ABI3 | | AT3G24650 | enhance |
Hormone ABA |
12231895;19754639 |
Arabidopsis thaliana |
Genetic evidence |
abi3-5 |
Col-0 |
T-DNA |
recessive |
The Arabidopsis mutants abscisic acid insensitive3-5 (abi3-5) and leafy cotyledon1-3 (lec1-3) have impaired seed maturation and quickly lose seed viability. abi3-5 and lec1-3 were used as sensitized genetic backgrounds for the study of seed longevity. |
AP2 | | AT4G36920 | enhance |
testa pigmentation |
10677433 |
Arabidopsis thaliana |
Genetic evidence |
ap2-1 |
Ler |
EMS |
recessive |
Testa mutants generally showed a reduced germination capacity and a higher rate of seedling abnormalities than their WTs |
ASPG1 | | AT3G18490 | enhance |
Aspartic Protease |
29648652 |
Arabidopsis thaliana |
Genetic evidence |
aspg1-1 |
Col-0 |
T-DNA |
recessive |
Aspg1-1 mutants have enhanced seed dormancy and reduced seed viability |
AtAP2/EREBP | | AT4G36920 | enhance |
|
23929721 |
Arabidopsis thaliana |
Molecular evidence |
|
|
|
|
ETHYLENE RESPONSE ELEMENT BINDING PROTEIN (AtAP2/EREBP) |
AtCHL | | AT3G47860 | enhance |
peroxidation |
23837879 |
Arabidopsis thaliana |
Genetic evidence |
AtCHL KO |
Col-0 |
T-DNA |
recessive |
Seeds of the AtCHL-overexpressing Comp line were even more resistant to ageing than WT seeds |
AtDLAH | | AT1G30370 | enhance |
phospholipase |
21856645 |
Arabidopsis thaliana |
Genetic evidence |
35S:AtDLAH |
Col-0 |
transgene |
dominance |
AtDLAH-overexpressing transgenic seeds (35S:AtDLAH) were markedly tolerant to accelerated-ageing treatment and thus had higher germination percentages than wild-type seeds |
AtFAHD1a | | AT4G15940 | decrease |
ROS |
33804275 |
Arabidopsis thaliana |
Genetic evidence |
Atfahd1a-1 |
Col-0 |
T-DNA |
recessive |
Compared to the WT, an A. thaliana T-DNA insertional line (Atfahd1a-1) had extended seed longevity and shallower thermo-dormancy. |
ATHA2-1 | | AT3G08030 | unclear |
molecular marker |
22975286 |
Arabidopsis thaliana |
Molecular evidence |
|
|
|
|
The mRNA of this gene is expressed in viable seeds. Its detection in a dry seed lot has potential for use as a molecular marker for germination performance as absence of expression correlates with decreased germination. Encodes DUF642 cell wall protein. |
ATHB22 | | AT2G36610 | enhance |
Hormone, GA, HB TF |
24335333 |
Arabidopsis thaliana |
Genetic evidence |
athb22 |
Col-0 |
T-DNA |
recessive |
Simultaneous knockdown of ATHB25, ATHB22, and ATHB31 expression decreases seed longevity |
ATHB25 | | AT5G65410 | enhance |
Hormone, GA, HB TF |
24335333 |
Arabidopsis thaliana |
Genetic evidence |
athb25-1D |
Col-0 |
transgene |
dominance |
Overexpression of ATHB25 Increases Seed Longevity |
ATHB31 | | AT1G14440 | enhance |
Hormone, GA, HB TF |
24335333 |
Arabidopsis thaliana |
Genetic evidence |
athb31 |
Col-0 |
T-DNA |
recessive |
Simultaneous knockdown of ATHB25, ATHB22, and ATHB31 expression decreases seed longevity |
AtHSFA9 | | AT5G54070 | enhance |
TF HSF |
32683703 |
Arabidopsis thaliana |
Genetic evidence |
hsfa9 |
Col-0 |
T-DNA |
recessive |
Decreased germination of mature seeds from athsfa9 compared with Col-0 after accelerated aging. |
AtHSL1 | | AT1G28440 | enhance |
LRR-RLK |
35763091 |
Arabidopsis thaliana |
Genetic evidence |
hsk1 |
Col-0 |
T-DNA |
recessive |
Arabidopsis HAESA-like 1 (AtHSL1) positively regulated seed longevity.LRR-RLK protein involved in seed longevity. Induced by aging, mutant seeds show decreased germination rate upon aging treatment |
AtOGG1 | | AT1G21710 | enhance |
DNA repair |
22473985 |
Arabidopsis thaliana |
Genetic evidence |
AtOGG1-OE |
Col-0 |
transgene |
dominance |
Overexpression of AtOGG1 in Arabidopsis enhanced seed resistance to controlled deterioration treatment. |
AtPARP3 | | AT5G22470 | enhance |
DNA repair |
24533577 |
Arabidopsis thaliana |
Genetic evidence |
parp3-1 |
Col-0 |
T-DNA |
recessive |
Stored parp3-1 mutant seeds lacking AtPARP3 expression displayed a delay in germination as compared to Col-0 wild-type seeds. A controlled deterioration test showed that the mutant seeds were hypersensitive to unfavourable storage conditions. The results demonstrate that AtPARP3 is an important component of seed storability and viability. |
ATS | | AT5G42630 | enhance |
testa pigmentation |
10677433 |
Arabidopsis thaliana |
Genetic evidence |
ats |
Ler |
EMS |
recessive |
Recessive aberrant testa shape (ats) gene showed a reduced germination capacity and a higher rate of seedling abnormalities than their WT |
AtSIP2 | | AT3G57520 | decrease |
Raffinose family oligosaccharides |
34553917 |
Arabidopsis thaliana |
Genetic evidence |
atsip2 |
Col-0 |
T-DNA |
recessive |
AtSIP2encodes alkaline α-galactosidase. Knock out of the AtSIP2 (the ZmAGA1 homolog) in Arabidopsis enhanced the seed aging tolerance. |
AtTIL | | AT5G58070 | enhance |
peroxidation |
23837879 |
Arabidopsis thaliana |
Genetic evidence |
AtTIL KO |
Col-0 |
T-DNA |
recessive |
TEMPERATURE-INDUCED LIPOCALIN |
BG14 | | AT2G27500 | enhance |
Hormone ABA |
36625794 |
Arabidopsis thaliana |
Genetic evidence |
bg14 |
Col-0 |
T-DNA |
recessive |
The loss of function of BG14 significantly decreased seed longevity, whereas functional reversion (RE) and overexpression (OE) lines reversed and increased the impaired phenotype, respectively. T |
BSRA5 | | AT2G18030 | unclear |
Protein repair |
23401556 |
Arabidopsis thaliana |
Molecular evidence |
|
|
|
|
METHIONINE SULFOXIDE REDUCTASE A5, MSRA5 |
CDF4 | | AT2G34140 | enhance |
Hormone GA |
27227784 |
Arabidopsis thaliana |
Genetic evidence |
cdf4-1D |
Col-0 |
activation-tagging |
dominance |
two activation-tagging mutants of Arabidopsis thaliana, cog1-2D and cdf4-1D, with improved seed tolerance to deterioration linked to increased expression of COG1/DOF1.5 and CDF4/DOF2.3, respectively |
COG1 | | AT1G29160 | enhance |
ROS,DOF TF |
31600827;27227784 |
Arabidopsis thaliana |
Genetic evidence |
cog1-2D |
Col-0 |
transgene |
dominance |
cog1-2D, a gain-of-function mutant with increased seed longevity |
CRUA | | AT5G44120 | enhance |
seed storage protein |
26184996 |
Arabidopsis thaliana |
Genetic evidence |
crua crub cruc |
Col-0 |
T-DNA |
recessive |
The effect of cruciferin content on seed longevity was even more apparent in the?crua crub cruc?triple mutant which was very sensitive to artificial ageing |
CRUB | | AT1G03880 | enhance |
seed storage protein |
26184996 |
Arabidopsis thaliana |
Genetic evidence |
crua crub cruc |
Col-0 |
T-DNA |
recessive |
The effect of cruciferin content on seed longevity was even more apparent in the?crua crub cruc?triple mutant which was very sensitive to artificial ageing |
CRUC | | AT4G28520 | enhance |
seed storage protein |
26184996 |
Arabidopsis thaliana |
Genetic evidence |
crua crub cruc |
Col-0 |
T-DNA |
recessive |
The effect of cruciferin content on seed longevity was even more apparent in the?crua crub cruc?triple mutant which was very sensitive to artificial ageing |
CYP86A8 | | AT2G45970 | enhance |
seed permeability |
32519347 |
Arabidopsis thaliana |
Genetic evidence |
cyp86a8 |
Col-0 |
T-DNA |
recessive |
Seeds of cyp86a8 showed a drastic reduction in their germination after 1?year of seed dry storage, which is also observed during AAT and CDT treatments |
DHAR1 | | AT1G19570 | enhance |
ROS |
32519347 |
Arabidopsis thaliana |
Genetic evidence |
dhar1 |
Col-0 |
T-DNA |
recessive |
After 1?year of NAT treatment, dhar1 seeds already lost part of their germination ability, while dhar2 and dhar3 mutant seeds did not. |
DOF4.1 | | AT4G00940 | decrease |
DOF TF |
35845633 |
Arabidopsis thaliana |
Genetic evidence |
dof4.1 |
Col-0 |
T-DNA |
recessive |
Dof-type zinc finger DNA-binding family protein. Mutants show enhanced seed longevity due to increased seed storage protein accumulation and reduced seed coat permeabilty.. dof4.1 loss-of-function plants generate seeds exhibiting higher germination after accelerated aging assays |
DOG1 | | AT5G45830 | enhance |
Hormone, ABA |
17065317 |
Arabidopsis thaliana |
Genetic evidence |
dog1 |
Col-0 |
EMS |
recessive |
The non-dormant dog1 (delay of germination1) mutant showed reduced seed longevity phenotypes |
ERCC1 | | AT3G05210 | enhance |
DNA repair |
35858436 |
Arabidopsis thaliana |
Genetic evidence |
ercc1-1 |
Col-0 |
T-DNA |
recessive |
After accelerated aging, mutant seed exhibited lower levelsof germination than wild-type controls. |
GA3OX2 | | AT1G80340 | enhance |
Hormone, GA |
24335333 |
Arabidopsis thaliana |
Genetic evidence |
GA3OX2-OE |
Col-0 |
transgene |
dominance |
GIBBERELLIC ACID3-OXIDASE2 |
GAAS5 | | AT5G45830 | enhance |
Hormone, ABA |
23085841 |
Arabidopsis thaliana |
Molecular evidence |
|
|
|
|
GERMINATION ABILITY AFTER STORAGE 5 |
