Transcriptomic perspective on extracellular ATP signaling: a few curious trifles

References

• Verkhratsky A, Burnstock G. Biology of purinergic signalling: its ancient evolutionary roots, its omnipresence and its multiple functional significance. Bioessays. 2014;36:697–705. doi:10.1002/bies.201400024.
   PubMed Web of Science ®Google Scholar
• Choi J, Tanaka K, Cao Y, Qi Y, Qiu J, Liang Y, Lee SY, Stacey G. Identification of a plant receptor for extracellular ATP. Science. 2014;343:290–294. doi:10.1126/science.343.6168.290.
   PubMed Web of Science ®Google Scholar
• Glazebrook J. Contrasting mechanisms of defense against biotrophic and necrotrophic pathogens. Annu Rev Phytopathol. 2005;43:205–227. doi:10.1146/annurev.phyto.43.040204.135923.
   PubMed Web of Science ®Google Scholar
• Chivasa S, Murphy AM, Hamilton JM, Lindsey K, Carr JP, Slabas AR. Extracellular ATP is a regulator of pathogen defence in plants. Plant J. 2009;60:436–448. doi:10.1111/j.1365-313X.2009.03968.x.
   PubMed Web of Science ®Google Scholar
• Bouwmeester K, De Sain M, Weide R, Gouget A, Klamer S, Canut H, Govers F, Howlett BJ. The lectin receptor kinase LecRK-I.9 is a novel Phytophthora resistance component and a potential host target for a RXLR effector. PLoS Pathog. 2011;7:e1001327. doi:10.1371/journal.ppat.1001327.
   PubMed Web of Science ®Google Scholar
• Chen D, Cao Y, Li H, Kim D, Ahsan N, Thelen J, Stacey G. Extracellular ATP elicits DORN1-mediated RBOHD phosphorylation to regulate stomatal aperture. Nat Commun. 2017;8:2265. doi:10.1038/s41467-017-02340-3.
   PubMed Web of Science ®Google Scholar
• Balagué C, Gouget A, Bouchez O, Souriac C, Haget N, Boutet-Mercey S, Govers F, Roby D, Canut H. The arabidopsis thaliana lectin receptor kinase LecRK-I.9 is required for full resistance to pseudomonas syringae and affects jasmonate signalling. Mol Plant Pathol. 2017;18:937–948. doi:10.1111/mpp.12457.
   PubMed Web of Science ®Google Scholar
• Tripathi D, Zhang T, Koo AJ, Stacey G, Tanaka K. Extracellular ATP acts on jasmonate signaling to reinforce plant defense. Plant Physiol. 2018;176:511–523. doi:10.1104/pp.17.01477.
   PubMed Web of Science ®Google Scholar
• Jewell JB, Sowders JM, He R, Willis MA, Gang DR, Tanaka K. Extracellular ATP shapes a defense-related transcriptome both independently and along with other defense signaling pathways. Plant Physiol. 2019;179:1144–1158. doi:10.1104/pp.18.01301.
   PubMed Web of Science ®Google Scholar
• Robinson JT, Thorvaldsdóttir H, Winckler W, Guttman M, Lander ES, Getz G, Mesirov JP. Integrative genomics viewer. Nat Biotechnol. 2011;29:24. doi:10.1038/nbt.1867.
   PubMed Web of Science ®Google Scholar
• Tripathi D, Tanaka K. A crosstalk between extracellular ATP and jasmonate signaling pathways for plant defense. Plant Signal Behav. 2018;13:e1432229. doi:10.1080/15592324.2018.1432229.
   PubMed Web of Science ®Google Scholar
• Mersmann S, Bourdais G, Rietz S, Robatzek S. Ethylene signaling regulates accumulation of the FLS2 receptor and is required for the oxidative burst contributing to plant immunity. Plant Physiol. 2010;154:391–400. doi:10.1104/pp.110.154567.
