(−)‐Loliolide is a general signal of plant stress that activates jasmonate‐related responses

Summary The production of defensive metabolites in plants can be induced by signaling chemicals released by neighboring plants. Induction is mainly known from volatile aboveground signals, with belowground signals and their underlying mechanisms largely unknown. We demonstrate that (−)‐loliolide tri...

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Published inThe New phytologist Vol. 238; no. 5; pp. 2099 - 2112
Main Authors Li, Lei‐Lei, Li, Zheng, Lou, Yonggen, Meiners, Scott J., Kong, Chui‐Hua
Format Journal Article
LanguageEnglish
Published England Wiley Subscription Services, Inc 01.06.2023
Subjects
(−)‐loliolide
abiotic stress
belowground signaling interactions
benzoxazinoids
biotic and abiotic stressors
Chemical defence
Chemical defense
chemical defenses
Competitors
cyanogenic glycosides
Cyclopentanes - metabolism
defense‐related genes
defensive metabolites
Flavonoids
Flowers & plants
Gene expression
genes
Glycosides
Herbivores
Hydrogen peroxide
Jasmonic acid
jasmonic acid (JA)
Metabolites
Oxylipins - metabolism
Pathogens
Phenolic acids
Phenols
Plant species
Plant stress
Plants
Plants - metabolism
reactive oxygen species (ROS)
rice
root transcriptome
Signal transduction
Signaling
Terpenes
terpenoids
transcription (genetics)
transcriptome
Transcriptomes
wheat
jasmonic acid (JA)
defense-related genes
defensive metabolites
root transcriptome
(−)-loliolide
reactive oxygen species (ROS)
belowground signaling interactions
biotic and abiotic stressors
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Abstract Summary The production of defensive metabolites in plants can be induced by signaling chemicals released by neighboring plants. Induction is mainly known from volatile aboveground signals, with belowground signals and their underlying mechanisms largely unknown. We demonstrate that (−)‐loliolide triggers defensive metabolite responses to competitors, herbivores, and pathogens in seven plant species. We further explore the transcriptional responses of defensive pathways to verify the signaling role of (−)‐loliolide in wheat and rice models with well‐known defensive metabolites and gene systems. In response to biotic and abiotic stressors, (−)‐loliolide is produced and secreted by roots. This, in turn, induces the production of defensive compounds including phenolic acids, flavonoids, terpenoids, alkaloids, benzoxazinoids, and cyanogenic glycosides, regardless of plant species. (−)‐Loliolide also triggers the expression of defense‐related genes, accompanied by an increase in the concentration of jasmonic acid and hydrogen peroxide (H2O2). Transcriptome profiling and inhibitor incubation indicate that (−)‐loliolide‐induced defense responses are regulated through pathways mediated by jasmonic acid, H2O2, and Ca 2+. These findings argue that (−)‐loliolide functions as a common belowground signal mediating chemical defense in plants. Such perception‐dependent plant chemical defenses will yield critical insights into belowground signaling interactions. See also the Commentary on this article by Frost, 238: 1749–1751.
AbstractList The production of defensive metabolites in plants can be induced by signaling chemicals released by neighboring plants. Induction is mainly known from volatile aboveground signals, with belowground signals and their underlying mechanisms largely unknown.We demonstrate that (−)‐loliolide triggers defensive metabolite responses to competitors, herbivores, and pathogens in seven plant species. We further explore the transcriptional responses of defensive pathways to verify the signaling role of (−)‐loliolide in wheat and rice models with well‐known defensive metabolites and gene systems.In response to biotic and abiotic stressors, (−)‐loliolide is produced and secreted by roots. This, in turn, induces the production of defensive compounds including phenolic acids, flavonoids, terpenoids, alkaloids, benzoxazinoids, and cyanogenic glycosides, regardless of plant species. (−)‐Loliolide also triggers the expression of defense‐related genes, accompanied by an increase in the concentration of jasmonic acid and hydrogen peroxide (H2O2). Transcriptome profiling and inhibitor incubation indicate that (−)‐loliolide‐induced defense responses are regulated through pathways mediated by jasmonic acid, H2O2, and Ca 2+.These findings argue that (−)‐loliolide functions as a common belowground signal mediating chemical defense in plants. Such perception‐dependent plant chemical defenses will yield critical insights into belowground signaling interactions.
