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leaf senescence

28945 relationships annotated with this phrase. Showing first 500 of 28945.
Source entity Relationship Target entity Species
SbWRKY50 functions as negative regulator in leaf senescence Sorghum bicolor
general response of (AtEIN3, EIN3, AT3G20770) /SbWRKY50 module to multiple phytohormones implied crosstalk between ET and other hormones in senescence Sorghum bicolor
WHIRLY1 (ATWHY1, PTAC1, WHY1, AT1G14410) functions as upstream suppressor of (ATWRKY53, WRKY53, AT4G23810) Arabidopsis thaliana
(ATWHY1, PTAC1, WHY1, AT1G14410) mutant shows altered (ATWRKY53, WRKY53, AT4G23810) promoter activity at different developmental stages Arabidopsis thaliana
Vcmax changed over lifetime of tropical leaves
leaf senescence involves reduction in cell sizes
functional redundancy between (H2B, HTB2, AT5G22880) and (HTB6, AT3G53650) may explain lack of early senescence phenotype in single mutants Arabidopsis thaliana
awhy1-1 antisense line shows early senescence phenotype Arabidopsis thaliana
rice homolog of (AtC3H23, ATCTH, ATTZF1, TZF1, AT2G25900) (OsTZF1) was recently shown to be involved in stress response and leaf senescence Oryza sativa
(ATWHY1, PTAC1, WHY1, AT1G14410) mutant shows elevated GUS activity from (ATWRKY53, WRKY53, AT4G23810) promoter Arabidopsis thaliana
overt visual sign of senescence (i.e. yellowing at tip of leaves) was observed only around 31 DAS Arabidopsis thaliana
(ATWRKY53, WRKY53, AT4G23810) positively participates in regulation of leaf senescence Arabidopsis thaliana
transcription factors (TFs) act as core control elements to drive drastic changes in senescence-associated gene (SAG) expression
plants grown on Fe-deficient media showed an early senescence phenotype Arabidopsis thaliana
study of Yang et al. provides a molecular framework by which mineral nutrients such as iron can interfere with leaf senescence Arabidopsis thaliana
(CBNAC, NTL9, AT4G35580) enters nucleus
WRKY family members play central roles in controlling leaf senescence Arabidopsis thaliana
transcriptional regulation plays a critical role in controlling initiation and progression of leaf senescence
(H2B, HTB2, AT5G22880) and (HTB6, AT3G53650) may be involved in the HTB4-regulated leaf senescence process Arabidopsis thaliana
HTB4-bHLH TFs-FRO2/IRT1-Fe homeostasis signaling pathway regulates the onset and progression of leaf senescence Arabidopsis thaliana
why1-2 mutant shows decreased photochemical efficiency of PSII (F_v/F_m) in leaf 7 Arabidopsis thaliana
SbWRKY50-OE sorghum show lower expression of SbSAG39 Sorghum bicolor
(HTB4, AT5G59910) comp plants displays WT-like senescence phenotype Arabidopsis thaliana
(ATWHY1, PTAC1, WHY1, AT1G14410) mutant shows weaker up-regulation of (ATWRKY33, WRKY33, AT2G38470) Arabidopsis thaliana
SbWRKY50 can antagonize plant senescence caused by other phytohormones Sorghum bicolor
(AtWRKY22, WRKY22, AT4G01250) positively participates in regulation of leaf senescence Arabidopsis thaliana
other phytohormones may act through SbWRKY50 Sorghum bicolor
(BAH1, NLA, SYG1, AT1G02860) mutant plants display rapid senescence when starved of nitrogen
transcription factors are reprogrammed during leaf senescence
sor1-d mutation suppressed delayed senescence phenotypes of (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) Arabidopsis thaliana
leaf senescence involves active degeneration of cellular metabolism
SbWRKY50-RNAi sorghum show similar effect as SbWRKY50-KO sorghum under different hormone treatments Sorghum bicolor
compromised chlorophyll synthesis leads to interveinal chlorosis in developing leaves Arabidopsis thaliana
release of (CBNAC, NTL9, AT4G35580) from the membrane regulates expression of a series of senescence-associated genes
(ATWHY1, PTAC1, WHY1, AT1G14410) overexpression line shows significant decline in GUS activity from (ATWRKY53, WRKY53, AT4G23810) promoter at 8-week-old stage Arabidopsis thaliana
Arabidopsis homologues of SbWRKY50 ( (ATWRKY59, WRKY59, AT2G21900) and (ATWRKY50, WRKY50, AT5G26170) ) is involved in leaf senescence Arabidopsis thaliana
SbNYC1 overexpression in sorghum results in more sensitive phenotype to dark treatment Sorghum bicolor
WRKY transcription factor family forms second-largest TF group in responses to leaf senescence
(HTB4, AT5G59910) loss-of-function led to premature leaf senescence
htb4-cr mutant displays early senescence phenotypes Arabidopsis thaliana
Cys level in mutant leaves is not cause for leaf senescence Solanum lycopersicum
BiP-overexpressing lines show lower malondialdehyde content Glycine max
GmNAC1 and GmCystP transcript levels display similar profiles in wild-type and BiP-overexpressing lines Glycine max
SlSAG12, SlSAG113, and SlSGR1 expression is significantly higher in third true leaf of 12-week-old SlNAP2-OX lines Solanum lycopersicum
(ATXDH1, XDH1, AT4G34890) mutant exhibits early senescence in older leaves Arabidopsis thaliana
higher degradation rate of proteins Rubisco and D1 is cause of senescence symptoms in older leaves of nitrate-starved (ATXDH1, XDH1, AT4G34890) Arabidopsis thaliana
senescence-associated genes (SAGs) limited information available for crop plants including maize, rice, wheat, and barley Zea mays; Oryza sativa; Triticum aestivum; Hordeum vulgare
dark incubation for 5 days induced senescence in (MEX1, RCP1, AT5G17520) leaves
SbWRKY50-OE lines show significantly lower expression of AtSAG13 Arabidopsis thaliana
SbWRKY42 shows expression slightly induced by dark-induced senescence Sorghum bicolor
overexpression of Ib (bHLH, AT5G51780) transcription factors suppresses premature senescence phenotype of (HTB4, AT5G59910) mutant
reduced Fe content due to low expressions of (BHLH038, bHLH38, ORG2, AT3G56970) (BHLH039, bHLH39, ORG3, AT3G56980) (BHLH100, AT2G41240) or (BHLH101, AT5G04150) may be cause of early senescence in (HTB4, AT5G59910) mutant Arabidopsis thaliana
Fe application in WT plants did not cause evident changes senescence phenotype Arabidopsis thaliana
(HTB4, AT5G59910) loss-of-function mutants display early leaf senescence phenotype Arabidopsis thaliana
NAC family members play central roles in controlling leaf senescence Arabidopsis thaliana
suppressor of (AtMAX2, MAX2, ORE9, PPS, AT2G42620) dominant (sor1-d) mutation was identified in activation-tagging-based screen for suppressors of the delayed leaf senescence phenotype of (AtMAX2, MAX2, ORE9, PPS, AT2G42620) Arabidopsis thaliana
SbWRKY50 may potentially function in leaf senescence Sorghum bicolor
