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seed development

64000 relationships annotated with this phrase. Showing first 500 of 64000.
Source entity Relationship Target entity Species
RNAi lines and edited pPLAIIγ lines show increased aborted seeds Arabidopsis thaliana
nrt1.6–3 mutant plants display strong seed abortion phenotypes under regular and HN conditions Arabidopsis thaliana
ZmRCL1 mutation leads to underdeveloped endosperm Zea mays
ABA-GE levels substantially increase during specific seed developmental stages
developing IKU2-OE seeds have slightly higher protein content until 19 DAF (d after flowering) Arabidopsis thaliana
(IKU2, AT3G19700) activity for seed development can also be exerted in embryo Arabidopsis thaliana
overexpression of (SHB1, AT4G25350) gene was found to result in increase in seed size, weight, and oil content Arabidopsis thaliana
differentially expressed probe sets were selected from complete seed development Medicago truncatula
embryogenesis and early maturation phase is marked by overrepresentation of functional classes related to growth and metabolic activities Medicago truncatula
eIF4E1-OE plants show significantly higher yield per plant Arabidopsis thaliana
temporal shifts in sugar transporter type profiles are shared between Gramineae permanent endosperms and Fabaceae and Brassicaceae embryos Gramineae; Fabaceae; Brassicaceae
abscisic acid (ABA) is involved in seed dormancy
DEK58 mutation causes embryo lethality Zea mays
(GOM8, RHD3, AT3G13870) −/− (RL2, AT5G45160) −/− plants had no seed production Arabidopsis thaliana
endosperm in mutant ovules of heterozygous (FIE, FIE1, FIS3, AT3G20740) plants finally dries out and forms extremely small, infertile seeds Arabidopsis thaliana
IKU2-OE1 line has total fatty acid content indistinguishable from wild type at 7 DAF but higher at 11, 15, and 19 DAF seed fatty acid accumulation during development Arabidopsis thaliana
total weight of seeds per plant is reduced in IKU2-OE plants Arabidopsis thaliana
global regulatory network is composed of large core module with 16 transcription factors and 292 putative target genes Medicago truncatula
loss-of-function allele of MSP1 leads to seed abortion Arabidopsis thaliana
(TGS1, AT1G45231) mutants can achieve viable seeds Arabidopsis thaliana
MINISEED3 (ATWRKY10, MINI3, WRKY10, AT1G55600) is involved in regulation of seed development Arabidopsis thaliana
phe1-7 mutant slightly reduces seed length Arabidopsis thaliana
phe1-7 mutant strongly reduces seed weight Arabidopsis thaliana
starch accumulates in early phase of seed development Arabidopsis thaliana
mutants have elevated starch content at 19 DAF (d after flowering) Arabidopsis thaliana
Medicago truncatula seed development is divided into late maturation Medicago truncatula
29 out of 32 Medicago truncatula putative (ABI3, AtABI3, SIS10, AT3G24650) targets were significantly down-regulated in Mtabi3 mutant Medicago truncatula
oastlAC B +/+ mutant shows number of fully developed seeds decreased by more than 85% compared to wild type Arabidopsis thaliana
(ATHSFA2, HSFA2, AT2G26150) expression restored at least partially seed size Arabidopsis thaliana
overexpression of (ATHD2A, HD2A, HDA3, HDT1, AT3G44750) severely affected seed development Arabidopsis thaliana
volume of oil bodies (V OB) increased during embryo growth Arabidopsis thaliana
ACPs as a class increase over early development Glycine max
GA signaling pathway is pivotal in seed germination
phe1-7 mutant shows residual (AGL37, PHE1, AT1G65330) expression Arabidopsis thaliana
heterozygous IKU2-OE1 line has siliques thicker than Col-0 empty vector control siliques Arabidopsis thaliana
oastlAB C +/− mutant shows number of fully developed seeds at 38% of wild type Arabidopsis thaliana
Tnt1 element in CT4:33 possibly landed in gene essential to embryo/seed development Solanum chacoense
mutations in Fertilization-Independent Endosperm1 (FIE, FIE1, FIS3, AT3G20740) cause reduced seed size Arabidopsis thaliana; Oryza sativa
OPM activity interacts with known pathways influencing seed size Hordeum vulgare
AMF inoculation with Glomus etuniacatum in nutrient-poor soils associated with more seeds per fruit Abutilon theophrasiti
At later stages of seed development (16 to 29 DAP) had scale leaf primordia and compound leaf primordia developing on the embryo axis Pisum sativum
nitric oxide (NO) mediates seed germination
dek58 mutant exhibits defective kernel and embryo-lethal phenotype Zea mays
phe1-1 mutant slightly reduces seed width Arabidopsis thaliana
(ATWRKY10, MINI3, WRKY10, AT1G55600) mutant reduces total fatty acids Arabidopsis thaliana
glycinin promoter is active during mid to late phase of seed development Arabidopsis thaliana
maternal effect of (IKU2, AT3G19700) overexpression in heterozygous siliques affects nontransgenic progeny Arabidopsis thaliana
large core module includes most of late embryogenesis abundant (LEA) probe sets Medicago truncatula
(ABI3, AtABI3, SIS10, AT3G24650) regulons in Arabidopsis include late embryogenesis abundant (LEA) proteins Arabidopsis thaliana
Dior Kelley performed genetic screen to identify 'big seed' mutants Arabidopsis thaliana
urb2 mutant shows retarded seed development Zea mays
(CPD45, FHY3, AT3G22170) transcript accumulates in dry seeds Arabidopsis thaliana
seed endosperm is triploid tissue with two maternal and one paternal genomes Arabidopsis thaliana
HAIKU2 (IKU2, AT3G19700) is expressed in developing endosperm during the early stage Arabidopsis thaliana
homozygous mutant seeds of (SHB1, AT4G25350) loss of function allele are smaller Arabidopsis thaliana
mini3-3 mutant reduces seed weight Arabidopsis thaliana
starch degradation is retarded in (AGL37, PHE1, AT1G65330) mutant seeds Arabidopsis thaliana
fie-11 mutant has drastically reduced amounts of TAG molecular species Arabidopsis thaliana
MINI3-OE line has seed size very similar to Col-0 empty vector control Arabidopsis thaliana
heterozygous IKU2-OE1 line has siliques thicker than homozygous IKU2-OE1 line siliques Arabidopsis thaliana
overexpression of (IKU2, AT3G19700) resulted in decrease in total amount of seeds per plant Arabidopsis thaliana
iku2-4 mutant produces smaller seeds with reduced weight Arabidopsis thaliana
cofactors levels were quantified over development Glycine max
inhibition of phosphorylation of OsbZIP10 precursors by OsPP2C51 promotes plant seed germination
