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senescence

15931 relationships annotated with this phrase. Showing first 500 of 15931.
Source entity Relationship Target entity Species
abscission at later developmental stages involves chloroplast degradation Setaria viridis
ERF101 (ETHYLENE RESPONSE FACTOR 101) gene is clearly reduced in expression in coi2 mutants compared with WT plants after MeJA treatments Oryza sativa
itpa mutant plants show slightly earlier senescence Arabidopsis thaliana
other housekeeping genes show increased transcript abundance during senescence Arabidopsis thaliana
surprising decline in expression of several AM markers could indicate inception of symbiosis senescence Medicago truncatula
catabolism of K-3,7-di-R increases during developmental senescence
acbp3-2 did not exhibit delayed progression of senescence Arabidopsis thaliana
NAP (ANAC098, ATCUC2, CUC2, AT5G53950) gene is clearly reduced in expression in coi2 mutants compared with WT plants after MeJA treatments Oryza sativa
proofreading of damaged metabolites is likely not as important in senescent plants Arabidopsis thaliana
multiple protease genes were actively expressed in senescent leaves and nodules
SENESCENCE-ASSOCIATED GENE12 (AtSAG12, SAG12, AT5G45890) expression is up-regulated in old leaves of mutants supplemented with lowest nitrate level Arabidopsis thaliana
high degree of overlap between nodule and leaf senescence transcriptomes argues for recruitment of similar pathways Medicago truncatula
whole chloroplast degradation occurs via autophagy
itpa mutants show increased senescence at 8 weeks with approximately 50% less chlorophyll in oldest leaves Arabidopsis thaliana
regulatory and proteolytic processes suggests appearance of senescence-related processes
coi2 mutants remain green compared to other coi mutants and WT plants after MeJA treatment Oryza sativa
higher SA levels in itpa plants may present an explanation for early senescence phenotype Arabidopsis thaliana
down-regulation of key cellular metabolic pathways and induction of gene classes related to remobilization is reminiscent of transcriptional changes described for senescence Arabidopsis thaliana
suppressor of (AtMAX2, MAX2, ORE9, PPS, AT2G42620) 1 (SMAX1, AT5G57710) mutant does not affect senescence phenotype of (AtMAX2, MAX2, ORE9, PPS, AT2G42620) Arabidopsis thaliana
coi2 mutants have much higher chlorophyll contents than WT plants after MeJA treatment Oryza sativa
plants with higher frequency of unrepaired DNA double-strand breaks show early senescence phenotype Arabidopsis thaliana
CaMV 35S promoter-driven MtPHR2 expression downregulates expression of MtCP3 Medicago truncatula
leaf senescence and nodule senescence are two comparable biological processes that share responsive genes
fucoxanthin in P. globosa declined when cells aged cell aging Phaeocystis globosa
incomplete resorption of nutrients by plants during senescence results in chemical composition and structure of presenesced leaves
degradation of chloroplast, chlorophyll, and chlorophyll-binding proteins in senescent leaves functionally corresponds to degradation of symbiosome, heme, and heme-binding proteins (mostly leghemoglobin) in senescent nodules
auxin signaling is upstream of chlorophyll breakdown and ROS generation Setaria viridis
Gene Ontology (GO) gene class "aging" becomes overrepresented in latter part of germination time course in micropylar and chalazal endosperm (MCE) Arabidopsis thaliana
Haberlea rhodopensis shows no visible senescence symptoms Haberlea rhodopensis
(ANAC072, ANAC72, AtRD26, RD26, AT4G27410) positively regulates senescence by stimulating chlorophyll degradation Arabidopsis thaliana
plants with decreased expression of GLUTATHIONE REDUCTASE2 display early onset of age- and dark-induced senescence Arabidopsis thaliana
dark-induced leaf senescence (DILS) involves disintegration of chloroplasts Hordeum vulgare
xanthine accumulation could contribute to hastening of senescence phenotype in (ATXDH1, XDH1, AT4G34890) old leaves supplemented with low nitrogen Arabidopsis thaliana
senescence symptoms are observed in rice Oryza sativa
early senescence is evidenced by enhanced bleaching Arabidopsis thaliana
mutation of (ANAC029, ATNAP, NAP, AT1G69490) delays senescence symptoms Arabidopsis thaliana
(AOX1D, AT1G32350) transcript level abundance is associated with senescence
Senescence-inducible chloroplast stay-green protein 2 shows three-fold induction in Os-LBD37/ASL39-overexpressor line RK16331–13 Oryza sativa
strength and duration of nutrient limitation determine whether senescence-related processes become dominant
NAC transcription factors have been shown to be positive regulators of DEVS Arabidopsis thaliana
(ANAC029, ATNAP, NAP, AT1G69490) inducible overexpression lines exhibit promoted silique senescence Arabidopsis thaliana
darkness induces (ANAC029, ATNAP, NAP, AT1G69490) Arabidopsis thaliana
abiotic stresses induce premature senescence angiosperms
(AtPIF4, PIF4, SRL2, AT2G43010) and (A-PUT2, bHLHb1, PIF5, PIL6, AT3G59060) are required for dark-induced senescence Arabidopsis thaliana
accumulation of ROS is important factor during senescence
(AtSWEET15, SAG29, SWEET15, AT5G13170) is involved in senescence Arabidopsis thaliana
K2 displays only 4% identical senescence-associated genes Arabidopsis thaliana
senescence is controlled by multiple transcription factors and global epigenetic programming
(ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) plants exhibited delayed senescence Arabidopsis thaliana
phloem sap feeders modulate senescence
mutations in (PAP3, PIF3, POC1, AT1G09530) and (A-PUT2, bHLHb1, PIF5, PIL6, AT3G59060) delay dark-induced senescence Arabidopsis thaliana
senescence-associated chlorophyll catabolites are not present in chlorotic (MEX1, RCP1, AT5G17520) leaves
(ALN, ATALN, AT4G04955) and (AAH, ATAAH, AT4G20070) mutants display enhanced senescence symptoms relative to wild type under low-nitrate conditions Arabidopsis thaliana
senescing breeding line of barley shows senescence phenotype under terminal drought stress Hordeum vulgare
MORE AXILLARY GROWTH2 (AtMAX2, MAX2, ORE9, PPS, AT2G42620) functions in senescence pathway Arabidopsis thaliana
(ANAC029, ATNAP, NAP, AT1G69490) null mutants exhibit delayed silique senescence Arabidopsis thaliana
dark-induced leaf senescence (DILS) involves loss of chlorophyll Hordeum vulgare
loss of chlorophyll, decrease in photosynthesis, and nuclear DNA fragmentation together with gradual disintegration of chloroplast Hordeum vulgare