SbWRKY50 overexpression in Arabidopsis results in obviously delayed leaf senescence Arabidopsis thaliana
(CESA6, E112, IXR2, PRC1, AT5G64740) activity weakens ethylene-induced leaf senescence Sorghum bicolor
JA treatment results in senescence of detached sorghum leaves Sorghum bicolor
loss of (ATIRT1, IRT1, AT4G19690) function results in severe leaf chlorosis Arabidopsis thaliana
early leaf senescence phenotype in (HTB4, AT5G59910) mutants can be reverted by overexpressing (ATIRT1, IRT1, AT4G19690) Arabidopsis thaliana
(AtSAG12, SAG12, AT5G45890) is target gene directly regulated by (ATWRKY53, WRKY53, AT4G23810) Arabidopsis thaliana
mitochondrial stress exhibits highly significant ROS transcriptome signature Arabidopsis thaliana
SbWRKY50-OE lines show significantly lower expression of (AtSAG12, SAG12, AT5G45890) Arabidopsis thaliana
SbWRKY50-OE Arabidopsis show less senescent phenotypes than wild-type upon various hormone treatments Arabidopsis thaliana
transcript levels of senescence-associated genes (SAGs) alter as leaves age
WRKY family transcription factors participate in the regulation of leaf senescence Arabidopsis thaliana
Fe-treated (HTB4, AT5G59910) mutant plants shows green leaves with higher chlorophyll content and photochemical efficiency Arabidopsis thaliana
functional complementation of (HTB4, AT5G59910) driven by its native promoter rescues premature leaf senescence phenotype Arabidopsis thaliana
SbWRKY50 may respond to phytohormones
control (HTB4, AT5G59910) mutant plants shows more dramatically induced (AtSAG12, SAG12, AT5G45890) expression Arabidopsis thaliana
(ATWHY1, PTAC1, WHY1, AT1G14410) repression on (ATWRKY53, WRKY53, AT4G23810) promoter activity occurs mainly during early stage of senescence Arabidopsis thaliana
leaf senescence acts through expression of senescence-associated genes (SAGs)
nitrogen deficiency will accelerate senescence of source leaves
(BIP, BIP2, AT5G42020) attenuated N-rich protein (NRP)-mediated cell death signaling during leaf senescence by inhibiting Tyr-Val-Ala-Asp (YVAD) proteolytic activity Glycine max
N-rich protein (NRP, NRP1, AT5G42050) -mediated cell death signaling is induced during leaf senescence Glycine max
nitrogen (N) deficiency leads to accelerated yellowing and senescence of old leaves
catabolic processes during leaf senescence occur in chloroplasts
(ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) (also termed ) is induced by multiple endogenous and environmental cues, including aging, darkness, and salinity Arabidopsis thaliana
SbWRKY42 shows expression kept almost unchanged under natural senescence Sorghum bicolor
functional complementation rescued early leaf senescence phenotype
MYB family transcription factors participate in the regulation of leaf senescence Arabidopsis thaliana
(HTB5, AT2G37470) (H2B, HTB9, AT3G45980) and (HTB11, AT3G46030) cannot complement the (HTB4, AT5G59910) phenotype Arabidopsis thaliana
(APX3, AT4G35000) and (APX4, TL29, AT4G09010) co-silencing could cause early leaf senescence Oryza sativa
WHIRLY1 (ATWHY1, PTAC1, WHY1, AT1G14410) suppression of (ATWRKY53, WRKY53, AT4G23810) occurs in developmental stage-dependent manner Arabidopsis thaliana
(ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) and (ATEIN2, CKR1, EIN2, ERA3, ORE2, ORE3, PIR2, AT5G03280) are thought to act in different pathway than (AtMAX2, MAX2, ORE9, PPS, AT2G42620) Arabidopsis thaliana
(ATWRKY45, WRKY45, AT3G01970) positively participates in regulation of leaf senescence Arabidopsis thaliana
(AtEIN3, EIN3, AT3G20770) /SbWRKY50 module illustrates clear regulatory mechanism of leaf senescence repression Sorghum bicolor
ET-responsive SbWRKY50 illustrated vital role of plant senescence regulation Sorghum bicolor
(CESA6, E112, IXR2, PRC1, AT5G64740) and PRC2 may work parallelly in different pathways for plant senescence regulation
(ATWHY1, PTAC1, WHY1, AT1G14410) directly regulates leaf senescence Arabidopsis thaliana
SbWRKY50-OE sorghum show lower expression of SbSAG20 Sorghum bicolor
leaf senescence is regulated by nutrient deficiency
ORESARA 1 (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) loss-of-function delays nitrogen deficiency-triggered leaf senescence
function-restored transgenic plant PWHY1-HA shows restored (ATWRKY53, WRKY53, AT4G23810) promoter activity at different developmental stages Arabidopsis thaliana
oeWHY1-HA5 overexpression line maintains photochemical efficiency of PSII (F_v/F_m) above 0.8 in leaf 7 Arabidopsis thaliana
natural leaf senescence results in sharply downregulated SbWRKY50 expression Sorghum bicolor
SbWRKY50-RNAi sorghum detached leaves show more senescent phenotype than wild-type after ethylene combined with dark treatment Sorghum bicolor
SbWRKY50 overexpression shows obvious stay-green phenotypes Sorghum bicolor
drought stress can accelerate leaf senescence process
pathogen infection can accelerate leaf senescence process
reduced (ATIRT1, IRT1, AT4G19690) expression may cause premature senescence of (HTB4, AT5G59910) mutant Arabidopsis thaliana
oeWHY1-HA6 overexpression line shows delayed senescence phenotype Arabidopsis thaliana
PWHY1-HA complementation line shows wild-type leaf senescence phenotype Arabidopsis thaliana
tocopherols are particularly abundant in gerontoplasts
(ATKO1, CYP701A3, GA3, AT5G25900) could repress SbWRKY50 Sorghum bicolor
iron (Fe) deficiency induces premature leaf senescence
comprehensive metabolome and transcriptome data contribute to high-quality reference genome sequence and in-depth exploration of molecular mechanisms during leaf coloration and senescence Quercus dentata
NAC QD08G038820 and MYC QD08G028710 TF genes may act as positive regulators of leaf senescence Quercus dentata
SbWRKY42 is not involved in leaf senescence Sorghum bicolor
(NYC1, AT4G13250) pSbNYC1:SbNYC1 line show similar senescent phenotype as Col-0 Arabidopsis thaliana
SbNYC1 knockdown leads to insensitive phenotype to dark treatment Sorghum bicolor
(ATWRKY54, WRKY54, AT2G40750) plays negative role in leaf senescence Arabidopsis thaliana
SbWRKY42 shows no increased expression during late senescent stage Sorghum bicolor
histone variant (HTB4, AT5G59910) functions as novel negative regulator of leaf senescence
inducing overexpression of the four Ib (bHLH, AT5G51780) transcription factors delays the early senescence of the (HTB4, AT5G59910) mutant Arabidopsis thaliana
PWHY1-HA complementation line restores wild-type senescence phenotype Arabidopsis thaliana
