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wound response

9105 relationships annotated with this phrase. Showing first 500 of 9105.
Source entity Relationship Target entity Species
wounding affects vascular pools of bound oxylipins Arabidopsis thaliana
ethylene emanation upon wounding is transient and peaks within 12 h before returning to baseline values Arabidopsis thaliana
wounding increases levels of dnOPDA-MGMG and OPDA-MGMG forms Arabidopsis thaliana
short-term wounding treatment reveals rapid increase in MACC (N-malonyl-ACC) levels Arabidopsis thaliana
lox6B mutant greatly reduces wound-induced increases in JA-Ile levels Arabidopsis thaliana
homogenized fresh WBPH egg extract application to fresh wounds results in higher levels of JA Oryza sativa; Sogatella furcifera
genes with higher expression in response to elevated red light:far-red light ratio in bud n-2 enriched for wounding Gene Ontology terms Arabidopsis thaliana
wound sites release ATP
jasmonate precursor pools undergo damage-response remodelling in Arabidopsis thaliana leaf vasculature Arabidopsis thaliana
synthesis of jasmonoyl-isoleucine (JA-Ile) in leaves is initiated upon wounding Arabidopsis thaliana
12-hydroxyjasmonic acid (12-OH-JA) is detected in response to wounding
ACC (1-aminocyclopropane-1-carboxylic acid) levels is significant at 60 min after wounding and increases sixfold in first 3 h wounding response Arabidopsis thaliana
homogenized fresh SBPH egg extract application to fresh wounds results in higher levels of JA-Ile Oryza sativa; Laodelphax striatellus
cluster 7 includes 128 early and strong JA- and wound-responsive genes Arabidopsis thaliana
homogenized BPH eggshell extract application to fresh wounds significantly induces biosynthesis of JA Oryza sativa; Nilaparvata lugens
inducible CRISPR-Kill lines may provide method to elucidate consequences of wound response Arabidopsis thaliana
homogenized fresh BPH egg extract application to fresh wounds significantly induces biosynthesis of JA Oryza sativa; Nilaparvata lugens
wounding causes decrease in sn-1-OPDA-MGMG levels in distal veins Arabidopsis thaliana
recombinant protein NlVgN application to fresh wounds induces higher levels of JA Oryza sativa
conversion of ACC to MACC is part of regulatory mechanism of ethylene emanation Arabidopsis thaliana
wounding causes decrease in sn-2-OPDA-MGMG levels in distal veins Arabidopsis thaliana
CAG breakdown occurs following tissue disruption Zea mays
Group 3 SUTs express in wounded tissues
Sl-LIP8 is not involved in wounding responses Solanum lycopersicum
callose accumulation can be induced by wounding
SlMPK3 is activated upon stress responses caused by wound-signaling peptide systemin Solanum lycopersicum
lymphocytes become quiescent unless exposed to tissue wounding
SlMPK2 is activated upon stress responses caused by wound-signaling peptide systemin Solanum lycopersicum
bioinformatic analysis identified overrepresented cis-element in promoters of rapid wound-responsive genes
atjat3-1;4-1 plants show significantly decreased wound-induced JA burst in distal leaves Arabidopsis thaliana
wall swelling in kelp sieve tubes might be wounding response elicited by preparation procedures for microscopy Laminariales
callose occurs in wounded cells
wounding treatment induces strong increase in SlAOC transcript abundance Solanum lycopersicum
(ANAC059, ATNAC3, NAC3, ORS1, AT3G29035) and (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) genes expression is controlled by stress, wound, or salicylic acid factors Arabidopsis thaliana
wounding treatment elevates SlDXS2 transcript levels Solanum lycopersicum
atjat3-1;4-1; (ATGLR3.3, GLR3.3, AT1G42540) triple mutant shows significantly decreased wound-induced JA burst in distal leaves Arabidopsis thaliana
actively transporting sieve element when punctured, its CF-stained contents contract within a minute into thread with wavy outlines Gerrardanthus macrorhizus
swelling of inner wall layer in severed sieve elements of Gerrardanthus grandiflorus is so intense that inner wall layer detaches from outer one and produces filament of wall material protruding from cut Gerrardanthus grandiflorus
cnr lesions cannot be initiated by pinpricks Zea mays
(ATPEPR1, PEPR1, AT1G73080) is transcriptionally induced by wounding Arabidopsis thaliana
(AtMC4, AtMCP2d, MC4, MCA4, MCP2d, AT1G79340) is activated in a Ca 2+ -dependent manner upon wound damage Arabidopsis thaliana
wounding stress resulted in concomitant increased unsaturation of phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2) Arabidopsis thaliana
wound-responsiveness of SlDXS2 in RNAi plants occurs at significantly reduced overall transcript abundance Solanum lycopersicum
AtPLAIIA gene becomes activated upon wounding Arabidopsis thaliana
wounding of leaves causes down-regulation of invertase inhibitor (ATC, AT2G27550) /VIF2 mRNA steady-state level Arabidopsis thaliana
complex wounding responses in sieve tubes include rapid swelling of inner cell wall layers following turgor loss Gerrardanthus macrorhizus
(SKU6, SPR1, AT2G03680) plants exhibit normal PI induction in response to oligosaccharide signals
(ATGLR3.3, GLR3.3, AT1G42540) mutant shows significantly decreased wound-induced JA-Ile in distal leaves Arabidopsis thaliana
wound response induces glutamate accumulation in leaves
Inactivation of TCPs by oncogenic 6B proteins could lead to prolonged cell division at the wound site
simple observation focused on processes following wounding
insect attack or wounding triggers cleavage of systemin from prosystemin Solanum lycopersicum
space formerly occupied by lumen of punctured sieve element showed irregular cellulose-linked staining of strongly varying intensity Gerrardanthus macrorhizus
MPK8-mediated (ATRBOHD, DELT1, RBOHD, AT5G47910) expression modulation represses wound-induced ROS production
(ANAC059, ATNAC3, NAC3, ORS1, AT3G29035) expression is wound-inducible in tobacco leaves Nicotiana tabacum