day 7 of dark-induced leaf senescence (DILS) was the point of no return when pigment loss, down-regulation of photosynthesis, and cell ultrastructure changes could not be reversed by re-exposure of plants to light Hordeum vulgare
transgenic plants overexpressing activated form of (CBNAC, NTL9, AT4G35580) up-regulate senescence-associated genes (SAGs)
induction of total Arabidopsis (TOR, AT1G50030) (AtTOR) silencing results in premature senescence Arabidopsis thaliana
SWEET transporter proteins participate in senescence Arabidopsis thaliana
(ANAC059, ATNAC3, NAC3, ORS1, AT3G29035) (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) and (ANAC029, ATNAP, NAP, AT1G69490) control senescence under severe nitrogen-limiting conditions Arabidopsis thaliana
low-nitrate-supplied mutants impaired in (ATXDH1, XDH1, AT4G34890) (ALN, ATALN, AT4G04955) or (AAH, ATAAH, AT4G20070) genes display similar senescence symptoms in older leaves Arabidopsis thaliana
stress-induced leaf senescence in barley occurs in two phases Hordeum vulgare
young plant tissues lack additional factors required for senescence-induced gene expression Arabidopsis thaliana
(VUP1, AT3G21710) OX plants exhibit extreme longevity of more than 10 months before senescence Arabidopsis thaliana
higher degradation rate of chloroplastic proteins such as Rubisco large subunit and D1, and enhanced remobilization of degradation product indicated by increased ATG8A and ATG5 cause premature senescence symptoms in older leaves of nitrate-starved (ATXDH1, XDH1, AT4G34890) plants Arabidopsis thaliana
(AtWRKY42, WRKY42, AT4G04450) activates expression of senescence-induced receptor-like kinase Arabidopsis thaliana
chlorophyll degradation occurs as visible symptom of premature aging
chloroplasts but not mitochondria seem to play the regulatory role in Arabidopsis leaf senescence Arabidopsis thaliana
(CBNAC, NTL9, AT4G35580) or Ca2+/CaM binding to may positively regulate (AtSWEET15, SAG29, SWEET15, AT5G13170)
senescence processes include reserve metabolite mobilization
ANAC gene family regulation differs between DEVS, NuDIS, and senescence in quadruple mutants Arabidopsis thaliana
(ANAC059, ATNAC3, NAC3, ORS1, AT3G29035) and (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) RNAi lines show stronger delay of senescence than respective T-DNA insertion mutants Arabidopsis thaliana
swirled thylakoid membranes and residual membrane patches presumably causing special nucleoid conformation
NuDIS is clearly differentiated from developmentally induced senescence (DEVS)
(ATNHL10, NHL10, YLS9, AT2G35980) (YELLOW-LEAF-SPECIFIC GENE 9) is ORS1-dependent up-regulated gene Arabidopsis thaliana
ors1-1 mutant shows approximately three-fold higher percentage of green leaves compared to control Arabidopsis thaliana
UV-C irradiation in (AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) mutants manifests as hastened senescence Arabidopsis thaliana
application of 0.3 mM trans-2-nonenal resulted in similar damage symptoms in (AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) knockout mutants Arabidopsis thaliana
DEVS involves lipid degradation
(ANAC059, ATNAC3, NAC3, ORS1, AT3G29035) is less strongly expressed in late-senescent accession N13 Arabidopsis thaliana
group 2 quadruple mutants match to 82% (Q2;1) and 70% (Q3;2) of senescence-associated genes Arabidopsis thaliana
senescence-associated genes show match of 70%, 63%, and 68% to N, P, and K nutrient starvation Arabidopsis thaliana
DEVS involves free amino acid accumulation
induction of SAGs might reveal specific mechanisms in common between nutrient-induced secondary effects and DEVS
SAGs are overrepresented in transcriptome of quadruple mutants
(MERI-5, MERI5B, SEN4, XTH24, AT4G30270) is involved in senescence Arabidopsis thaliana
nutrient depletion-induced senescence (NuDIS) displays wide overlap with developmental senescence (DEVS)
abscission of floral organs is senescence process Arabidopsis thaliana
ring-like nucleoid arrangement apparently linked to reorganization of thylakoid system during senescence
(ANAC059, ATNAC3, NAC3, ORS1, AT3G29035) triggers expression of senescence-associated genes (SAGs) Arabidopsis thaliana
natural senescence and UV-C irradiation led to higher chlorophyll degradation in (AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) knockout mutants but not in (ABA2, ATABA2, ATSDR1, GIN1, ISI4, SDR1, SIS4, SRE1, AT1G52340) and nced3-2 mutants compared with wild-type (WT) Arabidopsis thaliana
(ANAC059, ATNAC3, NAC3, ORS1, AT3G29035) RNAi lines show low (AtSAG12, SAG12, AT5G45890) expression Arabidopsis thaliana
(AtSAG12, SAG12, AT5G45890) is under control of (ATWRKY53, WRKY53, AT4G23810) transcription factor Arabidopsis thaliana
senescence is a finely tuned process modulated by hormonal and environmental inputs
pea plants bearing the alleles ar and n underwent full senescence only after further growth Pisum sativum
DEVS involves protein degradation
K-deficiency induces expression of senescence-related genes
(ANAC059, ATNAC3, NAC3, ORS1, AT3G29035) RNAi lines show significantly higher chlorophyll content in leaves no. 7 and 8 at 40 days after sowing compared to EV lines Arabidopsis thaliana
CND41 is involved in senescence Arabidopsis thaliana
NuDIS involves chlorophyll degradation
ANAC42 (ANAC042, AtJUB1, JUB1, NAC042, AT2G43000) is up-regulated in all mutants Arabidopsis thaliana
(ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) controls senescence Arabidopsis thaliana
(ANAC059, ATNAC3, NAC3, ORS1, AT3G29035) and (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) NAC transcription factors control gene sets that only partly overlap senescence-associated genes Arabidopsis thaliana
triacylglycerol (TAG) lipase has an important role in senescence Arabidopsis thaliana
ectopic expression of Os- (ASL39, LBD37, AT5G67420) in Arabidopsis leads to senescence Arabidopsis thaliana
chlorophyll degradation results in yellow-leaf phenotype Oryza sativa
DEVS involves chlorophyll degradation
ethylene regulates leaf senescence
downstream gene regulatory networks are governed by senescence transcription factors Arabidopsis thaliana
(ANAC059, ATNAC3, NAC3, ORS1, AT3G29035) regulates fewer genes than (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) Arabidopsis thaliana
metabolome does not reflect developmental state of the cell Arabidopsis thaliana