awhy1-1 antisense line shows increased transcript levels of (AtSAG12, SAG12, AT5G45890) Arabidopsis thaliana
changes in temperature and sunshine duration in autumn are thought to be important in triggering leaf senescence and anthocyanin synthesis in deciduous trees
(ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) (also termed ) directly activates expression of genes involved in ethylene biosynthesis Arabidopsis thaliana
dark-induced leaf senescence results in slightly increased SbWRKY42 expression Sorghum bicolor
(AtbZIP, bZIP, AT1G68880) family transcription factors participate in the regulation of leaf senescence Arabidopsis thaliana
(HTB4, AT5G59910) mutant displays premature leaf senescence Arabidopsis thaliana
SbWRKY50 overexpression in sorghum results in stay-greener phenotype compared to wild-type sorghum Sorghum bicolor
jasmonic acid (JA) treatment promotes senescence Sorghum bicolor
JA could repress SbWRKY50 Sorghum bicolor
ABA biosynthesis functions for plant senescence
(HTB4, AT5G59910) mutant shows more dramatically induced (AtSAG12, SAG12, AT5G45890) expression Arabidopsis thaliana
Zn, Mn, or Co application did not suppress early senescence phenotype of (HTB4, AT5G59910) Arabidopsis thaliana
maintenance of Fe homeostasis helps to increase plant longevity Arabidopsis thaliana
photochemical efficiency of PSII (F_v/F_m) decreases below 0.8 during leaf senescence onset Arabidopsis thaliana
awhy1-1 antisense line shows decreased chlorophyll content in leaf 7 Arabidopsis thaliana
(SMAX1, AT5G57710) (AtMAX2, MAX2, ORE9, PPS, AT2G42620) leaves exhibit no yellowing when grown in dark for 6 days Arabidopsis thaliana
10-h illumination condition postpones and extends leaf senescence Arabidopsis thaliana
(ANAC029, ATNAP, NAP, AT1G69490) inducible overexpression lines exhibit promoted leaf senescence Arabidopsis thaliana
reduced expression of SlNAP2 in knockdown plants results in substantial delay of natural senescence Solanum lycopersicum
harvested plants have the ability to repress senescence under storage conditions
(AAH, ATAAH, AT4G20070) mutant exhibits leaf senescence hallmarks Arabidopsis thaliana
EIN3-mediated leaf senescence is the combined result of multiple physiological effects Arabidopsis thaliana
clade Ib (bHLH, AT5G51780) and FIT heterodimers delay leaf senescence Arabidopsis thaliana
WHIRLY1 (ATWHY1, PTAC1, WHY1, AT1G14410) is upstream regulator of (ATWRKY53, WRKY53, AT4G23810) Arabidopsis thaliana
(ATWHY1, PTAC1, WHY1, AT1G14410) is senescence regulator Arabidopsis thaliana
GmNAC81-mediated induction of vacuolar processing enzyme (VPE) during leaf senescence was associated with specific increase in Tyr-Val-Ala-Asp (YVAD) proteolytic activity Glycine max
SlNAP2-IOE plants show up-regulated expression of SlSAG12, SlSAG113, and SlSGR1 Solanum lycopersicum
Glu and Asp levels are greater in SlNAP2-KD and dKD lines Solanum lycopersicum
leaf senescence starts from inhibition of leaf expansion
(DML3, AT4G34060) mutation delays leaf senescence
nitrogen deficiency induces rapid leaf senescence
early leaf senescence phenotype in (HTB4, AT5G59910) mutants can be reverted by providing extra iron to the (HTB4, AT5G59910) mutants Arabidopsis thaliana
nuclear isoform of (ATWHY1, PTAC1, WHY1, AT1G14410) protein developmentally controls expression of (ATWRKY53, WRKY53, AT4G23810) Arabidopsis thaliana
(BIP, BIP2, AT5G42020) may delay leaf senescence Glycine max
ABA-deficient mutants display delayed senescence Oryza sativa; Arabidopsis thaliana
degradation of Rubisco accounts for up to 35% of nitrogen in a mature leaf
(ATXDH1, XDH1, AT4G34890) mutant exhibits leaf senescence hallmarks Arabidopsis thaliana
tobacco shows decrease of assimilation capacity during leaf aging closely correlates with ontogenetic loss of cytochrome b 6 f complex (cyt-bf) Nicotiana tabacum
darkness conditions suppress leaf senescence Arabidopsis thaliana
(ALN, ATALN, AT4G04955) mutant exhibits leaf senescence hallmarks Arabidopsis thaliana
casein lytic proteinase (Clp) complex is involved in controlling leaf senescence
SlNAP2 directly controls expression of SlSAG113 Solanum lycopersicum
general developmental arrest is likely the survival strategy resulting from suppression of leaf senescence under darkness Arabidopsis thaliana
dark-induced leaf senescence (DILS) differs qualitatively from developmental leaf senescence (DLS) Hordeum vulgare
reduced phospholipase D alpha (PLDα) activity in mature leaves could delay leaf senescence
chloroplasts during leaf senescence marked by decreased photosynthetic activities
bean (Phaseolus vulgaris) shows loss of cytochrome b 6 f complex (cyt-bf) preceding degradation of photosystem II (PSII) Phaseolus vulgaris
degradation of Rubisco is hallmark of senescent leaves
stress-induced N-rich protein (NRP, NRP1, AT5G42050) -mediated cell death signaling likely operates during developmentally programmed leaf senescence Glycine max
individually darkened leaf (IDL) conditions triggers rapid leaf senescence
(RPL10C, SAG24, uL16x, AT1G66580) showed opposite expression patterns in (AtWRKY42, WRKY42, AT4G04450) mutants and overexpression lines Arabidopsis thaliana
salicylic acid (SA) is inducer of leaf senescence
BiP-overexpressing plants display delayed senescence after flowering Glycine max
endogenous ABA levels increase during senescence Avena sativa; Oryza sativa; Zea mays; Arabidopsis thaliana
inhibition of SlNAP2 leads to delayed leaf senescence Solanum lycopersicum
SIR Ri plants are characterized by fast yellowing of older (lower) leaves
(AVB1, IFL, IFL1, REV, AT5G60690) mutants exhibit delayed leaf senescence Arabidopsis thaliana
coordinated induction of N-rich protein (NRP, NRP1, AT5G42050) -mediated cell death response and unfolded protein response (UPR) by developmentally programmed leaf senescence contrasts with salicylic acid (SA)-mediated induction of N-rich protein (NRP, NRP1, AT5G42050) cell death signaling Glycine max
(ANAC029, ATNAP, NAP, AT1G69490) is central positive regulator of leaf senescence Arabidopsis thaliana
GmNAC1 and GmCystP transcript levels show higher expression at later developmental stages Glycine max
activity-based probes have been used by other plant research laboratories to investigate wheat leaf senescence Triticum aestivum
(BIP, BIP2, AT5G42020) attenuated N-rich protein (NRP)-mediated cell death signaling during leaf senescence by inhibiting induction of GmNAC81 Glycine max
down-regulation of meristem identity and leaf patterning genes and up-regulation of oxidative stress pathways indicates precocious senescence Vitis spp.