VIVIPAROUS1 (VP1) mutant displays reduced sensitivity to ABA during seed development Zea mays
phe1-1 mutant strongly reduces seed weight Arabidopsis thaliana
(AGL37, PHE1, AT1G65330) mutant contains increased amount of sucrose (Suc) Arabidopsis thaliana
(IKU2, AT3G19700) overexpression results in increase in seed size Arabidopsis thaliana
truncated versions of napin promoter made possible separation of effects of (AtLEC1, EMB 212, EMB212, LEC1, NF-YB9, AT1G21970) overexpression Brassica napus
use of truncated versions of glycinin promoter can result in generation of transgenic IKU2-OE plants which produce larger seeds without reduction of total seed yield per plant Arabidopsis thaliana
seed abortion rate in (AtHSBP, HCR2, HSBP, AT4G15802) KO mutant is higher than seed abortion rate in QK mutant Arabidopsis thaliana
gene expression during seed germination was compared with gene expression during seed development Arabidopsis thaliana
abscisic acid (ABA) is involved in seed germination
mini3-1 mutant seeds contained less glucose (Glc) Arabidopsis thaliana
IKU2-OE line has glucose content similar to wild type at all time points Arabidopsis thaliana
nontransgenic segregants of IKU2-OE1 line have length similar to large fluorescent (heterozygous) seeds Arabidopsis thaliana
(IKU2, AT3G19700) expression is also low in homozygous IKU2-OE siliques Arabidopsis thaliana
fie-11 mutant is seed development gene mutant Arabidopsis thaliana
germination capacity was acquired from 16 days after pollination onward Medicago truncatula
(AtHDA7, HDA7, AT5G35600) oe mutant shows similar silique fertility Arabidopsis thaliana
(AT.EIF4E1, CUM1, EIF4E, eIF4E1, AT4G18040) mutants show reduced seed weight Arabidopsis thaliana
(AtMYB55, MYB55, AT4G01680) is expressed during embryogenesis and germination Arabidopsis thaliana
At 12 DAP had PsPALM1a, PsPALM1b and (UNI, AT1G61180) gene expression detected in the embryo Pisum sativum
ABA accumulation occurs during seed maturation
seed development in Arabidopsis is organized into two phases Arabidopsis thaliana
FIE-OE line has total protein similar to wild type Arabidopsis thaliana
IKU2-OE2 line has total fatty acid content indistinguishable from wild type at 7 DAF but higher at 11, 15, and 19 DAF seed fatty acid accumulation during development Arabidopsis thaliana
phe1-1 homozygous seeds have slightly reduced weight Arabidopsis thaliana
phe1-6 homozygous seeds have slightly reduced weight Arabidopsis thaliana
MtABI4 transcription factor is highly connected with desiccation tolerance (DT) probe sets Medicago truncatula
MtHSF transcription factor is highly connected with late embryogenesis abundant (LEA) probe sets Medicago truncatula
Medicago truncatula basic leucine zipper transcription factors are highly connected with P50 probe sets Medicago truncatula
double knockout of (ATHSP17.4, HSP17.4, AT3G46230) and (AT-HSP17.6A, HSP17.6, HSP17.6A, AT5G12030) leads to seed abortion Arabidopsis thaliana
phenotypic similarity between (AtHSBP, HCR2, HSBP, AT4G15802) KO and QK mutants suggests HSFA1s and (AtHSBP, HCR2, HSBP, AT4G15802) may function in concert in seed development Arabidopsis thaliana
seed maturation-repressed genes (reactivated during germination) are, in contrast, mostly specific to either radicle (RAD) or micropylar and chalazal endosperm (MCE) Arabidopsis thaliana
(AtMAX2, MAX2, ORE9, PPS, AT2G42620) transcript was abundant in dry seeds Arabidopsis thaliana
(ATZFP2, ZFP2, AT5G57520) has expression in developing seeds Arabidopsis thaliana
fertilization-independent embryo and endosperm formation occurs in aposporous female gametophytes soon after egg differentiates and fusion of two polar nuclei in central cell occurs Hieracium spp.
(SAUR62, AT1G29430) /75 RNA interference (RNAi) knockdown line produces aborted seeds Arabidopsis thaliana
seeds undergo dehydration upon maturation
seed-specific genes are enriched for H3K27me3 after germination
LEC genes play a role in morphogenesis phase of seed development
decrease in number of ovules could explain seed drop observed during crossing Brassica rapa
iku2-4 mutant reduces seed weight Arabidopsis thaliana
phe1-6 mutant slightly reduces seed length Arabidopsis thaliana
(IKU2, AT3G19700) mutant reduces total fatty acids Arabidopsis thaliana
fatty acid content increased from approximately 0 to approximately 5 µg per seed in wild-type seeds during development Arabidopsis thaliana
sucrose (Suc) accumulation accumulated in wild type from approximately 0.2 µg per seed at 7 DAF to approximately 0.4 µg per seed at 19 DAF in a linear way wild-type seeds during development Arabidopsis thaliana
small increase in expression of (IKU2, AT3G19700) in maternal tissue may have positive effect on development of seeds Arabidopsis thaliana
phe1-7 homozygous seeds have similar length and width to wild type Arabidopsis thaliana
embryogenesis module corresponds to embryogenesis Medicago truncatula
seed metabolism at 56 and 66 days after sowing (DAS) mainly characterized by processes involved in seed storage Hordeum vulgare
(AtHSBP, HCR2, HSBP, AT4G15802) knockout mutant showed seed abortion phenotype Arabidopsis thaliana
embryo sac (ES) collapse before fertilization contributes to seed failures in Athda7-2 Arabidopsis thaliana
seed coat protects embryo Arabidopsis thaliana
(ACP, ACP1, AtACP1, AT3G05020) profile varied considerably between R5 and R6 stages of development Glycine max
reduction in seed weight of seed development mutants is mainly based on reduction in oil Arabidopsis thaliana
(IKU2, AT3G19700) mutant seeds have sucrose content similar to wild type Arabidopsis thaliana
(IKU2, AT3G19700) expression is found in young ovules after fertilization and in the endosperm of developing seeds Arabidopsis thaliana
IKU2-OE plants produced seeds with increase in size, weight, and oil content Arabidopsis thaliana
global regulatory network is composed of smaller core module with 6 transcription factors and 76 putative targets Medicago truncatula
MtHSF transcription factor connects P50 probe sets cluster Medicago truncatula
oil production rate increased sharply at 11 days after pollination (DAF) (U-shaped embryo stage) Arabidopsis thaliana
coi mutants show no significant difference in single-plant yield compared to WT plants in the field Oryza sativa
angiosperm seeds share broadly similar developmental pattern