reduction of invertase (INV) expression and activity relates to senescence
ANAC92 (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) is not up-regulated in mutants and nutrient-starved plants Arabidopsis thaliana
Senescence-associated protein 24 is up-regulated in Os-LBD37/ASL39-overexpressor line RK16331–13 Oryza sativa
T-DNA insertion mutant of (CBNAC, NTL9, AT4G35580) slightly but reproducibly down-regulate senescence-associated genes (SAGs)
ORS1-up-regulated genes are previously shown to be up-regulated during senescence Arabidopsis thaliana
programmed cell death (PCD) at final stage of leaf senescence is typical symptom resulting from disintegration of plasma and vacuolar membranes
ANAC12 (ANAC012, AtSND1, NAC012, NST3, SND1, AT1G32770) is down-regulated in quadruple mutants Arabidopsis thaliana
jasmonic acid methyl ester (JAME) exhibits senescence-promoting effect
(ATWRKY45, WRKY45, AT3G01970) directly targets (AtSAG12, SAG12, AT5G45890) (SAG13, AT2G29350) (HAI1, SAG113, AT5G59220) and (MERI-5, MERI5B, SEN4, XTH24, AT4G30270) Arabidopsis thaliana
application of 3 mM benzaldehyde solution for 3 h revealed necrosis and chlorophyll degradation within 48 h in (AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) knockout mutant leaves Arabidopsis thaliana
wild-type (WT) leaves hardly showed damage symptoms compared with (AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) knockout mutants Arabidopsis thaliana
(AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) knockout mutants exhibited visible senescence symptoms in rosette leaves 3 days after exposing 25-day-old plants to 150 mJ of UV-C irradiation Arabidopsis thaliana
impairment in tomato (SIR, AT5G04590) expression resulted in accelerated yellowing of cotyledons Solanum lycopersicum
(AtPIF4, PIF4, SRL2, AT2G43010) and (A-PUT2, bHLHb1, PIF5, PIL6, AT3G59060) activate expression of NAC transcription factor ORESARA1 Arabidopsis thaliana
day 7 of dark-induced leaf senescence (DILS) was found to be the point of no return Hordeum vulgare
DcWRKY75 activates expression of Senescence associated genes (SAGs) Dianthus caryophyllus
DcSAG12 exhibits elevated expression with ethylene treatment
SG is heritable delayed foliar senescence
application of 3 mM benzaldehyde solution for 3 h showed wild-type (WT) hardly showed damage symptoms wild-type (WT) leaves Arabidopsis thaliana
chlorophyll loss in cinnamaldehyde-treated (AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) knockout mutants is likely the consequence of acrolein and propionaldehyde increase as result of cinnamaldehyde application Arabidopsis thaliana
petunia corollas at 72 h after pollination (72 P) are severely wilted Petunia×hybrida
vacuolar invertase had isoforms that were up-regulated during senescence Petunia×hybrida
early initiation of regulation senescence is illustrated by rapid development of flowers and pods Pisum sativum
sugar-induced senescence of source leaves may be signal of low nitrogen availability
carbon:nitrogen and hormonal balances of the plant lead to senescence
ors1-1 mutant infrequently shows more pronounced delay of senescence than anac092-1 mutant Arabidopsis thaliana
maturation of reproductive floral organs is senescence process Arabidopsis thaliana
UV-C-induced aldehydes accumulation and resulting senescence of siliques lacking aldehyde oxidase 4 (AAO4, AO4, ATAO-4, ATAO2, AT1G04580) prompted examination of effect of UV-C on (AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) knockout mutants Arabidopsis thaliana
WRKY transcription factors (TFs) are one of the most important regulators in senescence process
(AAO1, AO1, AOalpha, AT-AO1, ATAO, AtAO1, AT5G20960) and (AAO2, AO3, AOgamma, atAO-2, AtAO3, AT3G43600) knockout mutants exhibited absence of senescence symptoms in oldest rosette leaves Arabidopsis thaliana
carnation genome contains 18 SAG genes
BnaNAC60 positively modulates leaf senescence Brassica napus
antisense suppression of LX RNase delays leaf senescence Solanum lycopersicum
senescence-associated genes (SAGs) includes 827 genes Arabidopsis thaliana
group 1 quadruple mutants show identical response in 34% (Q2;2) and 39% (Q1;1) of senescence-associated genes Arabidopsis thaliana
senescence-associated protein is similarly changed in transgenic plants and oxidative stress plant models
(ANAC059, ATNAC3, NAC3, ORS1, AT3G29035) is a novel senescence-regulatory transcription factor Arabidopsis thaliana
senescence processes are developmentally pre-programmed to initiate and control senescence during reproductive growth
35S:DcEIL3-1 transgenic plants show significant acceleration of flower senescence and abscission Arabidopsis thaliana
enhanced concentrations of abscisic acid (ABA) activate senescence-related cysteine protease
35S:DcWRKY75 transgenic plants show significant acceleration of leaf senescence Arabidopsis thaliana
wild-type (WT) plants grown in agar plates containing 0.5 Murashige and Skoog (MS) media did not show senescence symptoms in rosette leaves of 33 days post-germination (DPG) plants Arabidopsis thaliana
leaf cells during senescence carry out orderly changes in metabolism
H3K27me3 levels showed weak reduction in old leaves
perennial plants undergo more gradual senescence
(BFN1, ENDO1, AT1G11190) promoter activation shows good association with tissue senescence Arabidopsis thaliana
MaSAG is senescence-associated molecular marker Musa acuminata; Brassica oleracea
application of 2 mM acetaldehyde for 3 h revealed significantly higher tissue damage and chlorophyll degradation in (AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) knockout mutants compared with wild-type (WT) Arabidopsis thaliana
(AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) knockout (KO) mutants exhibit premature senescence symptoms Arabidopsis thaliana
application of 0.75 mM nonanal resulted in similar damage symptoms in (AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) knockout mutants Arabidopsis thaliana
toxic aldehyde level likely also contributed to enhanced tissue damage in mutant's leaves Arabidopsis thaliana
progressive loss of H3K27me3 marks was associated with transcriptional activation of SAGs human cells
PRC2 may participate in age-associated senescence
jasmonic acid (JA) is important signal for senescence
petal senescence is typically characterized by loss of fresh weight
developmental senescence in Alstroemeria has been shown to be almost completely ethylene independent Alstroemeria