developmental leaf senescence and individually darkened leaves (IDL) both demonstrate rapid decline in photosynthetic capacity concomitant with maintained mitochondrial respiration
confounding factors in developmental senescence include bolting or flowering
Cys level in mutant leaves is consequence of senescence-related processes in the mutant Solanum lycopersicum
prolonged dark conditions initiates synchronized senescence
development of male sterile mutants in Arabidopsis does not result in extension of life of individual leaves Arabidopsis thaliana
BiP-overexpressing plants retain green leaves for longer time than wild-type controls Glycine max
NAC transcription factor family members are functionally involved in regulation of leaf senescence Arabidopsis thaliana; Triticum aestivum; Gossypium hirsutum; Oryza sativa
ETHYLENE-INSENSITIVE3-mediated negative regulation of (EEP1, MIR164, MIR164C, AT5G27807) results in decreased expression of (EEP1, MIR164, MIR164C, AT5G27807) and increased expression of (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) in aging leaves Arabidopsis thaliana
SlNAP2pro:GUS transgenic plants show elevated GUS activity in older parts of leaves Solanum lycopersicum
current food supply and distribution practices rely on ability of harvested plants to repress senescence under storage conditions
lower glutathione contributes to premature senescence Solanum lycopersicum
(SIR, AT5G04590) (sulfite reductase) reduction to approximately 50% to 65% of wild-type activity results in premature senescence Solanum lycopersicum
BiP-mediated inhibition of programmed cell death (PCD) signal and unfolded protein response (UPR) occurred at 72 days after germination (DAG) Glycine max
SlNAP2 activation of downstream targets promotes leaf senescence Solanum lycopersicum
SlNAP2-IOE plants show induction of 15 out of 22 senescence-related genes Solanum lycopersicum
24 of 827 senescence-associated genes were more than three-fold up-regulated in (MEX1, RCP1, AT5G17520) compared with wild-type
SIR Ri impaired sulfite reductase expression due to RNA interference (SIR Ri) plants display early necrosis and chlorophyll degradation in cotyledons at age 2 to 3 weeks
expression of bacterial Tre6P phosphatase (otsB) affects leaf senescence Arabidopsis thaliana
SlORE1S02, SlORE1S03, and SlORE1S06 are closest tomato putative orthologs of Arabidopsis (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) Solanum lycopersicum
SlNAP2 plays central role in regulating leaf senescence Solanum lycopersicum
senescence regulatory module controlled by SlNAP2 is highly conserved between tomato and other plant species Solanum lycopersicum; Arabidopsis thaliana; Oryza sativa; Triticum aestivum; Gossypium hirsutum
N-rich protein A (NRP-A), N-rich protein B (NRP-B), GmNAC81, and vacuolar processing enzyme (VPE) homologs were induced during leaf senescence Glycine max
(BIP, BIP2, AT5G42020) attenuated N-rich protein (NRP)-mediated cell death signaling during leaf senescence by inhibiting induction of N-rich proteins (NRPs) Glycine max
(ANAC029, ATNAP, NAP, AT1G69490) null mutants exhibit delayed leaf senescence Arabidopsis thaliana
(HAI1, SAG113, AT5G59220) knockout delays developmental senescence Arabidopsis thaliana
Gln (glutamine) level is significantly lower in SlNAP2-KD plants Solanum lycopersicum
γ-Aminobutyric acid level is significantly higher in SlNAP2-OX Solanum lycopersicum
SlNAP2 regulates leaf senescence Solanum lycopersicum
SIR Ri mutants developed early leaf senescence Solanum lycopersicum
SIR Ri impaired sulfite reductase expression due to RNA interference (SIR Ri) displays yellow spots on older leaves
SlNAP2 (Solanum lycopersicum NAC-like, activated by Apetala3/Pistillata) expression increases during dark-induced leaf senescence Solanum lycopersicum
death of the organ is necessary or advantageous to rest of the plant
transcriptomic, cytological, and physiological data reveal events in dark-induced leaf senescence (DILS) Hordeum vulgare
sufficient supply of nitrate resulted in disappearance of premature senescence symptoms Arabidopsis thaliana
differential and global gene expression during dark-induced senescence demonstrates multifaceted nature of leaf senescence Arabidopsis thaliana
67 of 827 senescence-associated genes were more than two-fold up-regulated in (MEX1, RCP1, AT5G17520) compared with wild-type
SIR Ri37 line demonstrates more pronounced symptoms of early leaf senescence
35S::BiP4 leaves show significant differences in total chlorophyll content Glycine max
(BIP, BIP2, AT5G42020) may modulate developmentally programmed leaf senescence Glycine max
SlNAP2 (Solanum lycopersicum NAC-like, activated by Apetala3/Pistillata) expression increases during age-dependent leaf senescence Solanum lycopersicum
reduced expression of SlORE1s in RNAi lines led to delayed leaf senescence Solanum lycopersicum
Pro (proline) level is higher in SlNAP2-KD Solanum lycopersicum
leaf senescence is paralleled by decrease in RNA
vacuolar processing enzyme (VPE)-mediated programmed cell death (PCD) may be functional during leaf senescence Glycine max
SlNAP1 and SlNAP2 double knockdown line dKD results in significant delay of leaf senescence Solanum lycopersicum
senescence-associated genes (SAGs) are upregulated in individually darkened leaves (IDL)
Os- (ASL39, LBD37, AT5G67420) expression is closely related to senescence Arabidopsis thaliana
(AtWRKY42, WRKY42, AT4G04450) plays positive role in leaf senescence Arabidopsis thaliana
(AtWRKY42, WRKY42, AT4G04450) directly regulates transcription of senescence-associated genes (SAGs) Arabidopsis thaliana
loss of (SIR, AT5G04590) function leads to premature leaf senescence Solanum lycopersicum
enhanced XDH activity in the top and third leaves likely reflects senescence-related processes in these leaves Solanum lycopersicum
OsNAP/ (ATPS1, PS1, AT1G34355) directly activates transcription of Osh69 Oryza sativa
three-quarters of senescence-induced genes in (MEX1, RCP1, AT5G17520) had most changes less than two-fold
(NYC1, AT4G13250) mutant exhibits stay-green phenotype Arabidopsis thaliana
salicylic acid (SA) treatment promotes senescence Sorghum bicolor
SbWRKY50 overexpression delays leaf senescence Sorghum bicolor
(ATNPR1, NIM1, NPR1, SAI1, AT1G64280) was involved in leaf senescence regulation when both SA and ET were applied
(ATWHY1, PTAC1, WHY1, AT1G14410) mutant increases expression levels of (ATWRKY53, WRKY53, AT4G23810) Arabidopsis thaliana
why1why3 double mutant shows increased transcript levels of (AtSAG12, SAG12, AT5G45890) Arabidopsis thaliana
(ATWRKY53, WRKY53, AT4G23810) regulates genes important for plant aging and leaf senescence Arabidopsis thaliana
(AtWRKY42, WRKY42, AT4G04450) overexpression accelerates leaf senescence Arabidopsis thaliana