real-time and in planta imaging of sugar pool sizes and transport fluxes in developing seeds technical challenges require resolution understanding sugar loading in developing seeds
Arabidopsis (Arabidopsis thaliana) is one of plant species that produces myxospermous seed Arabidopsis thaliana
(FIE, FIE1, FIS3, AT3G20740) mutant alleles contain decrease in α-linolenic acid (18:3) Arabidopsis thaliana
(IKU2, AT3G19700) overexpression results in increase in seed weight Arabidopsis thaliana
seeds of heterozygous IKU2-OE plant contain embryos of different sizes embryo size variation Arabidopsis thaliana
increase in oil became visible as early as 7 to 11 DAF (d after flowering) Arabidopsis thaliana
(TGS1, AT1G45231) heterozygous and homozygous plants showed high proportions of aborted seeds Arabidopsis thaliana
oil levels were quantified over development Glycine max
(ATWRKY10, MINI3, WRKY10, AT1G55600) mutant slightly reduces total protein content Arabidopsis thaliana
(FIE, FIE1, FIS3, AT3G20740) was overexpressed in transgenic Arabidopsis plants under control of seed-specific glycinin promoter Arabidopsis thaliana; Glycine max
developing (ATWRKY10, MINI3, WRKY10, AT1G55600) seeds have similar Suc content to wild type Arabidopsis thaliana
seed size is correlated with abundance of (IKU2, AT3G19700) transcript during seed development Arabidopsis thaliana
Medicago truncatula seed development is divided into seed filling Medicago truncatula
sgpPLAIIγ lines show reduced seed sets by seed production Arabidopsis thaliana
(NFD6, AT2G20585) is required for normal seed development and maturation Ipomoea purpurea
PsPALM1a, PsPALM1b and (UNI, AT1G61180) gene expression was detected in the embryo when cotyledons are expanding Pisum sativum
second phase of seed development is characterized by embryo growth and expansion Arabidopsis thaliana
IKU2-OE line increases seed weight by approximately 30% seed weight Arabidopsis thaliana
MtAP2/ (ATERF13, EREBP, ERF13, AT2G44840) transcription factor connects late embryogenesis abundant (LEA) and desiccation tolerance (DT) probe sets cluster Medicago truncatula
A subunit genes of (PP2A, AT1G69960) have highest transcript levels in developing rape seeds Brassica napus
(ABI3, AtABI3, SIS10, AT3G24650) (ABI4, ATABI4, GIN6, ISI3, SAN5, SIS5, SUN6, AT2G40220) and (ABI5, AtABI5, DPBF1, GIA1, AT2G36270) control seed maturation
most of these genes were highly expressed in developing seeds of transgenic rice, especially TDC and T5H in HFL1 rice Oryza sativa
extensive membrane remodeling occurs during seed maturation Arabidopsis thaliana
RNAi-1 mutant showed fewer seeds per silique Arabidopsis thaliana
ABA regulates seed germination
expression cluster 3 shows transcript expression specificity in micropylar endosperm Arabidopsis thaliana
seeds derived from (TGS1, AT1G45231) FGs showed variety of defects, including mixed cellular identities in fertilization products Arabidopsis thaliana
phe1-7 mutant is derived from (AGL37, PHE1, AT1G65330) Arabidopsis thaliana
(FIE, FIE1, FIS3, AT3G20740) mutant alleles contain increase in palmitic acid (16:0) Arabidopsis thaliana
IKU2-OE line has seed width similar to control Arabidopsis thaliana
number of seeds per silique remained unchanged in IKU2-OE plants Arabidopsis thaliana
Arabidopsis (ABI3, AtABI3, SIS10, AT3G24650) regulon promoters were enriched for RY element-like (RYL) motifs Arabidopsis thaliana
ovules exert maternal influence on seed size
(AT.EIF4E1, CUM1, EIF4E, eIF4E1, AT4G18040) mutants show reduced yield per plant Arabidopsis thaliana
endosperm organisation of plasma-membrane influxers and effluxers is more complex spatiotemporal Fabaceae; Brassicaceae
seed accumulates large amounts of starch Arabidopsis thaliana
(IKU2, AT3G19700) overexpression results in increase in oil content Arabidopsis thaliana
Medicago truncatula seed development is divided into pod abscission Medicago truncatula
(ABI3, AtABI3, SIS10, AT3G24650) regulons in Arabidopsis include seed storage proteins Arabidopsis thaliana
(COI1, AT2G39940) mutants have higher grain weight than WT plants Oryza sativa
selfed pPLAIIγ diploid mutant lines show significantly reduced seed sets Arabidopsis thaliana
sgpPLAIIγ line #4 shows significantly increased proportion of aborted seeds Arabidopsis thaliana
grain size is influenced by spikelet hull growth
soybean events carrying transgenic alleles were examined for effects on metabolism Glycine max
this latter point likely limits extent of changes to storage reserve composition observed here Glycine max
heterozygous (FIE, FIE1, FIS3, AT3G20740) mutants develop endosperm in ovules carrying maternal fie allele without fertilization, leading to abortion Arabidopsis thaliana
seed coat is derived from inner and outer integument cells Arabidopsis thaliana
(AGL37, PHE1, AT1G65330) expression is strongly suppressed in (AGL37, PHE1, AT1G65330) homozygous mutants Arabidopsis thaliana
(AGL37, PHE1, AT1G65330) mutant shows tendency to increase α-linolenic acid (18:3) content Arabidopsis thaliana
(IKU2, AT3G19700) mutant slightly reduces total protein content Arabidopsis thaliana
aborted (FIE, FIE1, FIS3, AT3G20740) mutant seeds has oil content extremely low at around 0.05 µg per seed oil content Arabidopsis thaliana
IKU2-OE line increases seed length by approximately 20% seed length Arabidopsis thaliana
IKU2-OE line has total protein similar to wild type Arabidopsis thaliana
FIE-OE line has sucrose content similar to control Arabidopsis thaliana
(AGL37, PHE1, AT1G65330) seeds have reduced seed weight Arabidopsis thaliana
(ATWRKY10, MINI3, WRKY10, AT1G55600) lines have slightly reduced protein content Arabidopsis thaliana
transient starch accumulating during Arabidopsis seed development localizes to embryo Arabidopsis thaliana
OVULE PECTIN MODIFIER 1 (OPM1) is absent from seed Hordeum vulgare
embryo-specific overexpression of Fertilization Independent Endosperm (FIE, FIE1, FIS3, AT3G20740) has no influence on seed weight Arabidopsis thaliana
MINISEED3 (ATWRKY10, MINI3, WRKY10, AT1G55600) is expressed in developing endosperm during the early stage Arabidopsis thaliana
(ATWRKY10, MINI3, WRKY10, AT1G55600) is seed development gene Arabidopsis thaliana
MtABI5 transcription factor is highly connected with desiccation tolerance (DT) probe sets Medicago truncatula
coi mutants have larger grain length and width compared to WT plants Oryza sativa
ZmBELL10-OE plants exhibit increased kernel size Zea mays L.
