| GmIPT3pro-GUS signal |
shows same expression patterns in |
lateral root primordium, root maturation zone, and root tip |
Glycine max |
| OsMTP1 |
is preferentially expressed in |
roots, aleurone layer, and embryo of seeds |
Oryza sativa |
| ZmRCAα and ZmRCAβ transcripts |
showed no or very low signal in |
roots |
Zea mays |
| ZmBELL10 |
has especially high transcript levels in |
stalk |
Zea mays L. |
| OsMTP1 expression |
is high in |
root cell sap, lateral root, whole roots, aleurone layer, and embryo of seeds |
Oryza sativa |
| ProBpMADS11:GUS transgenic plants |
show expression of BpMADS11 in |
leaf margins |
Betula pendula |
| miR4407 |
is expressed in |
all cell types in elongation and meristematic regions |
Glycine max |
| ProOsMTP1:GFP transgenic line |
shows strong GFP signal in |
lateral roots |
Oryza sativa |
| SlCIPK23 and SlCBL1 |
were expressed to a higher extent in |
roots than SlCBL9 |
Solanum lycopersicum |
| GOLVEN2 (CLEL 9, GLV2, RGF9, AT5G64770) |
is |
shoot-specific gene |
Arabidopsis thaliana |
| DTN1 transcripts |
show low levels in |
tiller bud, spikelet, or root |
Oryza sativa |
| OsMTP1 level in root |
is 10-fold higher than |
OsMTP1 level in leaf |
Oryza sativa |
| TcGDS transcripts |
are most abundant in |
bract and receptacles |
Tanacetum cinerariifolium |
| (NRT1.12, AT3G16180) expression |
could be found in |
major vein of cauline leaves, junction of silique and pedicel, and apex of silique |
Arabidopsis thaliana |
| (ML3, AT5G23820) expression |
is restricted to |
epidermis |
Arabidopsis thaliana |
| GDS expression |
occurs in |
cortex cells surrounding vascular bundle |
Chrysanthemum morifolium |
| (AtNPF1.2, NPF1.2, NRT1.11, AT1G52190) expression |
could be found in |
major vein of cauline leaves, junction of silique and pedicel, and apex of silique |
Arabidopsis thaliana |
| pGLV2::GUS |
showed |
more robust GUS signal in shoots than in roots |
Arabidopsis thaliana |
| OsHMGB1 |
is expressed in |
variety of tissues |
Oryza sativa |
| OsMTP1 level in roots |
is significantly lower in |
(GCS1, HAP2, AT4G11720) accessions |
Oryza sativa |
| GDS promoter activity |
is visible in |
veins of leaves and petiole |
Chrysanthemum morifolium |
| DTN1 transcripts |
show relatively high levels in |
leaf, sheath, and stem |
Oryza sativa |
| (NRT1.12, AT3G16180) pro:GUS transgenic plants |
showed GUS staining mainly in |
major veins |
Arabidopsis thaliana |
| OsMTP1 |
shows markedly higher expression in |
bran |
Oryza sativa |
| BpMADS11 |
is expressed at highest level in |
mature leaves |
Betula pendula |
| ProBpMADS11:GUS transgenic plants |
show expression of BpMADS11 in |
apical buds |
Betula pendula |
| ProBpMADS11:GUS transgenic plants |
show expression of BpMADS11 in |
roots |
Betula pendula |
| OsMTP1 |
is expressed in |
root |
Oryza sativa |
| strong GUS activity |
was detected in |
xylem, phloem, parenchyma, and mesophyll cells of leaves |
Oryza sativa |
| OsMTP1 |
is expressed in |
leaf sheath |
Oryza sativa |
| SlSKOR |
was primarily expressed in |
tomato roots |
Solanum lycopersicum |
| pBdTHX1::GUS |
is absent or expressed at very low levels in |
mature leaves |
Brachypodium distachyon |
| OsOle18 |
is primarily expressed in |
bran |
Oryza sativa |
| ProOsMTP1:GFP transgenic line |
shows no GFP signal in |
endosperm |
Oryza sativa |
| PER transcript levels |
are 10-fold higher in roots than in |
other organs |
Oryza sativa |
| pBdTHX1::GUS |
is expressed in |
young internodes |
Brachypodium distachyon |
| EPP transcript levels |
are 300-fold higher in roots than in |
other organs |
Oryza sativa |
| pBdTHX1::GUS |
shows no GUS staining in |
mature vascular bundles |
Brachypodium distachyon |
| 5' and 3' genomic regions flanking phas gene |
are sufficient to confer |
seed-specific expression pattern |
Phaseolus vulgaris |
| (ATMSRB1, MSRB1, AT1G53670) |
is preferentially expressed in |
leaves and other green organs |
Arabidopsis thaliana |
| Os03bZIP |
is expressed in |
shoot and leaf |
Oryza sativa |
| (TAR1, AT1G23320) expression in vegetative tissues |
is exceedingly low, less than 100–500-fold compared to |
(TAR1, AT1G23320) expression in developing endosperm |
Zea mays |
| (ATFH8, FH8, FORMIN 8, AT1G70140) promoter |