(ATNHL10, NHL10, YLS9, AT2G35980) (yellow leaf-specific 9/ (NDR1, AT4G14350) /HIN1-like 10) is one of the SAG group Arabidopsis thaliana
WRKY42-ICS1 module modulates SA biosynthesis and leaf senescence Arabidopsis thaliana
(SAG13, AT2G29350) showed opposite expression patterns in (AtWRKY42, WRKY42, AT4G04450) mutants and overexpression lines Arabidopsis thaliana
oldest leaves of phosphorus (P)-limited plants had photosynthetic pigment fraction declined by 30 percent compared with mature leaves Hakea prostrata
GhNAP is positive regulator of ABA-mediated leaf senescence Gossypium hirsutum
metabolic shift between SlNAP2 overexpression and knockdown lines corresponds to contrasting senescence phenotypes Solanum lycopersicum
dark-induced leaf senescence (DILS) induces leaf senescence similar to that observed during normal plant development
DILS model eliminates confounding factors overlapping with developmental senescence
chlorophyll content reduction in (MEX1, RCP1, AT5G17520) is most significant in older leaves
bean (Phaseolus vulgaris) shows loss of cytochrome b 6 f complex (cyt-bf) preceding degradation of photosystem I (PSI) Phaseolus vulgaris
ceased synthesis of cyt-bf occurs weeks before any symptoms of leaf senescence
SlSAG12, SlSAG15, SlSAG113, SlSGR1, SlAGT1, SlSGR1, SlNYC1, SlPAO, SlNCED1, SlABA3, SITIENS, SlAAO3, SlCYP707A2, SlCYP707A4, and SlABCG40 are induced (log2 fold change > 1) 6 h after estradiol treatment in SlNAP2-IOE plants Solanum lycopersicum
SlSAG12, SlSAG15, SlSAG113, SlSGR1, SlAGT1, SlSGR1, SlNYC1, SlPAO, SlNCED1, SlABA3, SITIENS, SlAAO3, SlCYP707A2, SlCYP707A4, and SlABCG40 suggest early and positive regulation by SlNAP2 Solanum lycopersicum
(AtWRKY42, WRKY42, AT4G04450) loss-of-function mutation delayed leaf senescence Arabidopsis thaliana
senescence-associated genes (SAGs) are highly induced in K19624 line Arabidopsis thaliana
trichomes most of them disappeared in late growth stage (FL and FLNY) Phyllostachys edulis
(AtSWEET15, SAG29, SWEET15, AT5G13170) is related to early stage of leaf senescence Arabidopsis thaliana
sugar signaling is involved in the regulation of senescence
mutation of (ATRBOH F, ATRBOHF, RBOH F, RBOHAP108, RBOHF, AT1G64060) suppressed early senescence phenotype caused by (AtWRKY42, WRKY42, AT4G04450) overexpression Arabidopsis thaliana
Overexpression of NCEDs encoding carotenoid cleavage dioxygenases has been found to accelerate leaf senescence
(NOL, AT5G04900) cloned from perennial ryegrass suppressed leaf senescence Lolium perenne
(AtWRKY42, WRKY42, AT4G04450) is senescence-associated gene Arabidopsis thaliana
(FRK1, SIRK, AT2G19190) is target gene of (ATWRKY6, WRKY6, AT1G62300) Arabidopsis thaliana
hydrogen peroxide (H2O2) is inducer of leaf senescence
WRKY42-mediated ROS and SA signaling integration controls onset and progression of leaf senescence Arabidopsis thaliana
leaf senescence has important implications on carbon nitrogen (CN) balance of the leaf
leaf ageing may result in chloroplast and cell expansion with DNA divided among higher numbers of small nucleoid spots Beta vulgaris; Arabidopsis thaliana; Nicotiana tabacum; Zea mays
7 days from heat-stress initiation stay-green was visually scored as stay-green rating (ATNYE1, NYE1, SGR, SGR1, AT4G22920) Oryza sativa
(AtWRKY42, WRKY42, AT4G04450) transcription is induced during leaf aging Arabidopsis thaliana
senescence is critical in the regulation of carbon nitrogen (CN) balance in leaves
cytokinins delay leaf aging Nicotiana tabacum
(ANAC059, ATNAC3, NAC3, ORS1, AT3G29035) overexpression accelerates senescence Arabidopsis thaliana
35S:ORS1 overexpression lines has strongly elevated SAG12 expression (>30-fold) in shoots compared to control lines Arabidopsis thaliana
nitrogen mobilization occurs during leaf senescence Arabidopsis thaliana
(AtWRKY42, WRKY42, AT4G04450) is novel transcription factor positively regulating leaf senescence Arabidopsis thaliana
CND41 is induced in K16331 line Arabidopsis thaliana
silencing of ELP2-like gene (SlELP2L) in tomato promotes leaf senescence Solanum lycopersicum
RNA-seq profiling uncovered well-known senescence-associated genes (SAGs) and transcription factor genes Arabidopsis thaliana
(ATWRKY53, WRKY53, AT4G23810) plays central role in promoting leaf senescence Arabidopsis thaliana
(ATWRKY75, WRKY75, AT5G13080) can promote leaf senescence Arabidopsis thaliana
accumulation of sucrose and starch can accelerate leaf senescence
decreased CWIN activity in aging leaves is characteristic of aging leaves Solanum lycopersicum
(ANAC059, ATNAC3, NAC3, ORS1, AT3G29035) and (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) are important for control of leaf senescence Arabidopsis thaliana; Brassicaceae
35S:ORS1 overexpressor has considerably lower chlorophyll content in oldest rosette leaves (leaves no. 1-4) Arabidopsis thaliana
(AtLEA5, LEA38, LEA5, SAG21, AT4G02380) is one of the SAG group Arabidopsis thaliana
(ATWRKY6, WRKY6, AT1G62300) is first WRKY gene reported to regulate leaf senescence Arabidopsis thaliana
(AtWRKY42, WRKY42, AT4G04450) integrates reactive oxygen species (ROS) and salicylic acid (SA) signaling Arabidopsis thaliana
(ANAC059, ATNAC3, NAC3, ORS1, AT3G29035) inhibition delays senescence Arabidopsis thaliana
(ATWRKY6, WRKY6, AT1G62300) is one of the well-known sen-TF genes Arabidopsis thaliana
nutrient deficiency accelerates leaf senescence
(ARF1-BP, ARF2, AtARF2, HSS, ORE14, AT5G62000) gene was suggested to play a role in senescence Arabidopsis thaliana
loss-of-function mutation of a given gene may not alter senescence phenotype to a detectable level, although that gene may be important for regulating senescence senescence phenotype Arabidopsis thaliana
most (AtRAV1, EDF4, RAV1, AT1G13260) overexpressor transgenic lines showed early senescence phenotype Arabidopsis thaliana
ethylene is senescence-accelerating hormone
YUCCA6 allele with mutations in NADPH cofactor binding site exhibited neither delayed leaf senescence phenotypes Arabidopsis thaliana
(SAG13, AT2G29350) is strongly induced in K16331 line Arabidopsis thaliana
transcripts related to leaf senescence are already induced in Os-LBD37/ASL39-overexpressor lines Arabidopsis thaliana
35S:ORS1 transgenic lines has much more pronounced ion leakage in older leaves than EV control lines Arabidopsis thaliana
WRKY42-OE plants resulted in higher ion leakage Arabidopsis thaliana
silencing of xanthine dehydrogenase in transgenic Arabidopsis plants accelerates leaf senescence Arabidopsis thaliana
(AtLEA5, LEA38, LEA5, SAG21, AT4G02380) is strongly induced in K16331 line Arabidopsis thaliana
ptDNA may remain functionally active until senescence
shading and enrichment in far-red light activate leaf senescence programs Nicotiana tabacum