paternal (TGS1, AT1G45231) alleles do not rescue defects in (TGS1, AT1G45231) /+ seeds Arabidopsis thaliana
GLABRA2 (GL2, AT1G79840) is critical for seed mucilage biosynthesis Arabidopsis thaliana
GRMZM2G120575 is causal gene for the dek58 seed-defective phenotype Zea mays
(AtGATL5, GATL5, AT1G02720) expression is highest in 7-DPA siliques Arabidopsis thaliana
ABSCISIC ACID INSENSITIVE 5 (ABI5, AtABI5, DPBF1, GIA1, AT2G36270) is mainly expressed in seeds
(ATWRKY10, MINI3, WRKY10, AT1G55600) and (IKU2, AT3G19700) pathway has unknown exact mechanism and downstream factors Arabidopsis thaliana
mini3-1 mutant is derived from (ATWRKY10, MINI3, WRKY10, AT1G55600) Arabidopsis thaliana
MtAP2/ (ATERF13, EREBP, ERF13, AT2G44840) transcription factor connects P50 probe sets cluster Medicago truncatula
hull tissues (lemma and palea) provide physical constraints to limit seed size
seed coat protects embryo
(FAR1, AT5G22500) transcript accumulates in dry seeds Arabidopsis thaliana
fie-14 mutant is derived from (FIE, FIE1, FIS3, AT3G20740) Arabidopsis thaliana
(FIE, FIE1, FIS3, AT3G20740) mutant alleles contain decrease in linoleic acid (18:2) Arabidopsis thaliana
FIE-OE line has seed size very similar to Col-0 empty vector control Arabidopsis thaliana
increased seed size phenotype is observed only in heterozygous IKU2-OE seeds Arabidopsis thaliana
nucellus has impact on grain size
late embryogenesis in seed plants is an example of new developmental context for desiccation tolerance mechanisms
(AtMYB55, MYB55, AT4G01680) shows strong negative correlation with (ABI3, AtABI3, SIS10, AT3G24650) during seed development Arabidopsis thaliana
(AAP2, AT5G09220) seeds show decrease of protein content
(XXT5, AT1G74380) expression is also high at initial stages of seed development Arabidopsis thaliana
carbon flow from glutamine via malate occurs into fatty acid biosynthesis Glycine max
embryo-specific overexpression of Fertilization Independent Endosperm (FIE, FIE1, FIS3, AT3G20740) has no influence on seed size Arabidopsis thaliana
overexpression of HAIKU2 (IKU2, AT3G19700) results in seeds with increased seed weight Arabidopsis thaliana
increased Suc content in (AGL37, PHE1, AT1G65330) seeds can be explained by decreased sink strength associated with reduced conversion of Suc into fatty acids Arabidopsis thaliana
Medicago truncatula promoter sequences revealed presence of at least one RYL or one GBL motif Medicago truncatula
AtME4 and AtME2 genes are highly expressed during phase R6 of seed development Glycine max
ZmTFCB driven by 35S promoter did not completely rescue aborted seeds Arabidopsis thaliana
phe1-1 mutant is derived from (AGL37, PHE1, AT1G65330) Arabidopsis thaliana
(ATWRKY10, MINI3, WRKY10, AT1G55600) mutant shows tendency to reduce linoleic acid (18:2) content Arabidopsis thaliana
(AGL37, PHE1, AT1G65330) gene is expressed in preglobular embryo and in the endosperm during early development Arabidopsis thaliana
rpl27ac-2 and rpl27ac-3 mutant siliques have reduced number of seed Arabidopsis thaliana
cuticular structures on developing embryo are important to prevent organ fusion Arabidopsis thaliana
transgenic rice seeds expressing bacterial (DHPS, HPPK, AT1G69190) morphological changes were observed in transgenic rice seeds Oryza sativa
type I MADS-box genes are preferentially expressed in seed Arabidopsis thaliana
water stress during flowering and grain filling periods results in severe reduction in seed quality canola
arabinose accumulates in pronounced manner during seed development Arabidopsis thaliana
cell proliferation was active during 10–20 DAF (days after flowering) Brassica napus
coi1b mutants have higher grain weight than WT plants Oryza sativa
585 kb highly differentiated region on chromosome 6 contained nuclear fission defective 6 (NFD6, AT2G20585) and NAC transcription factor 25 (anac025, NAC025, NAC25, AT1G61110) genes Ipomoea purpurea
derepression of the maternal (AGL37, PHE1, AT1G65330) allele in polycomb group (PcG) mutants is believed to cause endosperm overproliferation and seed abortion Arabidopsis thaliana
mini3-1 mutant reduces seed width Arabidopsis thaliana
starch degradation in mutant seeds was retarded starch metabolism Arabidopsis thaliana
MINI3-OE line has sucrose content similar to control Arabidopsis thaliana
IKU2-OE line has starch content strongly increased at 7 DAF to 8 to 10 µg per seed starch accumulation at early seed development Arabidopsis thaliana
transgenic LEC1-overexpressing rapeseed plants produce larger seeds without detrimental effects on plant development Brassica napus
gene regulatory network of developing M. truncatula seeds visualized the presence of tightly coregulated modules of gene expression Medicago truncatula
different seed compartments control seed germination Arabidopsis thaliana
oleosin proteins are involved in total lipid and protein accumulation Arabidopsis thaliana
endosperm-associated cuticle is localized to outer side of mature endosperm Arabidopsis thaliana
mature endosperm-associated cuticle is of maternal ii1 cellular origin Arabidopsis thaliana
dark-brown HFL1 seeds had slight increase in chalkiness Oryza sativa
maternal (AGL37, PHE1, AT1G65330) mutation improves fertility in species crosses Arabidopsis thaliana; Arabidopsis arenosa
embryo proliferation in the second phase is accompanied with accumulation of seed storage compounds Arabidopsis thaliana
IKU2-OE line has sucrose accumulation pattern opposite to starch sucrose and starch metabolism Arabidopsis thaliana
(IKU2, AT3G19700) expression is silenced in homozygous IKU2-OE seeds Arabidopsis thaliana
wrinkled1 mutant shows reduction in oil accumulation accompanied with retardation in starch degradation Arabidopsis thaliana
(ATWRKY10, MINI3, WRKY10, AT1G55600) expression is detected in endosperm and embryo until the globular stage Arabidopsis thaliana
(ATWRKY10, MINI3, WRKY10, AT1G55600) expression is absent from heart stage embryos Arabidopsis thaliana
oastlAC B +/− mutant shows number of fully developed seeds decreased by more than 85% compared to wild type Arabidopsis thaliana
histone (H2B, HTB2, AT5G22880) monoubiquitination (H2Bub) affects seed dormancy Arabidopsis thaliana
volume of oil bodies (V OB) in ole1ole2ole4 mutant reached average of 2.5 µm³ at 11 DAF Arabidopsis thaliana
ii1 maternal cells are located on outer side of developing endosperm cells Arabidopsis thaliana