is restricted to |
vascular tissue in hypocotyl and roots |
Arabidopsis thaliana |
| BdCSLF6 |
is highly expressed in |
endosperm |
Brachypodium distachyon |
| S. foetida homolog |
had |
56 occurrences in cotyledon and embryo of developing seeds |
Steculia foetida |
| pBdTHX1::GUS |
is expressed in |
seedlings |
Brachypodium distachyon |
| pBdTHX1::GUS |
is absent or expressed at very low levels in |
internodes |
Brachypodium distachyon |
| cDNA sample preparation method |
was successfully adopted to compare |
gene expression responses in vascular and nonvascular regions in cotyledons |
|
| pBdTHX1::GUS |
is expressed in |
endosperm |
Brachypodium distachyon |
| stably transformed lines of tobacco and Arabidopsis containing reporter gene β-glucuronidase (GUS) flanked by 5' and 3' genomic regions of phas |
exhibit |
same pattern of developmental expression of GUS as phas in its native context |
Nicotiana tabacum; Arabidopsis thaliana |
| S. foetida LPAT (SfLPAT) |
is |
preferentially seed-expressed |
Sterculia foetida |
| Ghd7 transcripts in emerged leaf blade |
display gradient with higher accumulation in |
leaf tip than leaf base |
Oryza sativa |
| shortest transcriptional variant of PtREV |
is prevalent in |
xylem tissue |
Populus trichocarpa |
| BdCSLF6 |
is highly expressed in |
elongating stem internodes |
Brachypodium distachyon |
| β-phaseolin (phas) |
is completely silenced in |
vegetative tissue |
Phaseolus vulgaris |
| (ATMSRB7, MSRB7, AT4G21830) |
is more specifically expressed in |
roots |
Arabidopsis thaliana |
| (PSS1, AT3G59640) expression |
is highest in |
siliques |
Arabidopsis thaliana |
| RET transcript levels |
are more than 2,000-fold higher in roots than in |
other organs |
Oryza sativa |
| pBdTHX1::GUS |
shows GUS staining in all cells except |
vascular bundles |
Brachypodium distachyon |
| Os07RISBZ1 |
is expressed in |
pistil |
Oryza sativa |
| TcADH1, TcADH2, TcALDH1, TcCDS, and TcGLIP transcripts |
are less abundant in |
leaves, roots, or stems |
Tanacetum cinerariifolium |
| OsMED14_1 |
shows highest accumulation of mRNA in |
early anther and Y-leaf |
Oryza sativa |
| (S8H, AT3G12900) |
expression is |
root specific |
Arabidopsis thaliana |
| ProOsMTP1:GFP transgenic line |
shows strong GFP signal in |
embryo and aleurone |
Oryza sativa |
| BpMADS11 |
is expressed in |
roots |
Betula pendula |
| intron 3 of LeSUT1 |
is necessary for |
expression in trichomes |
Solanum lycopersicum |
| seven out of 13 PR-10 gene loci in birch |
encode proteins that are |
specifically expressed in pollen |
Betula pendula |
| RBOH1 |
is more abundant in |
tomato root and stamen |
Solanum lycopersicum |
| X. viscosa (ABI3, AtABI3, SIS10, AT3G24650) paralogues |
showed expression analysis with |
only XvABI3B expressed at appreciable levels in leaves |
Xerophyta viscosa |
| PIVC:uidA |
is absent in |
seedlings and adult root and leaf tissues |
Arabidopsis thaliana |
| shorter iso-forms |
are expressed in |
specific tissues |
Arabidopsis thaliana |
| mannan synthase (ManS) gene |
was specifically expressed in |
endosperm |
Cyamopsis tetragnoloba |
| (ATFH8, FH8, FORMIN 8, AT1G70140) promoter |
shows staining in |
root apical meristem |
Arabidopsis thaliana |
| XhLEC1 genes |
had mean normalised read counts |
< 10 across all RWC |
Xerophyta humilis |
| remaining two copies of BnaZEP |
are found mainly in |
leaves |
Brassica napus |
| XhLEC1 genes |
were barely expressed in |
leaf tissue irrespective of RWC |
Xerophyta humilis |
| transcript expression of VvRops |
were mainly expressed in |
pre-véraison berries and young leaves |
Vitis vinifera |
| R1G1B promoter |
is active in |
whole grain |
Oryza sativa |
| HCC1:GUS transgenic plants |
show GUS expression in |
embryo |
Arabidopsis thaliana |
| HAHB10 |
is almost undetectable in |
other tissues |
Helianthus annuus |
| (ATFH8, FH8, FORMIN 8, AT1G70140) promoter |
shows staining in |
root cap cells |
Arabidopsis thaliana |
| PIVC:uidA |
is strong in |
flower tissues, specifically stigma, ovary, and funiculus |
Arabidopsis thaliana |
| levels of OsFKBP20-1b transcripts in 1–2-week-old seedlings |
were higher in |
endosperm than in roots and shoots |
Oryza sativa |