The production of defensive metabolites in plants can be induced by signaling chemicals released by neighboring plants. Induction is mainly known from volatile aboveground signals, with belowground signals and their underlying mechanisms largely unknown. We demonstrate that (−)‐loliolide triggers defensive metabolite responses to competitors, herbivores, and pathogens in seven plant species. We further explore the transcriptional responses of defensive pathways to verify the signaling role of (−)‐loliolide in wheat and rice models with well‐known defensive metabolites and gene systems. In response to biotic and abiotic stressors, (−)‐loliolide is produced and secreted by roots. This, in turn, induces the production of defensive compounds including phenolic acids, flavonoids, terpenoids, alkaloids, benzoxazinoids, and cyanogenic glycosides, regardless of plant species. (−)‐Loliolide also triggers the expression of defense‐related genes, accompanied by an increase in the concentration of jasmonic acid and hydrogen peroxide (H 2 O 2 ). Transcriptome profiling and inhibitor incubation indicate that (−)‐loliolide‐induced defense responses are regulated through pathways mediated by jasmonic acid, H 2 O 2 , and Ca 2+ . These findings argue that (−)‐loliolide functions as a common belowground signal mediating chemical defense in plants. Such perception‐dependent plant chemical defenses will yield critical insights into belowground signaling interactions. See also the Commentary on this article by Frost, 238 : 1749–1751 .
The production of defensive metabolites in plants can be induced by signaling chemicals released by neighboring plants. Induction is mainly known from volatile aboveground signals, with belowground signals and their underlying mechanisms largely unknown. We demonstrate that (−)‐loliolide triggers defensive metabolite responses to competitors, herbivores, and pathogens in seven plant species. We further explore the transcriptional responses of defensive pathways to verify the signaling role of (−)‐loliolide in wheat and rice models with well‐known defensive metabolites and gene systems. In response to biotic and abiotic stressors, (−)‐loliolide is produced and secreted by roots. This, in turn, induces the production of defensive compounds including phenolic acids, flavonoids, terpenoids, alkaloids, benzoxazinoids, and cyanogenic glycosides, regardless of plant species. (−)‐Loliolide also triggers the expression of defense‐related genes, accompanied by an increase in the concentration of jasmonic acid and hydrogen peroxide (H₂O₂). Transcriptome profiling and inhibitor incubation indicate that (−)‐loliolide‐induced defense responses are regulated through pathways mediated by jasmonic acid, H₂O₂, and Ca ²⁺. These findings argue that (−)‐loliolide functions as a common belowground signal mediating chemical defense in plants. Such perception‐dependent plant chemical defenses will yield critical insights into belowground signaling interactions.
Summary The production of defensive metabolites in plants can be induced by signaling chemicals released by neighboring plants. Induction is mainly known from volatile aboveground signals, with belowground signals and their underlying mechanisms largely unknown. We demonstrate that (−)‐loliolide triggers defensive metabolite responses to competitors, herbivores, and pathogens in seven plant species. We further explore the transcriptional responses of defensive pathways to verify the signaling role of (−)‐loliolide in wheat and rice models with well‐known defensive metabolites and gene systems. In response to biotic and abiotic stressors, (−)‐loliolide is produced and secreted by roots. This, in turn, induces the production of defensive compounds including phenolic acids, flavonoids, terpenoids, alkaloids, benzoxazinoids, and cyanogenic glycosides, regardless of plant species. (−)‐Loliolide also triggers the expression of defense‐related genes, accompanied by an increase in the concentration of jasmonic acid and hydrogen peroxide (H2O2). Transcriptome profiling and inhibitor incubation indicate that (−)‐loliolide‐induced defense responses are regulated through pathways mediated by jasmonic acid, H2O2, and Ca 2+. These findings argue that (−)‐loliolide functions as a common belowground signal mediating chemical defense in plants. Such perception‐dependent plant chemical defenses will yield critical insights into belowground signaling interactions. See also the Commentary on this article by Frost, 238: 1749–1751.
The production of defensive metabolites in plants can be induced by signaling chemicals released by neighboring plants. Induction is mainly known from volatile aboveground signals, with belowground signals and their underlying mechanisms largely unknown. We demonstrate that (-)-loliolide triggers defensive metabolite responses to competitors, herbivores, and pathogens in seven plant species. We further explore the transcriptional responses of defensive pathways to verify the signaling role of (-)-loliolide in wheat and rice models with well-known defensive metabolites and gene systems. In response to biotic and abiotic stressors, (-)-loliolide is produced and secreted by roots. This, in turn, induces the production of defensive compounds including phenolic acids, flavonoids, terpenoids, alkaloids, benzoxazinoids, and cyanogenic glycosides, regardless of plant species. (-)-Loliolide also triggers the expression of defense-related genes, accompanied by an increase in the concentration of jasmonic acid and hydrogen peroxide (H O ). Transcriptome profiling and inhibitor incubation indicate that (-)-loliolide-induced defense responses are regulated through pathways mediated by jasmonic acid, H O , and Ca . These findings argue that (-)-loliolide functions as a common belowground signal mediating chemical defense in plants. Such perception-dependent plant chemical defenses will yield critical insights into belowground signaling interactions.