GL2 | | AT1G79840 | enhance |
testa pigmentation |
10677433 |
Arabidopsis thaliana |
Genetic evidence |
gl2-1 |
Ler |
EMS |
recessive |
Testa mutants generally showed a reduced germination capacity and a higher rate of seedling abnormalities than their WTs |
GOLS1 | | AT2G47180 | enhance |
marker |
26993241 |
Arabidopsis thaliana |
Genetic evidence |
gols1 gols2 |
Col-0 |
T-DNA |
recessive |
The mutants gols2 and gols1gols2 were the only mutants that showed a significantly reduced seed longevity, |
GOLS2 | | AT1G56600 | enhance |
marker |
26993241 |
Arabidopsis thaliana |
Genetic evidence |
gols2 |
Col-0 |
T-DNA |
recessive |
The mutants gols2 and gols1gols2 were the only mutants that showed a significantly reduced seed longevity, |
KNAT7 | | AT1G62990 | decrease |
TF |
32519347 |
Arabidopsis thaliana |
Genetic evidence |
knat7 |
Col-0 |
T-DNA |
recessive |
Loss of function increases seed longevity. |
KU70 | | AT1G16970 | enhance |
DNA repair |
35858436 |
Arabidopsis thaliana |
Genetic evidence |
ku70-1 |
Col-0 |
T-DNA |
recessive |
After accelerated aging, mutant seed exhibited lower levelsof germination than wild-type controls. |
LEC1 | | AT1G21970 | enhance |
NF-YB TF |
19754639 |
Arabidopsis thaliana |
Genetic evidence |
lec1-3 |
|
|
|
The Arabidopsis mutants abscisic acid insensitive3-5 (abi3-5) and leafy cotyledon1-3 (lec1-3) have impaired seed maturation and quickly lose seed viability. abi3-5 and lec1-3 were used as sensitized genetic backgrounds for the study of seed longevity. |
LIG4 | | AT5G57160 | enhance |
DNA repair |
20584150 |
Arabidopsis thaliana |
Genetic evidence |
lig4lig6 |
Col-0 |
T-DNA |
recessive |
High sensitivity of the lig6 mutant and the lig6 lig4 double mutant to seed ageing |
LIG6 | | AT1G66730 | enhance |
DNA repair |
20584150 |
Arabidopsis thaliana |
Genetic evidence |
lig4 |
Col-0 |
T-DNA |
recessive |
High sensitivity of the lig6 mutant and the lig6 lig4 double mutant to seed ageing |
LOX1 | | AT1G55020 | decrease |
Lipid Oxidation |
28371855 |
Arabidopsis thaliana |
Genetic evidence |
lox1 |
Col-0 |
T-DNA |
recessive |
the germination of aged lox1 seeds was slightly higher than in the wild type |
MSRA1 | | AT5G61640 | unclear |
Protein repair |
23401556 |
Arabidopsis thaliana |
Molecular evidence |
|
|
|
|
METHIONINE SULFOXIDE REDUCTASE 1, MSRA1 |
MSRA2 | | AT5G07460 | unclear |
Protein repair |
23401556 |
Arabidopsis thaliana |
Genetic evidence |
pmsr2-1 |
Col-0 |
Em/Spm transposon |
recessive |
METHIONINE SULFOXIDE REDUCTASE 2, MSRA2 |
MSRA3 | | AT5G07470 | unclear |
Protein repair |
23401556 |
Arabidopsis thaliana |
Molecular evidence |
|
|
|
|
METHIONINE SULFOXIDE REDUCTASE 3, MSRA3 |
MSRA4 | | AT4G25130 | unclear |
Protein repair |
23401556 |
Arabidopsis thaliana |
Molecular evidence |
|
|
|
|
METHIONINE SULFOXIDE REDUCTASE A4, MSRA4 |
MSRB1 | | AT1G53670 | unclear |
Protein repair |
23401556 |
Arabidopsis thaliana |
Molecular evidence |
|
|
|
|
METHIONINE SULFOXIDE REDUCTASE B 1, MSRB1 |
MSRB3 | | AT4G04800 | unclear |
Protein repair |
23401556 |
Arabidopsis thaliana |
Molecular evidence |
|
|
|
|
METHIONINE SULFOXIDE REDUCTASE B3, MSRB3 |
MSRB4 | | AT4G04810 | unclear |
Protein repair |
23401556 |
Arabidopsis thaliana |
Molecular evidence |
|
|
|
|
METHIONINE SULFOXIDE REDUCTASE B4, MSRB4 |
MSRB5 | | AT4G04830 | unclear |
Protein repair |
23401556 |
Arabidopsis thaliana |
Molecular evidence |
|
|
|
|
METHIONINE SULFOXIDE REDUCTASE B5, MSRB5 |
MSRB6 | | AT4G04840 | unclear |
Protein repair |
23401556 |
Arabidopsis thaliana |
Molecular evidence |
|
|
|
|
METHIONINE SULFOXIDE REDUCTASE B6, MSRB6 |
MSRB7 | | AT4G21830 | unclear |
Protein repair |
23401556 |
Arabidopsis thaliana |
Molecular evidence |
|
|
|
|
METHIONINE SULFOXIDE REDUCTASE B7, MSRB7 |
MSRB8 | | AT4G21840 | unclear |
Protein repair |
23401556 |
Arabidopsis thaliana |
Molecular evidence |
|
|
|
|
METHIONINE SULFOXIDE REDUCTASE B8, MSRB8 |
MSRB9 | | AT4G21850 | unclear |
Protein repair |
23401556 |
Arabidopsis thaliana |
Molecular evidence |
|
|
|
|
METHIONINE SULFOXIDE REDUCTASE B9, MSRB9 |
MYB47 | | AT1G18710 | enhance |
MYB TF |
32519347 |
Arabidopsis thaliana |
Genetic evidence |
myb47 |
Col-0 |
T-DNA |
recessive |
Loss of function decreases seed longevity. |
NADP-ME | | AT2G19900 | enhance |
Enzyme |
29744896 |
Arabidopsis thaliana |
Genetic evidence |
nadp-me1 |
Col-0 |
T-DNA |
recessive |
nadp-me1 also showed a significant reduction in seed longevity |
NYC1 | | AT4G13250 | enhance |
Hormone ABA |
22751379 |
Arabidopsis thaliana |
Genetic evidence |
nyc1 |
Col-0 |
T-DNA |
recessive |
chlorophyll degradation is induced by ABA during seed maturation to produce storable seeds |
PARP1 | | AT2G31320 | enhance |
DNA repair |
35858436 |
Arabidopsis thaliana |
Genetic evidence |
arp1-1 |
Col-0 |
T-DNA |
recessive |
After accelerated aging, mutant seed exhibited lower levelsof germination than wild-type controls. |
PHYA | | AT1G09570 | decrease |
light |
27227784 |
Arabidopsis thaliana |
Genetic evidence |
phyA |
Col-0 |
T-DNA |
recessive |
phyA and phyB mutants exhibit increased seed tolerance to deterioration |
PHYB | | AT2G18790 | decrease |
light |
27227784 |
Arabidopsis thaliana |
Genetic evidence |
phyB |
Col-0 |
T-DNA |
recessive |
phyA and phyB mutants exhibit increased seed tolerance to deterioration |
PIMT1 | | AT3G48330 | enhance |
Protein repair |
19011119 |
Arabidopsis thaliana |
Genetic evidence |
pimt1-1 |
Col-0 |
T-DNA |
recessive |
Over-expression of PROTEIN-L-ISOASPARTATE METHYLTRANSFERASE1 (PIMT1) enhances seed longevity and germination vigour in Arabidopsis |
PRX2 | | AT1G05250 | enhance |
ROS |
31600827 |
Arabidopsis thaliana |
Genetic evidence |
prx2 prx25 prx71? |
Col-0 |
T-DNA |
recessive |
After controlled deterioration treatment, seeds from the prx2 prx25 double and prx2 prx25 prx71 triple mutant plants presented lower germination than wild-type plants |
PRX25 | | AT2G41480 | enhance |
ROS |
31600827 |
Arabidopsis thaliana |
Genetic evidence |
prx2 prx25 prx71? |
Col-0 |
T-DNA |
recessive |
After controlled deterioration treatment, seeds from the prx2 prx25 double and prx2 prx25 prx71 triple mutant plants presented lower germination than wild-type plants |
PRX71 | | AT5G64120 | enhance |
ROS |
31600827 |
Arabidopsis thaliana |
Genetic evidence |
prx2 prx25 prx71? |
Col-0 |
T-DNA |
recessive |
After controlled deterioration treatment, seeds from the prx2 prx25 double and prx2 prx25 prx71 triple mutant plants presented lower germination than wild-type plants |
PSAD1 | | AT4G02770 | enhance |
photosystem |
32519347 |
Arabidopsis thaliana |
Genetic evidence |
psad1 |
Col-0 |
T-DNA |
recessive |
Loss of function decreases seed longevity. |
RBOHD | | AT5G47910 | decrease |
ROS |
32519347 |
Arabidopsis thaliana |
Genetic evidence |
rbohd |
Col-0 |
T-DNA |
recessive |
Seeds of rbohd, rbohe and rbohf mutant plants exhibited increased longevity and the double mutant, rbohd,f has even more seed longevity |
RBOHE | | AT1G19230 | decrease |
ROS |
32519347 |
Arabidopsis thaliana |
Genetic evidence |
rbohe |
Col-0 |
T-DNA |
recessive |
Seeds of rbohd, rbohe and rbohf mutant plants exhibited increased longevity and the double mutant, rbohd,f has even more seed longevity |
RBOHF | | AT1G64060 | decrease |
ROS |
32519347 |
Arabidopsis thaliana |
Genetic evidence |
rbohf |
Col-0 |
T-DNA |
recessive |
Seeds of rbohd, rbohe and rbohf mutant plants exhibited increased longevity and the double mutant, rbohd,f has even more seed longevity |
RGA1 | | AT2G01570 | decrease |
Hormone, GA |
24335333 |
Arabidopsis thaliana |
Genetic evidence |
gai-t6 rga-t2 rgl1-1 |
Col-0 |
T-DNA |
recessive |
GA3-treated plants and the quintuple DELLA mutant, which shows constitutive activation of the GA signaling pathway, produced seeds that are more resistant to accelerated aging, as compared with their respective controls. |
RGA2 | | AT1G14920 | decrease |
Hormone, GA |
24335333 |
Arabidopsis thaliana |
Genetic evidence |
gai-t6 rga-t2 rgl1-1 |
Col-0 |
T-DNA |
recessive |
GA3-treated plants and the quintuple DELLA mutant, which shows constitutive activation of the GA signaling pathway, produced seeds that are more resistant to accelerated aging, as compared with their respective controls. |
RGL1 | | AT1G66350 | decrease |
Hormone, GA |
24335333 |
Arabidopsis thaliana |
Genetic evidence |
gai-t6 rga-t2 rgl1-1 |
Col-0 |
T-DNA |
recessive |
GA3-treated plants and the quintuple DELLA mutant, which shows constitutive activation of the GA signaling pathway, produced seeds that are more resistant to accelerated aging, as compared with their respective controls. |
RGL2 | | AT3G03450 | decrease |
Hormone, GA |
24335333 |