regulatory elements in (ANAC059, ATNAC3, NAC3, ORS1, AT3G29035) and (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) promoters have function in stress, wound, or salicylic acid responses Arabidopsis thaliana
wounding treatment significantly increased PM protein yields Zea mays
SlDXS2-RNAi lines retain wound-responsiveness of SlDXS2 Solanum lycopersicum
wounding induces AtJAT3 (AtABCG6) and AtJAT4 (AtABCG20) transcript levels in local damaged leaves Arabidopsis thaliana
xylem parenchyma play roles in wound signalling
nacreous walls may function in wounding-induced sieve tube occlusion
bundle sheath play roles in wound signalling
methyl jasmonate (MeJA) can overcome inhibitory effect of ASA Solanum lycopersicum
simultaneous coagulation of sieve element proteins occurs shortly after burning stimulus Cucurbita maxima
earlier wounding studies employed simple observation
tissue and organ regeneration gets triggered in response to mechanical injury
single cell ablation allowed identifying wound response processes
JAZ genes display differing expression patterns and induction strength in response to mechanical wounding Arabidopsis thaliana
wounding is able to modify chromatin configurations
primary wound signal activates adjacent cells
(AtPEPR2, PEPR2, AT1G17750) is transcriptionally induced by wounding Arabidopsis thaliana
tomato GA xylosyltransferase is not apparently involved in response to wounding tomato
wound response processes occurs at systemic level
stress signaling directly links to ectopic activation of developmental programs
AtGSNOR transcript and protein levels are down-regulated after wounding Arabidopsis thaliana
wounding responses appear to involve cell wall enzyme activity
GmFAD7-1 mRNA levels rapidly accumulated after wounding with 2.5–3-fold increase at 30 min after treatment Glycine max
NaGSNOR transcripts regained levels seen in non-treated plants by 3 h after treatment Nicotiana attenuata
increased auxin biosynthesis occurs in wounded leaves
InsP3 signalling relates to other signalling pathways mediating wound response
pinprick induces (ACD1, LLS1, PAO, AT3G44880) lesions Zea mays
early jasmonic acid (JA) release may occur in wounded tissue Arabidopsis thaliana
wounding-induced gene expression in InsP5-ptase plants is overall attenuated in compared with wild-type plants Arabidopsis thaliana
histone deacetylase (ATHD1, ATHDA19, HD1, HDA1, HDA19, HDAC19, RPD3A, AT4G38130) expression is induced after wounding Arabidopsis thaliana
RPLD1 was induced rapidly but transiently in wounded leaf tissues Oryza sativa
chitinase class IV is upregulated in PtMYB14 overexpression lines Picea glauca; Pinus taeda
AtProT2:GUS staining is detectable in leaves only after wounding Arabidopsis thaliana
multiple signals are involved in response to wounding
inositol 1,4,5-trisphosphate (InsP3) levels are elevated over remaining period of study beyond 30 min of stimulation sustained accumulation state
wounding decreased amount of carbon monoxide (CO)
wounding treatment caused significant decrease in intensity of pmPOX2b Zea mays
RNA levels of (ATLOX2, LOX2, AT3G45140) increase after wounding Brassica oleracea
(AtRAV1, EDF4, RAV1, AT1G13260) and (AtRAV2, EDF2, RAP2.8, RAV2, TEM2, AT1G68840) expression are up-regulated by wounding Arabidopsis thaliana
wounding decreases abundance of pmPOX2b
AFS transcript accumulates in response to mechanical wounding Pinus taeda; Picea glauca
phosphatidylcholine (PtdCho) levels are greatly reduced after 30 minutes of stimulation Arabidopsis thaliana
(ATCAD4, CAD, CAD-C, CAD4, AT3G19450) transcript accumulates in response to mechanical wounding Picea glauca
wounding induces expression of PtrWRKY genes Populus trichocarpa
inositol 1,4,5-trisphosphate (InsP3) levels show second increase to 22 ± 1 nmol g−1 fresh weight after 4–5 h secondary accumulation phase
transfer of 2-week-old soybean plants from Perlite to new containers for soybean cyst nematode (SCN) inoculation or mock inoculation may cause wounding Glycine max
mechanically wounded seedlings show transcript accumulation for defensin (DEF) Pinus taeda; Picea glauca
wounding decreases total guaiacol activity of washed plasma membrane
wounding triggers filling xylem conduits with tyloses and gels
monogalactosyldiacylglycerol (MGDG) levels decreased at later time points after wounding Arabidopsis thaliana
GAGT gene does not respond to wounding Solanum lycopersicum
NaGSNOR transcripts were slightly reduced 30 min after W+W and W+OS treatment Nicotiana attenuata
wounding and wounding supplemented with insect-derived elicitor 18:3-Glu show similar levels of induction of NaHD20 mRNA levels at 24 h Nicotiana attenuata
wound response element (TTGTTGAAATATA) is located in LIN6 promoter Solanum lycopersicum
phosphatidylcholine (PtdCho) levels decreased during first 15 minutes of wounding Arabidopsis thaliana
wounding shows no effect on washed plasma membrane
wild-type leaves exhibit red GGT activity staining around wounded region Arabidopsis thaliana
(MYC3, AT5G46760) may only participate in activation of wound response Arabidopsis thaliana
9-lipoxygenase-derived colnelenic acid dominates 24 h after wounding in transgenic Arabidopsis Arabidopsis thaliana
de-achened green fruit (G2 stage) causes strong increase in Fa (ATWRKY1, WRKY1, ZAP1, AT2G04880) gene expression Fragaria × ananassa
InsP 5-ptase plants show distinct maxima of IAA at 5 to 15 minutes and 4 to 5 hours after wounding
wounding induces NaHD20 mRNA levels slower compared with JA application Nicotiana attenuata
(ERF115, AT5G07310) expression in ablations outside stem cell niche is confined to cells directly adjacent to killed cell Arabidopsis thaliana
tomato RNase LE is induced by wounding Solanum lycopersicum
protease inhibitors (PIs) accumulate upon wounding
GmFAD7-1 mRNA levels remained high (more than 2-fold) 4 h after wounding Glycine max