high-Lys transgenic rice plant performance and seed germination were unchanged between wild type Oryza sativa
(MUCI70, AT1G28240) and (GAUT11, AT1G18580) were transcribed in developing Arabidopsis siliques from 3 to 10 (DPA, AT5G02470) Arabidopsis thaliana
absence of (EMB173, FIS1, MEA, SDG5, AT1G02580) and (FIE2, FIS2, AT2G35670) orthologs in rice suggests that repression of central cell nuclei mediated by FIS complex in Arabidopsis does not operate in rice Oryza sativa; Arabidopsis thaliana
(AtLHP1, LHP1, TFL2, AT5G17690) role in repression of seed-specific genes remains to be determined seed-specific genes Arabidopsis thaliana
overexpressor or mutant lines and wild type did not show significant differences in germination rates after 2 to 4 d of incubation with excess (ATBHLH029, ATBHLH29, ATFIT1, BHLH029, FIT, FIT1, FRU, AT2G28160) Arabidopsis thaliana
Kalanchoe fedtschenkoi does not produce viable seed Kalanchoe fedtschenkoi
M2 ears were screened for dominant seed mutant phenotypes Zea mays
ostga10 mutant exhibits lower seed set Oryza sativa
35S-15 and GR-14 transgenic lines showed comparable appearance to wild-type dehulled mature seeds Oryza sativa
BADC proteins play role in normal seed development Arabidopsis thaliana
67% of genes from set that were down-regulated during seed maturation showed inverse expression pattern (were induced) during germination Arabidopsis thaliana
(HSA32, AT4G21320) and (ATHSP101, HOT1, HSP101, AT1G74310) interplay takes place during seed development Oryza sativa
DEX itself hardly affects germination of control seeds Solanum lycopersicum
oil body accumulation pattern in double mutants changed especially after 9 DAF Arabidopsis thaliana
nitric oxide (NO) is involved in alleviation of seed dormancy
abscisic acid (ABA) plays critical roles in seed germination
germination is more sensitive to cyclopropane fatty acid (CPA) accumulation than seed maturation
seed-specific expression of feedback-insensitive (DHPS, HPPK, AT1G69190) and AK resulted in wrinkled seeds Glycine max
autonomous pseudoseeds result from nucellar cell proliferation Oryza sativa
endosperm provides nutrients to embryo
abscisic acid (ABA) promotes synthesis of seed storage proteins
environment, such as temperature, during grain filling differs among caryopses from the same panicle Oryza sativa
siliques from (SAUR75, AT5G27780) mutant pollination showed aborted seeds dispersing randomly from the top to the base Arabidopsis thaliana
genes expressed only in developing seeds are expressed during specific phase of seed development Arabidopsis thaliana
gibberellin (GA) plays a significant role in seed development
genes that exhibit seed-specific expression are preferentially de-repressed in the presence of uniconazole Arabidopsis thaliana
seed maturation involves gradual desiccation process
Brassica napus seeds reach approximately 45% lipid content after maturation Brassica napus
SDG728 RNAi plants had reduced seed size and weight Oryza sativa
(AAP1, AtAAP1, NAT2, AT1G58360) has function in seed loading Arabidopsis thaliana
fiber accounts for 45% of total seed biomass at maturity in AD genome species
different plant strategies in response to water stress resulted in several similar outcomes when comparing equal seed weights Arabidopsis thaliana
structure at surface of ii1 cells during globular and heart stages has inverted electron density relative to structure at endosperm surface in mature seeds
CR-slida CRISPR-Cas9 gene knockout lines show 86%, 70% and 79% reduction in seed number Solanum lycopersicum
SEED STORAGE ALBUMIN1 (AT2S1, SESA1, AT4G27140) was down-regulated in cer9-2 mutant Arabidopsis thaliana
germination of (AtROS1, DML1, ROS1, AT2G36490) /DEL seeds of lines 4 and 11 was strongly delayed on DEX medium compared to non-DEX medium Solanum lycopersicum
free Lys content in 35S-15 and GR-14 lines showed similar decrease as wild-type rice Oryza sativa
different grains of the same plant experience diverse environmental conditions during seed development Oryza sativa
severe defects in pollen tube growth result in reduced seed set Arabidopsis thaliana
(GAUT11, AT1G18580) showed dramatic increase in expression at 7 (DPA, AT5G02470) Arabidopsis thaliana
siliques from (SAUR62, AT1G29430) mutant pollination showed aborted seeds dispersing randomly from the top to the base Arabidopsis thaliana
(ABI3, AtABI3, SIS10, AT3G24650) seeds exhibit viviparous germination
seed development signals play a role in increase of lignocellulosic biomass in (ATGRP8, CCR1, GR-RBP8, GRP8, RBGA6, AT4G39260) ProSNBE lines Arabidopsis thaliana
decline of free Lys from 10 to 15 DAF might be related to expansion via deposition of storage proteins in developing seeds about 12 DAF Oryza sativa
time and processing of grain filling can be quite different among caryopses from the same panicle Oryza sativa
(SAUR62, AT1G29430) /− is a knockdown mutant and (SAUR75, AT5G27780) /− is a knockout mutant might explain impaired seed development observed only with wild-type pollen on (SAUR75, AT5G27780) /− but not (SAUR62, AT1G29430) /− and RNAi pistils Arabidopsis thaliana
water stress during flowering and grain filling periods results in severe reduction in seed yield canola
LEC genes act early in seed development during morphogenesis
de-repression of seed-specific transcripts includes all three LEC genes Arabidopsis thaliana
wild-type plants show less than 2% seed abortion compared to heterozygous (ATOBGC, ATOBGL, CPSAR1, EMB269, EMB3138, Obg A-2, OBGC, OBGL, AT5G18570) mutant plants Arabidopsis thaliana
cuticle continuing development could be inferred from continuous presence of dense particles in ii1 cell walls Arabidopsis thaliana
(PAC, AT2G48120) treatment does not rupture testa or endosperm Arabidopsis thaliana
abscisic acid (ABA) plays critical roles in seed maturation
emb2279-2 heterozygote siliques contained about 25% of the seeds that were albino and aborted Arabidopsis thaliana
PHERES1 repression occurs during gametophyte and endosperm development Arabidopsis thaliana
initiation of the synthesis of storage substances results in decreased cell division Brassica napus
reduced IAA levels in de-B18 mutant is attributed to altered cellular morphology of BETL and reduced seed mass Zea mays
flange wall ingrowths are present by 15 days after anthesis Gossypium hirsutum
seed coat utilizes dry weight