Arabidopsis thaliana |
Genetic evidence |
gai-t6 rga-t2 rgl1-1 |
Col-0 |
T-DNA |
recessive |
GA3-treated plants and the quintuple DELLA mutant, which shows constitutive activation of the GA signaling pathway, produced seeds that are more resistant to accelerated aging, as compared with their respective controls. |
RGL3 | | AT5G17490 | decrease |
Hormone, GA |
24335333 |
Arabidopsis thaliana |
Genetic evidence |
gai-t6 rga-t2 rgl1-1 |
Col-0 |
T-DNA |
recessive |
GA3-treated plants and the quintuple DELLA mutant, which shows constitutive activation of the GA signaling pathway, produced seeds that are more resistant to accelerated aging, as compared with their respective controls. |
ROF1 | | AT3G25230 | enhance |
Protein isomerization |
22268595 |
Arabidopsis thaliana |
Genetic evidence |
rof1 rof2 |
Col-0 |
T-DNA |
recessive |
ROTAMASE FKBP 1, ROF1. Only the double loss-of-function mutant rof1 rof2 was more sensitive than wild-type in the controlled deterioration test for seed longevity, while single rof1 or rof2 mutants and lines over-expressing ROF2 exhibited similar germination to wild-type after accelerated aging of seeds. |
ROF2 | | AT5G48570 | enhance |
Protein isomerization |
22268595 |
Arabidopsis thaliana |
Genetic evidence |
rof1 rof2 |
Col-0 |
T-DNA |
recessive |
ROTAMASE FKBP 2, ROF2. Only the double loss-of-function mutant rof1 rof2 was more sensitive than wild-type in the controlled deterioration test for seed longevity, while single rof1 or rof2 mutants and lines over-expressing ROF2 exhibited similar germination to wild-type after accelerated aging of seeds. |
RSL1 | | AT2G26130 | enhance |
Protein degradtion |
24388521 |
Arabidopsis thaliana |
Genetic evidence |
rsl1 |
Col-0 |
T-DNA |
recessive |
RING FINGER OF SEED LONGEVITY 1, RSL1.Encodes a RING-type zinc finger ubiquitin ligase involved in seed longevity.Gain of function (35S promoter) increases, and loss of function decreases, seed longevity. |
SEP | | AT5G15800 | decrease |
TF |
32519347 |
Arabidopsis thaliana |
Genetic evidence |
sep |
Col-0 |
T-DNA |
recessive |
Loss of function increases seed longevity. |
SKIP31 | | AT5G45360 | enhance |
|
37462265 |
Arabidopsis thaliana |
Genetic evidence |
skip31 |
Col-0 |
T-DNA |
recessive |
skip31 T-DNA insertion mutants and RNAi lines show a defect in seed maturation and germination vigor and/or viability, while seed-specific OE lines show improved seed vigor in Arabidopsis |
SOG1 | | AT1G25580 | decrease |
DNA repair |
35858436 |
Arabidopsis thaliana |
Genetic evidence |
sog1 |
Col-0 |
EMS |
recessive |
After accelerated aging,sog1mutant seed exhibited higher levelsof germination than wild-type controls. |
SPCH1 | | AT5G53210 | enhance |
TF |
32519347 |
Arabidopsis thaliana |
Genetic evidence |
spch1 |
Col-0 |
T-DNA |
recessive |
Loss of function decreases seed longevity. |
SSLEA | | AT3G17520 | enhance |
LEA |
32519347 |
Arabidopsis thaliana |
Genetic evidence |
sslea |
Col-0 |
T-DNA |
recessive |
Loss of function decreases seed longevity. |
SSTPR | | AT4G02750 | enhance |
tetratricopeptide repeat |
32519347 |
Arabidopsis thaliana |
Genetic evidence |
sstpr |
Col-0 |
T-DNA |
recessive |
Loss of function decreases seed longevity. |
TAP46 | | AT5G53000 | enhance |
PP2A |
25399018 |
Arabidopsis thaliana |
Genetic evidence |
TAP46OE |
Col-0 |
transgene |
dominance |
TAP46 overexpression also enhanced seed size and viability under accelerated ageing conditions. |
TIP3;1 | | AT1G73190 | enhance |
|
26019256 |
Arabidopsis thaliana |
Genetic evidence |
tip3;1 tip3;2 |
Col-0 |
T-DNA |
recessive |
The tip3;1/tip3;2 double mutant was affected in seed longevity and accumulated high levels of hydrogen peroxide compared with the wild type, suggesting that TIP3s function in seed longevity. |
TIP3;2 | | AT1G17810 | enhance |
|
26019256 |
Arabidopsis thaliana |
Genetic evidence |
tip3;1 tip3;2 |
Col-0 |
T-DNA |
recessive |
The tip3;1/tip3;2 double mutant was affected in seed longevity and accumulated high levels of hydrogen peroxide compared with the wild type, suggesting that TIP3s function in seed longevity. |
TT1 | | AT1G34790 | enhance |
testa pigmentation |
10677433 |
Arabidopsis thaliana |
Genetic evidence |
tt1-1 |
Ler |
EMS |
recessive |
Testa mutants generally showed a reduced germination capacity and a higher rate of seedling abnormalities than their WTs |
TT10 | | AT5G48100 | enhance |
testa pigmentation |
10677433 |
Arabidopsis thaliana |
Genetic evidence |
tt10-1 |
Ler |
EMS |
recessive |
Testa mutants generally showed a reduced germination capacity and a higher rate of seedling abnormalities than their WTs |
TT3 | | AT5G42800 | enhance |
testa pigmentation |
10677433 |
Arabidopsis thaliana |
Genetic evidence |
tt3-1 |
Ler |
EMS |
recessive |
Testa mutants generally showed a reduced germination capacity and a higher rate of seedling abnormalities than their WTs |
TT5 | | AT3G55120 | enhance |
testa pigmentation |
10677433 |
Arabidopsis thaliana |
Genetic evidence |
tt5-1 |
Ler |
EMS |
recessive |
Testa mutants generally showed a reduced germination capacity and a higher rate of seedling abnormalities than their WTs |
TT7 | | AT5G07990 | enhance |
testa pigmentation |
10677433 |
Arabidopsis thaliana |
Genetic evidence |
tt7-1 |
Ler |
EMS |
recessive |
Testa mutants generally showed a reduced germination capacity and a higher rate of seedling abnormalities than their WTs |
TT8 | | AT4G09820 | enhance |
testa pigmentation |
10677433 |
Arabidopsis thaliana |
Genetic evidence |
tt8-1 |
Enkheim (En) |
EMS |
recessive |
BHLH42/TT8. Testa mutants generally showed a reduced germination capacity and a higher rate of seedling abnormalities than their WTs |
TT9 | | AT3G28430 | enhance |
testa pigmentation |
10677433 |
Arabidopsis thaliana |
Genetic evidence |
tt9-1 |
Ler |
EMS |
recessive |
Testa mutants generally showed a reduced germination capacity and a higher rate of seedling abnormalities than their WTs |
VTE1 | | AT4G32770 | enhance |
vitamin E |
15155886 |
Arabidopsis thaliana |
Genetic evidence |
vte1-1 |
Col-0 |
EMS |
recessive |
Mutants in vitamin E synthesis genes (vte1 and vte2) showed decreased seed longevity |
VTE2 | | AT2G18950 | enhance |
vitamin E |
15155886 |
Arabidopsis thaliana |
Genetic evidence |
vte2-1 |
Col-0 |
EMS |
recessive |
Mutants in vitamin E synthesis genes (vte1 and vte2) showed decreased seed longevity |
WHY1 | | AT1G14410 | enhance |
ROS |
37351567 |
Arabidopsis thaliana |
Genetic evidence |
why1why3 |
Col-0 |
T-DNA |
recessive |
Loss of WHY1 and WHY3 functions decreases the ability of Arabidopsis seeds to resist the adverse effects of seed aging. |
WHY3 | | AT2G02740 | enhance |
ROS |
37351567 |
Arabidopsis thaliana |
Genetic evidence |
why1why3 |
Col-0 |
T-DNA |
recessive |
Loss of WHY1 and WHY3 functions decreases the ability of Arabidopsis seeds to resist the adverse effects of seed aging. |
XRCC2 | | AT5G64520 | enhance |
DNA repair |
35858436 |
Arabidopsis thaliana |
Genetic evidence |
xrcc2-1 |
Col-0 |
T-DNA |
recessive |
After accelerated aging, mutant seed exhibited lower levelsof germination than wild-type controls. |
βVPE | | AT1G62710 | enhance |
marker |
30782971 |
Arabidopsis thaliana |
Genetic evidence |
βvpe |
Col-0 |
T-DNA |
recessive |
The mutant seeds did not show statistical differences from the wild type, although both β-vpe and the quadruple vpe mutant were slightly more sensitive to the ageing treatment |
AaDOG1 | KFK28541 | Aa_G419960 | unclear |
|
30712274 |
Arabis alpina |
Molecular evidence |
|
|
|
|
Gene ID of A. thaliana Ortholog is AT5G45830 |
AaGA20ox2 | KFK26790 | Aa_G598100 | unclear |
Hormone GA |
30712274 |
Arabis alpina |
Molecular evidence |
|
|
|
|
Gene ID of A. thaliana Ortholog is AT5G51810 |
AaGA2ox1 | KFK42227 | Aa_G470650 | unclear |
Hormone GA |
30712274 |
Arabis alpina |
Molecular evidence |
|
|
|
|
Gene ID of A. thaliana Ortholog is AT1G78440 |
AaGA2ox2 | KFK44827 | Aa_G655020 | unclear |
Hormone GA |
30712274 |
Arabis alpina |
Molecular evidence |
|
|
|
|
Gene ID of A. thaliana Ortholog is AT1G30040 |
AaGA2ox3 | KFK36353 | Aa_G291640 | unclear |
Hormone GA |
30712274 |
Arabis alpina |
Molecular evidence |
|
|
|
|
Gene ID of A. thaliana Ortholog is AT2G34555 |
AaGA2ox6 | KFK42605 | Aa_G6340 | unclear |
Hormone GA |
30712274 |
Arabis alpina |
Molecular evidence |
|
|
|
|
Gene ID of A. thaliana Ortholog is AT1G02400 |
AaGA2ox8 | KFK28698 | Aa_G37650 | unclear |
Hormone GA |
30712274 |
Arabis alpina |
Molecular evidence |
|
|
|
|
Gene ID of A. thaliana Ortholog is AT4G21200 |
AaPEP1 | JX310558 | Aa_G579940 | enhance |
Flowering |
30712274 |
Arabis alpina |
Genetic evidence |
pep1-1 |
|
|
|