jasmonic acid (JA) levels are elevated over remaining period of study beyond 30 min of stimulation sustained accumulation state
chloroplast-produced reactive oxygen species (ROS) have been shown to be capable of transmitting spread of wound-induced Programmed cell death (PCD) through maize tissue Zea mays
mechanical wounding in wild-type spruce and pine plantlets led to coordinated accumulation of Pt/PgMYB14 transcripts Picea; Pinus
wPR4e is induced following wounding Triticum aestivum
mechanical injury triggers plant defence and healing responses
jasmonic acid (JA) levels precede increases in inositol 1,4,5-trisphosphate (InsP3) levels
hydrogen peroxide (H2O2) production leads to IbMAPK phosphorylation
pectinase treatment activates TARGET OF MONOPTEROS6 (DOF5.3, TMO6, AT5G60200) pro:erRFP and (DOF5.6, HCA2, AT5G62940) pro:erRFP in cut tissues Arabidopsis thaliana
auxinole treatment (auxin receptor blocker) greatly reduces TARGET OF MONOPTEROS6 (DOF5.3, TMO6, AT5G60200) pro:erRFP and (DOF5.6, HCA2, AT5G62940) pro:erRFP expression Arabidopsis thaliana
PMEI5oe line shows strong (ERF115, AT5G07310) and (anac096, NAC096, AT5G46590) induction in intact plants Arabidopsis thaliana
(DOF5.3, TMO6, AT5G60200) induction by auxin appeared non-overlapping with (DOF5.3, TMO6, AT5G60200) induction by cellulase
(AtFAD7, FAD7, FADD, AT3G11170) wound induction is mediated by distinct promoter domains
LIN6 expression in leaves/stem is responsive to wound induction
marked increase in Fa (ATWRKY1, WRKY1, ZAP1, AT2G04880) gene expression after achene removal suggests Fa (ATWRKY1, WRKY1, ZAP1, AT2G04880) gene responds to physical damage (wounding) Fragaria × ananassa
spindle-like protein bodies (forisomes) disperse upon wounding
(ATVSP2, VSP2, AT5G24770) expression was examined in 35S::MYC3 and 35S::MYC4 overexpression plants Arabidopsis thaliana
(AtFAD2, FAD2, AT3G12120) is wound-inducible wounding stress Gossypium hirsutum
ablations can result in local cell shape changes Arabidopsis thaliana
auxin accumulates at wound site
NAC DOMAIN-CONTAINING PROTEIN071 (anac071, NAC071, AT4G17980) promotes cell-wall remodeling
asymmetric expression pattern of (DOF5.6, HCA2, AT5G62940) and TARGET OF MONOPTEROS6 (DOF5.3, TMO6, AT5G60200) suggests mobile substance, such as sugar or auxin, could be responsible Arabidopsis thaliana
(DOF5.6, HCA2, AT5G62940) and (DOF5.3, TMO6, AT5G60200) were exceptional since they also showed ectopic expression in epidermis
acetyl salicylic acid (ASA) efficiently suppresses accumulation of invertase activity Solanum lycopersicum
Arabidopsis lectin receptor kinase lecRK-a1 expression is induced during wounding Arabidopsis thaliana
wounding increased expression in GmEREBP1 Glycine max
LIN6 promoter is up-regulated by mechanical wounding Solanum lycopersicum
suberin deposition can occur in response to wounding
putrescine plays a role in wound repair
DAMPs have been regarded as wound-inducing proteins
wounding induces expression of Ipomoelin (IPO) Ipomoea batatas
ethylene acts as important modulator of plant responses to mechanical damage
wounding stress induced increased activation of MAPKs Solanum lycopersicum
zinc protoporphyrin IX (ZnPP) addition the more added, the more observed ipomoelin (IPO) expression
hyperpolarization after burning reflects sudden, transient turgor disbalance of the system Cucurbita maxima
TaWRKY78 is almost unaffected by wounding Triticum aestivum
GUS expression is higher in veins located more closely to cutting edge Nicotiana tabacum
spatial distribution of invertase activity matches histochemical GUS expression pattern Solanum lycopersicum; Nicotiana tabacum
wounding stress induced systemic response to insect attack Solanum lycopersicum
wounding reduced haem oxygenase (HO) and carbon monoxide (CO) contents
(AtRAV1, EDF4, RAV1, AT1G13260) and (AtRAV2, EDF2, RAP2.8, RAV2, TEM2, AT1G68840) expression is induced by wounding Arabidopsis thaliana
auxin accumulation upregulates (anac096, NAC096, AT5G46590)
an auxin response to promote DOF activation and regeneration
NaHD20 expression is induced by wounding Nicotiana attenuata
non-wounded leaf areas do not show GUS expression Nicotiana tabacum
WIPK is transducer of the wounding signal
AG motif-binding protein-1 is positive regulator of wounding and elicitor response Solanum tuberosum
wounding in Arabidopsis causes almost equal increase in 13- and 9-hydroperoxides Arabidopsis thaliana
JA-insensitive jai1-1 mutant is impaired in lesion responses
(GGT1, AT4G39640) knockout leaves do not exhibit GGT activity staining around wounded region Arabidopsis thaliana
phloem parenchyma play roles in wound signalling
empty vector (EV) application to fresh wounds results in higher JA level Oryza sativa
homogenized dsNlVg-BPH ovary extract application to fresh wounds exhibits impaired induction of JA-Ile Oryza sativa; Nilaparvata lugens
artificial injury with razor blade or microneedle in Tradescantia leaf epidermal cells causes actin filaments in neighbouring cells to become parallel to slit wound Tradescantia
wounding triggers increase in JA-Ile (jasmonoyl-isoleucine) levels Arabidopsis thaliana
CAG breaks down to catechol following tissue disruption Zea mays
(AOS, CYP74A, DDE2, AT5G42650) (AOC2, AT3G25770) (AtOPR3, DDE1, OPR3, AT2G06050) (AtGH3.11, FIN219, JAR1, AT2G46370) (CYP94B3, AT3G48520) (JMT, AT1G19640) and (ATST2A, ST2A, AT5G07010) expression enhanced in jam x3 plants after wounding Arabidopsis thaliana
SEOR agglomerations involvement in wound sealing appears questionable
cytoskeleton governs response of the cell to wounding
wounding induces changes in reactive oxygen species levels
cellular damage from bleomycin, cutting, or cell ablation causes expansion of ETHYLENE RESPONSE FACTOR115 (ERF115, AT5G07310) expression
dominant-negative ERF113-SRDX plants fail to heal stem cuts
cellulose degradation can overcome auxin receptor inhibition Arabidopsis thaliana