isochorismate synthase 1 (ATICS1, EDS16, ICS1, SID2, AT1G74710) mutant suppresses early senescence phenotype evoked by (AtWRKY42, WRKY42, AT4G04450) overexpression Arabidopsis thaliana
(AtWRKY42, WRKY42, AT4G04450) modulates leaf senescence through a complex regulatory network Arabidopsis thaliana
(ATWRKY57, WRKY57, AT1G69310) regulates leaf senescence Arabidopsis thaliana
total content of chlorophylls and carotenoids decreased more drastically in wild-type plants than in mutant Arabidopsis thaliana
knockdown or null mutation of (NYC1, AT4G13250) led to cosmetic stay-green phenotype
(AtWRKY42, WRKY42, AT4G04450) is expressed in a spatial gradient along long axis (tip, middle and base) of late senescent leaves Arabidopsis thaliana
(ATWRKY53, WRKY53, AT4G23810) has targets that are positive or negative regulators in leaf senescence process Arabidopsis thaliana
(ATWRKY28, WRKY28, AT4G18170) play key roles in light signal mediated leaf senescence Arabidopsis thaliana
TEM play regulatory roles in leaf senescence Arabidopsis thaliana
plastoglobule-localized metallopeptidase 48 (PGM48, AT3G27110) is positive regulator of leaf senescence Arabidopsis thaliana
Black Gora has genotype mean SGR of 3.75 Oryza sativa
acs2-1 leaves show faster senescence Solanum lycopersicum
carotenoid stability results in red and yellow colors of senescent leaves
sugar accumulation during leaf senescence was reported in Arabidopsis Arabidopsis thaliana
OsNAP RNA interference (RNAi) lines exhibit impeded leaf senescence Oryza sativa
suppression of (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) homologs (SlORE1S02, SlORE1S03, and SlORE1S06) results in delay of leaf senescence Solanum lycopersicum
SlNAP2 activation of target genes through direct promoter binding promotes leaf senescence Solanum lycopersicum
leaf senescence occurs in coordinated manner
differential and global gene expression during natural senescence demonstrates multifaceted nature of leaf senescence Arabidopsis thaliana
AtBFN1 was significantly induced in BnaNAC60ΔTM overexpression lines (OE-28# and OE-31#) Arabidopsis thaliana
rice osnol mutant displayed strong cosmetic stay-green phenotype lacking photosynthetic activity Oryza sativa
ethylene is upstream of ORESARA1 (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610)
nitrogen-remobilization processes is closely related to senescence Arabidopsis thaliana
cell wall invertase (CWIN) is essential for hormone-controlled leaf senescence
ABA-mediated leaf senescence is dependent on decreased CWIN due to post-translational inhibition Solanum lycopersicum
(ANAC059, ATNAC3, NAC3, ORS1, AT3G29035) promoter drives expression in older leaf parts during senescence Arabidopsis thaliana
(AtWRKY42, WRKY42, AT4G04450) transcript level is significantly increased in early senescence (ES) stage Arabidopsis thaliana
acs2-1 detached leaves show faster loss of colouration Solanum lycopersicum
zeatin/ACC ratio correlates with onset and progression of leaf senescence Solanum lycopersicum
ANAC089ΔTM overexpression caused chlorophyll degradation Nicotiana tabacum
lower ROS accumulation in (AtTEM1, EDF1, TEM1, AT1G25560) (AtRAV2, EDF2, RAP2.8, RAV2, TEM2, AT1G68840) mutants correlated with observed lower expression of genes involved in stress-induced senescence Arabidopsis thaliana
incubation of wheat leaves (Triticum aestivum) with 6-benzylaminopurine (BAP) reduced degradation of Rubisco small subunit during dark-induced senescence Triticum aestivum
redistribution of sulfur (S) compounds to young developing leaves and roots was without any acceleration of leaf senescence processes oilseed rape
ore14-1 mutant shows delayed senescence symptoms under phytohormone treatment Arabidopsis thaliana
ore14-2 mutant shows delayed senescence symptoms under phytohormone treatment Arabidopsis thaliana
ore14-1/arf2-10 mutant leaves showed slower increases in membrane ion leakage Arabidopsis thaliana
wild-type leaves treated with ABA showed rapid decrease in chlorophyll Arabidopsis thaliana
decline in Amax with leaf senescence was rather sudden in control plants compared with plants growing with low Ca supply Ipomoea pes-caprae
SSH screen was undertaken to isolate genes involved in triggering the onset of leaf senescence
low hexose-to-sucrose ratio in the leaf apoplasm may trigger or allow ABA-induced senescence Solanum lycopersicum
plants overexpressing (ATMKK9, MKK9, AT1G73500) display precocious senescence Arabidopsis thaliana
triacylglycerols (TAGs) accumulate during senescence
(AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) is essential in preventing premature senescence Arabidopsis thaliana
NOLi lines have greater numbers of green leaves per tiller Lolium perenne
Unknown SAG protein is senescence-associated gene product Arabidopsis thaliana
(ATWRKY55, WRKY55, AT2G40740) promotes leaf senescence Arabidopsis thaliana
senescence-related genes (Osl85, Osl57, Osh36) are upregulated in (ELL1, FK, HYD2, AT3G52940) mutant Oryza sativa
Arabidopsis atnol mutant did not have stay-green phenotype Arabidopsis thaliana
Arabidopsis and rice (NYC1, AT4G13250) and/or (NOL, AT5G04900) mutants showed no functional stay-green at all Arabidopsis thaliana; Oryza sativa
LpNOL was only highly expressed in senescent leaves Lolium perenne
heat shock-inducible promoter leakiness in tobacco causes delayed senescence Nicotiana tabacum
senescence-induced expression is specific for (KAT2, AT4G18290) Arabidopsis thaliana
darkened leaves displayed strong GUS staining by fourth day under darkness Arabidopsis thaliana
(KAT2, AT4G18290) transcript levels were 8-fold higher than (KAT2, AT4G18290) transcript levels in light-grown leaves by fourth day Arabidopsis thaliana
cut leaf senescence experiments have little relevance to leaf senescence in intact plants in the light
photosynthesis genes encoding chlorophyll a/b binding protein and Rubisco subunits are classed as senescence down-regulated genes
(ATWRKY28, WRKY28, AT4G18170) play key roles in SA mediated leaf senescence Arabidopsis thaliana
physiological indicators of chloroplast degeneration and degradation of photosynthetic pigments mark onset of senescence Arabidopsis thaliana
abscisic acid (ABA) could induce senescence of leaves
(ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) is regulator of leaf senescence Arabidopsis thaliana
SAG103 is one of the SAG group Arabidopsis thaliana
(ATRBOH F, ATRBOHF, RBOH F, RBOHAP108, RBOHF, AT1G64060) mutants had delayed senescence Arabidopsis thaliana
2-nitrodebranone (2NOD) after 8 days of exogenous application, decreased chlorophyll levels of Col-0 and max3-11 leaves Arabidopsis thaliana
LpNOL might also be involved in other metabolic regulation pathways related to leaf senescence Lolium perenne