| BnaA09.ZEP (zeaxanthin epoxidase) |
is predominantly expressed in |
floral tissues |
Brassica napus |
| GUS signal |
could hardly be detected in |
roots |
Oryza sativa |
| bHLH6 expression |
is higher in leaves than in |
roots |
Oryza sativa |
| transcriptional profiling |
can detect |
molecular signatures of different biological samples |
|
| (TAR1, AT1G23320) gene |
is |
endosperm-specific in expression |
Zea mays |
| GUS signal |
is undetectable in |
other tissues |
Arabidopsis thaliana |
| epigenetic profiling |
can detect |
molecular signatures of different biological samples |
|
| cell identities |
are established at the mechanistic level by |
transcription factors and epigenetic regulators |
|
| BnaC09.ZEP (zeaxanthin epoxidase) |
is predominantly expressed in |
floral tissues |
Brassica napus |
| NtCAT1 promoter |
is used as |
endosperm-specific promoter |
Arabidopsis thaliana |
| tobacco nectarin NEC3 |
is expressed in |
nectaries and a few other floral tissues |
Nicotiana langsdorffii × Nicotiana sanderae var. L×S8; Nicotiana tabacum |
| GFP fluorescence |
was observed in |
region behind the root tip |
Hordeum vulgare |
| OeACS2 |
is found at highest level in |
leaf and flower tissue in ARB |
|
| OeERS1 |
is expressed differentially within and between |
fruit abscission zone–adjacent cells of two cultivars |
|
| GUS signal |
could hardly be detected in |
leaves |
Oryza sativa |
| bHLH6 |
is expressed in |
leaf mesophyll cells |
Oryza sativa |
| ZmYS1 |
expression in crown and seminal roots is lower than in |
leaf blades |
Zea mays |
| G-box mutation |
causes decreased expression in |
aerial parts |
Arabidopsis thaliana |
| (ATCYTC-A, CYTC-1, AT1G22840) and (CYTC-2, AT4G10040) promoters |
display |
different expression patterns |
Arabidopsis thaliana |
| bHLH6pro::GUS transgenic plants |
show bHLH6 expression in |
spikelets |
Oryza sativa |
| (ABA1, ATABA1, ATZEP, IBS3, LOS6, NPQ2, ZEP, AT5G67030) expression in roots |
is lowest in |
roots |
Capsicum annuum |
| transgenic rice lines harboring the OsTOD1j::OsTOD1jg-GUS transgene |
showed strong β-glucuronidase (GUS) signals in |
pollen grains |
Oryza sativa |
| Zm00001d052047 |
is highly expressed in |
pollen in the background of (B73, CHL6, CNX, CNX1, SIR4, AT5G20990) |
Zea mays |
| buds |
showed highest expression of |
F3′H |
Cosmos sulphureus |
| RNase Phy4 |
is also highly expressed in |
petals |
Petunia hybrida |
| OsCc1 promoter |
is highly active in |
reproductive tissues |
Oryza sativa |
| (ATCNGC19, CNGC19, AT3G17690) |
is expressed in |
phloem |
Arabidopsis thaliana |
| Northern blot analysis |
showed |
TaCAD1 transcript was most abundant in stem tissues |
Triticum aestivum |
| pollen grains |
show no |
GUS staining |
Arabidopsis thaliana |
| transcripts of putative VvRop- and VvRab-interacting proteins |
were found to be expressed in |
various organs |
Vitis vinifera |
| RNase Phy5 |
is mostly expressed in |
styles |
Petunia hybrida |
| weak GUS activity |
was also found in |
flowers of transgenic plants |
Oryza sativa |
| OsNRT2.4 |
was expressed mainly in |
leaves |
Oryza sativa |
| BjCET3 and BjCET4 |
accumulate relatively more in |
the root than the other tissues |
Brassica juncea |
| NaHD20 mRNA |
shows highest levels in |
corolla, sepals, and stamens |
Nicotiana attenuata |
| some PR-10 gene members |
are |
constitutively expressed in defined tissues |
|
| OsPUB65 |
is expressed only in |
calli tissue |
Oryza sativa |
| RNase Phy1 expression |
seems higher in |
floral organs than in vegetative tissues |
Petunia hybrida |
| GFP fluorescence |
was observed in |
roots of barley grown in hydroponics |
Hordeum vulgare |
| GluB-5 and (BGLU25, GLUC, AT3G03640) promoters |
directed GUS expression in |
whole mature endosperm |
Oryza sativa |
| bHLH6pro::GUS transgenic plants |
show bHLH6 expression in |
leaves |
Oryza sativa |
| three VvRabGDIs |
were not detected in |
berry tissues |
Vitis vinifera |
| RNase Phy3 and RNase Phy4 |
have patterns consistent with |
nectarins |
Petunia hybrida |
| S-RNases |
are expressed mainly in |
pistil |
|
| tissue specialization |
could be associated with |
transcript profiles |
Citrus clementina |
| (PGD1, AT1G64190) promoter |
is particularly active in |