Upon wounding, all four transcriptional reporters showed strong vascular induction of all four transcriptional reporters
This activation occurred even when turgor pressure was reduced with mannitol treatment (DOF5.6, HCA2, AT5G62940) and (DOF5.3, TMO6, AT5G60200) activation
LIN6::GUS transgenic plants show GUS expression upon mechanical wounding Nicotiana tabacum
wound induction of LIN6 promoter reaches a level of more than 50-fold over the control Nicotiana tabacum
ABA and MeJA are signals known to modulate mechanical wounding
lox6B mutant attenuates wound-response increase in JA levels in leaf 13 vein Arabidopsis thaliana
pYUC8::GUS reporter lines show no detectable reporter activity in response to wounding Arabidopsis thaliana
IbMYB expression is repressed by microRNA (miR828, MIR828A, AT4G27765)
mechanical damage induces rapid production of jasmonates (JAs)
leucine aminopeptidase (LAP) shows a slower increase in mRNA accumulation in both damaged and distal leaves Solanum tuberosum
mechanical wounding activates CaPIMP1 expression Capsicum annuum
wounding promotes (ML3, AT5G23820) gene expression Arabidopsis thaliana
ML3p:GUS transgenic lines show increased staining at sites of wounding Arabidopsis thaliana
wounding causes large increase in synthesis of all measured volatiles Solanum lycopersicum
large increase in TomloxD RNA in wounded tissues indicates 13-LOX is not involved in GLV synthesis Solanum lycopersicum
carbon monoxide (CO) contents were decreased in sweet potato after wounding
carbon monoxide (CO) might regulate hydrogen peroxide (H2O2) contents to affect ipomoelin (IPO) induction
carbon monoxide (CO) could activate ascorbate peroxidase (APX), catalase (CAT), and peroxidase (POX) to scavenge hydrogen peroxide (H2O2) induced by wounding
IbMAPK phosphorylation leads to ipomoelin (IPO) expression
peptide derived from tomato pathogenesis-related protein 1 (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) is wound induced in the same way as systemin Solanum lycopersicum
carbon monoxide (CO) main reduction in at 3h after wounding
wild-type tomato leaves show invertase activity distribution upon wounding Solanum lycopersicum
methyl jasmonate (MeJA) restores invertase activity Solanum lycopersicum
multiple hormones and signals regulate wound response
four related DOF transcription factors promoted callus formation
wounding significantly reduces TomloxC RNA contents Solanum lycopersicum
wound response to grafting induces PR proteins Vitis vinifera
wounding-induced decrease in carbon monoxide (CO) content activates phosphorylation of IbMAPK through IbMEK1
wounding very significantly increases TomloxD RNA contents Solanum lycopersicum
wound-induced GLV synthesis is significantly reduced in LoxC-AS lines Solanum lycopersicum
peptide derived from tomato pathogenesis-related protein 1 (AtCAPE9, ATPR1, PR 1, PR1, AT2G14610) is wound induced Solanum lycopersicum
confocal laser ablation of vascular cells in hypocotyl causes upregulation of (DOF5.6, HCA2, AT5G62940) fluorescent reporter Arabidopsis thaliana
auxin and cell-wall-degrading enzyme treatments appear additive for (ERF115, AT5G07310) pro:GUS-GFP expression Arabidopsis thaliana
PMEI5oe cells are so stiff that growth results in self-inflicted wounding by shearing of the cell wall
wounding induces anisotropic cell growth
salicylic acid treatment has no effect upon TARGET OF MONOPTEROS6 (DOF5.3, TMO6, AT5G60200) induction Arabidopsis thaliana
wounding induces changes in hormone levels
cell-wall breakdown products suppress growth
auxin induced TMO6 close to the cut
carbon monoxide (CO) activation of ascorbate peroxidase (APX), catalase (CAT), and peroxidase (POX) further interfered in ipomoelin (IPO) expression
methyl jasmonate (MJ) further induces ipomoelin (IPO) expression
infiltration process may have caused wounding that activated phospholipase Ds (PLDs)
OsHPL2 is not wound-induced Oryza sativa
expression levels of genes involved in the phenylpropanoid pathway are up- or down-regulated after wounding
LIN6 promoter activity is detected adjacent to the cutting edge Nicotiana tabacum
PD98059 blocked IbMAPK phosphorylation in the wounding response
C5 volatile synthesis increases in leaves following mechanical wounding Solanum lycopersicum
wound healing is affected in mutants lacking the PSK receptor
active JA pathway is required for wound-induced growth retardation
TARGET OF MONOPTEROS6 (DOF5.3, TMO6, AT5G60200) pro:erRFP and (DOF5.6, HCA2, AT5G62940) pro:erRFP show expanded fluorescence into endodermis and cortex Arabidopsis thaliana
tissue disruption causes maize plants to accumulate catechol Zea mays
StCCR gene expression shows induced expression pattern similar to StPAL1 gene expression Solanum tuberosum
wounding and defence responsive genes (LCR77, PDF1.2, PDF1.2A, AT5G44420) were chosen as target promoter candidates Arabidopsis thaliana
auxin treatment increases ETHYLENE RESPONSE FACTOR115 (ERF115, AT5G07310) expression
TARGET OF MONOPTEROS6 (DOF5.3, TMO6, AT5G60200) behaves similarly to (DOF5.6, HCA2, AT5G62940) Arabidopsis thaliana
wounding induces changes in cell-wall integrity
confocal laser ablation of cortex cells in hypocotyl causes upregulation of TARGET OF MONOPTEROS6 (DOF5.3, TMO6, AT5G60200) and (DOF5.6, HCA2, AT5G62940) expression Arabidopsis thaliana
PMEI5oe line increases (DOF5.6, HCA2, AT5G62940) transcript levels Arabidopsis thaliana
cellulose and pectin degradation or changes are sufficient to induce wound-responsive ERFs and ANACs Arabidopsis thaliana
(DOF5.6, HCA2, AT5G62940) and (DOF5.3, TMO6, AT5G60200) were exceptional since they also showed ectopic expression in endodermis
modifications to cellulose microfibrils and pectic matrix polysaccharides induce downstream genes, the DOFs
(anac096, NAC096, AT5G46590) showed similar expression pattern to DOF expression
oligogalacturonides (OGs) are released upon wounding
wounding induces changes in turgor pressure