unpollinated plants senescence did proceed even though it was delayed Spinacia oleracea
vernalization accelerated senescence in late-flowering lines with functional (FLA, FRI, RSB7, AT4G00650) and (AGL25, FLC, FLF, RSB6, AT5G10140) alleles Arabidopsis thaliana
TRV-DcWRKY75 silenced plants show delayed petal senescence
(AtSAG12, SAG12, AT5G45890) expression is much higher in 35S:DcWRKY75 plants Arabidopsis thaliana
six senescence-associated or stress-responsive NAC TFs were upregulated in autumn Picea abies
direct exposure to aldehydes results in damage and senescence phenotype in mutant rosette leaves Arabidopsis thaliana
STAY GRAY PROTEIN2 (SGN2) showed higher relative expression in (AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) knockout mutants than in wild-type (WT) Arabidopsis thaliana
many genes are induced during progress of leaf senescence Arabidopsis thaliana
(ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) (ORESARA1, ) is positive regulator of leaf senescence
significantly higher level of hexanal in (AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) knockout mutants compared with wild-type (WT) are attributed to significantly higher damage and lower remaining chlorophyll level in (AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) mutant leaves Arabidopsis thaliana
HLB-induced physiological changes result in leaf senescence Citrus spp.
proanthocyanidin helps to combat aging
MADS box protein expression was high in buds at stage S1 and then again from stage S4 bimodal expression pattern Alstroemeria
pre-anthesis (sequential) leaf senescence progresses more slowly in low-GPC lines barley
co-silencing plants showed early senescence Solanum lycopersicum
genetic regulation of senescence most probably relies on only a few loci
stresses in leaves induce early onset of developmental senescence
silencing of Sl-EBF1 and Sl-EBF2 expression caused accelerated plant senescence Solanum lycopersicum
PhADF1 spot 50-10 was not detectable in unpollinated corollas (0 h to 72 h) or at 24 h after pollination Petunia×hybrida
diminution of leaves in inflorescence of spinach can be explained by shift in hormonal and nutrient balance Spinacia oleracea
apical senescence in peas can be explained by shift in hormonal and nutrient balance Pisum sativum
exogenous treatments with cytokinin may delay senescence of cut flowers
DcWRKY75 promotes flower senescence Arabidopsis thaliana
putative lipase/thioesterase is highly up-regulated in high-GPC germplasm barley
co-silenced plants show accelerated senescence Solanum lycopersicum
UTP-glucose-1-phosphate uridyltransferase (PhUGP) was senescence-specific protein Petunia×hybrida
glucose has been shown to cause induction of senescence-specific gene (AtSAG12, SAG12, AT5G45890)
leaf senescence proceeds basipetally
(ASP3, YLS4, AT5G11520) is involved in senescence Arabidopsis thaliana
Senescence-inducible chloroplast stay-green protein 2 is up-regulated in Os-LBD37/ASL39-overexpressor line RK16331–13 Oryza sativa
(CBNAC, NTL9, AT4G35580) or Ca2+/CaM binding to may positively regulate (SAG13, AT2G29350)
phospholipase D ZmPLD1 is involved in floret abortion response Zea mays
tissue from senescent leaf material should contain no, very little, and/or heavily damaged DNA according to DNA
senescence involves decrease in photosynthesis Arabidopsis thaliana
nuclease is senescence-induced catabolic enzyme Arabidopsis thaliana
slow growth phenotype resembles pre-senescence state Daucus carota L.
stress treatments appear to accelerate processes associated with developmental senescence Alstroemeria
transcription factors associated with petal senescence have been identified in wallflower Erysimum
two leucine-rich repeat (LRR) transmembrane protein kinases are highly up-regulated in high-GPC germplasm barley
proteins in largest up-regulated subcluster represented senescence-specific proteins detected only in 48 P and 72 P corollas Petunia×hybrida
overproduction of cytokinins in petunia flowers transformed with PSAG12-IPT delays corolla senescence
identified modules integrated with leaf expression profiling in senescence stage to investigate module expression and coexpression patterns Arabidopsis thaliana
leaf cells during senescence carry out orderly changes in gene expression
(ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) represses GOLDEN2-LIKE 2 (ATGLK2, GLK2, GPRI2, AT5G44190) expression
breakdown of chlorophylls leads to impaired photosynthesis
post-harvest stress accelerates petal wilting
petal senescence is typically characterized by turgor loss
metallothionein expression was up-regulated by stress treatments and increased in expression during developmental senescence Alstroemeria
senescence-associated transcripts normally only evident after stage S4 are switched on in petals that have the appearance of stage S2–S3 flowers Alstroemeria
decline in nitrogen fixation is often connected to briskly progressing senescence of leaves
developing seed crop fails to cause plant senescence and death Pisum sativum
genes encoding NAC transcription factors are frequently up-regulated during normal developmental petal senescence
chlorophyll degradation is induced by stress in leaves and parallels chlorophyll degradation during natural senescence
remobilization of nutrients previously associated with leaf and petal senescence
senescence occurs rapidly in floral tissues
senescence is controlled at post-transcriptional level
methionine synthase had isoforms that were down-regulated during senescence Petunia×hybrida
flower removal has been consistently misinterpreted as counter-example to nutrient drain hypothesis Spinacia oleracea
chlorophyll (Chl) content is physiological senescence marker
α-amylase is senescence-induced catabolic enzyme Arabidopsis thaliana
OGs and flg22 appear to initiate a senescence program
reactive oxygen species (ROS) have been shown to influence senescence in tobacco Nicotiana tabacum
zinc finger ( (AtZAT6, C2H2, CZF2, ZAT6, AT5G04340) type) family protein analysis by RT-PCR reveals bimodal expression pattern Alstroemeria
nucleases are involved in senescence
older leaves maintained some function for longer period of time in pistillate plants Spinacia oleracea
(AtMAD1, MAD1, NES1, AT5G49880) induction pattern was generally induced in both cotyledons and true leaves Arabidopsis thaliana
engineering of plants with different autophagic capacities would facilitate advances in comprehension of role of autophagy during leaf senescence