flowers |
Oryza sativa |
| HCC1:GUS transgenic plants |
show GUS expression in |
cotyledon primordia |
Arabidopsis thaliana |
| OUTER CELL LAYER1 (OCL1) |
is expressed in |
endosperm epidermis |
Zea mays |
| RNase Phy5 |
shows weak expression in |
petals, stamens (anthers), and ovaries |
Petunia hybrida |
| all class A ssDETDFs |
were present in |
all organs analysed of apomictic plants |
Paspalum simplex |
| AtACBP1pro::GUS transgenic line |
is expressed in |
cortex |
Arabidopsis thaliana |
| (AGP1, ATAGP1, AT5G64310) promoter |
drives strong GFP expression in |
chalazal region of ovules |
Arabidopsis thaliana |
| GUS staining of pPROAtCAPE1:GUS transgenic lines |
reflected |
mRNA expression pattern in shoots and roots shown by qRT-PCR |
Arabidopsis thaliana |
| transgenic rice lines harboring the OsTOD1j::OsTOD1jg-GUS transgene |
showed strong β-glucuronidase (GUS) signals in |
pollen tubes |
Oryza sativa |
| novel TE insertion |
may change |
tissue-specific patterns of expression |
|
| R1G1B promoter |
is active in |
endosperm |
Oryza sativa |
| HCC1:GUS transgenic plants |
show GUS expression in |
funicular attachment site of ovules |
Arabidopsis thaliana |
| MtNoa1/ (ATNOA1, ATNOS1, NOA1, NOS1, RIF1, SVR10, AT3G47450) promoter activity |
was detected mainly in |
vascular bundles |
Medicago truncatula |
| HT-M3 |
is rare or absent in |
SC N. plumbaginifolia pistils |
Nicotiana plumbaginifolia |
| VvRabGEF1 |
was expressed in |
wide diversity of organs |
Vitis vinifera |
| NtIRT1 transcript |
was detected in |
all root samples |
Nicotiana tabacum |
| glucose 6-phosphate (Glc6P)/phosphate translocator (GPT) |
is preferentially expressed in |
non-green tissues |
|
| MtNOA1/ (ATNOA1, ATNOS1, NOA1, NOS1, RIF1, SVR10, AT3G47450) |
is expressed more in |
Medicago truncatula leaves |
Medicago truncatula |
| uncoupling protein 1 (ATPUMP1, ATUCP1, PUMP1, UCP, UCP1, AT3G54110) expression level |
is similar between |
root and shoot tissues |
Arabidopsis thaliana |
| GUS activity |
was not observed in |
flower petals |
Solanum lycopersicum |
| SiAREB1 and SiAREB2 |
highly expressed in |
leaf tissue |
Setaria italica |
| OsNRAMP5 |
shows high expression levels in |
plumules and young shoots |
Oryza sativa |
| OsNRAMP5 |
shows little or no expression in |
endosperm |
Oryza sativa |
| OsCc1 promoter |
is highly active in |
vegetative tissues |
Oryza sativa |
| OeACO2 |
is not |
fruit abscission zone specific |
|
| OeACO2 |
transcripts are more abundant in |
flower and fruit tissue |
|
| OeEIL2 |
is expressed differentially within and between |
fruit abscission zone–adjacent cells of two cultivars |
|
| VvRabGEF1 transcripts |
were expressed in |
wide diversity of organs |
Vitis vinifera |
| putative Rop- and Rab-GAP-, GEF-, and GDI-interacting proteins |
were generally not restricted to |
specific tissues |
|
| Expression in stems |
was higher than in |
roots and shoot apices |
Dendranthema grandiflorum |
| DgCCD8b |
was detected only in |
stem and root tissues |
Dendranthema grandiflorum |
| GUS staining |
showed OsNRT2.4 was specially expressed in |
base of lateral root primodia |
Oryza sativa |
| OeERS1 |
is not |
fruit abscission zone specific |
|
| lcy-β1 and lcy-β2 genes |
were measured in |
Tainung and Hybrid 1B leaves, flowers and fruit |
Carica papaya |
| 17-bp signatures from 18 libraries |
represent |
12 different tissues/organs |
Oryza sativa |
| three VvRabGDIs |
was not expressed in |
berry tissues |
Vitis vinifera |
| DgCCD8b |
was not detected in |
shoot apices |
Dendranthema grandiflorum |
| transverse section through the root |
showed fluorescence in |
all cell layers |
Hordeum vulgare |
| (AAc1, ACT1, AT2G37620) promoter |
is highly active in |
reproductive tissues |
Oryza sativa |
| pyruvate,orthophosphate dikinase (PPDK, AT4G15530) |
is only moderately expressed in |
mature leaves |
|
| OeACS2 |
is expressed at low level in |
shoot tissue |
|
| MtNoa1/ (ATNOA1, ATNOS1, NOA1, NOS1, RIF1, SVR10, AT3G47450) expression |
occurs in |
vascular tissues |
Medicago truncatula |
| rice allergenic RAG-1 promoter |
is expressed in |
inner starchy endosperm |
Oryza sativa |
| ZmYS1 |
expression in crown and seminal roots is similar |
crown and seminal roots |