Pro35S:CaUBP12 Arabidopsis plants displayed accelerated leaf senescence after ABA treatment Arabidopsis thaliana
(ATWRKY30, WRKY30, AT5G24110) can interact with (ATWRKY53, WRKY53, AT4G23810) Arabidopsis thaliana
(AtSAG12, SAG12, AT5G45890) was expressed in late senescent leaves Arabidopsis thaliana
LpNOL expression level increases during leaf senescence progression Lolium perenne
(ATWRKY55, WRKY55, AT2G40740) was validated by qRT-PCR Lolium perenne
sugar accumulation during leaf senescence was reported in tobacco Nicotiana benthamiana
transcriptional networks regulate competence to senesce
KAT2as leaves showed strongly attenuated yellowing symptoms after 7 days in darkness Arabidopsis thaliana
(AtSAG12, SAG12, AT5G45890) cysteine proteinase is highly senescence-specific SAG
(SUT1, AT5G63020) mutant plants show chlorotic, senescent, and necrotic leaves Zea mays
age-related reductions in the hydraulic conductance of leaf blade junctions were measured from the base up, over a period of weeks and accompanied sequential onset of leaf senescence in whole plants
downregulation of selected JA biosynthesis genes and SAGs in mutant suggests that senescence could be delayed in tem plants Arabidopsis thaliana
comparative transcriptomic analysis of NOLi and WT leaves revealed many DEGs associated with NOL-mediated stay-green phenotypes Lolium perenne
(ATWRKY18, WRKY18, AT4G31800) is upstream regulator and protein interactor of (ATWRKY53, WRKY53, AT4G23810) Arabidopsis thaliana
Loss of SPL33 function causes accelerated leaf senescence Oryza sativa
2-nitrodebranone (2NOD) decreased chlorophyll levels to much lower levels than leaves treated with rac-GR24 (GR24) Arabidopsis thaliana
carotenoid degradation is slower than chlorophyll degradation
(NOL, AT5G04900) could act as negative regulator of leaf senescence
overexpression of (NOL, AT5G04900) led to accelerated leaf senescence Arabidopsis thaliana
increased Chl b / a ratio might extend leaf longevity
age-dependent mechanisms control onset of senescence
(ATWRKY6, WRKY6, AT1G62300) and (ATWRKY45, WRKY45, AT3G01970) participate in gibberellin mediated leaf senescence Arabidopsis thaliana
(ATWRKY6, WRKY6, AT1G62300) play key roles in light signal mediated leaf senescence Arabidopsis thaliana
AtSAG13 was significantly induced in OE-31# line Arabidopsis thaliana
leaf senescence involves degradation of chlorophyll and carotenoids
NAC10 was validated by qRT-PCR Lolium perenne
CND41 functions as senescence-related marker Arabidopsis thaliana
CND41 plays an important role in nitrogen remobilization Arabidopsis thaliana
(SAG13, AT2G29350) is related to early stage of leaf senescence Arabidopsis thaliana
35S-ANAC092 overexpression lines had generally more pronounced senescence than 35S:ORS1 overexpression lines Arabidopsis thaliana
TE-2-6b plants at even later stages have leaves that remain green Arabidopsis thaliana
complex negative feedback network fine-tunes leaf senescence and growth in Arabidopsis Arabidopsis thaliana
stay-green mutants have potential to increase plant productivity
wild-type leaves had chlorophyll content reduced to 27% of that of 12 DAE leaves Arabidopsis thaliana
ore14-1/arf2-10 mutant leaves retained more than 80% of chlorophyll at 5 days after incubation with MJ, ABA, or ethylene Arabidopsis thaliana
ore14-1/arf2-10 mutant showed delay of leaf senescence during plant hormone-accelerated senescence Arabidopsis thaliana
developmental age shares common senescence pathway Arabidopsis thaliana
leaf calcium (Ca) content increased as the leaf became older in both treatments Ipomoea pes-caprae
(AtRAV1, EDF4, RAV1, AT1G13260) T-DNA insertion line (SALK_021865) did not significantly alter senescence process during age-dependent and darkness-induced senescence Arabidopsis thaliana
(AtRAV1, EDF4, RAV1, AT1G13260) inducible overexpression sufficiency for promoting leaf senescence suggests (AtRAV1, EDF4, RAV1, AT1G13260) plays an important role in positively controlling leaf senescence Arabidopsis thaliana
(ATWRKY57, WRKY57, AT1G69310) can integrate with jasmonic acid and auxin signaling pathway Arabidopsis thaliana
senescence-associated maker genes showed lower expression in age-dependent leaves of NOLi lines Lolium perenne
molecular components underlie onset of senescence
newly identified genes in each ARM tend to be upregulated and coexpressed during senescence stage of Arabidopsis Arabidopsis thaliana
BnaNAC60ΔTM overexpression caused loss of chlorophyll Nicotiana benthamiana
2NOD performs better than GR24 in accelerating leaf senescence Arabidopsis thaliana
leaf senescence occurs in an orderly manner beginning with degeneration of the chloroplast
oxidative stress shares common senescence pathway Arabidopsis thaliana
ethylene has major effect on leaf senescence Arabidopsis thaliana
ore12-1 mutant confers extended leaf longevity Arabidopsis thaliana
auxin is negatively acting factor of leaf senescence Arabidopsis thaliana
(ARF1, AT1G59750) acts in partially redundant manner Arabidopsis thaliana
(ARF7, BIP, IAA21, IAA23, IAA25, MSG1, NPH4, TIR5, AT5G20730) and (ARF11, ARF19, IAA22, AT1G19220) genes are induced in senescing leaves Arabidopsis thaliana
SSH screening followed by RNA gel blot analysis identified 132 cDNAs with increased transcripts during early leaf senescence
RAV genes might play an important role during age-dependent senescence Arabidopsis thaliana
(AtRAV1, EDF4, RAV1, AT1G13260) might control senescence by transcriptional activation and/or repression of genes involved in the execution of leaf senescence
(ATWRKY53, WRKY53, AT4G23810) is up-regulated during progression of leaf senescence Arabidopsis thaliana
(AtRAV1, EDF4, RAV1, AT1G13260) inducible overexpression caused precocious leaf senescence Arabidopsis thaliana
salicylic acid (SA) accelerates leaf senescence
ore14-2 mutant causes reduced expression of senescence-associated genes Arabidopsis thaliana
(ATEIN2, CKR1, EIN2, ERA3, ORE2, ORE3, PIR2, AT5G03280) mutants have delayed leaf senescence phenotype Arabidopsis thaliana
auxin levels decline with leaf age Arabidopsis thaliana
leaf half-life (t50) was 94 d in plants grown for 3 weeks Ipomoea pes-caprae
low-calcium plants had 19-d shorter leaf half-life (t50) than leaves of control plants Ipomoea pes-caprae
(AtRAV1, EDF4, RAV1, AT1G13260) mRNA decreased during late senescence Arabidopsis thaliana
(AtRAV1, EDF4, RAV1, AT1G13260) plays an important role in senescence mediated by darkness or senescence-enhancing hormones as well as in age-mediated senescence Arabidopsis thaliana
(ATMKK9, MKK9, AT1G73500) is senescence-associated molecular marker Arabidopsis thaliana
Arabidopsis atnol mutant did not exhibit stay-green phenotype Arabidopsis thaliana
(ATCBF2, CBF2, DREB1C, FTQ4, AT4G25470) overexpression extends time until onset of leaf senescence Arabidopsis thaliana