dismantling of the photosynthetic apparatus of leaf chloroplasts is hallmark of the senescence process
TaNPF6.2 transcript increased much earlier, already at 3–4 weeks post-anthesis Triticum aestivum
characterized transcriptional regulators have shown overlap in expression between petal senescence and stress
actin depolymerizing factor 1 (PhADF1) had isoforms with opposite expression patterns Petunia×hybrida
floral initiation and leaf senescence of Arabidopsis accessions are linked Arabidopsis accessions Arabidopsis thaliana
senescence is most strongly induced by Flg22 at later time points Arabidopsis thaliana
cold dehydration stress (72 h) reduces time to 50% tepal abscission by flower longevity
beta-ureidopropionase (PhBUP) was senescence-specific protein Petunia×hybrida
early shift to support reproductive process was apparently sufficient to lead to eventual senescence Spinacia oleracea
plant degrades leaf mesophyll cells
gene expression between developmental senescence and stress-induced senescence in petals is poorly characterized in any species
genes related to proteolysis expression was up-regulated by stress treatments and increased in expression during developmental senescence Alstroemeria
PhADF1 spot 50-10 was newly detected in senescing corollas at 48 h and 72 h after pollination Petunia×hybrida
PhADF2 spots (49-22 and 51-14) showed similar patterns to PhADF1 Petunia×hybrida
grain protein content (GPC) locus in barley strongly influences timing of post-anthesis flag leaf senescence Hordeum vulgare
initial senescence response activated (AtSAG12, SAG12, AT5G45890) promoter creeping bentgrass
selective stabilization of LHCII mainly contributes to non-functional stay-green phenotype
peroxisomal processes are involved in amino acid and lipid metabolism Hordeum vulgare
mitochondrial functions are mainly related to electron transport chain Hordeum vulgare
alternative oxidase participates in dissipating processes Hordeum vulgare
transcription factor families are conserved in senescence process across plant kingdom Hordeum vulgare; Arabidopsis thaliana
qRT-PCR experiment showed up-regulation of an additional 8–10 NAC genes Hordeum vulgare
797 salinity-up-regulated genes are known developmental senescence-up-regulated genes Arabidopsis thaliana
RubiscoSSU relative expression showed reduction compared to anthesis Triticum aestivum
increased cytokinin levels delays senescence
petal senescence is typically characterized by changes in pigmentation
severely co-silenced plants display pale green spots Solanum lycopersicum
ore14-1 mutation causes delay in stem senescence Arabidopsis thaliana
Kunitz-type protease inhibitor family protein had isoforms that were up-regulated during senescence Petunia×hybrida
RECEPTOR FOR ACTIVATED C KINASE 1A (ATARCA, AtRACK1, RACK1A, RACK1A_AT, RACK1z, SAC53, AT1G18080) interacts with ETHYLENE INSENSITIVE 3 (AtEIN3, EIN3, AT3G20770)
ascorbate-deficient Arabidopsis mutant vitamin c-1 enters senescence prematurely Arabidopsis thaliana
transcription factors associated with petal senescence have been identified in petunia Petunia
TCA cycle is significantly drained for N assimilation might constitute an additional factor in overstretching nodule activity and adding to emerging nodule senescence at pod formation
senescence-associated vacuoles (SAVs) are lytic compartments containing senescence-associated proteases Arabidopsis thaliana
largest up-regulated subcluster included proteins with highest abundance at 48 and 72 h after pollination Petunia×hybrida
actin depolymerizing factor 2 (PhADF2) had isoforms with opposite expression patterns Petunia×hybrida
mechanical prevention of pod expansion delayed senescence of soybean Glycine max
senescence programme initiation occurs early in flowering period
abscisic acid (ABA) level issue did not play role in early senescence symptoms of (AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) mutants Arabidopsis thaliana
senescing leaves are characterized by reduced levels of photosynthesis-related genes
nodulation accelerates decline in antioxidant capacity of leaves during senescence Pisum sativum
EST collection included genes relating to remobilization of nutrients Alstroemeria
one of GPC genes may be functional homologue of Arabidopsis glycine-rich RNA-binding protein 7
(AtSAG12, SAG12, AT5G45890) expression is regulated in senescence-specific mode Arabidopsis thaliana
NAC family transcription factors are shown to be involved in senescence Arabidopsis thaliana
transfer to darkness had no marked effect on senescence of GFP–AtAtg8f-HA plants Arabidopsis thaliana
genes related to remobilization expression was reduced by latest stage of senescence Alstroemeria
pathogenesis-related and stress-response proteins may protect tissues from pathogen attack or accumulation of damaging reactive oxygen species Petunia × hybrida
senescence programme allows mobilization of nutrients and metabolites from source to sink organs
senescence involves physiological, biochemical, and gene expression changes
amino acids deriving from Rubisco net degradation are transported to sinks
WRKY transcription factor family have been reported to have possible regulatory role in senescence
ethylene initiates senescence programme
delay in leaf yellowing in RNAi line suggests delayed degradation of chloroplasts
(ATWRKY6, WRKY6, AT1G62300) has been associated with senescence
genes encoding specific classes of transcription factors (NAC, MYB, MYC, MADS-box, WRKY, zinc finger) may play regulatory role
WRKY transcription factors are important in leaf senescence in monocotyledonous plants
low-GPC tetraploid or hexaploid germplasm has functional NAC transcription factor wheat
pistillate plants show yellowing and withering of lowest leaves
leaf senescence causes glutamine (Gln) to become predominant free amino acid in leaf and phloem extracts
some of the SAGs encode proteases
ABA-activated Sucrose non-fermenting 1-Related protein Kinases (SnRKs) have implication in activating Senescence associated genes (SAGs) Arabidopsis thaliana
higher chlorophyll degradation in (AAO3, AOdelta, At-AO3, AtAAO3, AT2G27150) knockout mutants is not the result of water loss Arabidopsis thaliana
senescence involves degradation of starches Arabidopsis thaliana
induction of a senescence program is a common response to pathogen infection
genes whose expression changed following dehydration stress and between stages S0 and S5 included transcription factors and metallothioneins and armadillo domain protein