Zea mays |
| lcy-β1 and lcy-β2 genes |
are expressed in |
yellow fruit |
|
| OsNAR2.1 expression |
included the same tissue types as |
OsNRT2.1, OsNRT2.2, and OsNRT2.3 expression |
Oryza sativa |
| HT-M1 |
is rare or absent in |
SC N. plumbaginifolia pistils |
Nicotiana plumbaginifolia |
| putative (MIR159, MIR159A, AT1G73687) target genes expressed throughout the root |
may not show |
a change in steady-state mRNA levels when whole roots are assayed |
Arabidopsis thaliana |
| GFP fluorescence |
was observed in |
newly emerged lateral roots |
Hordeum vulgare |
| (PGD1, AT1G64190) promoter |
is particularly active in |
mature roots |
Oryza sativa |
| HCC1:GUS transgenic plants |
show GUS expression in |
vascular tissue |
Arabidopsis thaliana |
| expression of type I HD-Zip genes |
is specific to |
different tissues and organs of the plant |
|
| OsCEST |
is detected at high levels in |
leaf tissues |
Oryza sativa |
| rice glutelin |
is expressed exclusively in |
endosperm |
Oryza sativa |
| ZmCKX10 transcript levels |
are highest in |
tassels and silks |
Zea mays |
| OsNRT2.2 |
was strongly expressed not only in roots, but also in |
caryopsis |
Oryza sativa |
| HCC1:GUS transgenic plants |
show GUS expression in |
guard cells |
Arabidopsis thaliana |
| bHLH6 expression |
is higher in leaves than in |
stem bases |
Oryza sativa |
| PtoPIN3a |
only expressed in |
leaves |
Populus tomentosa |
| (AGP1, ATAGP1, AT5G64310) |
was selected for further analysis based on |
presence of transcripts in pistil tissues and absence in stamen tissues |
Arabidopsis thaliana |
| (AGP23, ATAGP23, AT3G57690) |
is downregulated in |
pistil tissues compared with pollen |
Arabidopsis thaliana |
| HvALMT1 promoter::GFP fusion in transgenic barley leaves |
showed strong GFP fluorescence specifically in |
guard cells of stomata |
Hordeum vulgare |
| BjCET3 and BjCET4 accumulation pattern |
is similar to |
(ATMTP3, ATMTPA2, MTP3, MTPA2, AT3G58810) transcript abundance |
Brassica juncea; Arabidopsis thaliana |
| (AtCEST, CEST, Y3IP1, AT5G44650) |
is expressed in |
rosette and cauline leaves and flowers |
Arabidopsis thaliana |
| CAN24 |
is expressed 1600-fold higher in |
glands compared to leaves |
Cannabis sativa |
| rice allergenic Glb-1 promoter |
is expressed in |
inner starchy endosperm |
Oryza sativa |
| site II elements |
are required for maximal expression mainly in |
reproductive tissues |
Arabidopsis thaliana |
| rice U-box protein genes |
are expressed in |
flower tissue |
Oryza sativa |
| (AGP9, AT2G14890) |
was selected for further analysis based on |
presence of transcripts in pistil tissues and absence in stamen tissues |
Arabidopsis thaliana |
| (AGP15, ATAGP15, AT5G11740) |
is downregulated in |
seedlings |
Arabidopsis thaliana |
| SiARDP |
transcript levels lower in |
inflorescence |
Setaria italica |
| OsNRAMP5 |
shows enrichment in |
vascular bundles |
Oryza sativa |
| GL3::SCM-GFP construct |
drives SCM-GFP expression in |
differentiating hair cells |
Arabidopsis thaliana |
| (LGO, SMR1, AT3G10525) gene expression |
occurs in |
epidermal and mesophyll cell layers |
Arabidopsis thaliana |
| ZmXTH1 mRNA in hydroponic conditions |
mainly accumulates in |
leaves |
Zea mays |
| ZmCKX1 expression |
is almost undetectable in |
young leaves |
Zea mays |
| ZmCKX1 expression |
is predominant in |
developing kernel and reproductive organs |
Zea mays |
| JEKYLL |
is |
transfer cell-specific gene |
Hordeum vulgare |
| Ntann12 |
is principally expressed in |
roots |
Nicotiana tabacum |
| ZmXTH5 |
expressed preferentially in |
leaves |
Zea mays |
| ZmYS1 |
is expressed in |
shoots |
Zea mays |
| GluA-3 promoter |
expression pattern was similar to |
previously reported GluA-3 promoter expression pattern |
Oryza sativa |
| ZmXTH1 mRNA in soil-grown plants |
accumulates predominantly in |
roots |
Zea mays |
| ZmYS1 |
almost no expression detected in |
hypocotyl |
Zea mays |
| ZmCKX10 transcript accumulation |
is exception in |
embryo and endosperm |
Zea mays |
| PwTUA1 |
is not detected in |
needles |
Picea wilsonii |
| PwTUA1 |
is not detected in |
stems |
Picea wilsonii |
| OsCEST |
is detected at moderate levels in |
flowers |
Oryza sativa |
| rice U-box protein genes |