   PubMed Web of Science ®Google Scholar
• Yao Y, He RJ, Xie QL, Zhao XH, Deng XM, He JB, Song L, He J, Marchant A, Chen X-Y, et al. ETHYLENE RESPONSE FACTOR 74 (ERF74) plays an essential role in controlling a respiratory burst oxidase homolog D (RbohD)-dependent mechanism in response to different stresses in Arabidopsis. New Phytol. 2017;213:1667–1681. doi:10.1111/nph.14278.
   PubMed Web of Science ®Google Scholar
• Watkins JM, Hechler PJ, Muday GK. Ethylene-induced flavonol accumulation in guard cells suppresses reactive oxygen species and moderates stomatal aperture. Plant Physiol. 2014;164:1707–1717. doi:10.1104/pp.113.233528.
   PubMed Web of Science ®Google Scholar
• Marcec MJ, Gilroy S, Poovaiah BW, Tanaka K. Mutual interplay of Ca(2+) and ROS signaling in plant immune response. Plant Sci. 2019;283:343–354. doi:10.1016/j.plantsci.2019.03.004.
   PubMed Web of Science ®Google Scholar
• Waadt R, Krebs M, Kudla J, Schumacher K. Multiparameter imaging of calcium and abscisic acid and high-resolution quantitative calcium measurements using R-GECO1-mTurquoise in Arabidopsis. New Phytologist. 2017;216:303–320. doi:10.1111/nph.14706.
   PubMed Web of Science ®Google Scholar
• Yang T, Poovaiah BW. A calmodulin-binding/CGCG box DNA-binding protein family involved in multiple signaling pathways in plants. J Biol Chem. 2002;277:45049–45058. doi:10.1074/jbc.M207941200.
   PubMed Web of Science ®Google Scholar
• Lorenzo O, Piqueras R, Sanchez-Serrano JJ, Solano R. ETHYLENE RESPONSE FACTOR1 integrates signals from ethylene and jasmonate pathways in plant defense. Plant Cell. 2003;15:165–178. doi:10.1105/tpc.007468.
   PubMed Web of Science ®Google Scholar
• Zhu Z, An F, Feng Y, Li P, Xue L, A M, Jiang Z, Kim J-M, To TK, Li W, et al.. Derepression of ethylene-stabilized transcription factors (EIN3/EIL1) mediates jasmonate and ethylene signaling synergy in Arabidopsis. Proc Natl Acad Sci U S A. 2011;108: 12539–44. doi:10.1073/pnas.1103959108.
   Web of Science ®Google Scholar
• Kazan K. Diverse roles of jasmonates and ethylene in abiotic stress tolerance. Trends Plant Sci. 2015;20:219–229. doi:10.1016/j.tplants.2015.02.001.
   PubMed Web of Science ®Google Scholar
• Song S, Huang H, Gao H, Wang J, Wu D, Liu X, Yang S, Zhai Q, Li C, Qi T, et al.. Interaction between MYC2 and ETHYLENE INSENSITIVE3 modulates antagonism between jasmonate and ethylene signaling in Arabidopsis. Plant Cell. 2014;26:263–279. doi:10.1105/tpc.113.120394.
   PubMed Web of Science ®Google Scholar
• Ohta M, Matsui K, Hiratsu K, Shinshi H, Ohme-Takagi M. Repression domains of class II ERF transcriptional repressors share an essential motif for active repression. Plant Cell. 2001;13:1959–1968. doi:10.1105/tpc.010127.
   PubMed Web of Science ®Google Scholar
• Choi J, Tanaka K, Liang Y, Cao Y, Lee SY, Stacey G. Extracellular ATP, a danger signal, is recognized by DORN1 in Arabidopsis. Biochem J. 2014;463:429–437. doi:10.1042/BJ20130619.
   PubMed Web of Science ®Google Scholar
• Tanaka K, Choi J, Cao Y, Stacey G. Extracellular ATP acts as a damage-associated molecular pattern (DAMP) signal in plants. Front Plant Sci. 2014;5:446. doi:10.3389/fpls.2014.00446.
   PubMed Web of Science ®Google Scholar