ore14-1 mutant causes delay in membrane ion leakage Arabidopsis thaliana
relative decrease in stomatal conductance (gs) with leaf ageing was higher than that occurring in maximum CO2 assimilation rate (Amax) Ipomoea pes-caprae
leaf senescence can be affected by cellular differentiation
SAG spectrum provides new insights into the complex mechanisms that regulate leaf senescence
Arabidopsis genes encoding transcription factors show at least a 3-fold up-regulation in senescing leaves Arabidopsis thaliana
constitutive overexpression of (AtRAV1, EDF4, RAV1, AT1G13260) accelerates the onset of various senescence symptoms during darkness-induced senescence Arabidopsis thaliana
(AtRAV1, EDF4, RAV1, AT1G13260) induction caused precocious leaf senescence during age-dependent senescence Arabidopsis thaliana
(AtRAV1, EDF4, RAV1, AT1G13260) is senescence-associated gene (SAG)
temporal expression patterns of SAGs may indicate role of each gene during various steps from initiation signal to terminal phase of cell death
(AtWRKY42, WRKY42, AT4G04450) directly binds promoter of senescence-associated genes (SAGs) Arabidopsis thaliana
(SAG13, AT2G29350) is one of the SAG group Arabidopsis thaliana
(ANAC055, ANAC55, ATNAC3, NAC055, NAC3, AT3G15500) is one of the well-known sen-TF genes Arabidopsis thaliana
overexpression of (ATCBF2, CBF2, DREB1C, FTQ4, AT4G25470) and (ATCBF3, CBF3, DREB1A, AT4G25480) transcriptional activators elicits delay in leaf senescence Arabidopsis thaliana
transgenic tobacco plants that produced more (AtCKS, CKS, KDSB, AT1G53000) showed delayed senescence-related decline in Rubisco Nicotiana tabacum
ore14-1/arf2-10 mutant had chlorophyll content declined much more slowly; retained over 70% after 6 days of dark incubation Arabidopsis thaliana
calcium (Ca) may alter leaf senescence process
(AtRAV1, EDF4, RAV1, AT1G13260) expression profile during leaf development indicates (AtRAV1, EDF4, RAV1, AT1G13260) might play a role in regulating the onset of leaf senescence
(ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) has reduced transcript abundance during senescence in yuc6-1D compared with wild type senescence process Arabidopsis thaliana
elevated free auxin levels in planta protect against leaf senescence Arabidopsis thaliana
leaf senescence required perception of jasmonic acid (JA)
developmental leaf senescence in intact plants is hypothesized to be induced by carbohydrate starvation in the leaf cells
low sugar levels can induce leaf senescence
cut leaves placed in darkness is condition for sugar prevention of senescence
leaf girdling indicates that accumulation of sugars in leaves might induce leaf senescence
cellular remobilization during senescence has purpose of production of sugars that can be transported out of the leaf
carotenoid-to-chlorophyll ratio became larger in senescing leaves Acer platanoides; Cornus alba; Parthenocissus quinquefolia; Cornus alaunica; Corylus avellana
specific responses in gene expression related to development and to the N-deficient and S-deficient crops indicate importance of shifts in expression of amino acid metabolism and other genes during leaf senescence
LS-HN treatment old leaves show chlorophyll concentration similar to control old leaves
reducing sulphate supply effect on foliar senescence was highly dependent on nitrate availability Brassica napus
salicylic acid (SA) accelerates progression of leaf senescence Arabidopsis thaliana
Arabidopsis lectin receptor kinase lecRK-a1 expression is induced during senescence of leaves Arabidopsis thaliana
sugar executes opposite effect in darkness versus light
(AtWRKY42, WRKY42, AT4G04450) promotes leaf senescence Arabidopsis thaliana
senescence symptoms in (AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) mutants included increase in transcript expression of NAC-LIKE Arabidopsis thaliana
NAC, WRKY, and TCP family members are senescence-associated transcription factors
total content of photosynthetic pigments declined rapidly in wild-type but more slowly in tem mutants in response to salt stress Arabidopsis thaliana
carotenoid remobilization occurs in response to disassembly of thylakoid membrane and turnover of photosynthetic machinery Arabidopsis thaliana
ethylene/zeatin ratio is key determinant regulating leaf senescence Solanum lycopersicum
(ATWRKY45, WRKY45, AT3G01970) can promote leaf senescence Arabidopsis thaliana
senescence symptoms in (AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) mutants included increase in transcript expression of Senescence-Related-Gene1 Arabidopsis thaliana
TEMs could act in positive regulation of leaf senescence in addition to negative regulation of plant growth Arabidopsis thaliana
delaying the degradation rate of photosystem complexes could contribute to stay-green phenotype
in vitro application of ABA could enhance leaf senescence
differences in leaf senescence became measurable starting with leaves 4 and 5
(ARF1-BP, ARF2, AtARF2, HSS, ORE14, AT5G62000) might be regulator in controlling the senescence process in age-dependent and dark-induced senescence Arabidopsis thaliana
leaf senescence can be affected by plant growth regulators
(ATWRKY6, WRKY6, AT1G62300) may target senescence-induced receptor kinase gene (FRK1, SIRK, AT2G19190)
(AtRAV1, EDF4, RAV1, AT1G13260) transcript was also induced when leaf senescence was accelerated by methyl jasmonate (MJ) Arabidopsis thaliana
NAC family genes are senescence-related transcription factors
WRKY family genes are senescence-related transcription factors
Initiation and dynamics of foliar senescence depend on leaf age
leaf half-life (t50) was 60 d in plants grown for 10 months Ipomoea pes-caprae
negative slopes of Amax decline are similar to those reported in two tropical tree species with mean leaf longevity between 74 d and 94 d
elevated CO2 delayed senescence of the soybean canopy
(AtRAV1, EDF4, RAV1, AT1G13260) functions as positive regulator of leaf senescence Arabidopsis thaliana
(AtSAG12, SAG12, AT5G45890) transcripts in wild-type leaves started to accumulate at 22 DAE Arabidopsis thaliana
pathogen infection accelerates leaf senescence
chlorophyll loss in '10_11' leaves 4 and 5 at 42 d is significantly faster than in 'Karl' leaves 4 and 5 at 42 d Hordeum vulgare
(ARF1-BP, ARF2, AtARF2, HSS, ORE14, AT5G62000) might be regulator in controlling the senescence process modulated by phytohormones Arabidopsis thaliana
(ARF1-BP, ARF2, AtARF2, HSS, ORE14, AT5G62000) might be central regulator of leaf senescence Arabidopsis thaliana
hormones shares common senescence pathway Arabidopsis thaliana
(ARF1-BP, ARF2, AtARF2, HSS, ORE14, AT5G62000) transcripts increase in senescing leaves when induced by darkness Arabidopsis thaliana