are expressed in |
root tissue |
Oryza sativa |
| PpSFBB 4-u1–u4 and PpSFBB 4-d1–d2 |
were all specifically expressed in |
pollen, but not in pistils or leaves |
Pyrus pyrifolia |
| OsNRAMP5 |
shows highest GUS activity in |
stele and sclerenchyma layer cells of roots |
Oryza sativa |
| PtoPIN8a and 8b |
highly transcribed in |
catkins and pollen |
Populus tomentosa |
| (ANU10, AT1G28530) gene |
is expressed in |
roots |
Arabidopsis thaliana |
| (AGP10, ATAGP10, AT4G09030) |
shows higher level of overexpression in |
pistils compared with pollen |
Arabidopsis thaliana |
| OsNRAMP5 |
shows strong expression in |
hulls |
Oryza sativa |
| GluA subfamily gene promoters (GluA-1, GluA-2, and GluA-3) |
were specific to |
outer endosperm |
Oryza sativa |
| (AGP1, ATAGP1, AT5G64310) |
was selected for further analyses |
upregulated AGP group |
Arabidopsis thaliana |
| (AGP12, ATAGP12, AT3G13520) promoter |
shows very weak GFP expression along |
internal tissues of funiculus and septum |
Arabidopsis thaliana |
| tissue-specific differentiation of gene expression |
relates to |
DNA methylation |
|
| (AtCEST, CEST, Y3IP1, AT5G44650) expression |
is at higher level than that at |
roots |
Arabidopsis thaliana |
| other two genes encoding the same subunit |
are expressed in |
vegetative tissues |
Arabidopsis thaliana |
| lcy-β2 gene |
is expressed at much higher level in |
yellow fruit |
|
| OeEIL2 |
shows high expression level in |
leaf tissue |
|
| rice U-box protein genes |
are expressed in |
calli tissue |
Oryza sativa |
| β2 transcript level in red papaya fruit |
is reduced |
red papaya fruit |
|
| tobacco nectarins (NEC1, NEC4, NEC5) |
are expressed exclusively in |
nectaries that are actively secreting nectar |
Nicotiana langsdorffii × Nicotiana sanderae var. L×S8; Nicotiana tabacum |
| rice 26 kDa globulin (Glb-1) promoter |
is |
only inner endosperm-specific promoter |
Oryza sativa |
| ZmYS1 |
expression is much lower in |
leaf sheaths |
Zea mays |
| mitochondrial proteins |
show preferential expression in |
anthers and roots |
|
| OsMTP1 |
shows lower expression in |
endosperm |
Oryza sativa |
| (NRT1.12, AT3G16180) |
is expressed in |
both shoot and root |
Arabidopsis thaliana |
| OsHMA3 expression |
is high in |
root hair |
Oryza sativa |
| SlSKOR |
expression was higher in |
stele than in cortex |
Solanum lycopersicum |
| miR4407 expression |
is highest in |
stems |
Glycine max |
| weaker GUS activity |
was detected in |
anthers and glumes |
Oryza sativa |
| ZmPRP transcripts |
were found in |
xylem in the root maturation region |
Zea mays |
| FaMYB10 |
shows negligible expression levels in |
vegetative tissues (leaves, crowns, roots, runners) |
Fragaria × ananassa |
| GUS activity |
was not detected in |
seedlings, roots, stems, and leaves |
Solanum lycopersicum |
| pAGP23:GUS fusion-expressing plants |
show GUS activity in |
pollen tubes |
Arabidopsis thaliana |
| (AGP9, AT2G14890) |
is upregulated in |
pistil |
Arabidopsis thaliana |
| both pAG23:GUS and pAGP23:NLS:3GFP reporters |
were detected in |
pollen |
Arabidopsis thaliana |
| PpSFBB 2-u1–u5 and PpSFBB 2-d1–d5 |
were all specifically expressed in |
pollen, but not in pistils or leaves |
Pyrus pyrifolia |
| TcGDS transcripts |
have lower levels in |
disk flowers and leaves |
Tanacetum cinerariifolium |
| GDS promoter activity |
is primarily localized in |
parenchyma cells surrounding vascular bundles of stem |
Chrysanthemum morifolium |
| (AtNPF1.2, NPF1.2, NRT1.11, AT1G52190) expression levels in shoot |
are about 4-fold higher than |
(NRT1.12, AT3G16180) expression levels in shoot |
Arabidopsis thaliana |
| two genes orthologous to (ALMT9, AtALMT9, AT3G18440) (Aco003023.1 and Aco010725.1) |
were |
most highly expressed members of ALMT gene family in green tissue |
Ananas comosus |
| allelic expression difference between (ATSS1, SS1, AT5G24300) and (ATNS1, NS1, OVA8, AT4G17300) alleles |
was observed in |
immature ear tissue |
Zea mays |
| (AGP12, ATAGP12, AT3G13520) |
was selected for further analysis based on |
presence of transcripts in pistil tissues and absence in stamen tissues |
Arabidopsis thaliana |
| OsNRAMP5 |
shows GUS activity in |
vascular tissues of hulls |