The production of defensive metabolites in plants can be induced by signaling chemicals released by neighboring plants. Induction is mainly known from volatile aboveground signals, with belowground signals and their underlying mechanisms largely unknown. We demonstrate that (-)-loliolide triggers defensive metabolite responses to competitors, herbivores, and pathogens in seven plant species. We further explore the transcriptional responses of defensive pathways to verify the signaling role of (-)-loliolide in wheat and rice models with well-known defensive metabolites and gene systems. In response to biotic and abiotic stressors, (-)-loliolide is produced and secreted by roots. This, in turn, induces the production of defensive compounds including phenolic acids, flavonoids, terpenoids, alkaloids, benzoxazinoids, and cyanogenic glycosides, regardless of plant species. (-)-Loliolide also triggers the expression of defense-related genes, accompanied by an increase in the concentration of jasmonic acid and hydrogen peroxide (H2 O2 ). Transcriptome profiling and inhibitor incubation indicate that (-)-loliolide-induced defense responses are regulated through pathways mediated by jasmonic acid, H2 O2 , and Ca 2+ . These findings argue that (-)-loliolide functions as a common belowground signal mediating chemical defense in plants. Such perception-dependent plant chemical defenses will yield critical insights into belowground signaling interactions.The production of defensive metabolites in plants can be induced by signaling chemicals released by neighboring plants. Induction is mainly known from volatile aboveground signals, with belowground signals and their underlying mechanisms largely unknown. We demonstrate that (-)-loliolide triggers defensive metabolite responses to competitors, herbivores, and pathogens in seven plant species. We further explore the transcriptional responses of defensive pathways to verify the signaling role of (-)-loliolide in wheat and rice models with well-known defensive metabolites and gene systems. In response to biotic and abiotic stressors, (-)-loliolide is produced and secreted by roots. This, in turn, induces the production of defensive compounds including phenolic acids, flavonoids, terpenoids, alkaloids, benzoxazinoids, and cyanogenic glycosides, regardless of plant species. (-)-Loliolide also triggers the expression of defense-related genes, accompanied by an increase in the concentration of jasmonic acid and hydrogen peroxide (H2 O2 ). Transcriptome profiling and inhibitor incubation indicate that (-)-loliolide-induced defense responses are regulated through pathways mediated by jasmonic acid, H2 O2 , and Ca 2+ . These findings argue that (-)-loliolide functions as a common belowground signal mediating chemical defense in plants. Such perception-dependent plant chemical defenses will yield critical insights into belowground signaling interactions.
Author Meiners, Scott J.
Li, Zheng
Lou, Yonggen
Li, Lei‐Lei
Kong, Chui‐Hua
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  surname: Kong
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  organization: China Agricultural University
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Cites_doi 10.1016/j.indcrop.2009.10.008
10.1038/ncomms7273
10.1016/j.devcel.2020.10.012
10.1093/emboj/16.16.4806
10.1146/annurev.phyto.44.070505.143425
10.1093/nsr/nwaa149
10.1038/s41467-018-06429-1
10.1111/pce.14083
10.1016/j.tplants.2020.12.006
10.1111/tpj.15102
10.1146/annurev-arplant-042817-040322
10.1111/j.1469-8137.2008.02599.x
10.1146/annurev-arplant-042817-040047
10.1186/s40168-018-0537-x
10.1146/annurev-arplant-042110-103854
10.1146/annurev-arplant-042916-041132
10.1002/pld3.426
10.1016/j.cub.2019.06.028
10.1093/jxb/ern259
10.1126/science.1147455
10.1016/j.tplants.2008.03.005
10.1104/pp.18.00837
10.1111/pce.13892
10.1021/jf8034034
10.1016/S1360-1385(02)02244-6
10.1146/annurev-phyto-082718-095959
10.1146/annurev.ecolsys.110308.120314
10.1038/d41586-020-00403-y
10.1002/ps.5355
10.1146/annurev-arplant-050718-095910
10.1126/science.aat7744
10.1016/j.plantsci.2021.110903
10.1038/s41576-021-00413-0
10.1111/nph.16135
10.1093/aob/mcw152
10.1093/jxb/erw175
10.1021/jf035467i
10.1111/pce.13897
10.1146/annurev-phyto-080516-035544
10.1177/1934578X1400900428
10.1046/j.1365-313X.1997.11040773.x