Perpetual flowering accessions and pep1 mutants have low seed longevity. Gene ID of A. thaliana Ortholog is AT5G10140 |
AaRGL2 | KFK38060 | Aa_G47610 | unclear |
Hormone GA |
30712274 |
Arabis alpina |
Molecular evidence |
|
|
|
|
Gene ID of A. thaliana Ortholog is AT3G03450 |
AaSLP2 | KFK28394 | Aa_G180420 | unclear |
|
30712274 |
Arabis alpina |
Molecular evidence |
|
|
|
|
Gene ID of A. thaliana Ortholog is AT4G34980 |
CaABI3.1 | XM_016721996.2 | CAN.G771.55 | unclear |
Seed coat lignification |
34796959 |
Capsicum annuum |
Molecular evidence |
|
|
|
|
Capsicum annuum B3 domain-containing transcription factor ABI3 (LOC107875324) |
CaABI3.2 | XM_047414275.1 | CAN.G771.56 | unclear |
Seed coat lignification |
34796959 |
Capsicum annuum |
Molecular evidence |
|
|
|
|
Capsicum annuum B3 domain-containing transcription factor ABI3 (LOC107875325) |
CaABI5 | XM_016701108.2 | CAN.G397.17 | unclear |
Seed coat lignification |
34796959 |
Capsicum annuum |
Molecular evidence |
https://bioinformati |
|
|
|
Capsicum annuum protein ABSCISIC ACID-INSENSITIVE 5 (LOC107856113) |
CaASPG1 | XM_016700454.2 | CAN.G587.80 | unclear |
Seed coat lignification |
34796959 |
Capsicum annuum |
Molecular evidence |
|
|
|
|
Capsicum annuum protein ASPARTIC PROTEASE IN GUARD CELL 1 (LOC107855434) |
CaFUS3 | XM_016706302.2 | CAN.G473.153 | unclear |
Seed coat lignification |
34796959 |
Capsicum annuum |
Molecular evidence |
|
|
|
|
Capsicum annuum B3 domain-containing transcription factor FUS3 (LOC107860813) |
CaGOLS2 | NM_001324776.1 | CAN.G358.49 | unclear |
Seed coat lignification |
34796959 |
Capsicum annuum |
Molecular evidence |
|
|
|
|
Capsicum annuum galactinol synthase 2 (LOC107859925) |
CaHB25 | XM_016705161.2 | CAN.G358.72 | unclear |
Seed coat lignification |
34796959 |
Capsicum annuum |
Molecular evidence |
|
|
|
|
Capsicum annuum zinc-finger homeodomain protein 2 (LOC107859980) |
CaLEA14 | XM_016682673.2 | CAN.G78.132 | unclear |
Seed coat lignification |
34796959 |
Capsicum annuum |
Molecular evidence |
|
|
|
|
Capsicum annuum desiccation protectant protein Lea14 homolog (LOC107839261) |
CaLEC1 | XM_016694818.2 | CAN.G1156.20 | unclear |
Seed coat lignification |
34796959 |
Capsicum annuum |
Molecular evidence |
|
|
|
|
Capsicum annuum nuclear transcription factor Y subunit B-6 (LOC107850352) |
CaOGG1 | XM_047402030.1 | CAN.G1391.3 | unclear |
Seed coat lignification |
34796959 |
Capsicum annuum |
Molecular evidence |
|
|
|
|
Capsicum annuum N-glycosylase/DNA lyase OGG1 (LOC107854385) |
CaPIMT1 | XM_016708244.2 | CAN.G126.92 | unclear |
Seed coat lignification |
34796959 |
Capsicum annuum |
Molecular evidence |
|
|
|
|
Capsicum annuum protein-L-isoaspartate O-methyltransferase 1 (LOC107862612) |
CaSnRK2.6 | XM_016705648.2 | CAN.G836.53 | unclear |
Seed coat lignification |
34796959 |
Capsicum annuum |
Molecular evidence |
|
|
|
|
Capsicum annuum serine/threonine-protein kinase SRK2I (LOC107860330) |
CaVTE1 | XM_016682501.2 | CAN.G21.50 | unclear |
Seed coat lignification |
34796959 |
Capsicum annuum |
Molecular evidence |
|
|
|
|
Capsicum annuum probable tocopherol cyclase, chloroplastic (LOC107839135) |
CaVTE2 | XM_016694630.2 | CAN.G33.20 | unclear |
Seed coat lignification |
34796959 |
Capsicum annuum |
Molecular evidence |
|
|
|
|
Capsicum annuum homogentisate phytyltransferase 1, chloroplastic (LOC107850218) |
CaGolS1 | KU189226 | | enhance |
ROS |
27725707 |
Chickpea (Cicer arietinum) |
Genetic evidence |
CaGolS1OE |
|
transgene |
dominance |
Seed-specific overexpression of CaGolS1 and CaGolS2 in Arabidopsis results improved seed vigor and longevity through limiting the age induced excess ROS and consequent lipid peroxidation. |
CaGolS2 | KU189226 | | enhance |
ROS |
27725707 |
Chickpea (Cicer arietinum) |
Genetic evidence |
CaGolS2OE |
|
transgene |
dominance |
Seed-specific overexpression of CaGolS1 and CaGolS2 in Arabidopsis results improved seed vigor and longevity through limiting the age induced excess ROS and consequent lipid peroxidation. |
CaPIMT1 | GQ421817 | | enhance |
Protein repair |
23284083 |
Chickpea (Cicer arietinum) |
Genetic evidence |
CaPIMT1-OE |
Col-0 |
transgene |
dominance |
Seed-Specific Overexpression of CaPIMT1 and CaPIMT2 Genes in Arabidopsis Enhances Seed Vigor and Longevity |
CaPIMT2 | JQ690076 | | enhance |
Protein repair |
23284083 |
Chickpea (Cicer arietinum) |
Genetic evidence |
CaPIMT2-OE |
Col-0 |
transgene |
dominance |
Seed-Specific Overexpression of CaPIMT1 and CaPIMT2 Genes in Arabidopsis Enhances Seed Vigor and Longevity |
UpGAPDH | MK046694.1 | | decrease |
Hormone NO |
34244712 |
Elm (Ulmus pumila) |
Genetic evidence |
oxUpGAPDH |
|
transgene |
dominance |
Seeds of oxUpGAPDH lines showed cell death and lost seed vigor rapidly during controlled deterioration treatment-triggered seed aging |
NADP-ME | AK248526.1 | | enhance |
|
29744896 |
Hordeum vulgare |
transcriptome and pr |
nadp-me1 |
|
|
|
Both the NADP-ME MLOC_35785.1 and the UDP-glycosyltransferase MLOC_11661.1 were able to rescue the nadp-me1 seed longevity phenotype. |
ZmAGA1 | XM_008667421.4 | | decrease |
Raffinose family oligosaccharides |
34553917 |
Maize (Zea mays) |
Genetic evidence |
ZmAGA1-OE |
Col-0 |
transgene |
dominance |
Overexpressing ZmAGA1 in Arabidopsis decreased seed aging tolerance |
ZmDREB2A | NM_001112406.2 | GRMZM2G006745 | enhance |
|
32662115 |
Maize (Zea mays) |
Genetic evidence |
zmdreb2a |
|
mutator (Mu)-inserte |
recessive |
The zmdreb2a seeds, with decreased expression of RAFFINOSE SYNTHASE (ZmRAFS) and less raffinose in their embryo, exhibit decreased seed aging tolerance, than the NS controls. |
ZmLPA | EF586878 | | enhance |
ROS |
36614175 |
Maize (Zea mays) |
Genetic evidence |
lpa1-1 |
|
Transposon |
recessive |
LPA1 gene encodes a multidrug-associated protein (MRP) named ZmMRP4. lpa1-1 seeds aged faster as compared to wildtype |
ZmMCCα | NM_001371674.1 | GRMZM2G019926 | enhance |
protein repair |
36999611 |
maize (Zea mays) |
Genetic evidence |
ZmMCCαOE |
|
transgene |
dominance |
3-METHYLCROTONYL COA CARBOXYLASE α-subunit (MCCα). Knockdown of ZmMCCα decreased maize seed aging tolerance. |
ZmPIMT2 | XM_008668898 | GRMZm2G100315 | enhance |
protein repair |
36999611 |
maize (Zea mays) |
Genetic evidence |
ZmPIMT2 OE |
|
transgene |
dominance |
overexpression of ZmPIMT2 decreased the accumulation of isoAsp of ZmMCCα protein in seed embryos that underwent accelerated aging treatment.ZmPIMT2 binds ZmMCCα in mitochondria, repairs isoAsp damage, and positively affects maize seed vigor |
AGAL2 | | At5g08370 | enhance |
|
26410298 |
Medicago truncatula |
Cross-species networ |
aga12 |
Col-0 |
T-DNA |
recessive |
Loss-of-function mutant displays decreased longevity |
CAF-1 | | At2g32070 | enhance |
|
26410298 |
Medicago truncatula |
Cross-species networ |
caf-1 |
Col-0 |
T-DNA |
recessive |
Loss-of-function mutant displays decreased longevity |
CYP81D3 | | At4g37340 | enhance |
|
26410298 |
Medicago truncatula |
Cross-species networ |
cyp81d3 |
Col-0 |
T-DNA |
recessive |
Loss-of-function mutant displays decreased longevity |
MtABI3 | XM_039828061.1 | Medtr7g059330 | enhance |
|
23929721 |
Medicago truncatula |
Network |
Mt-abi3 |
|
Tnt1 insertion |
recessive |
ABSCISIC ACID-INSENSITIVE3 (MtABI3) |
MtABI4 | XM_003616618.3 | Medtr5g082950 | enhance |
|
23929721 |
Medicago truncatula |
Network |
|
|
|
|
ABSCISIC ACID-INSENSITIVE3 (MtABI4) |
MtABI5 | | Medtr7g104480 | enhance |
ABA |
27956585 |
Medicago truncatula |
Genetic evidence |
Mt-abi5 |
|
|
|
bZIP transcription factor ABSCISIC ACID INSENSITIVE5 (ABI5) in Medicago truncatula |
MtHSFA9 | XM_024782179.2 | Medtr4g126070 | enhance |
Hormone ABA |
32683703 |
Medicago truncatula |
Genetic evidence |
Mthsfa9 |
|
|
recessive |
Decreased germination of mature seeds after accelerated aging compared with WT seeds. |
MtMSRA2 | | MTR_135s0002 | unclear |
Protein repair |
23401556 |
Medicago truncatula |
Enzymatic capacity |
|
|
|
|
Medicago truncatula methionine sulfoxide reductase (MSR). MSR enzymatic capacity decreased as seed ageing. |
MtMSRA4.1L | | MTR_5g092680 | unclear |
Protein repair |
23401556 |
Medicago truncatula |
Enzymatic capacity |
|
|
|
|
Medicago truncatula methionine sulfoxide reductase (MSR). MSR enzymatic capacity decreased as seed ageing. |
MtMSRA4.1S | | MTR_5g092680 | unclear |
Protein repair |
23401556 |
Medicago truncatula |
Enzymatic capacity |
|
|
|
|
Medicago truncatula methionine sulfoxide reductase (MSR). MSR enzymatic capacity decreased as seed ageing. |
MtMSRA4.2 | | MTR_3g051460 | unclear |
Protein repair |
23401556 |
Medicago truncatula |
Enzymatic capacity |
|
|
|
|
Medicago truncatula methionine sulfoxide reductase (MSR). MSR enzymatic capacity decreased as seed ageing. |