free amino acids (FAAs) play important roles in seed desiccation
water stress inhibits cell division in endosperm cells
nitric oxide (NO) is involved in promotion of seed germination
(ABI3, AtABI3, SIS10, AT3G24650) mutant results in reduced seed dormancy
(ABI3, AtABI3, SIS10, AT3G24650) (ABI4, ATABI4, GIN6, ISI3, SAN5, SIS5, SUN6, AT2G40220) and (ABI5, AtABI5, DPBF1, GIA1, AT2G36270) transcription factors positively regulate expression in seeds Arabidopsis thaliana
embryo is surrounded by single-cell endosperm layer Arabidopsis thaliana
cuticle acquires globular organization during globular and heart stages Arabidopsis thaliana
OsFDML1 transcripts are not detected in 10-d-old ovary Oryza sativa
FIS2–MEA complex presumably affects other, as yet unidentified, genes involved in seed development Arabidopsis thaliana
(EMB173, FIS1, MEA, SDG5, AT1G02580) functions specifically in seed development Arabidopsis thaliana
de-repression of (AGL37, PHE1, AT1G65330) is likely to contribute to seed abortion phenotype of (EMB173, FIS1, MEA, SDG5, AT1G02580) Arabidopsis thaliana
majority of genes induced in seed maturation and subsequently removed during germination are shared by micropylar and chalazal endosperm (MCE) and radicle (RAD) (72%) Arabidopsis thaliana
exogenous L-NMMA decreased germination in wild-type seeds Arabidopsis thaliana
germination process accumulates delay of approximately 2 to 3 days in (ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) mutants Arabidopsis thaliana
transcript elevation of genes involved in serotonin biosynthesis existed only at medium and late stages in developing seeds of transgenic rice but not in early stage Oryza sativa
(AGL23, AT1G65360) functions in female gametophyte and during seed development
SAMS protein is absent in dry mature seed Medicago truncatula
activation of (CHD3, CHR6, CKH2, EPP1, GYM, HRB2, LWR1, PKL, SSL2, AT2G25170) after germination is insufficient to repress expression of seed-associated traits
(OLE1, OLEO1, AT4G25140) mutant is major oleosin found in developing seeds Arabidopsis thaliana
seed storage proteins were down-regulated in cer9-2 mutant Arabidopsis thaliana
fusion of central cell and sperm nuclei produces endosperm
Atgint1 seeds were slightly but significantly larger than wild type seeds Arabidopsis thaliana
LEAFY COTYLEDON 2 (AtLEC2, LEC2, AT1G28300) is key transcriptional regulator of seed development Arabidopsis thaliana
(SAUR62, AT1G29430) mutant showed higher seed abortion rates than wild type Arabidopsis thaliana
seed germination is transition state between quiescent embryo and photosynthetically active plant
abscisic acid (ABA) plays crucial role in embryo development
(FIE, FIE1, FIS3, AT3G20740) functions in regulating seed development following fertilization Hieracium piloselloides
HvTrxh1 was observed in dissected endosperm of mature barley seeds Hordeum vulgare
LORELEI functions in early seed development Arabidopsis thaliana
largest decreases in seed weight occurred in lines that accumulate the most cyclopropane fatty acid (CPA) Arabidopsis thaliana
cuticle is associated with endosperm outer cell wall Arabidopsis thaliana
gaps at micropylar and chalazal poles might play role in seed development and seed germination
segregation of endosperm color among HFL mature seeds might be considered a response to environmental factors Oryza sativa
(AGL23, AT1G65360) expressed predominantly paternally within endosperm after fertilization
loss of activity of any of the four FIS complex genes results in overgrowth of fertilized endosperm Arabidopsis thaliana
chromatin-associated factors restrict expression of seed-specific genes
(GAUT11, AT1G18580) has a role in seed wall composition Arabidopsis thaliana
794 proteins from B. napus developing seed provide resource linking transcriptional and post-transcriptional regulatory network of seed development Brassica napus
AtLPLA is strongly expressed during embryo development Arabidopsis thaliana
single-cell endosperm layer is surrounded by seed coat (testa) Arabidopsis thaliana
electron-lucent and electron-dense layers of cuticle thickened significantly by mature embryo stage Arabidopsis thaliana
cuticle is fully associated with endosperm cell wall Arabidopsis thaliana
pyramid HFL1 rice (35S-15/GR-14) had dehulled seeds with dark-brown endosperm phenotype Oryza sativa
(BADC1, BLP3, AT3G56130) (BADC3, BLP2, AT3G15690) double mutant shows significant decrease in weight per seed Arabidopsis thaliana
EMBRYO SURROUNDING FACTOR1 (ESF1) regulates nutrient transfer into embryo
chromatin remodelers are required for repression of seed expression programs
(ATELP, ATELP1, ATVSR1, BP-80, BP80, BP80-1;1, BP80B, GFS1, MTV18, VSR1, VSR1;1, AT3G52850) (AtVSR2, BP80-1;2, VSR1;2, VSR2, AT2G30290) (BP80-2;1, MTV2, MTV4, VSR2;1, VSR4, AT2G14720) (BP80-3;2, VSR3;2, VSR5, AT2G34940) (BP80-3;3, VSR3;3, VSR6, AT1G30900) (BP80-3;1, VSR3;1, VSR7, AT4G20110) single mutants show no obvious difference in seed germination Arabidopsis thaliana
cuticle became more frequently associated with endosperm cells than ii1 cells at heart stage Arabidopsis thaliana
seed coat defects of (TT1, WIP1, AT1G34790) and (ATCHS, CHS, TT4, AT5G13930) mutants are maternally derived maternal origin Arabidopsis thaliana
tight association between dark-brown color emerging and Lys accumulation occurred at late stage of endosperm development in HFL rice Oryza sativa
endosperm appearance in harvested seeds from HFL lines is quite different and color is segregated Oryza sativa
hybrid endosperm harvested at five days post pollination Oryza sativa
phenotype of (AGD1, VAL1, AT5G61980) (HSI2-L1, HSL1, VAL2, AT4G32010) seedlings bears striking similarities to phenotype of (CHD3, CHR6, CKH2, EPP1, GYM, HRB2, LWR1, PKL, SSL2, AT2G25170) seedlings
HvTrxh1 was observed in aleurone layer of mature barley seeds Hordeum vulgare
female gametophyte of HSFA1 QK mutant associated with higher seed abortion rate Arabidopsis thaliana
(OLE1, OLEO1, AT4G25140) protein is detected following OLE5 protein Arabidopsis thaliana
(VUP1, AT3G21710) promoter drives expression in developing seeds Arabidopsis thaliana
endosperm nourishes developing embryo and seedling
endosperm cuticle is produced by maternal inner integument 1 layer Arabidopsis thaliana
abscisic acid (ABA) inhibits seed germination
master regulators promote developmental program of seeds