10.1073/pnas.89.6.2389
10.1016/j.tree.2020.04.001
10.1104/pp.125.4.2189
10.1111/tpj.15124
10.1093/pcp/pcz161
10.1093/jxb/erac439
10.1146/annurev-ecolsys-010421-020045
10.3389/fpls.2019.00751
10.1111/nph.12747
10.3390/molecules25214952
10.1111/nph.18552
10.1016/j.phytochem.2016.08.013
10.1007/s11738-015-1927-3
10.1016/j.phytochem.2009.05.012
10.1111/1365-2435.13627
10.1111/pce.13910
10.1073/pnas.2003742117
10.1016/j.foodchem.2018.07.131
10.1016/j.tplants.2021.08.009
10.3390/molecules27031007
10.1038/ncomms15324
10.1104/pp.114.252700
10.1126/sciadv.aat6797
10.1093/jxb/erv367
10.1073/pnas.87.19.7713
10.1016/j.tplants.2016.01.008
10.1146/annurev-ento-020117-043507
10.1104/pp.107.112169
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Keywords jasmonic acid (JA)
defense-related genes
defensive metabolites
root transcriptome
(−)-loliolide
reactive oxygen species (ROS)
belowground signaling interactions
biotic and abiotic stressors
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References 2018; 361
2015; 37
2017; 8
2021; 26
2009; 40
2019; 10
2019; 57
2022; 23
2020; 55
2008; 146
2022; 27
2018; 6
2018; 9
1990; 87
2009; 57
2019; 60
2018; 4
1997; 11
2016; 118
2020; 578
2019; 29
1997; 16
2014; 9
2019; 270
1992; 89
2014; 202
2012; 63
2021; 308
2021; 8
2010; 31
2015; 6
2019; 70
2021; 44
2019; 75
2015; 167
2021; 105
2002; 7
2017; 68
2020; 105
2008; 59
2020; 225
2008; 13
2020; 35
2018; 63
2020; 34
2021; 52
2001; 125
2018; 69
2008; 180
2004; 52
2007; 317
2009; 70
2022
2006; 44
2022; 6
2017; 55
2020; 71
2015; 66
2016; 21
2023; 237
2019; 179
2020; 117
2020; 25
2016; 131
2016; 67
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37010034 - New Phytol. 2023 Jun;238(5):1749-1751
References_xml – volume: 31
  start-page: 214
  year: 2010
  end-page: 218
  article-title: Effects of exogenous methyl jasmonate on artemisinin biosynthesis and secondary metabolites in L
  publication-title: Industrial Crops and Products
– volume: 27
  start-page: 1007
  year: 2022
  article-title: Evolution of DIMBOA‐Glc ‐methyltransferases from flavonoid ‐methyltransferases in the grasses
  publication-title: Molecules
– volume: 70
  start-page: 527
  year: 2019
  end-page: 557
  article-title: Molecular interactions between plants and insect herbivores
  publication-title: Annual Review of Plant Biology
– volume: 63
  start-page: 433
  year: 2018
  end-page: 452
  article-title: Tritrophic interactions mediated by herbivore‐induced plant volatiles: mechanisms, ecological relevance, and application potential
  publication-title: Annual Review of Entomology
– volume: 70
  start-page: 1645
  year: 2009
  end-page: 1651
  article-title: Benzoxazinoid biosynthesis, a model for evolution of secondary metabolic pathways in plants
  publication-title: Phytochemistry
– volume: 68
  start-page: 485
  year: 2017
  end-page: 512
  article-title: Defense priming: an adaptive part of induced resistance
  publication-title: Annual Review of Plant Biology
– volume: 89
  start-page: 2389
  year: 1992
  end-page: 2393
  article-title: Jasmonic acid is a signal transducer in elicitor‐induced plant cell cultures
  publication-title: Proceedings of the National Academy of Sciences, USA
– year: 2022
  article-title: Root‐secreted (–)‐loliolide modulates both belowground defense and aboveground flowering in Arabidopsis and tobacco
  publication-title: Journal of Experimental Botany
– volume: 6
  year: 2022
  article-title: Belowground and aboveground herbivory differentially affect the transcriptome in roots and shoots of maize
  publication-title: Plant Direct
– volume: 202
  start-page: 1335
  year: 2014
  end-page: 1345
  article-title: Root jasmonic acid synthesis and perception regulate folivore‐induced shoot metabolites and increase resistance
  publication-title: New Phytologist
– volume: 308
  year: 2021
  article-title: OsIAA20, an Aux/IAA protein, mediates abiotic stress tolerance in rice through an ABA pathway
  publication-title: Plant Science
– volume: 225
  start-page: 621
  year: 2020
  end-page: 636
  article-title: Fellowship of the rings: a saga of strigolactones and other small signals
  publication-title: New Phytologist
– volume: 179
  start-page: 1822
  year: 2019
  end-page: 1833
  article-title: Loliolide, a carotenoid metabolite, is a potential endogenous inducer of herbivore resistance