MtMSRA5 | | MTR_8g076060 | unclear |
Protein repair |
23401556 |
Medicago truncatula |
Enzymatic capacity |
|
|
|
|
Medicago truncatula methionine sulfoxide reductase (MSR). MSR enzymatic capacity decreased as seed ageing. |
MtMSRB2 | | MTR_4g092800 | unclear |
Protein repair |
23401556 |
Medicago truncatula |
Enzymatic capacity |
|
|
|
|
Medicago truncatula methionine sulfoxide reductase (MSR). MSR enzymatic capacity decreased as seed ageing. |
MtMSRB5.1 | | MTR_2g020950 | unclear |
Protein repair |
23401556 |
Medicago truncatula |
Enzymatic capacity |
|
|
|
|
Medicago truncatula methionine sulfoxide reductase (MSR). MSR enzymatic capacity decreased as seed ageing. |
MtMSRB5.2 | | MTR_2g020930 | unclear |
Protein repair |
23401556 |
Medicago truncatula |
Enzymatic capacity |
|
|
|
|
Medicago truncatula methionine sulfoxide reductase (MSR). MSR enzymatic capacity decreased as seed ageing. |
MtMSRB5.3 | | MTR_2g020900 | unclear |
Protein repair |
23401556 |
Medicago truncatula |
Enzymatic capacity |
|
|
|
|
Medicago truncatula methionine sulfoxide reductase (MSR). MSR enzymatic capacity decreased as seed ageing. |
MtSNF4b | AY247270 | | enhance |
|
17488238 |
Medicago truncatula |
Genetic evidence |
RNAi MtSNF4b |
|
RNAi |
recessive |
Silencing of MtSNF4b using a RNA interference (RNAi) approach resulted in a phenotype with reduced seed longevity |
NFLX1 | | At1g10170 | enhance |
|
26410298 |
Medicago truncatula |
Cross-species networ |
nflx1 |
Col-0 |
T-DNA |
recessive |
Loss-of-function mutant displays decreased longevity |
NOT4 | | At3g45630 | enhance |
|
26410298 |
Medicago truncatula |
Cross-species networ |
not4 |
Col-0 |
T-DNA |
recessive |
Loss-of-function mutant displays decreased longevity |
PPC6-1 | | At3g02750 | enhance |
|
26410298 |
Medicago truncatula |
Cross-species networ |
ppc6-1 |
Col-0 |
T-DNA |
recessive |
Loss-of-function mutant displays decreased longevity |
SIP2 | | At3g57520 | enhance |
|
26410298 |
Medicago truncatula |
Cross-species networ |
sip2 |
Col-0 |
T-DNA |
recessive |
Loss-of-function mutant displays decreased longevity |
WRKY33 | | At2g38470 | enhance |
WRKY TF |
26410298 |
Medicago truncatula |
Cross-species networ |
wrky33 |
Col-0 |
T-DNA |
recessive |
Loss-of-function mutant displays decreased longevity |
VrRH1 | AF156667 | | unclear |
RNA helicase |
11785937 |
Mung bean (Vigna radiata) |
|
|
|
|
|
VrRH1 (Vigna radiata RNA helicase 1)The amount of these mRNAs reached a maximum in 24 h imbibed seeds after the treatment. The accumulation of VrRH transcripts was shown to lead to the appearance of 25S and 18S rRNAs in the imbibed aging mung bean seeds. The results suggest that VrRH1 may play a role in the viability of mung bean seeds. |
OcPIMT1-1 | MZ061932 | | enhance |
Protein repair |
35686643 |
Oryza coarctata |
Genetic evidence |
OcPIMT1-1 RNAi |
|
RNAi |
recessive |
Suppression of PIMT reduces, and its overexpression increases, seed desiccation tolerance and seed longevity in O. sativa. |
OcPIMT2-1 | MZ061933 | | enhance |
Protein repair |
35686643 |
Oryza coarctata |
Genetic evidence |
OcPIMT2-1 RNAi |
|
RNAi |
recessive |
Suppression of PIMT reduces, and its overexpression increases, seed desiccation tolerance and seed longevity in O. sativa. |
OcPIMT2-2 | MZ061934 | | enhance |
Protein repair |
35686643 |
Oryza coarctata |
Genetic evidence |
OcPIMT2-2 RNAi |
|
RNAi |
recessive |
Suppression of PIMT reduces, and its overexpression increases, seed desiccation tolerance and seed longevity in O. sativa. |
PsABI5 | | PsCam017634 | enhance |
ABA |
27956585 |
Pea (Pisum sativum) |
Genetic evidence |
|
|
|
|
bZIP transcription factor ABSCISIC ACID INSENSITIVE5 (ABI5) in Pisum sativum. |
PSLAG1 | XP_002322262 | | unclear |
Metabolism |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Acetolactate synthase |
PSLAG10 | XP_002329233 | | unclear |
Metabolism |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Hydroxyacylglutathione hydrolase |
PSLAG11 | ABK93990 | | unclear |
Metabolism |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Inorganic pyrophosphatase |
PSLAG12 | XP_002329233 | | unclear |
Metabolism |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Hydroxyacyiglutathione hydrolase |
PSLAG13 | XP_002314019 | | unclear |
Metabolism |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Ribonucleoprotein |
PSLAG14 | ABK96373 | | unclear |
Metabolism |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Ribonucleoprotein |
PSLAG15 | XP_002322981 | | unclear |
Metabolism |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Probable pyridoxal biosynthesis protein PDX1 |
PSLAG16 | XP_002326261 | | unclear |
Energy |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
2,3-Bisphosphoglycerate-independent phosphoglycerate mutase |
PSLAG17 | XP_002311517 | | unclear |
Energy |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Cytosolic phosphoglucomutase |
PSLAG18 | XP_002311090 | | unclear |
Energy |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Phosphoglucomutase |
PSLAG19 | XP_002322420 | | unclear |
Energy |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Enolase |
PSLAG2 | XP_002321728 | | unclear |
Metabolism |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Glutamate-1-semialdehyde 2,1-aminomutase |
PSLAG20 | BAA33801 | | unclear |
Energy |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Cytosolic phosphoglycerate kinase 1 |
PSLAG21 | XP_002315067 | | unclear |
Energy |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Phosphoglycerate kinase |
PSLAG22 | XP_002311168 | | unclear |
Energy |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Triosephosphate isomerase |
PSLAG23 | XP_002314179 | | unclear |
Energy |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Triosephosphate isomerase |
PSLAG24 | XP_002314631 | | unclear |
Energy |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Pyruvate dehydrogenase |
PSLAG25 | XP_002305090 | | unclear |
Energy |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Magnesium-chelatase subunit chll |
PSLAG26 | XP_002309064 | | unclear |
Energy |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Putative NAD-dependent |
PSLAG27 | ABK96553 | | unclear |
Energy |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Peptidyi-prolyl cis-trans isomer |
PSLAG28 | XP_002301171 | | unclear |
Protein synthesis and destination( |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Polyadenylate-binding protein |
PSLAG29 | XP_002306784 | | unclear |
Protein synthesis and destination( |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Nucleolar protein nop56 |
PSLAG3 | XP_002301683 | | unclear |
Metabolism |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Glutamine synthetase |
PSLAG30 | XP_002317118 | | unclear |
Protein synthesis and destination( |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
NSFL1 cofactor p47 |
PSLAG31 | XP_002319515 | | unclear |
Protein synthesis and destination( |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
26S proteasome AAA-ATPase |
PSLAG32 | XP_002318902 | | unclear |
Protein synthesis and destination( |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Proteasome subunit alpha type |
PSLAG33 | XP_002308263 | | unclear |
Protein synthesis and destination( |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Proteasome subunit alpha type |
PSLAG34 | ADG86642 | | unclear |
Protein synthesis and destination( |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Proteasome subunit beta type |
PSLAG35 | AAN60260 | | unclear |
Protein synthesis and destination( |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Aspartic proteinase |
PSLAG36 | XP_002328218 | | unclear |
Protein synthesis and destination( |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Chaperonin containing t-complexprotein 1 |
PSLAG37 | ABK93392 | | unclear |
Protein synthesis and destination( |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Protein disulfide isomerase |
PSLAG38 | XP_002326137 | | unclear |
Protein synthesis and destination( |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Groes chaperonin |
PSLAG39 | XP_002324138 | | unclear |
Protein synthesis and destination( |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
20 kDa chaperonin family protein |
PSLAG4 | XP_002311011 | | unclear |
Metabolism |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Argininosuccinate synthase |
PSLAG42 | XP_002329509 | | unclear |
Storage protein |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Glutelin type-A 3 |
PSLAG43 | XP_002306851 | | unclear |
Storage protein |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
11S globulin seed storage protein 2 |