second male gamete and diploid central cell fusion develops into triploid endosperm Arabidopsis thaliana
(ATNTRA, NTR2, NTRA, AT2G17420) (ATNTRB, NTR1, NTRB, AT4G35460) mutant shows slightly wrinkled seeds Arabidopsis thaliana
SOD isoform is exclusively identified in endosperm barley; Hordeum vulgare
parental fad2fae1 seeds weighed 20.0 ± 1.24 µg Arabidopsis thaliana
PIFs (PHYTOCHROME INTERACTING FACTORS) repress seed germination Arabidopsis thaliana
TIP3 isoforms expression is restricted to seeds Arabidopsis thaliana
activation of (CHD3, CHR6, CKH2, EPP1, GYM, HRB2, LWR1, PKL, SSL2, AT2G25170) prior to germination is sufficient to repress expression of seed-associated traits
(AGD1, VAL1, AT5G61980) (HSI2-L1, HSL1, VAL2, AT4G32010) double mutant shows accumulation of triacylglycerol
ABA establishes desiccation tolerance
neutral invertase was isolated and expression pattern analysis showed expression is significantly increased during seed development
oil content increased sharply at 11 days after pollination (DAF) (U-shaped embryo stage) Arabidopsis thaliana
triple mutant plants displayed markedly reduced seed set Arabidopsis thaliana
QPM mutant maize endosperm was hardened endosperm Zea mays
(BADC1, BLP3, AT3G56130) (BADC2, BLP1, AT1G52670) double mutant showed significant decrease in desiccated seed weight Arabidopsis thaliana
(ABI3, AtABI3, SIS10, AT3G24650) mutants germinate only after embryos mature
de-repression of LEC genes contributes substantially to generation of pickle root phenotype Arabidopsis thaliana
FIS genes are expressed in endosperm
immature siliques of heterozygous mutant plants contain approximately 25% white seeds white seeds Arabidopsis thaliana
(GAUT11, AT1G18580) is shown to be involved in production of Arabidopsis seed testa cell wall and mucilage Arabidopsis thaliana
outer seed coat cuticle is associated with water desiccation tolerance
dso-4 genotype exhibits seed fusion Arabidopsis thaliana
heritability of TS–GUS reactivation is highly sensitive to resetting at another stage of plant development during seed aging
altered BETL morphology in de-B18 mutant is due to greatly reduced ZmPIN RNA localization in BETL Zea mays
cotton transfer cells (TCs) are characterized by flange and reticulate wall ingrowths (WIs) forming sequentially during development Gossypium species
different plant strategies in response to water stress resulted in different outcomes at whole-seed level Arabidopsis thaliana
electron-lucent material corresponds to cuticle Arabidopsis thaliana
emb-type mutations mainly affect embryo Zea mays
oil body (OB) size decreases during seed maturation
expression pattern of (AtMAX2, MAX2, ORE9, PPS, AT2G42620) in dry seed and imbibition stages was similar to expression pattern of (AT3, ATEM1, EM1, GEA1, AT3G51810) a gene highly expressed in seeds Arabidopsis thaliana
ii1 cells undergo programmed cell death during final steps of testa maturation
cuticle could play role in preventing fusion between endosperm and integumental cells
developing seed at 10 DAF had limited number of differential metabolites (DMs) detected in transgenic rice compared with wild type Oryza sativa
sHSPs are involved in seed maturation
1:3 segregation ratio of aborted to normal seeds mimics defective kernel phenotype of maize (ASG6, CRK2, AT1G70520) mutant Arabidopsis thaliana; Zea mays
(ABI3, AtABI3, SIS10, AT3G24650) is expressed throughout maturation phase Arabidopsis thaliana
fie-11 mutant is derived from (FIE, FIE1, FIS3, AT3G20740) Arabidopsis thaliana
(AGL37, PHE1, AT1G65330) was overexpressed in transgenic Arabidopsis plants under control of seed-specific glycinin promoter Arabidopsis thaliana; Glycine max
IKU2-OE seeds have reduced Suc content at 7 DAF (d after flowering) Arabidopsis thaliana
seed developing has not finished at 19 DAF (d after flowering) Arabidopsis thaliana
SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE (SERK) acts as positive regulator of seed development program Arabidopsis thaliana
proteomic composition was preserved under most severe water limitation treatment (10% PC) Arabidopsis thaliana
35S:STK plants show wider seed area compared with wild-type and (AGL11, STK, AT4G09960) mutant Arabidopsis thaliana
cuticle is transferred to endosperm around the heart and torpedo stages of embryo development Arabidopsis thaliana
cv Nipponbare under LT conditions has significantly reduced seed-setting percentage Oryza sativa
excess sugars are known to inhibit seed germination Arabidopsis thaliana
(ABI3, AtABI3, SIS10, AT3G24650) (ABI4, ATABI4, GIN6, ISI3, SAN5, SIS5, SUN6, AT2G40220) and (ABI5, AtABI5, DPBF1, GIA1, AT2G36270) regulate overlapping subsets of seed-specific genes
free Lys level in wild-type rice was reduced to very low level after seed maturation Oryza sativa
seed abortion and reduced seed set was not observed in wild-type siliques Arabidopsis thaliana
endosperm and nucellar cells in fertilized seeds have distinct border Oryza sativa
ATP-dependent remodelers restrict expression of seed-specific genes
(LEA, AT2G21490) (Late Embryogenesis Abundant) genes named for abundant expression in desiccating seeds
two barley Trx h isoforms might be regulated differently and have seed tissue-specific functions Hordeum vulgare
loss of (ATOBGC, ATOBGL, CPSAR1, EMB269, EMB3138, Obg A-2, OBGC, OBGL, AT5G18570) causes seed lethality Arabidopsis thaliana
SALT-OVERLY SENSITIVE 5 (FLA4, SOS5, AT3G46550) is highly expressed at 4 days post-anthesis (DPA) Arabidopsis thaliana
ii1 primary cell wall is in continuity with cuticle and endosperm cell wall Arabidopsis thaliana
lrx mutants show reduced seed set Arabidopsis thaliana
ectopic expression of an enzyme that inactivates GAs leads to seed abortion Arabidopsis thaliana
ABSCISIC ACID INSENSITIVE3 (ABI3, AtABI3, SIS10, AT3G24650) is required at later stage than LEC genes
genes that exhibit seed-specific expression are preferentially de-repressed in the absence of PICKLE (CHD3, CHR6, CKH2, EPP1, GYM, HRB2, LWR1, PKL, SSL2, AT2G25170) Arabidopsis thaliana
protein translation was heavily inhibited at 17–21 DAF stage Brassica napus
(ATTPS2, TPS2, AT1G16980) is expressed in seeds Arabidopsis thaliana
VfAAP1 has function in seed size Vicia faba
overexpression of (BZR1, AT1G75080) enhanced seed number Solanum lycopersicum
expression levels of Chr4.2307.KCS, Chr4.2308.KCS, and Chr4.2311.KCS were indeed significantly upregulated from 85 DAF to 100 DAF Acer truncatum