  publication-title: Plant Physiology
– volume: 66
  start-page: 6591
  year: 2015
  end-page: 6603
  article-title: The wheat AGC kinase TaAGC1 is a positive contributor to host resistance to the necrotrophic pathogen
  publication-title: Journal of Experimental Botany
– volume: 59
  start-page: 4195
  year: 2008
  end-page: 4204
  article-title: Overexpression of TiERF1enhances resistance to sharp eyespot in transgenic wheat
  publication-title: Journal of Experimental Botany
– volume: 131
  start-page: 84
  year: 2016
  end-page: 91
  article-title: The natural plant stress elicitor cis‐jasmone causes cultivar‐dependent reduction in growth of the stink bug, and associated changes in flavonoid concentrations in soybean,
  publication-title: Phytochemistry
– volume: 75
  start-page: 2413
  year: 2019
  end-page: 2436
  article-title: Recent advances in allelopathy for weed control: from knowledge to applications
  publication-title: Pest Management Science
– volume: 63
  start-page: 431
  year: 2012
  end-page: 450
  article-title: Plant defense against herbivores: chemical aspects
  publication-title: Annual Review of Plant Biology
– volume: 125
  start-page: 2189
  year: 2001
  end-page: 2202
  article-title: Molecular interactions between the specialist herbivore (Lepidoptera, Sphingidae) and its natural host . IV. Insect‐induced ethylene reduces jasmonate‐induced nicotine accumulation by regulating putrescine ‐methyltransferase transcripts
  publication-title: Plant Physiology
– volume: 69
  start-page: 209
  year: 2018
  end-page: 236
  article-title: Reactive oxygen species in plant signaling
  publication-title: Annual Review of Plant Biology
– volume: 26
  start-page: 509
  year: 2021
  end-page: 523
  article-title: Shade avoidance: expanding the color and hormone palette
  publication-title: Trends in Plant Science
– volume: 34
  start-page: 1779
  year: 2020
  end-page: 1789
  article-title: Risky roots and careful herbivores: sustained herbivory by a root‐feeding herbivore attenuates indirect plant defences
  publication-title: Functional Ecology
– volume: 9
  start-page: 533
  year: 2014
  end-page: 537
  article-title: Variation of glucosinolate accumulation and gene expression of transcription factors at different stages of Chinese cabbage seedlings under light and dark conditions
  publication-title: Natural Product Communications
– volume: 8
  start-page: 15324
  year: 2017
  article-title: Sequencing and assembly of a near complete indica rice genome
  publication-title: Nature Communications
– volume: 4
  year: 2018
  article-title: Convergent evolution of a metabolic switch between aphid and caterpillar resistance in cereals
  publication-title: Science Advance
– volume: 44
  start-page: 135
  year: 2006
  end-page: 162
  article-title: Significance of inducible defense‐related proteins in infected plants
  publication-title: Annual Review of Phytopathology
– volume: 27
  start-page: 29
  year: 2022
  end-page: 38
  article-title: How do plants sense volatiles sent by other plants?
  publication-title: Trends in Plant Science
– volume: 35
  start-page: 716
  year: 2020
  end-page: 730
  article-title: Plant secondary compounds in soil and their role in belowground species interactions
  publication-title: Trends in Ecology and Evolution
– volume: 44
  start-page: 1044
  year: 2021
  end-page: 1058
  article-title: Root exudate signals in plant–plant interactions
  publication-title: Plant, Cell & Environment
– volume: 44
  start-page: 1165
  year: 2021
  end-page: 1177
  article-title: Indole primes defence signaling and increases herbivore resistance in tea plants
  publication-title: Plant, Cell & Environment
– volume: 167
  start-page: 1100
  year: 2015
  end-page: 1116
  article-title: Induced jasmonate signaling leads to contrasting effects on root damage and herbivore performance
  publication-title: Plant Physiology
– volume: 40
  start-page: 373
  year: 2009
  end-page: 391
  article-title: Belowground herbivory and plant defenses
  publication-title: Annual Review of Ecology, Evolution, and Systematics
– volume: 67
  start-page: 3573
  year: 2016
  end-page: 3585
  article-title: Silicon‐induced reversibility of cadmium toxicity in rice
  publication-title: Journal of Experimental Botany
– volume: 270
  start-page: 452