PSLAG44 | XP_002307645 | | unclear |
Storage protein |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Legumin family protein |
PSLAG45 | XP_002313331 | | unclear |
Storage protein |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Nutrient reservoir |
PSLAG46 | XP_002336547 | | unclear |
Storage protein |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Glutelin type-A 3 |
PSLAG47 | XP_002317577 | | unclear |
Storage protein |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
2S albumin family protein |
PSLAG48 | XP_002336547 | | unclear |
Storage protein |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Glutelin type-A 3 |
PSLAG49 | XP_006370926 | | unclear |
Storage protein |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Legumin family protein |
PSLAG5 | XP_002308219 | | unclear |
Metabolism |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Probable pyridoxal biosynthesis protein PDX1 |
PSLAG50 | XP_002329472 | | unclear |
Storage protein |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Hypothetical protein |
PSLAG52 | XP_002317682 | | unclear |
Signal transduction |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Serine/threonine-protein kinase |
PSLAG53 | XP_002312740 | | unclear |
Cell growth and structure |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Dienelactone hydrolase family protein |
PSLAG54 | XP_002311776 | | unclear |
Cell growth and structure |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
F5O8.30 protein |
PSLAG55 | XP_002301942 | | unclear |
Cell defense and rescue |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Phi class glutathione transferase GSTF2 |
PSLAG56 | XP_002313445 | | unclear |
Hormore CK |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Zeamatin |
PSLAG57 | XP_002299179 | | unclear |
Cell defense and rescue |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Cysteine proteinase inhibitor |
PSLAG58 | CAI43948 | | unclear |
ROS |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Catalase |
PSLAG59 | XP_002319637 | | unclear |
Cell defense and rescue |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Aldo/keto reductase |
PSLAG6 | XP 002325923 | | unclear |
Metabolism |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
ATP phosphoribosyltransferase |
PSLAG60 | XP_002330137 | | unclear |
Cell defense and rescue |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Late embryogenesis abundant |
PSLAG61 | XP_002328518 | | unclear |
Cell defense and rescue |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Late embryogenesis abundant |
PSLAG62 | XP_002326522 | | unclear |
Hormone ABA |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Abscisic acid receptor PYR1 |
PSLAG63 | XP_002331340 | | unclear |
Cell defense and rescue |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Heat shock factor binding protein |
PSLAG64 | XP_002324004 | | unclear |
Cell defense and rescue |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Universal stress family protein |
PSLAG7 | XP002312082 | | unclear |
Metabolism |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Thymidine diphospho-glucose-4-6-dehydratase |
PSLAG8 | XP_006388670 | | unclear |
Metabolism |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
GDSL esterase/ipase |
PSLAG9 | XP_002298803 | | unclear |
Metabolism |
26172265 |
Poplar (Populus × Canadensis Moench) |
Proteomic evidence |
|
|
|
|
Inorganic pyrophosphatase |
Os4BGlu14 | XM_015778859 | | decrease |
metabolism |
32833149 |
Rice (Oryza sativa) |
Genetic evidence |
Os4BGlu14-OE |
|
|
|
Os4BGlu14, a monolignol β-glucosidase, plays a negative role in seed longevity by affecting primary metabolism during seed development and aging. |
OsAGO1 | | Os02g0831600 | unclear |
miRNA |
30791202 |
Rice (Oryza sativa) |
Genetic evidence |
|
|
|
|
Rice Argonaute1 (AGO1) |
OsALDH7 | XM_015756349.1 | LOC_Os09g26880 | enhance |
detoxification |
19052152 |
Rice (Oryza sativa) |
Genetic evidence |
osaldh7 |
|
T-DNA |
recessive |
The osaldh7 mutant seeds were more sensitive to our accelerated aging treatment and accumulated more malondialdehyde than the wild type. |
Osa-miR164c | | MIMAT0001033 | decrease |
miRNA |
33281848;30791202 |
Rice (Oryza sativa) |
Genetic evidence |
OE164c |
|
transgene |
dominance |
Ovexpression of Osa-miR164c decreases seed longevity. https://mirbase.org/browse/results/?organism=osa |
Osa-miR168a | | MIMAT0001045 | enhance |
miRNA |
30791202 |
Rice (Oryza sativa) |
Genetic evidence |
MIM168a |
|
|
|
Osa-miR164c overexpression in OE164c transgenic seeds and osa-miR168a silencing in MIM168a transgenic seeds of the rice cultivar Kasalath led to lower germination rates, whereas osa-miR164c silencing in MIM164c and osa-miR168a overexpression in OE168a resulted in higher seed germination rates compared with wild-type seeds |
OsAOX1a | AB004864 | | enhance |
ROS |
37375909 |
Rice (Oryza sativa) |
Genetic evidence |
OsAOX1a-RNAi |
|
RNAi |
recessive |
Low AOX1a Impaired Seed Development and Storability |
OsBES | | LOC_Os02g03690 | unclear |
|
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
beta-amylase, putative, expressed.Transcriptional factor possesses over-representative targets among the genes differentially expressed during Kasalath and Jigeng88 seed ageing. |
OsbZIP23 | | LOC_Os02g52780 | enhance |
ROS,detoxification,ABA |
35217598 |
Rice (Oryza sativa) |
Genetic evidence |
35S::bZIP23 |
|
transgene |
dominance |
Overexpression of bZIP23 enhanced seed vigor, whereas its gene knockout reduced seed vigor, |
OsbZIP66 | | LOC_Os05g41070 | unclear |
bZIP TF |
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
bZIP transcription factor, putative, expressed.Transcriptional factor possesses over-representative targets among the genes differentially expressed during Kasalath and Jigeng88 seed ageing. |
OsCPuORF5 | | LOC_Os12g37410 | unclear |
|
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
CPuORF5 - conserved peptide uORF-containing transcript, expressed.Transcriptional factor possesses over-representative targets among the genes differentially expressed during Kasalath and Jigeng88 seed ageing. |
OsDREB2A | | LOC_Os01g07120 | unclear |
|
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
AP2 domain containing protein.Transcriptional factor possesses over-representative targets among the genes differentially expressed during Kasalath and Jigeng88 seed ageing. |
OsDREB2C | | LOC_Os08g45110 | unclear |
|
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
AP2 domain containing protein, expressed |
OsEIN3 | | LOC_Os03g20780 | unclear |
Ethylene |
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
ethylene-insensitive 3, putative, expressed.Transcriptional factor possesses over-representative targets among the genes differentially expressed during Kasalath and Jigeng88 seed ageing. |
OsEPSPS | XM_015787560.1 | LOC_Os06g04280 | enhance |
ROS |
34203092 |
Rice (Oryza sativa) |
Genetic evidence |
|
|
|
|
5-enolpyruvylshikimate 3-phosphate synthase (EPSPs) |
OsERF54 | | LOC_Os01g46870 | unclear |
ERF TF |
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
AP2 domain containing protein.Transcriptional factor possesses over-representative targets among the genes differentially expressed during Kasalath and Jigeng88 seed ageing. |
OsERF76 | | LOC_Os04g57340 | unclear |
ERF TF |
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
AP2 domain containing protein, expressed.Transcriptional factor possesses over-representative targets among the genes differentially expressed during Kasalath and Jigeng88 seed ageing. |
OsERN1 | | LOC_Os07g10410 | unclear |
|
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
AP2 domain containing protein, expressed.Transcriptional factor possesses over-representative targets among the genes differentially expressed during Kasalath and Jigeng88 seed ageing. |
OsGID1 | NM_001420504.1 | LOC_Os05g33730 | unclear |
Hormone GA |
35651763 |
Rice (Oryza sativa) |
Transcriptome |
|
|
|
|
Specific long-lived mRNAs in rice, including gibberellin receptor gene GID1, which may be associated with seed longevity. |
OsGLYI3 | XM_015773698.2 | LOC_Os03g16940 | enhance |
ROS |
35569169 |
Rice (Oryza sativa) |
Genetic evidence |
OsGLYI3-cr |
|
CRISP |
recessive |
The accelerated aging (AA) treatment results indicated significant roles of OsGLYI3 in seed longevity and vigor, as the seeds of the transgenic lines with overexpressed and knocked-out OsGLYI3 exhibited higher and lower germination, respectively. |
OsGT2 | | LOC_Os02g43300 | unclear |
|
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