fewer genes down-regulated compared with up-regulated may be due to fewer genes being expressed at stage S0 relative to later developmental stages Alstroemeria
ethylene is considered as senescing hormone in plants
1,4-benzoquinone reductase-like protein had isoforms that were up-regulated during senescence Petunia×hybrida
pistillate plants were mostly dead by week 8
sugars are known to extend vase-life of flowers
banana fruit at 20 °C after 6 d ripening shows membrane permeability value of 18% Musa acuminata
nitric oxide may differ in role between developmental senescence and stress-induced senescence
chloroplasts are dismantled in early phase of senescence
transcription factor genes includes MYB transcription factor genes Hordeum vulgare
conservation between Arabidopsis senescence processes and barley results suggests that visual senescence pathway map and expression data are likely representative for other cereals Hordeum vulgare; Arabidopsis thaliana
long-term (4 d), moderate (150mM) NaCl treatment induces leaf senescence Arabidopsis thaliana
β-oxidation is important during dark-induced senescence plants
physiological changes induced by stress in leaves parallel physiological changes during natural senescence
microarray analysis compared expression changes following stress treatments with developmental senescence (stage S0 to stage S5)
rate of cortical death was positively associated with root age Triticum aestivum
Sl-EBF1 and Sl-EBF2 are necessary for regulating senescence Solanum lycopersicum
S-adenosyl-L-methionine:benzoic acid/salicylic acid carboxyl methyltransferase (PhBSMT2) had isoforms with opposite expression patterns Petunia×hybrida
senescence-induced catabolic enzymes are targeted to secretory pathway Arabidopsis thaliana
adenine nucleotide translocator gene expression showed steady increase from stage S4 (early senescence) to stage S6 (mid to late senescence)
multiple spots representing a protein function had same pattern of either up- or down-regulation during corolla senescence Petunia×hybrida
leaves at senescence had adequate carbohydrate Spinacia oleracea
expression of senescence-promoting and senescence-retarding genes regulates active senescence process
ureides accumulate during senescence
bundle sheath cells participates in leaf senescence
molecular mechanisms governing senescence regulation are poorly understood senescence regulation
Rubisco is degraded by developmentally regulated cysteine endopeptidases and peptide hydrolases
carbon levels decrease during petal and leaf senescence
genes encoding phosphate transporter proteins have not been specifically reported in screens for senescence-enhanced genes in petals
AtPHT1;5 is up regulated during natural senescence of leaves Arabidopsis thaliana
glutamate and glutamine typically become more available during leaf senescence
ARABIDOPSIS HOMOLOG OF TRITHORAX 1 (ATX1, SDG27, AT2G31650) promotes H3K4me3 enrichment at petal-senescence-inducing genes Dianthus caryophyllus L.
(EEP1, MIR164, MIR164C, AT5G27807) targets ORESARA 1 (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610)
ambient dehydration stress (48 h) reduces time to 50% tepal abscission by flower longevity
genes whose expression was up-regulated by stress treatments would also increase in expression during developmental senescence Alstroemeria
early reallocation of phloem-transported fixed carbon to reproductive development can account for induction of senescence in vegetative tissues Spinacia oleracea
jasmonates are powerful promoters of plant senescence
cut tobacco flowers fed with sugars in MS media at stage 6 delayed senescence signs by about 1 day Nicotiana tabacum
71 novel putative target genes of NAC transcription factors are presented Hordeum vulgare
(ANAC054, ATNAC1, CUC1, AT3G15170) and (ANAC098, ATCUC2, CUC2, AT5G53950) genes are required for age-dependent cell death Arabidopsis thaliana
relative chlorophyll/senescence profile of SPAD analysis of middle part of leaf 2 indicates at least 50% senescence at 6 weeks post-anthesis Triticum aestivum
higher-than-WT JA-Ile levels in Spodoptera-attacked (ACA10, ATACA10, CIF1, AT4G29900) (ACA12, AT3G63380) double mutant may relate to senescence rather than to increased jasmonate pathway signaling Arabidopsis thaliana
natural and dark-induced senescence share some symptoms and molecular components
free amino acids in wheat leaves with reduced sink capacity may be washed out in rain during late senescence Triticum aestivum
autophagy has primary role in bulk macromolecule degradation during senescence
Glu dehydrogenase [69] (GDH) is associated with senescence in plant tissues Triticum aestivum
leaf during senescence becomes source of mobilized carbon, nitrogen, phosphate, and other minerals
banana fruit at 30 °C after 6 d ripening shows membrane permeability value of 37% Musa acuminata
tobacco flowers may have senescence-related processes starting before anthesis Nicotiana tabacum
tobacco sepals after corolla abscission remained green Nicotiana tabacum
programmed cell death (PCD) fulfils essential function in senescence connected with reutilization of nutrients
(BFN1, ENDO1, AT1G11190) promoter pattern of induction was analyzed in Arabidopsis Arabidopsis thaliana
increase in (BFN1, ENDO1, AT1G11190) promoter activity correlates with decrease in chlorophyll level Arabidopsis thaliana
elevated Chl levels and photooxidative stress were associated with stay-green mutation in the Navel Negra citrus mutant Citrus sinensis
decreases in nucleic acid content accompany petal and leaf senescence petunia
stage 9 in tobacco flowers shows high metabolic activity probably due to carbon mobilization Nicotiana tabacum
GDH activity increased in wheat leaves post-anthesis Triticum aestivum
MDA content in banana peel shows similar trends during fruit ripening at both temperatures Musa acuminata
decrease in carbon levels during leaf senescence is unclear whether it is the result of C recycling or tissue respiration
Evans blue staining did not stain all cells in tobacco corolla at stage 9 Nicotiana tabacum
delayed senescence trait is linked to OC-1 transgene expression Nicotiana tabacum
ZEN1 was not expressed in leaf senescence Zinnia
genetically controlled senescence programme allows the plant to dismantle macromolecules and organelles from dying corollas
MaSAG expression in banana fruit at 20 °C shows slight increase at day 1 but lower levels at days 2–3 compared with banana fruit at 30 °C Musa acuminata