temporary accumulation of starch is helpful as sink organ Brassica napus
high expression of auxin-related genes indicates that auxin may have possible roles in 17–21 DAF developmental processes Brassica napus
AN1 is involved in seed coat morphogenesis Petunia hybrida
reduced cell size in endosperm causes miniature seed phenotype Zea mays
flange wall ingrowth density in Gossypium hirsutum at 20 DAA is higher than flange wall ingrowth density in Gossypium arboreum Gossypium hirsutum; Gossypium arboreum
(TFL-1, TFL1, AT5G03840) mutants show larger seed phenotype Arabidopsis thaliana
microspore defects can lead to reduced seed set rate
MADS29 is expressed in early seed stages Oryza sativa
seed number and weight are not predetermined upon bolting and can be altered in response to stress water stress at almost any stage during seed setting Arabidopsis thaliana
PBAA relative composition is rigorously maintained under any water stress condition Arabidopsis thaliana
Arabidopsis thaliana mature seed contains embryo Arabidopsis thaliana
LeLID1 contributes to seed germination Solanum lycopersicum
Rubisco small subunit-encoding gene was not changed during seed development Brassica napus
(AtbZIP, bZIP, AT1G68880) family participate in seed maturation
cell wall invertase (CWIN) activity rate-limits seed development
anti-159 plants house smaller-sized seeds reduced in number compared to wild-type plants Arabidopsis thaliana
TIP3;1–YFP is abundant and fluoresces brightly in dry seeds Arabidopsis thaliana
ccc triple mutant seed germination failure may be due to embryo lethality Arabidopsis thaliana
knockout alleles of (ATSUC5, SUC5, AT1G71890) are slightly delayed in embryo development Arabidopsis thaliana
timing of endosperm cellularization is directly linked to seed size
redundant role of (ATBET11, ATBS14A, BET11, BS14A, MTV15, AT3G58170) and (ATBET12, ATBS14B, BET12, BS14B, AT4G14455) suggested by fertilization failure and seed developmental abortion in double mutants Arabidopsis thaliana
double-fertilization event leads to formation of diploid embryo
Differences in TE and imprinted genes expression between endosperm domains were observed between endosperm domains Arabidopsis thaliana
Failure in parental genome dosage regulation results in defective endosperm development Arabidopsis thaliana
expression cluster 1 shows transcript expression specificity in seed coat Arabidopsis thaliana
B. napus ESTs were detected as differentially expressed at 15 and 25 DAF (days after flowering) Brassica napus
50% decrease in lipid content of the seed is reduced along with embryo development Brassica napus
starch synthesis blocked in the embryo results in impaired formation of the embryo as a sink tissue Brassica napus
cruciferin is major storage protein of Brassica napus seeds Brassica napus
ZmTar1 gene shows highly divergent (antagonistic) response at 12 and 16 days after pollination (DAP) Zea mays
homozygous recessive mn1 mutant is seed-specific and bears one-fifth the weight of normal Mn1 seed at maturity Zea mays
entire complement of TIPs has been characterized Arabidopsis seeds Arabidopsis thaliana
immature seeds were separated from silique coats Brassica napus
SDG728 RNAi plants displayed reduced seed size and seed weight phenotype
(ATOPT3, OPT3, AT4G16370) has function in seed development Arabidopsis thaliana
8–12 days after pollination (DAP) stage coincident with early peak in IAA levels Zea mays
CYP724B1 RNAi plants show reduced seed size and weight Oryza sativa
seed weight in OsMED14_1 RNAi plants is lighter by up to 33% reduction compared with wild-type seeds Oryza sativa
alteration in seed weight can be traced to changes in seed filling rate Arabidopsis thaliana
proteomic rebalancing phenomenon has been previously reported in seed storage protein (SSP) mutants of soybean, corn, barley, and Arabidopsis
(ASK1, ATSKP1, SKP1, SKP1A, UIP1, AT1G75950) seeds are 1.4-fold bigger than WT seeds Arabidopsis thaliana
VfPTR1 expression occurs at later stages of seed development compared to amino acid transporter VfAAP1 Vicia faba
(AQP1, ATTIP2;1, DELTA-TIP, DELTA-TIP1, TIP2;1, AT3G16240) is expressed in outer integument of seed coat Arabidopsis thaliana
(GAMMA-TIP2, SITIP, TIP1;2, TIP2, AT3G26520) ;2–YFP and (PAT24, TIP1, AT5G20350) ;1–RFP have mutually exclusive expression patterns in seeds Arabidopsis thaliana
rigorous maintenance of PBAA relative composition strongly suggests that PBAA composition plays a key role in seed survival under any water stress condition Arabidopsis thaliana
ZmDREB2A mRNA accumulation in zygotic embryos increases dramatically during seed maturation from 21 to 35 DAP Zea mays
DREB/CBF play roles in seed development
testa surrounds embryo Arabidopsis thaliana
organic N compounds are utilized for biosynthesis of storage compounds
silencing of Lin5 expression reduced seed number Solanum lycopersicum
miniature1 (mn1) seed mutant leads to pleiotropic changes including altered sugar levels Zea mays
reticulate wall ingrowth density in Gossypium hirsutum at 20 DAA is higher than reticulate wall ingrowth density in Gossypium thurberi Gossypium hirsutum; Gossypium thurberi
fiber accounts for 40% of total seed biomass at maturity in A genome progenitor
(GAMMA-TIP2, SITIP, TIP1;2, TIP2, AT3G26520) ;1 (AQP1, ATTIP2;1, DELTA-TIP, DELTA-TIP1, TIP2;1, AT3G16240) is excluded from embryos Arabidopsis thaliana
spikelets in OsMED14_1 RNAi panicles remain green during seed maturation Oryza sativa
Arabidopsis thaliana mature seed consists of external dead seed coat Arabidopsis thaliana
(AAP8, ATAAP8, AT1G10010) mutant shows reduction in seeds per silique Arabidopsis thaliana
exogenous supply of hexoses was unable to recover miniature seed phenotype Zea mays
T1 seed from single copy suppression lines showed 20–27% reduction in average seed weight compared with wild-type plants Solanum lycopersicum
early embryogenesis stages occurs during 1 to 4 days after fertilisation (DAF1−DAF4) Xerophyta humilis
(ACBP4, AtACBP4, AT3G05420) functions in seed development Arabidopsis thaliana
GmEXPB2 overexpression line 1 produced 10.0% increase in 100 grain weight Glycine max
differences in proteolysis during seed development explains low correlation between alpha and beta chains Medicago truncatula
endosperm associated with maternal-filial boundaries is linked with nutritional dynamics
mature seed contains fully formed embryo