expressed protein.Transcriptional factor possesses over-representative targets among the genes differentially expressed during Kasalath and Jigeng88 seed ageing. |
OsHGGT | AY222862 | | enhance |
ROS |
26810451 |
Rice (Oryza sativa) |
Genetic evidence |
OsHGGT:RNAi |
|
RNAi |
recessive |
Deficiency of tocopherols and tocotrienols led to accelerated aging in OsHGGT:RNAi seeds |
OsHSFA2C | | LOC_Os10g28340 | unclear |
|
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
heat stress transcription factor, putative, expressed.Transcriptional factor possesses over-representative targets among the genes differentially expressed during Kasalath and Jigeng88 seed ageing. |
OsHSFB2C | | LOC_Os09g35790 | unclear |
|
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
HSF-type DNA-binding domain containing protein, expressed.Transcriptional factor possesses over-representative targets among the genes differentially expressed during Kasalath and Jigeng88 seed ageing. |
OsHSFC1B | | LOC_Os01g53220 | unclear |
|
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
HSF-type DNA-binding domain containing protein. Transcriptional factor possesses over-representative targets among the genes differentially expressed during Kasalath and Jigeng88 seed ageing. |
OsHSP18.2 | NM_001406238 | LOC_Os01g08860 | enhance |
ROS |
26442027 |
Rice (Oryza sativa) |
Genetic evidence |
OsHSP18.2 OE |
|
transgene |
dominance |
OsHSP18.2 has ability to improve seed vigor and longevity by reducing deleterious ROS accumulation in seeds |
OsLOX10 | XM_015759992 | | decrease |
|
36867321 |
Rice (Oryza sativa) |
Genetic evidence |
OsLOX10-Cr |
|
CRISP |
recessive |
CRISPR/Cas9 knockout of OsLOX10 increased seed longevity compared with the wild-type and OsLOX10 overexpression lines in response to artificial aging |
OsLOX2 | | Os03g0738600 | decrease |
Lipid Oxidation |
24792034 |
Rice (Oryza sativa) |
Genetic evidence |
OsLOX2 RNAi |
|
RNAi |
recessive |
RNA interference (RNAi) of OsLOX2 caused delayed germination and enhanced seed longevity. |
OsLOX3 | XM_052294053 | Os03g0700400 | decrease |
lipid oxidation |
26641666 |
Rice (Oryza sativa) |
Genetic evidence |
TA-lox3 |
|
TALENs |
recessive |
LOX3 knockout mutants show improved seed storability |
OsLOX3 | NM_001402220.1 | LOC_Os03g49260 | decrease |
Lipid Oxidation |
25545811 |
Rice (Oryza sativa) |
Genetic evidence |
OsLOX3 RNAi |
|
RNAi |
recessive |
The suppression of LOX3 expression in rice endosperm increased grain storability |
OsLTPL36 | | LOC_Os03g25350 | enhance |
lipid transport |
26398804 |
Rice (Oryza sativa) |
Genetic evidence |
OsLTPL36 RNAi |
|
RNAi |
recessive |
impeded seed germination and puny seedling were also observed in the OsLTPL36 RNAi lines |
OsMSRB5 | | LOC_Os03g24600 | enhance |
Protein repair |
35909309 |
Rice (Oryza sativa) |
Genetic evidence |
OsMSRB5 RNAi |
|
RNAi |
recessive |
OsMSRB5 preserves seed vigor and longevity by modulating ROS homeostasis in seeds. |
OsNAC78 | | LOC_Os08g44820 | unclear |
NAC TF |
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
no apical meristem protein, putative, expressed.Transcriptional factor possesses over-representative targets among the genes differentially expressed during Kasalath and Jigeng88 seed ageing. |
OsPIMT1 | XM_026027566.1 | LOC_Os08g44280 | enhance |
Protein repair |
26987457 |
Rice (Oryza sativa) |
Genetic evidence |
35S:OsPIMT1 |
|
transgene |
dominance |
PIMT repairs antioxidative enzymes and proteins which restrict ROS accumulation, lipid peroxidation, etc. in seed, particularly during aging, thus contributing to seed vigor and longevity. |
OsPIMT1 | | Os08g055700 | enhance |
Protein repair |
26438231 |
Rice (Oryza sativa) |
Genetic evidence |
|
|
|
|
The germination percentage of transgenic seeds overexpressing OsPIMT1 increased 9�C15 % compared to the WT seeds after 21-day of artificial aging, whereas seeds from the OsPIMT1 RNAi lines overaccumulated isoAsp in embryos and experienced rapid loss of seed germinability. |
OsPIMT2 | XM_015778385 | LOC_Os04g40540 | enhance |
Protein repair |
26987457 |
Rice (Oryza sativa) |
Genetic evidence |
35S:OsPIMT2 |
|
transgene |
dominance |
PIMT repairs antioxidative enzymes and proteins which restrict ROS accumulation, lipid peroxidation, etc. in seed, particularly during aging, thus contributing to seed vigor and longevity. |
OsPM27 | XM_015761726.2 | LOC_Os11g44940 | unclear |
miRNA |
30791202 |
Rice (Oryza sativa) |
Genetic evidence |
|
|
|
|
Seed maturation protein gene |
OsPSK5 | NM_001423322.1 | LOC_Os12g05260 | unclear |
miRNA |
30791202 |
Rice (Oryza sativa) |
Genetic evidence |
|
|
|
|
phytosulfokines precursor gene |
OsPTR2 | NM_001418486 | LOC_Os03g48180 | unclear |
miRNA |
30791202 |
Rice (Oryza sativa) |
Genetic evidence |
|
|
|
|
peptide transporter gene |
OsRAV1 | | LOC_Os01g49830 | unclear |
|
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
B3 DNA binding domain containing protein.Transcriptional factor possesses over-representative targets among the genes differentially expressed during Kasalath and Jigeng88 seed ageing. |
OsSLAG1 | | LOC_Os01g71930 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Glycosyl hydrolases family 17 protein. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG10 | | LOC_Os04g01140 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Cytochrome P450 93A2. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG11 | | LOC_Os04g01160 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Zinc finger family protein.Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG12 | | LOC_Os04g01230 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Phosphoglycerate mutase. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG13 | | LOC_Os04g01280 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Glycosyltransferase family 43 protein.Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG14 | | LOC_Os04g01290 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Proteasome subunit. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG15 | | LOC_Os04g01300 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
OsRhmbd10. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG16 | | LOC_Os09g37250 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
High mobility group.Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG17 | | LOC_Os09g37280 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Peroxisomal multifunctional enzyme type 2. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG18 | | LOC_Os09g37300 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Transporter, monovalent cation:proton antiporter-2 family. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG19 | | LOC_Os11g01439 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Chloroplast unusual positioning protein. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG2 | | LOC_Os01g71960 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Endonuclease.Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG20 | | LOC_Os11g01550 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
DUF260 domain containing protein.Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG21 | | LOC_Os11g01570 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
PMR5.Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG22 | | LOC_Os11g01590 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Nodulin. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG23 | | LOC_Os11g01600 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Macrophage migration inhibitory factor. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG24 | | LOC_Os03g06890 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
DUF593 domain containing protein. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG25 | | LOC_Os03g06900 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
DNA topoisomerase 3 protein. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG26 | | LOC_Os03g06930 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Homeodomain protein. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG27 | | LOC_Os03g06940 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Beta-galactosidase. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG28 | | LOC_Os03g09150 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Pumilio-family RNA binding repeat domain containing protein. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG29 | | LOC_Os03g09210 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
NADH dehydrogenase 1 alpha subcomplex subunit 13. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG3 | | LOC_Os01g71970 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