Constitutive overexpression of (AGL15, AT5G13790) delays flower senescence Arabidopsis thaliana
JA/ethylene pathway seems to participate in natural and dark-induced senescence
SA pathway plays a role in natural senescence
amino acids for remobilization are provided by proteolysis of leaf proteins
Cys endopeptidase [68] is associated with senescence in plant tissues Triticum aestivum
(BFN1, ENDO1, AT1G11190) gene transcript levels have been found to be induced during stem senescence Arabidopsis thaliana
delayed leaf senescence can be induced by altered hormone status
senescing leaves are characterized by reduced levels of chlorophyll
remobilization is associated in Alstroemeria and other systems with floral senescence Alstroemeria
overexpression of MADS box transcription factor delayed abscission Arabidopsis thaliana
ethylene regulates leaf senescence
expression of flowering- and senescence-associated genes correlation was found between flowering- and senescence-associated genes Arabidopsis thaliana
plum PsERF2a and PsERF2b accumulate in flowers after fertilization Prunus salicina
some of the SAGs encode hydrolytic enzymes
regulatory mechanism activates BFN1 promoter at specific late stage of senescence process Arabidopsis thaliana; Solanum lycopersicum
canopy density signal regulates, at least in part, senescence
banana fruit at 30 °C at end of ripening shows 2-fold higher MDA content than fruit at 20 °C Musa acuminata
mannitol exerted intermediate effect between presence or absence of sugars Nicotiana tabacum
(ATWRKY18, WRKY18, AT4G31800) expression is upregulated during leaf senescence Arabidopsis thaliana
flower bud vigour decrease in C. albidus plants suggests symptoms of senescence at the whole-plant level
line '10_11' shows development and senescence phenotype Hordeum vulgare
nitrogen released during protein degradation is translocated in the form of amino acids Hordeum vulgare
NaCl treatment (150mM) for 4 d triggers leaf senescence Arabidopsis thaliana
HvNAC001 was upregulated in senescing leaves from SN plots Hordeum vulgare
TaSAG12 expression increased eight-fold further with senescence Triticum aestivum
TaNAM-B1 expression showed earlier increase of expression compared to TaSAG12 Triticum aestivum
circadian clock is part of developmental programmes
proteases and nucleases are likely to be involved in macromolecule degradation during senescence
senescence-related genes regulate programmed cell death (PCD)
stay-green plants can be divided into functional and non-functional types
protease genes responsible for degradation of Rubisco
parallel up-regulation and dual targeting of PAPs and RNases was demonstrated in senescing tissues of both species Arabidopsis thaliana; Hakea prostrata
leaf senescence of harsh hakea and Arabidopsis was paralleled by pronounced induction of intracellular and cell wall-targeted APase and RNase activities
methionine sulfoxide reductases (MSRs) have been associated with senescence
exogenous sugars delay flower senescence
proteases are specifically induced during leaf senescence
glyoxylate pathway is probably part of anaplerotic pathways Hordeum vulgare
up-regulated transporter proteins include ZIP proteins Arabidopsis thaliana
banana fruit at 30 °C 3 d after treatment starts to display significantly higher MDA content Musa acuminata
MaSSU expression is high before ripening and markedly decreases with ripening process at both temperatures Musa acuminata
i1 (isocitrate lyase) and vpe3 (vacuolar processing enzyme 3) in sepals are greatly increased in stages 7 and 9 respectively Nicotiana tabacum
nitric oxide participates in senescence
chloroplastic (ATGSL1, GLN2, GS2, AT5G35630) gene shows strong down-regulation Hordeum vulgare
HvNAC013, -22, and -25 are up-regulated during late burst of degradation processes Hordeum vulgare
abscisic acid (ABA) is also known as hormone triggering senescence
HvWRKY12 was identified as upregulated during senescence Hordeum vulgare
elevated [CO2] delays senescence with marginal significance at R7 stage
abiotic or biotic stresses prematurely induce ethylene synthesis
faster decrease in Fv/Fm and faster increase in membrane permeability and MDA content in banana fruit at 30 °C strongly indicates high temperature accelerates fruit senescence process Musa acuminata
(PPDK, AT4G15530) (pyruvate orthophosphate dikinase) expression is enhanced in senescing broccoli florets Brassica oleracea
(PPDK, AT4G15530) (pyruvate orthophosphate dikinase) is not specifically induced at stage 7 Nicotiana tabacum
other transcripts, proteins, and metabolites at stage 9 are found at highest levels with remarkable increases in (AOX2, AT5G64210) and D1 protein Nicotiana tabacum
senescent leaves have high levels of anthocyanin Arabidopsis thaliana
photosystem II protein had isoforms with opposite expression patterns Petunia×hybrida
genes involved in remobilization are in keeping with primary function of the senescence programme Petunia × hybrida
macromolecule degradation during senescence is for nutrient re-allocation Arabidopsis thaliana
genes related to remobilization expression was up-regulated by stress treatments and increased in expression during developmental senescence Alstroemeria
caffeoyl CoA 3-O-methyltransferase had isoforms that were down-regulated during senescence Petunia×hybrida
(GGT1, AT4G39640) knockout mutants exhibits progressive senescence Arabidopsis thaliana
hypusinated eukaryotic translation initiation factor 5A (ATELF5A-1, EIF-5A, EIF5A, ELF5A-1, AT1G13950) plays a role in senescence Arabidopsis thaliana
mild osmotic stress of 50 mM mannitol manifested enhanced senescence of older leaves in GFP–AtAtg8f-HA-expressing plants Arabidopsis thaliana
PLDα is involved in mediating ABA- and ethylene-dependent senescence of detached leaves Arabidopsis thaliana
(BFN1, ENDO1, AT1G11190) function is probably required in latest stages of senescence process Arabidopsis thaliana
reactive oxygen species (ROS) impacts senescence processes
banana fruit at 30 °C after 6 d ripening shows Fv/Fm ratio decline to almost zero despite high chlorophyll level remaining Musa acuminata
(BFN1, ENDO1, AT1G11190) promoter pattern of induction was analyzed in tomato Solanum lycopersicum
senescence-enhanced genes encode catabolic enzymes
up-regulated transporter proteins include YSL proteins Arabidopsis thaliana
transcriptome analysis of leaves from plants undergoing different types of senescence revealed significant differences in gene expression profiles and signalling pathways