activities of catalase (CAT), ascorbate peroxidase (APX), and peroxidase (POX) were also elevated by carbon monoxide (CO) in wounding responses
mannitol treatment inhibits ETHYLENE RESPONSE FACTOR115 (ERF115, AT5G07310) induction
H2O2 treatment increases ETHYLENE RESPONSE FACTOR115 (ERF115, AT5G07310) expression
shoot-derived auxin is necessary for TARGET OF MONOPTEROS6 (DOF5.3, TMO6, AT5G60200) and (DOF5.6, HCA2, AT5G62940) induction Arabidopsis thaliana
pectin modifications require auxin signaling for wound induction Arabidopsis thaliana
Expression of genes involved in the general phenylpropanoid and specific lignin biosynthesis pathways, i.e. phenylalanine ammonia lyase (IbPAL), hydroxycinnamoyl CoA shikimate/quinate hydroxycinnamoyl transferase (IbHCT) and cinnamyl alcohol dehydrogenase 1 (IbCAD1) was induced upon wounding Ipomoea batatas
leaf 8 wounded mechanically by crushing apical 60% of the lamina
exogenous auxin (NAA) activates TARGET OF MONOPTEROS6 (DOF5.3, TMO6, AT5G60200) pro:erRFP in cut hypocotyls Arabidopsis thaliana
auxin treatment induces (ERF115, AT5G07310) pro:GUS-GFP expression in intact roots Arabidopsis thaliana
reducing auxin response with iaa18-1 prevented (DOF5.6, HCA2, AT5G62940) and (DOF5.3, TMO6, AT5G60200) wound activation
wounding caused DOF expression to spread laterally and to adjacent cell layers
wounding is required for auxin enhancement of (DOF5.6, HCA2, AT5G62940) and TARGET OF MONOPTEROS6 (DOF5.3, TMO6, AT5G60200) Arabidopsis thaliana
auxin combined with cellulase or pectinase is not additive for TARGET OF MONOPTEROS6 (DOF5.3, TMO6, AT5G60200) pro:erRFP intensity Arabidopsis thaliana
wound-induced [L-Glu] apo and [Ca2+] cyt increases propagate at speed of 472 ± 78 μm/s Arabidopsis thaliana
sensitively balanced and coordinated mechanisms result in wound healing
wounding induces expression of OsHPL3 Oryza sativa
(ATMAPK3, ATMPK3, MPK3, AT3G45640) is rapid wound-responsive gene Arabidopsis thaliana
(ATWRKY40, WRKY40, AT1G80840) expression in (A11, AtCHI, CFI, CHI, TT5, AT3G55120) −Nar plants is higher than in (A11, AtCHI, CFI, CHI, TT5, AT3G55120) +Nar plants at 60 min after wounding Arabidopsis thaliana
An increase of lignin content was observed in sweet potato after wounding Ipomoea batatas
cucumber stems when cut exude fluid more copiously from internal phloem (IP) Cucumis sativus
AtERF#111 expression shows 2.1-fold induction by H2O2 treatment Arabidopsis thaliana
resin cells development is wound inducible Taiwania cryptomerioides
ABA signaling has antagonistic interaction with jasmonate signaling Arabidopsis thaliana
(DAA1, AT1G64110) expression is induced by wounding Arabidopsis thaliana
StAOS2 mRNA is barely detected in damaged leaves Solanum tuberosum
MAPKs are involved in plant signal transduction in response to wounding
genes whose expression is induced by touch overlap with wound-responsive genes induced by JA
wounding induces changes in gene expression
sorbitol or mannitol treatment reduces jasmonic acid signaling in wounded tissues
(DOF5.6, HCA2, AT5G62940) and TARGET OF MONOPTEROS6 (DOF5.3, TMO6, AT5G60200) activation is much stronger above the cut than below the cut separated hypocotyls Arabidopsis thaliana
(DOF5.6, HCA2, AT5G62940) and (DOF5.3, TMO6, AT5G60200) were exceptional since they also showed ectopic expression in cortex
DOFs, ANACs, and ERFs transcription factors promotes tissue attachment
StTHT gene expression is significantly upregulated soon after wounding Solanum tuberosum
plant defensins were differentially expressed upon wounding Arabidopsis thaliana
wounding induces changes in calcium levels
confocal laser ablation of vascular cells in hypocotyl causes upregulation of (DOF6, AT3G45610) fluorescent reporter Arabidopsis thaliana
(DOF5.6, HCA2, AT5G62940) is activated above cut in separated hypocotyls Arabidopsis thaliana
carbon monoxide (CO) addition inhibited methyl jasmonate (MJ)-induced ipomoelin (IPO) expression
carbon monoxide (CO) decrease subsequently content of hydrogen peroxide (H2O2) and phosphorylation of ERK were induced
Driselase treatment rescues reduction in DOF activation caused by mannitol treatment Arabidopsis thaliana
AtPLAI gene becomes activated upon wounding Arabidopsis thaliana
W box is wounding, salicylic acid and stress response element
iaa18-1 dominant mutant inhibits expression of TARGET OF MONOPTEROS6 (DOF5.3, TMO6, AT5G60200) (DOF5.6, HCA2, AT5G62940) and (DOF2.1, AT2G28510) Arabidopsis thaliana
burning of one rosette leaf induces movement of the stem of the primary inflorescence Arabidopsis thaliana
extracellular ATP and NO are coplayers in wound response
wounding results in highly elevated in situ invertase activity Arabidopsis thaliana
complex wounding responses in sieve tubes include formation of plugs from P-proteins and other materials in adjacent sieve elements Gerrardanthus macrorhizus
(ATGLR3.3, GLR3.3, AT1G42540) (ATGLR3.6, GLR3.6, AT3G51480) double mutant does not show decrease in OPDA levels after wounding Arabidopsis thaliana
FD treatment does not alter StC4H gene expression Solanum tuberosum
(AGC2, AGC2-1, AtOXI1, OXI1, AT3G25250) regulates wound-inducible (ATMAPK6, ATMPK6, MAPK6, MPK6, AT2G43790) activation Arabidopsis thaliana
(CKRC2, YUC8, YUCCA8, AT4G28720) and (YUC9, YUCCA9, AT1G04180) are induced by wounding Arabidopsis thaliana
sRNA8105 is wounding-induced small RNA Ipomoea batatas
Scots pine and larch may excrete large quantities of pitch in response to wounding
homogenized fresh BPH egg extract application to fresh wounds significantly induces biosynthesis of JA-Ile Oryza sativa; Nilaparvata lugens
(DALL2, AT1G51440) mutant background shows slightly induced JA and JA-Ile after wounding Arabidopsis thaliana
(ML3, AT5G23820) expression is induced after wounding Arabidopsis thaliana
wounding triggers phase changes in populations of oxygenated lipids (O) Arabidopsis thaliana
homogenized BPH eggshell extract application to fresh wounds significantly induces biosynthesis of JA-Ile Oryza sativa; Nilaparvata lugens