GRAS family transcription factor containing protein.Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG30 | | LOC_Os03g09220 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Stage II sporulation protein E. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG31 | | LOC_Os03g03790 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
AMP-binding domain containing protein. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG32 | | LOC_Os03g03820 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Adenylate kinase. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG33 | | LOC_Os03g03850 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
GATA zinc finger domain containing protein. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG34 | | LOC_Os03g03870 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
DNA-binding bromodomain-containing protein. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG35 | | LOC_Os11g11500 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Serpin domain containing protein. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG36 | | LOC_Os11g11580 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
NB-ARC domain containing protein.Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG4 | | LOC_Os01g71980 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
rho-GTPase-activating protein-like.Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG5 | | LOC_Os03g51030 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Phytochrome A.Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG6 | | LOC_Os03g51050 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Peptide transporter PTR2. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG7 | | LOC_Os03g51080 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Glutamate decarboxylase. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG8 | | LOC_Os03g51110 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
MYB family transcription factor.Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSLAG9 | | LOC_Os04g01130 | unclear |
|
31180503 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
Chromatin modification-related protein EAF3.Chromatin modification-related protein EAF3. Candidate genes associated with seed longevity traits of 299 Indica rice accessions. |
OsSPL15 | | LOC_Os08g40260 | unclear |
|
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
OsSPL15 - SBP-box gene family member, expressed.Transcriptional factor possesses over-representative targets among the genes differentially expressed during Kasalath and Jigeng88 seed ageing. |
OsSPL9 | | LOC_Os05g33810 | unclear |
SPL TF |
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
OsSPL9 - SBP-box gene family member, expressed.Transcriptional factor possesses over-representative targets among the genes differentially expressed during Kasalath and Jigeng88 seed ageing. |
OsTCX2 | | LOC_Os07g07974 | unclear |
|
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
tesmin/TSO1-like CXC domain containing protein, expressed.Transcriptional factor possesses over-representative targets among the genes differentially expressed during Kasalath and Jigeng88 seed ageing. |
OsWRKY13 | | LOC_Os01g54600 | unclear |
WRKY TF |
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
WRKY13.Transcriptional factor possesses over-representative targets among the genes differentially expressed during Kasalath and Jigeng88 seed ageing. |
OsWRKY51 | | LOC_Os04g21950 | unclear |
WRKYTF |
35217598 |
Rice (Oryza sativa) |
Molecular evidence |
|
|
|
|
WRKY51, expressed.Transcriptional factor possesses over-representative targets among the genes differentially expressed during Kasalath and Jigeng88 seed ageing. |
SNAT1 | AK059369 | | enhance |
melatonin |
31952365 |
Rice (Oryza sativa) |
Genetic evidence |
snat1 |
|
RNAi |
recessive |
Seed-aging testing revealed that snat1 was the most severely deteriorated, followed by snat1+2 and snat2, suggesting that melatonin is positively involved in seed longevity. |
SNAT2 | AK068156 | | enhance |
melatonin |
31952365 |
Rice (Oryza sativa) |
Genetic evidence |
snat2 |
|
RNAi |
recessive |
Seed-aging testing revealed that snat1 was the most severely deteriorated, followed by snat1+2 and snat2, suggesting that melatonin is positively involved in seed longevity. |
OsGH3-2 | NM_001408978.1 | LOC_Os01g55940 | decrease |
Hormone Auxin |
33570603 |
Rice (Oryza sativa) |
Genetic evidence |
OsGH3-2 OE |
|
transgene |
dominance |
Overexpression of OsGH3-2 significantly decreased seed storability, while knockout or knockdown of the gene enhanced seed storability compared with the wild-type. |
OsSAUR33 | XM_015793499.2 | LOC_Os08g35110 | enhance |
Hormone Auxin |
33557166 |
Rice (Oryza sativa) |
Genetic evidence |
ossaur33-1 |
|
CRISPR |
recessive |
Disruption of OsSAUR33 Results in Low Seed Vigor |
NnHSP17.5 | EF100453.1 | | enhance |
HSP |
22009054 |
Sacred lotus (Nelumbo nucifera Gaertn.) |
Genetic evidence |
NnHSP17.5-YFP |
Col-0 |
transgene |
dominance |
Transgenic Arabidopsis seeds ectopically expressing NnHSP17.5 displayed enhanced seed germination vigor and exhibited increased superoxide dismutase activity after accelerated aging treatment. |
NnMT2a | EF421200.1 | | enhance |
ROS |
21971996 |
Sacred lotus (Nelumbo nucifera Gaertn.) |
Genetic evidence |
NnMT2a-YFP |
Col-0 |
transgene |
dominance |
Transgenic Arabidopsis seeds overexpressing NnMT2a and NnMT3 displayed improved resistance to accelerated aging (AA) treatment, indicating their significant roles in seed germination vigor. |
NnMT3 | EF421199.1 | | enhance |
ROS |
21971996 |
Sacred lotus (Nelumbo nucifera Gaertn.) |
Genetic evidence |
NnMT3-YFP |
Col-0 |
transgene |
dominance |
Transgenic Arabidopsis seeds overexpressing NnMT2a and NnMT3 displayed improved resistance to accelerated aging (AA) treatment, indicating their significant roles in seed germination vigor. |
NnPER1 | XM_010272626.2 | | enhance |
ROS |
27464651 |
Sacred lotus (Nelumbo nucifera Gaertn.) |
Genetic evidence |
NnPER1-OE |
Col-0 |
transgene |
dominance |
Ectopic expression of NnPER1enhances seed longevity |
GmATX1 | NM_001251167 | | enhance |
Copper Chaperone |
35631750 |
Soybean (Glycine max) |
Genetic evidence |
GmATX1ox |
Col-0 |
transgene |
dominance |
Copper Chaperone Protein Gene GmATX1 Promotes Seed Vigor and Seedling Tolerance under Heavy Metal and High Temperature and Humidity Stresses |
GmPAL1.1 | NM_001357056 | | enhance |
PAL |
36501278 |
Soybean (Glycine max) |
Genetic evidence |
GmPAL1ox |
Col-0 |
transgene |
dominance |
GmPAL1.1 Promotes Seed Vigor under High-Temperature and -Humidity Stress and Enhances Seed Germination under Salt and Drought Stress |
GmPLDα1 | NR_163829.1 | Glyma.15G008500 | decrease |
|
30622651 |
Soybean (Glycine max) |
Genetic evidence |
GmPLDα1KD |
|
RNAi |
recessive |
Phospholipase Dα1.PLDα1-knockdown soybean seeds display higher unsaturated glycerolipid contents and seed vigor in high temperature and humidity environments |
BvCRT | CAA05161 | | unclear |
Ca2+ |
21432998 |
Sugarbeet (Beta vulgaris) |
Proteomic evidence |
|
|
|
|
Calreticulin |
BvEF2 | CAB09900 | | unclear |
Translation |
21432998 |
Sugarbeet (Beta vulgaris) |
Proteomic evidence |
|
|
|
|
Translation elongation factor 2 (EF-2) |
BvFRK | AAA80675 | | unclear |
Methodology,biomarker |
21432998 |
Sugarbeet (Beta vulgaris) |
Proteomic evidence |
|
|
|
|
Fructokinase |
BvSAMS | BAE07179 | | unclear |
Hormone ACC |
21432998 |
Sugarbeet (Beta vulgaris) |
Proteomic evidence |
|
|
|
|
S-adenosyl-L-methionine synthetase |
HaDREB2 | AY508007 | | enhance |
DREB TF |
19545370 |
Sunflower (Helianthus annuus) |
Genetic evidence |
CaMV35S: HaDREB2 |
|
transgene |
dominance |
HaDREB2 and HaHSFA9 were conjointly overexpressed in seeds to enhance seed longevity. |
HaHSFA9 | AY099451.1 | | enhance |
Heat, HSF TF |
16998084 |
Sunflower (Helianthus annuus) |
Genetic evidence |
DS10::HaHSFA9 |
|
transgene |
dominance |
Tobacco (Nicotiana tabacum) seeds over-expressing HaHSFA9 (a heat shock transcription factor isolated from sunflower Helianthus annuus) accumulate elevated levels of heat shock proteins and are more tolerant to CDT |
HaIAA27 | FR669188 | | decrease |
Hormone Auxin |
21115822 |
Sunflower (Helianthus annuus) |
Genetic evidence |
|
|
|
|
HaHSFA9 transcription factor was reported to interact with the auxin/IAA (Aux/IAA) protein HaIAA27, leading to its repression. Auxin would therefore act downstream of ABI3 to enhance seed longevity by alleviating HaIAA27-mediated HaHSFA9 repression in sunflower |
HaHSFA9 | AY099451 | | enhance |
HSP |
20444218;12228226 |
Sunflower(Helianthus annuus) |
Genetic evidence |
HaHSFA9-SRDX |
|
SRDX |
recessive |
HaHSFA9-SRDX showed a highly significant reduction of seed longevity |