various SAGs exhibit differential expression in response to dark incubation
itpa background shows higher incidence of PCD during senescence Arabidopsis thaliana
OsCOI2 plays a dominant role in rice senescence Oryza sativa
lines or varieties with functional Gpc-1 genes demonstrate earlier senescence wheat; barley
glyoxylate pathway is probably not connected to gluconeogenesis Hordeum vulgare
HvNAC005, -23, -27, -29, and -30 show relatively early up-regulation Hordeum vulgare
model NACBSs could be detected in 333 out of 1106 available promoter sequences of up-regulated genes Hordeum vulgare
>800 genes are distinctively up-regulated during senescence
(BFN1, ENDO1, AT1G11190) is associated with senescence Arabidopsis thaliana
photosynthetic capacity was quite stable in summer before autumn senescence
up-regulated transporter proteins include OPT proteins Arabidopsis thaliana
inosine in RNA of older itpa plants indicates that problems may become more severe with age Arabidopsis thaliana
damage to DNA and RNA by aberrant nucleotide incorporation may be the cause for earlier senescence and increased PCD rate Arabidopsis thaliana
(ATPSKR1, PSKR1, AT2G02220) mutants exhibit weak early senescence phenotype
(GGT1, AT4G39640) mutants show slight progressive senescence Arabidopsis thaliana
AtBCAT1 under darkness delays dark-induced senescence Arabidopsis thaliana
genetic regulation of the complex senescence process is executed via spatial and temporary patterns of gene expression
(ANAC029, ATNAP, NAP, AT1G69490) regulates senescence Arabidopsis thaliana
(ANAC059, ATNAC3, NAC3, ORS1, AT3G29035) regulates senescence Arabidopsis thaliana
carbon skeletons can be utilized in re-assimilation of nitrogen Hordeum vulgare
increased reactive oxygen species (ROS) levels promote leaf senescence Hordeum vulgare
stay-green mutants showed that in mutants with defect in chlorophyll catabolism pathway
TaNPF6.3 expression remained level until week 5 Triticum aestivum
H2O2 is generated during senescence
down-regulation of SAGs contributes to functional stay-green phenotype of (APG5, ATATG5, ATG5, AT5G17290) leaves under mild abiotic-stress conditions
analysis of genes coregulated/coexpressed across a series of experimental conditions with known senescence regulators basis for identification of additional regulatory genes
NaCl treatment (150mM) for 4 d induces expression of (AtSAG12, SAG12, AT5G45890) Arabidopsis thaliana
cluster 14 includes 1704 genes Arabidopsis thaliana
senescence time series data is taken from Breeze et al. (2011) Arabidopsis thaliana
proteases have been described to be associated with protein degradation during senescence Hordeum vulgare; Arabidopsis thaliana; Oryza sativa
senescing Arabidopsis leaves induce cell wall-targeted and vacuolar APase activity, which is primarily due to action of (ATPAP26, PAP26, PUP3, AT5G34850) Arabidopsis thaliana
(AtWRKY22, WRKY22, AT4G01250) /29 expression is upregulated during leaf senescence Arabidopsis thaliana
nitric oxide induces cotyledon senescence Arabidopsis thaliana
functional stay-green involves slow progression of senescence syndrome
3867 differentially regulated genes shows overlap of ~700 genes with 2927 genes from Jukanti et al. (2008) Hordeum vulgare
(HAI1, SAG113, AT5G59220) is specifically involved in control of water loss during leaf senescence Arabidopsis thaliana
three previously characterized cis-regulatory elements (CREs) and four novel putative CREs are probably involved in both types of senescence Arabidopsis thaliana
histone modifications occur during plant senescence
high nitrogen supply can diminish/suppress chlorophyll degradation Hordeum vulgare
harsh hakea proteoid roots have time interval from senescence initiation to death of 5–7 days
RubiscoSSU is used as marker of senescence Triticum aestivum
NahG transgenic plants show reduced necrosis during developmental senescence Arabidopsis thaliana
NAC-like genes have functions including regulation of senescence
(APG5, ATATG5, ATG5, AT5G17290) shows early leaf yellowing phenotype during dark-induced senescence
autophagic processes involved in plastidial protein degradation
dismantling of the photosynthetic apparatus of leaf chloroplasts results in degradation and conversion of plastidic proteins
accelerated senescence in wheat is due to the presence of NAC transcription factor gene Triticum aestivum
(ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) regulates senescence Arabidopsis thaliana
HvPAP14 was one of the most upregulated genes during development of flag leaves from SN field plots Hordeum vulgare
TaNPF7.2 post-anthesis relative expression levels were very similar with no change or only slightly increased transcript levels until 5 weeks post-anthesis Triticum aestivum
transport pathway between maternal and filial tissues necessary to delineate nitrogen remobilization
transcription factor genes includes (bHLH, AT5G51780) transcription factor genes Hordeum vulgare
NaCl treatment (150mM) for 6h does not affect expression of (AtSAG12, SAG12, AT5G45890) Arabidopsis thaliana
NAC transcription factors were shown to have high levels of expression in senescent leaves Hordeum vulgare; Arabidopsis thaliana; Oryza sativa
TaGS2 (plastidic protein localization) expression decreased as would be expected with increasing senescence Triticum aestivum
GFP–AtAtg8f-HA plants tended to be slightly greener than control plants Arabidopsis thaliana
genes associated with photosynthesis expression is repressed during senescence
promoters of senescence-associated genes (SAGs) retained senescence-specific expression in other plants
Line 2 with strongest transgene expression senesced early Arabidopsis thaliana
decrease in carbon levels during petal senescence is unclear whether it is the result of C recycling or tissue respiration
(ATPAD4, PAD4, AT3G52430) mutants show reduced necrosis during developmental senescence Arabidopsis thaliana
expression levels of four SAGs under strong abiotic-stress conditions were not significantly different in (APG5, ATATG5, ATG5, AT5G17290) leaves and wild-type leaves
engineering of plants with different autophagic capacities would facilitate advances in comprehension of role of autophagy during petal senescence
global alterations in chromatin structure occur during plant senescence
HvNAC001 was shown to have highest upregulation in senescent leaves from SN plots Hordeum vulgare