Oryza sativa |
| OsNRAMP5 |
is also detected in |
elongation zone of roots |
Oryza sativa |
| HvGS1_2 |
is more highly expressed in |
leaf |
Hordeum vulgare |
| HvRAF transcripts |
is more abundant in |
roots |
Hordeum vulgare |
| (AtEND1, END1, AT1G32280) promoter |
is |
seed and pollen specific |
Arabidopsis thaliana |
| PtoPIN3b, 5b, and 5c |
enriched in |
leaves |
Populus tomentosa |
| (AGP7, AT5G65390) |
is downregulated in |
pistil tissues compared with pollen |
Arabidopsis thaliana |
| OsNRAMP5 |
shows higher expression in |
older leaves |
Oryza sativa |
| PtoPIN1c, PtoPIN2, and PtoPIN5a |
only expressed in |
roots |
Populus tomentosa |
| (AGP9, AT2G14890) promoter |
leads to GFP expression in |
funiculus |
Arabidopsis thaliana |
| 46 selected PtrWRKY genes |
are expressed in |
roots, stems, and leaves |
Populus trichocarpa |
| BnaGLN1.2 gene |
is more expressed in |
leaf blades than in stems |
Brassica napus |
| (AGP9, AT2G14890) |
is downregulated in |
seedlings |
Arabidopsis thaliana |
| SiARDP |
transcript levels lower in |
root |
Setaria italica |
| OsNRAMP5 |
shows clearly higher expression in |
unexpanded part of the fourth leaf |
Oryza sativa |
| OsNRAMP5 |
is mainly detected in |
maturation zone of roots |
Oryza sativa |
| (AGP9, AT2G14890) promoter |
exhibits very weak GFP expression in |
chalazal pole of ovules |
Arabidopsis thaliana |
| FISH technique |
were performed with |
whole organs |
Arabidopsis thaliana |
| HvGS1_1 |
is more highly expressed in |
stem |
Hordeum vulgare |
| (ATCSP3, CSP3, AT2G17870) |
has very low levels of expression relative to |
(ATCSP2, CSDP2, CSP2, GRP2, AT4G38680) and (ATCSP4, ATGRP2B, GRP2B, AT2G21060) |
Arabidopsis thaliana |
| AtCSP homologues |
exhibit similar gene expression pattern except |
(AtCSP1, CSDP1, CSP1, AT4G36020) |
Arabidopsis thaliana |
| (GBF3, AT2G46270) |
is preferentially expressed in |
stamens at the F 12 stage and in mature pollen |
Arabidopsis thaliana |
| two transcription factors |
were found to be preferentially expressed in |
glands |
Cannabis sativa |
| (AGP9, AT2G14890) promoter |
leads to GFP expression in |
vascular tissues of pistil transmitting tract |
Arabidopsis thaliana |
| expression in flowers and siliques |
is |
lower |
Arabidopsis thaliana |
| (AGP12, ATAGP12, AT3G13520) promoter |
guides strong GFP expression to |
chalazal pole of ovules |
Arabidopsis thaliana |
| (AGP15, ATAGP15, AT5G11740) |
is upregulated in |
pistil |
Arabidopsis thaliana |
| OsNRAMP5 |
is moderately expressed in |
expanded leaves |
Oryza sativa |
| allelic expression difference between (ATSS1, SS1, AT5G24300) and (ATNS1, NS1, OVA8, AT4G17300) alleles |
was observed in |
seedling tissue |
Zea mays |
| WER::SCM-GFP construct |
expresses SCM-GFP in |
epidermis tissue |
Arabidopsis thaliana |
| alternative oxidase 1d (AOX1D, AT1G32350) transcript level |
is not enhanced in |
shoot of (AOX1A, ATAOX1A, AtHSR3, HSR3, AT3G22370) mutants |
Arabidopsis thaliana |
| AtACBP1pro::GUS expression |
is more abundant in |
stem epidermis than in leaf epidermis |
Arabidopsis thaliana |
| Seven PtoPINs (PtoPIN1a, 1b, 1d, 3b, 5c, 8a, and 8b) |
ubiquitously expressed |
all tissues |
Populus tomentosa |
| FT expression |
is higher in |
buds than leaves |
Citrus |
| AtPDF2.6 |
is mainly expressed in |
root xylem parenchyma cells |
Arabidopsis thaliana |
| (ATHSGBP, ATRAB11B, ATRABA1D, RABA1d, AT4G18800) |
is expressed high in |
stele |
Arabidopsis thaliana |
| ZmNF-Y16 |
was not expressed in |
different maize tissues |
Zea mays |
| clusters 24 and 31 |
show |
high levels of expression in green segments |
Ananas comosus |
| (VQ20, AT3G18360) |
is specifically expressed in |
anthers |
Arabidopsis thaliana |
| GUS expression directed by 1.6 kb GluD-1 promoter |
occurs in |
inner starchy endosperm |
Oryza sativa |
| site II elements |
act to enhance |
expression levels mainly in reproductive organs |
Arabidopsis thaliana |
| HvGS1_3 |
is more highly expressed in |
grain |
Hordeum vulgare |
| J0121 enhancer trap line |
drives gene transcription in |
all xylem parenchyma (XPP) cells from elongation zone upward |
Arabidopsis thaliana |
| J0634 enhancer trap line |
drives gene transcription in |