  year: 2019
  end-page: 458
  article-title: Spanish traditional tomato. Effect of genotype, location and agronomic conditions on the nutritional quality and evaluation of consumer preferences
  publication-title: Food Chemistry
– volume: 13
  start-page: 264
  year: 2008
  end-page: 272
  article-title: Long‐distance signalling in plant defence
  publication-title: Trends in Plant Science
– volume: 55
  start-page: 401
  year: 2017
  end-page: 425
  article-title: Evolution of hormone signaling networks in plant defense
  publication-title: Annual Review of Phytopathology
– volume: 16
  start-page: 4806
  year: 1997
  end-page: 4816
  article-title: Catalase is a sink for H O and is indispensable for stress defence in C plants
  publication-title: EMBO Journal
– volume: 317
  start-page: 1561
  year: 2007
  end-page: 1563
  article-title: Mutual feedbacks maintain both genetic and species diversity in a plant community
  publication-title: Science
– volume: 21
  start-page: 256
  year: 2016
  end-page: 265
  article-title: Metabolomics in the rhizosphere: tapping into belowground chemical communication
  publication-title: Trends in Plant Science
– volume: 146
  start-page: 867
  year: 2008
  end-page: 874
  article-title: Interactions between arthropod‐induced aboveground and belowground defenses in plants
  publication-title: Plant Physiology
– volume: 52
  start-page: 2861
  year: 2004
  end-page: 2865
  article-title: Release and activity of allelochemicals from allelopathic rice seedlings
  publication-title: Journal of Agricultural and Food Chemistry
– volume: 55
  start-page: 529
  year: 2020
  end-page: 543
  article-title: Thriving under stress: how plants balance growth and the stress response
  publication-title: Developmental Cell
– volume: 180
  start-page: 722
  year: 2008
  end-page: 734
  article-title: Priming defense genes and metabolites in hybrid poplar by the green leaf volatile ‐3‐hexenyl acetate
  publication-title: New Phytologist
– volume: 6
  start-page: 6273
  year: 2015
  article-title: Indole is an essential herbivore‐induced volatile priming signal in maize
  publication-title: Nature Communications
– volume: 57
  start-page: 505
  year: 2019
  end-page: 529
  article-title: Surviving in a hostile world: plant strategies to resist pests and diseases
  publication-title: Annual Review of Phytopathology
– volume: 237
  start-page: 562
  year: 2023
  end-page: 574
  article-title: Root placement patterns in allelopathic plant–plant interactions
  publication-title: New Phytologist
– volume: 23
  start-page: 104
  year: 2022
  end-page: 119
  article-title: Abiotic stress responses in plants
  publication-title: Nature Reviews Genetics
– volume: 117
  start-page: 12017
  year: 2020
  end-page: 12028
  article-title: Induction of defense in cereals by 4‐fluorophenoxyacetic acid suppresses insect pest populations and increases crop yields in the field
  publication-title: Proceedings of the National Academy of Sciences, USA
– volume: 8
  year: 2021
  article-title: The LRXs‐RALFs‐FER module controls plant growth and salt stress responses by modulating multiple plant hormones
  publication-title: National Science Review
– volume: 105
  start-page: 351
  year: 2021
  end-page: 375
  article-title: Plant apocarotenoids: from retrograde signaling to interspecific communication
  publication-title: The Plant Journal
– volume: 71
  start-page: 1540
  year: 2020
  end-page: 1550
  article-title: (–)‐Loliolide, the most ubiquitous lactone, is involved in barnyardgrass‐induced rice allelopathy
  publication-title: Journal of Experimental Botany
– volume: 105
  start-page: 489
  year: 2020
  end-page: 504
  article-title: Multiple levels of crosstalk in hormone networks regulating plant defense
  publication-title: The Plant Journal
– volume: 69
  start-page: 387
  year: 2018
  end-page: 415
  article-title: Modularity in jasmonate signaling for multistress resilience
  publication-title: Annual Review of Plant Biology
– volume: 57
  start-page: 1677
  year: 2009
  end-page: 1696
  article-title: Hydroxamic acids derived from 2‐hydroxy‐2 ‐1,4‐benzoxazin‐3(4 )‐one: key defense chemicals of cereals
  publication-title: Journal of Agricultural and Food Chemistry
– volume: 118
  start-page: 821
  year: 2016
  end-page: 831