wound-response decreases in OPDA, sn-2-OPDA-MGMG and sn-2-18:3-MGMG did not occur in wounded (ATGLR3.3, GLR3.3, AT1G42540) (ATGLR3.6, GLR3.6, AT3G51480) double mutant Arabidopsis thaliana
four related DOF transcription factors promoted stem incision
short-term wounding treatment reveals rapid increase in ACC (1-aminocyclopropane-1-carboxylic acid) levels Arabidopsis thaliana
small gene is inducible by wounding Arabidopsis thaliana
wounding does not significantly change levels of OPDA, sn-2-OPDA-MGMG, JA and JA-Ile in c1x11 mutant Arabidopsis thaliana
homogenized dsGFP-BPH ovary extract application to fresh wounds significantly induces biosynthesis of JA Oryza sativa; Nilaparvata lugens
(ATGLR3.3, GLR3.3, AT1G42540) (ATGLR3.6, GLR3.6, AT3G51480) double mutant does not show decrease in sn-2-OPDA-MGMG levels after wounding Arabidopsis thaliana
(ATGLR3.3, GLR3.3, AT1G42540) (ATGLR3.6, GLR3.6, AT3G51480) double mutant does not show increase in JA levels after wounding Arabidopsis thaliana
(ATGLR3.3, GLR3.3, AT1G42540) /GLR3.6-dependent electrical signals trigger phase changes in populations of oxygenated lipids (O) converting them to different phases (W) Arabidopsis thaliana
recombinant protein NlVgN application to fresh wounds induces higher levels of JA-Ile Oryza sativa
maize plants form catechol upon mechanical damage Zea mays
homogenized fresh SBPH egg extract application to fresh wounds results in higher levels of JA Oryza sativa; Laodelphax striatellus
wounding triggers rapid increase in vascular jasmonic acid (JA) levels Arabidopsis thaliana
homogenized dsNlVg-BPH ovary extract application to fresh wounds exhibits impaired induction of JA Oryza sativa; Nilaparvata lugens
sRNA8105 expression up-regulated wounding Ipomoea batatas
invertase inhibitor (ATC, AT2G27550) /VIF2 expression is not detectable at 24 and 48 hours after wounding Arabidopsis thaliana
atjat3-1;4-1; (ATGLR3.3, GLR3.3, AT1G42540) triple mutant shows significantly decreased wound-induced JA-Ile in distal leaves Arabidopsis thaliana
ACC (1-aminocyclopropane-1-carboxylic acid) levels returns to control level within 24 h after wounding Arabidopsis thaliana
damaged leaves accumulate both AOS1 and AOS2 proteins Solanum tuberosum
(ATMAPK3, ATMPK3, MPK3, AT3G45640) expression is activated at 5 min after wounding in (A11, AtCHI, CFI, CHI, TT5, AT3G55120) −Nar plants Arabidopsis thaliana
wounding leads to IbMYB1 DNA methylation Ipomoea batatas
wounding induces expression of sRNA8105 Ipomoea batatas
brassinosteroid treatment increases ETHYLENE RESPONSE FACTOR115 (ERF115, AT5G07310) expression
PMEI5oe line increases TARGET OF MONOPTEROS6 (DOF5.3, TMO6, AT5G60200) transcript levels Arabidopsis thaliana
Both PMEI5oe and pectin digestion were sufficient to activate (DOF5.6, HCA2, AT5G62940) and (DOF5.3, TMO6, AT5G60200)
rapid wound-responsive (RWR) genes respond quickly to mechanical wounding Arabidopsis thaliana
expression of IbANS, IbCHI, IbCHS, IbDFR and IbF3H was down-regulated wounding Ipomoea batatas
FD application results in significant delay in induced expression of StGPAT5 gene Solanum tuberosum
AtERF#111 expression decreases to basal levels after 6 h Arabidopsis thaliana
AtERF#111 expression is also highly induced upon wounding treatment Arabidopsis thaliana
division plane switch depends on cell expansion
(AGC2, AGC2-1, AtOXI1, OXI1, AT3G25250) expression pattern is different in (ATMPK8, MPK8, AT1G18150) mutant Arabidopsis thaliana
expression of all the IbMYB1 family genes at 3 h after wounding showed no obvious differences from plant without wounding Ipomoea batatas
StAOS1 mRNA is detected in parenchyma close to the wound site Solanum tuberosum
(ATNRT3.1, NRT3.1, WR3, AT5G50200) encodes wound-responsive protein (ATNRT3.1, NRT3.1, WR3, AT5G50200) Arabidopsis thaliana
rain, wind, pathogens and herbivores cause wounding to plants
sRNA8105 represses the IbMYB1 family genes to regulate the phenylpropanoid pathway following wounding Ipomoea batatas
oryzalin-treated roots displayed normal wound-responsive expansion
ETHYLENE RESPONSE FACTOR109 (ERF109, RRTF1, AT4G34410) mediates auxin synthesis
dominant-negative ANAC071-SRDX plants fail to heal stem cuts
adding auxin in the absence of wounding seemed to have little effect upon (DOF5.6, HCA2, AT5G62940) or (DOF5.3, TMO6, AT5G60200) induction
(ERF115, AT5G07310) did not require auxin or cell expansion for wound activation
DOFs, ANACs, and ERFs transcription factors promotes wound filling
OsHPL1 is not wound-induced Oryza sativa
ZmLOX8 is strongly induced by wounding at early time points Zea mays
sRNA8105 transcript remained present for up to 3 h after leaf wounding Ipomoea batatas
Wounding-induced sRNA8105 repressed expression of IbMYB1 family genes Ipomoea batatas
leaf wounding induces autophagy in roots Arabidopsis thaliana
indole glucosinolates (IGs) have role in root response to leaf wounding Arabidopsis thaliana
histone (H3.15, AT5G12910) is induced upon wounding in roots Arabidopsis thaliana
(ATWRKY40, WRKY40, AT1G80840) is rapid wound-responsive gene Arabidopsis thaliana
stem cells become quiescent unless exposed to tissue wounding
SlDXS2-RNAi lines exhibit wound-induced increase in SlDXS2 transcripts Solanum lycopersicum
sieve plates bordering punctured sieve element curved toward contracted cytoplasmic lumen Gerrardanthus macrorhizus
temporal pattern of JA-Ile and 9,10-KODA induction corresponds well with pattern of induction of JA-Ile and 9,10-KODA Zea mays
agarwood sesquiterpene synthase 1 (ASS1) is wound-induced gene Aquilaria sinensis
preformed OPDA pools are depleted rapidly in Arabidopsis leaves distal to wounds Arabidopsis thaliana
methyl jasmonate (MeJA) induces wound-responsive gene expression in plants
448 out of 1415 DEGs from our wounding array were also modified in expression in previous wounding array Arabidopsis thaliana
nicotine increases in response to wounding Nicotiana spp.
