
Thines B, Parlan EV, Fulton EC. Circadian Network Interactions with Jasmonate Signaling and Defense. Plants. 2019; 8(8):252. https://doi.org/10.3390/plants8080252
Chicago/Turabian StyleThines, Bryan, Emily V. Parlan, and Elena C. Fulton. 2019. "Circadian Network Interactions with Jasmonate Signaling and Defense" Plants 8, no. 8: 252. https://doi.org/10.3390/plants8080252