  article-title: Root‐mediated signal transmission of systemic acquired resistance against above‐ground and below‐ground pathogens
  publication-title: Annals of Botany
– volume: 25
  start-page: 4952
  year: 2020
  article-title: Production of defense phenolics in tomato leaves of different age
  publication-title: Molecules
– volume: 44
  start-page: 1030
  year: 2021
  end-page: 1043
  article-title: Plant volatiles as cues and signals in plant communication
  publication-title: Plant, Cell & Environment
– volume: 9
  start-page: 3867
  year: 2018
  article-title: Plant neighbor detection and allelochemical response are driven by root‐secreted signaling chemicals
  publication-title: Nature Communications
– volume: 6
  start-page: 156
  year: 2018
  article-title: Root exudates drive the soil‐borne legacy of aboveground pathogen infection
  publication-title: Microbiome
– volume: 7
  start-page: 210
  year: 2002
  end-page: 216
  article-title: Priming in plant–pathogen interactions
  publication-title: Trends in Plant Science
– volume: 37
  start-page: 176
  year: 2015
  article-title: The genetic background of benzoxazinoid biosynthesis in cereals
  publication-title: Acta Physiologiae Plantarum
– volume: 10
  start-page: 751
  year: 2019
  article-title: Presence of belowground neighbors activates defense pathways at the expense of growth in tobacco plants
  publication-title: Frontiers in Plant Science
– volume: 60
  start-page: 2638
  year: 2019
  end-page: 2647
  article-title: Plant specialized metabolism regulated by jasmonate signaling
  publication-title: Plant and Cell Physiology
– volume: 361
  start-page: 1112
  year: 2018
  end-page: 1115
  article-title: Glutamate triggers long‐distance, calcium‐based plant defense signaling
  publication-title: Science
– volume: 29
  start-page: 688
  year: 2019
  end-page: 690
  article-title: Evolution: an early role for flavonoids in defense against oomycete infection
  publication-title: Current Biology
– volume: 87
  start-page: 7713
  year: 1990
  end-page: 7716
  article-title: Interplant communication: airborne methyl jasmoante induces synthesis of proteinase inhibitors in plant leaves
  publication-title: Proceedings of the National Academy of Sciences, USA
– volume: 52
  start-page: 1
  year: 2021
  end-page: 24
  article-title: Plant communication
  publication-title: Annual Review of Ecology, Evolution, and Systematics
– volume: 44
  start-page: 3709
  year: 2021
  end-page: 3721
  article-title: Intra‐specific kin recognition contributes to inter‐specific allelopathy: a case study of allelopathic rice interference with paddy weeds
  publication-title: Plant, Cell & Environment
– volume: 11
  start-page: 773
  year: 1997
  end-page: 782
  article-title: Abscisic acid and jasmonic acid activate wound‐inducible genes in potato through separate, organ‐specific signal transduction pathways
  publication-title: The Plant Journal
– volume: 578
  start-page: 518
  year: 2020
  end-page: 519
  article-title: Making sense of hydrogen peroxide signals
  publication-title: Nature
– ident: e_1_2_9_56_1
  doi: 10.1016/j.indcrop.2009.10.008
– ident: e_1_2_9_17_1
  doi: 10.1038/ncomms7273
– ident: e_1_2_9_68_1
  doi: 10.1016/j.devcel.2020.10.012
– ident: e_1_2_9_61_1
  doi: 10.1093/emboj/16.16.4806
– ident: e_1_2_9_40_1
  doi: 10.1146/annurev.phyto.44.070505.143425
– ident: e_1_2_9_70_1
  doi: 10.1093/nsr/nwaa149
– ident: e_1_2_9_35_1
  doi: 10.1038/s41467-018-06429-1
– ident: e_1_2_9_63_1
  doi: 10.1111/pce.14083
– ident: e_1_2_9_20_1
  doi: 10.1016/j.tplants.2020.12.006
– ident: e_1_2_9_48_1
  doi: 10.1111/tpj.15102
– ident: e_1_2_9_59_1
  doi: 10.1146/annurev-arplant-042817-040322
– ident: e_1_2_9_26_1
  doi: 10.1111/j.1469-8137.2008.02599.x
– ident: e_1_2_9_31_1
  doi: 10.1146/annurev-arplant-042817-040047
– ident: e_1_2_9_66_1
  doi: 10.1186/s40168-018-0537-x
– ident: e_1_2_9_47_1
  doi: 10.1146/annurev-arplant-042110-103854
– ident: e_1_2_9_46_1
  doi: 10.1146/annurev-arplant-042916-041132
– ident: e_1_2_9_65_1
  doi: 10.1002/pld3.426
– ident: e_1_2_9_21_1
  doi: 10.1016/j.cub.2019.06.028
– ident: e_1_2_9_6_1
  doi: 10.1093/jxb/ern259
– ident: e_1_2_9_36_1
  doi: 10.1126/science.1147455
– ident: e_1_2_9_30_1
  doi: 10.1016/j.tplants.2008.03.005
– ident: e_1_2_9_49_1
  doi: 10.1104/pp.18.00837
– ident: e_1_2_9_57_1