coronatine (COR) treatment induces responses to wounding Arabidopsis thaliana
homogenized fresh WBPH egg extract application to fresh wounds results in higher levels of JA-Ile Oryza sativa; Sogatella furcifera
wounding of leaf 8 causes rapid decline in OPDA levels in primary vein and vein sheath Arabidopsis thaliana
ES7 (endosidin 7) does not inhibit callose accumulation in response to wounding Arabidopsis thaliana
(YUC9, YUCCA9, AT1G04180) expression responds strongly to wounding similar to wound-inducible ALLENE OXIDE SYNTHASE promoter Arabidopsis thaliana
processing and maturation of plant elicitor peptide 1 (ATPEP1, PEP1, PROPEP1, AT5G64900) triggers defense response in Arabidopsis Arabidopsis thaliana
(DORN1, LecRK-I.9, P2K1, AT5G60300) overexpression line shows elevated response to wounding
SlMPK1 is activated upon stress responses caused by wound-signaling peptide systemin Solanum lycopersicum
callose is generally wound-response polysaccharide
fibroblasts become quiescent unless exposed to tissue wounding
partial mechanical wounding triggers C6-alcohol production Arabidopsis thaliana
OsSAP1 transcript rapidly responds to mechanical wounding Oryza sativa
slight increase in sporogenous-like cells in water-treated wild-type anthers may have been triggered by wounding Oryza sativa
(ATLOX5, LOX5, AT3G22400) knockout mutants displayed greatly reduced wound-induced accumulation of oxylipins Zea mays
ASS1 expression is rapidly up-regulated in response to wounding Aquilaria sinensis
genes most highly induced by ERF#111-OE were also differentially expressed upon wounding Arabidopsis thaliana
single-cell ablation causes microtubules to orient in circumferential pattern around wound Arabidopsis thaliana
systemin amplifies jasmonate production in vascular tissues Solanum lycopersicum
(AtMC4, AtMCP2d, MC4, MCA4, MCP2d, AT1G79340) activation upon wound damage leads to processing and maturation of plant elicitor peptide 1 (ATPEP1, PEP1, PROPEP1, AT5G64900) Arabidopsis thaliana
remodeling of membrane lipids is caused by wounding
(AtNPF2.10, GTR1, NPF2.10, AT3G47960) is claimed to be multifunctional transporter with a role in stamen development and wound responses Arabidopsis thaliana
water-treated controls show accumulation of abscisic acid (ABA) Solanum tuberosum
(ATLOX6, LOX6, AT1G67560) mutant does not show rapid changes in JA and JA-Ile levels in distal leaves Arabidopsis thaliana
abscisic acid (ABA) accumulation begins within 2 days post-wounding Solanum tuberosum
StC4H gene expression does not show clear pattern of induced expression Solanum tuberosum
StGPAT5 gene expression shares same temporal expression pattern as genes involved in aliphatic metabolism Solanum tuberosum
AtERF#111 expression is strongly induced by wounding stress Arabidopsis thaliana
rapid wound-responsive (RWR) genes may be modulated by flavonoids Arabidopsis thaliana
wounding induces JA accumulation Arabidopsis thaliana
lignin content is increased to thicken the cell wall at the wounding site
leaf wounding induces I3C-dependent response in roots Arabidopsis thaliana
homogenized dsGFP-BPH ovary extract application to fresh wounds significantly induces biosynthesis of JA-Ile Oryza sativa; Nilaparvata lugens
enzymes necessary for rapid, wound-response jasmonate synthesis are preformed in Arabidopsis leaves Arabidopsis thaliana
ES7 (endosidin 7) does not affect callose accumulation in physically wounded plants Arabidopsis thaliana
FD treatment of tubers results in clear significant delay in induction of StFAR3 gene expression Solanum tuberosum
FD application results in significant delay in induced expression of StGPAT6 gene Solanum tuberosum
AtERF#111 shows strong induction upon wounding Arabidopsis thaliana
prAtERF#111:fLUC lines show wounding-dependent response of prAtERF#111 Arabidopsis thaliana
SPLAYED (CHR3, SYD, AT2G28290) is necessary for transcriptional induction of MYC2-dependent genes in response to wounding Arabidopsis thaliana
jasmonoyl-isoleucine (JA-Ile) synthesis is rapid and is initiated in < 3 min in undamaged leaves that are vascularly connected to wounded leaves Arabidopsis thaliana
defense response in external phloem (EP) of peripheral vascular bundle (PeVB) involves response to wounding Cucumis sativus
water-treated controls show induction of StCYP86A33 gene expression Solanum tuberosum
FD application results in significant delay in induced expression of StFHT gene Solanum tuberosum
Thioredoxin H-type 8 ( (ATH8, TH8, AT1G69880) ) was differentially expressed upon wounding Arabidopsis thaliana
CMT response after ablation in isoxaben-treated WT meristems was quantified for cells surrounding the wound
wound-adjacent cells underwent re-arrangement of cortical MT orientation
(ATMPK8, MPK8, AT1G18150) pathway leads to repression of ROS-related signaling response after mechanical wounding Arabidopsis thaliana
confocal laser ablation of vascular cells in hypocotyl causes upregulation of TARGET OF MONOPTEROS6 (DOF5.3, TMO6, AT5G60200) fluorescent reporter Arabidopsis thaliana
FD-treated tubers show significant upregulation of StTHT gene expression Solanum tuberosum
(ATH8, TH8, AT1G69880) were chosen as target promoter candidates Arabidopsis thaliana
ABA treatment does not alter StPAL1 gene expression patterns Solanum tuberosum
FD application results in significant delay in induced expression of StABCG1 gene Solanum tuberosum
FD + ABA treatment does not alter StC4H gene expression Solanum tuberosum
AtERF#111 expression reaches maximum (>300-fold increase) at 1 h after wounding stress Arabidopsis thaliana
supracellular alignments of CMTs are observed in WT meristems after wounding
cell wall damage in presence of auxin is sufficient for robust induction of (ERF115, AT5G07310) expression
ZmLOX5 transcript accumulation is detected between 1 h and 4 h after mild wounding Zea mays
submergence did not activate wound-inducible marker JASMONATE-ZIM-DOMAIN PROTEIN 10 Arabidopsis thaliana
inhibition of NADPH oxidase activity could be reason for observed inhibitory action of methyl viologen on the decrease in oxygen concentration after cell wall microperforation Chara corallina
large-scale lipid degradation in disintegrating damaged cells may explain transient phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2) decreases Arabidopsis thaliana
wounding induces increase in jasmonic acid (JA) levels
wounding causes strong decrease in guaiacol activity of unwashed plasma membrane preparations
extracellular soluble peroxidases are involved in wound response Triticum aestivum
PtMYB14 transcript accumulates strongly and rapidly in response to mechanical wounding Pinus taeda
gain-of-function (AVB1, IFL, IFL1, REV, AT5G60690) mutants show callus formation on the stem surface Populus trichocarpa
(ATMAPK3, ATMPK3, MPK3, AT3G45640) expression peaks significantly later at approximately 30 min after wounding in (A11, AtCHI, CFI, CHI, TT5, AT3G55120) +Nar plants Arabidopsis thaliana