  doi: 10.1111/pce.13892
– ident: e_1_2_9_50_1
  doi: 10.1021/jf8034034
– ident: e_1_2_9_8_1
  doi: 10.1016/S1360-1385(02)02244-6
– ident: e_1_2_9_60_1
  doi: 10.1146/annurev-phyto-082718-095959
– ident: e_1_2_9_10_1
  doi: 10.1146/annurev.ecolsys.110308.120314
– ident: e_1_2_9_23_1
  doi: 10.1038/d41586-020-00403-y
– ident: e_1_2_9_44_1
  doi: 10.1002/ps.5355
– ident: e_1_2_9_15_1
  doi: 10.1146/annurev-arplant-050718-095910
– ident: e_1_2_9_53_1
  doi: 10.1126/science.aat7744
– ident: e_1_2_9_67_1
  doi: 10.1016/j.plantsci.2021.110903
– ident: e_1_2_9_69_1
  doi: 10.1038/s41576-021-00413-0
– ident: e_1_2_9_43_1
  doi: 10.1111/nph.16135
– ident: e_1_2_9_52_1
  doi: 10.1093/aob/mcw152
– ident: e_1_2_9_19_1
  doi: 10.1093/jxb/erw175
– ident: e_1_2_9_34_1
  doi: 10.1021/jf035467i
– ident: e_1_2_9_64_1
  doi: 10.1111/pce.13897
– ident: e_1_2_9_4_1
  doi: 10.1146/annurev-phyto-080516-035544
– ident: e_1_2_9_33_1
  doi: 10.1177/1934578X1400900428
– ident: e_1_2_9_12_1
  doi: 10.1046/j.1365-313X.1997.11040773.x
– ident: e_1_2_9_29_1
  doi: 10.1073/pnas.89.6.2389
– ident: e_1_2_9_14_1
  doi: 10.1016/j.tree.2020.04.001
– ident: e_1_2_9_62_1
  doi: 10.1104/pp.125.4.2189
– ident: e_1_2_9_2_1
  doi: 10.1111/tpj.15124
– ident: e_1_2_9_7_1
  doi: 10.1093/pcp/pcz161
– ident: e_1_2_9_38_1
  doi: 10.1093/jxb/erac439
– ident: e_1_2_9_32_1
  doi: 10.1146/annurev-ecolsys-010421-020045
– ident: e_1_2_9_5_1
  doi: 10.3389/fpls.2019.00751
– ident: e_1_2_9_24_1
  doi: 10.1111/nph.12747
– ident: e_1_2_9_9_1
  doi: 10.3390/molecules25214952
– ident: e_1_2_9_55_1
  doi: 10.1111/nph.18552
– ident: e_1_2_9_27_1
  doi: 10.1016/j.phytochem.2016.08.013
– volume: 71
  start-page: 1540
  year: 2020
  ident: e_1_2_9_39_1
  article-title: (–)‐Loliolide, the most ubiquitous lactone, is involved in barnyardgrass‐induced rice allelopathy
  publication-title: Journal of Experimental Botany
– ident: e_1_2_9_45_1
  doi: 10.1007/s11738-015-1927-3
– ident: e_1_2_9_25_1
  doi: 10.1016/j.phytochem.2009.05.012
– ident: e_1_2_9_28_1
  doi: 10.1111/1365-2435.13627
– ident: e_1_2_9_51_1
  doi: 10.1111/pce.13910
– ident: e_1_2_9_58_1
  doi: 10.1073/pnas.2003742117
– ident: e_1_2_9_3_1
  doi: 10.1016/j.foodchem.2018.07.131
– ident: e_1_2_9_41_1
  doi: 10.1016/j.tplants.2021.08.009
– ident: e_1_2_9_22_1
  doi: 10.3390/molecules27031007
– ident: e_1_2_9_13_1
  doi: 10.1038/ncomms15324
– ident: e_1_2_9_42_1
  doi: 10.1104/pp.114.252700
– ident: e_1_2_9_37_1
  doi: 10.1126/sciadv.aat6797
– ident: e_1_2_9_71_1
  doi: 10.1093/jxb/erv367
– ident: e_1_2_9_18_1
  doi: 10.1073/pnas.87.19.7713
– ident: e_1_2_9_11_1
  doi: 10.1016/j.tplants.2016.01.008
– ident: e_1_2_9_54_1
  doi: 10.1146/annurev-ento-020117-043507
– ident: e_1_2_9_16_1
  doi: 10.1104/pp.107.112169
– reference: 37010034 - New Phytol. 2023 Jun;238(5):1749-1751
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Snippet Summary The production of defensive metabolites in plants can be induced by signaling chemicals released by neighboring plants. Induction is mainly known from...
The production of defensive metabolites in plants can be induced by signaling chemicals released by neighboring plants. Induction is mainly known from volatile...
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SubjectTerms (−)‐loliolide
abiotic stress
belowground signaling interactions
benzoxazinoids
biotic and abiotic stressors
Chemical defence
Chemical defense
chemical defenses
Competitors
cyanogenic glycosides
Cyclopentanes - metabolism
defense‐related genes
defensive metabolites
Flavonoids
Flowers & plants
Gene expression
genes
Glycosides
Herbivores
Hydrogen peroxide
Jasmonic acid
jasmonic acid (JA)
Metabolites
Oxylipins - metabolism
Pathogens
Phenolic acids
Phenols
Plant species
Plant stress
Plants
Plants - metabolism
reactive oxygen species (ROS)
rice
root transcriptome
Signal transduction
Signaling
Terpenes
terpenoids
transcription (genetics)
transcriptome
Transcriptomes
wheat
Title (−)‐Loliolide is a general signal of plant stress that activates jasmonate‐related responses
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fnph.18644
https://www.ncbi.nlm.nih.gov/pubmed/36444519
https://www.proquest.com/docview/2806326866
https://www.proquest.com/docview/2742656406
https://www.proquest.com/docview/2811968955
Volume 238
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