naringenin significantly delays and reduces induction of rapid wound-responsive (RWR) genes Arabidopsis thaliana
expression of IbMYB2 genes also decreased 0.5 and 1 h after wounding Ipomoea batatas
phosphoinositide levels decreased during first 15 minutes of wounding Arabidopsis thaliana
global lipid degradation may take place rapidly after wounding Arabidopsis thaliana
wound-inducible genes are manifested by expression of physiological responses to wounding Arabidopsis thaliana
cell wall enzyme activity is possibly related to suberin formation
FD treatment of tubers results in clear significant delay in induction of StCYP86B12 gene expression Solanum tuberosum
FD treatment of tubers results in clear significant delay in induction of StKCS6 gene expression Solanum tuberosum
15 direct target genes of AtERF#111 whose expression was also modified in response to wounding stress or in ERF#111-OE transgenic lines Arabidopsis thaliana
wounding treatment induces increase in SlDXS2 transcripts Solanum lycopersicum
irregular cellulose-linked staining matched the behaviour of nacreous walls in sieve tube sections Gerrardanthus macrorhizus
oligosaccharide signals are thought to play a role in local wound response
(PSY1, AT5G58650) is strongly expressed after wounding
WOUND-INDUCED DEDIFFERENTIATION1–4 is the name for four (AP2, AtAP2, FL1, FLO2, AT4G36920) /ERF transcription factors
Ca2+/CaMs–MKK3–MPK8 pathways are involved in perception of mechanical wounding Arabidopsis thaliana
phosphoinositide-signaling cascade roles for wound responses in Arabidopsis Arabidopsis thaliana
carnation DcEIL3 (54% identical to Arabidopsis (AtEIN3, EIN3, AT3G20770) at the amino acid level) expression was also influenced by wounding Dianthus caryophyllus
different types of wounding triggered expression of different class III peroxidases Oryza sativa
NaGSNOR transcript levels increased 2.2-fold after W+W treatment at 6 h Nicotiana attenuata
(AGC2, AGC2-1, AtOXI1, OXI1, AT3G25250) expression pattern is different in mkk3-1 + W7 Arabidopsis thaliana
P-proteins other than the forisome-forming SEO family have been postulated to prevent assimilate loss by sealing wounded sieve tubes
infiltration procedure causes wounding effect on leaves Arabidopsis thaliana
(ATGLR3.3, GLR3.3, AT1G42540) mutant shows significantly decreased wound-induced JA burst in distal leaves Arabidopsis thaliana
suberin is formed in response to wound damage
invertase inhibitor (ATC, AT2G27550) /VIF2 is strongly expressed at 8 hours past wounding Arabidopsis thaliana
jasmonic acid (JA) increases from 0.5 to 2.5 nmol g−1 fresh weight within first 5 min after wounding wound response signaling
abscisic acid (ABA) accumulation reaches maximum sustained level by 3 days post-wounding Solanum tuberosum
Sl-LIP8 knockout lines showed no difference in wound-associated C6 volatiles in leaves Solanum lycopersicum
root tips were cut to make wounding
(SKU6, SPR1, AT2G03680) impairs systemic PI expression
(ATGLR3.3, GLR3.3, AT1G42540) mutant shows decreased wound-induced JA burst in distal leaves Arabidopsis thaliana
atjat3-1;4-1 plants show significantly decreased wound-induced JA-Ile in distal leaves Arabidopsis thaliana
nacreous walls in G. macrorhizus might be response to wounding Gerrardanthus macrorhizus
multimerized cis-element CGCG TT confers rapid response to wounding
MAPKs are involved in plant signal transduction in response to wounding Arabidopsis thaliana
atjat3-1;4-1; (ATGLR3.3, GLR3.3, AT1G42540) triple mutant shows even greater reduction in wound-induced JA burst in distal leaves Arabidopsis thaliana
TCP proteins might play a role in arrest of wound-induced cell divisions
MgCl2 infiltration causes approximately 11-fold decrease in expression of invertase inhibitor (ATC, AT2G27550) /VIF2 Arabidopsis thaliana
adjacent sieve elements accumulate less densely stained, flexible streaks Gerrardanthus macrorhizus
JAT4OX plants show remarkable increases in wound-induced JA in distal leaves Arabidopsis thaliana
MgCl2 infiltration decreases expression of invertase inhibitor (ATC, AT2G27550) /VIF2 Arabidopsis thaliana
wounding induces AtJAT3 (AtABCG6) and AtJAT4 (AtABCG20) transcript levels in distal leaves Arabidopsis thaliana
Zinnia ZRNase II is induced by wounding Zinnia
PtMYB14 transcript accumulation is slightly delayed or simultaneous with isoprenoid and terpenoid pathway transcript accumulation Pinus taeda
histone deacetylase (ATHDA6, AXE1, HDA6, HDAC6, RPD3B, RTS1, SIL1, AT5G63110) expression is induced after wounding Arabidopsis thaliana
wounding induces the production of Arabidopsis thaliana (ATPEP1, PEP1, PROPEP1, AT5G64900) (a 23-amino acid peptide) Arabidopsis thaliana
hydrogen peroxide (H2O2) accumulates around wound
(ATMPK4, MAPK4, MPK4, AT4G01370) is activated by wounding Arabidopsis thaliana
depletion of both 13-AOS enzymes leads to alteration in wound-induced gene expression
ablation of a horizontal section of cells mimics macroscopic root tip excision
genes in cluster II-OUT associated with wounding Arabidopsis thaliana
bleomycin (BLM) treatment of pERF115:GFP-NLS/GUS seedlings in fer-4 background results in enhanced induction of (ERF115, AT5G07310) expression compared with wild-type
mechanoinduced oxygen response insensitive to DCMU Chara corallina
wounding-induced ETHYLENE RESPONSIVE FACTOR 115 (ERF115, AT5G07310) expression is related to changes in auxin accumulation Arabidopsis thaliana
(ATFLS2, FLS2, AT5G63580) upregulation occurs in elongation zone of the root Arabidopsis thaliana
increase in cell width followed by change of division plane orientation
ROS propagation is enhanced in mpk8 mutant and repressed in mpk8 rbohD mutant after mechanical wounding Arabidopsis thaliana
WT plants show clear induction of ZmLOX10 transcripts Zea mays
IbMYB1 and sRNA8105 are involved in the regulation of IbMYB2 genes Ipomoea batatas
cell ablation causes instantaneous pressure loss at wound site
division plane switch depends on cell's underlying physical deformations
(AGC2, AGC2-1, AtOXI1, OXI1, AT3G25250) shows moderate changes in expression in (ATMPK8, MPK8, AT1G18150) mutant Arabidopsis thaliana
RBOHD-mediated ROS production has been implicated in wound-induced ROS wave Arabidopsis thaliana
wounding alone does not cause differences in jasmonic acid-isoleucine conjugate accumulation Nicotiana attenuata
BR biosynthesis-defective dpy mutant showed intense increase in PI-I transcript accumulation after wounding
(SKU6, SPR1, AT2G03680) plants are deficient mainly in systemic proteinase inhibitor (PI) expression in response to wounding
ABA application to wounded tubers results in significantly earlier expression of StFHT gene Solanum tuberosum
inner cells deform more in response to cell ablation, taking priority in response to wounding
less densely stained, flexible streaks resemble wounding-induced P-protein plugs Gerrardanthus macrorhizus
ER bodies formation was induced in wounded cotyledons Arabidopsis thaliana