epidermis starting at beginning of differentiation zone |
Arabidopsis thaliana |
| ZAR7 |
is mainly expressed in |
root tissue |
Zea mays |
| (AGP23, ATAGP23, AT3G57690) |
is highly downregulated in |
seedlings |
Arabidopsis thaliana |
| HvGS1_2 |
is more highly expressed in |
root |
Hordeum vulgare |
| five peroxidases |
are expressed mainly in |
roots |
Arabidopsis thaliana |
| polygalacturonases |
have expression absent in |
other tissues |
Oryza sativa |
| (ZAR1, AT3G50950) |
showed highest expression in |
root and pericarp tissues |
Zea mays |
| OsNRAMP5 |
shows moderate expression level in |
stems at the heading stage |
Oryza sativa |
| BdCSLF6 |
is expressed at low levels in |
mature leaf |
Brachypodium distachyon |
| other genes |
are also expressed in |
the same tissue |
Oryza sativa |
| polygalacturonases |
have |
eight loci with ESTs displaying >6 (AIRP3, AtAIRP3, LOG2, AT3G09770) higher expression than in seedlings |
Oryza sativa |
| ZmRCAα and ZmRCAβ transcripts |
accumulated primarily in |
leaves |
Zea mays |
| pBdTHX1::GUS |
shows GUS staining in |
parenchyma cells |
Brachypodium distachyon |
| (ATMSRB6, MSRB6, AT4G04840) |
is preferentially expressed in |
leaves and other green organs |
Arabidopsis thaliana |
| StPPI1 expression |
is higher in |
leaves |
Solanum tuberosum L. |
| Aco011916.1 and Aco015779.1 |
are |
highly expressed in green tissue |
Ananas comosus |
| (AGP1, ATAGP1, AT5G64310) promoter |
drives strong GFP expression in |
funiculus |
Arabidopsis thaliana |
| SQUAMOSA PROMOTER BINDING PROTEIN-LIKE 7 (ATSPL7, SPL7, AT5G18830) expression |
shows a relative peak in |
pollen |
Arabidopsis thaliana |
| GmIPT3 |
is mainly expressed in |
root |
Glycine max |
| GmIPT3 expression |
is highest in |
roots |
Glycine max |
| miR4407 |
is found in |
all tissues tested |
Glycine max |
| PtrMYB6 transcripts |
are more abundant in all tissues tested than |
PtrMYB126 transcripts |
Populus trichocarpa |
| lncRNAs in cluster I |
highly or specifically expressed in |
at least one embryo tissue |
Ricinus communis |
| organ |
exhibits |
transcriptome specificities |
Glycine max; Arabidopsis thaliana; Solanum lycopersicum |
| OSR flowering time genes |
show apex-specific expression |
apex tissue |
Brassica napus |
| ChCAD4 (XP_010519292.1) |
was expressed in |
both seed coat and stem |
Cleome |
| tissue marker genes |
provided consistent results |
tissue-specific expression patterns |
|
| BdTHX1 promoter |
expression pattern is similar to |
BdTHX1 expression profile |
Brachypodium distachyon |
| (AGP10, ATAGP10, AT4G09030) |
was selected for further analysis based on |
presence of transcripts in pistil tissues and absence in stamen tissues |
Arabidopsis thaliana |
| (AGP1, ATAGP1, AT5G64310) transcripts |
were not detected in |
stigmatic cells |
Arabidopsis thaliana |
| (B73, CHL6, CNX, CNX1, SIR4, AT5G20990) allele of Tsh |
is favored in |
ear tissues |
Zea mays |
| SHR::SCM-GFP line |
generates |
stele-specific SCM-GFP |
Arabidopsis thaliana |
| GUS staining in (ATLOX6, LOX6, AT1G67560) pro:ACA10-GUS |
was intense in |
xylem regions |
|
| different (ATGSTU24, GST, GSTU24, AT1G17170) isoenzymes |
are expressed in |
different tissues |
Zea mays |
| HlALMT1 expression in outer tissues of root tips |
is higher than |
HlALMT1 expression in inner tissues of root tips |
Holcus lanatus |
| 46 co-expression clusters in white tissues |
have |
positively correlated co-expression in white tissues and no correlated expression in green tissues |
Ananas comosus |
| (ATAIG1, BHLH32, TMO5, AT3G25710) promoter |
directs expression in |
developing xylem cells |
Arabidopsis thaliana |
| PAL genes |
exhibited highest transcript levels in |
fibers |
Cleome |
| RIM-CR transcription factors |
show higher expression in |
ovules than in anthers |
Arabidopsis thaliana |
| GL2:GUS seedlings |
show GUS staining in |
defined cell files of growth region at root tip |
Arabidopsis thaliana |
| MtNoa1/ (ATNOA1, ATNOS1, NOA1, NOS1, RIF1, SVR10, AT3G47450) promoter activity |
was not observed in |
nitrogen-fixing zone |
Medicago truncatula |
| PwTUA1 |
is not detected in |
roots |
Picea wilsonii |
| (CLE45, AT1G69588) |
was preferentially expressed in |
stigma in the pistil at 22°C |
Arabidopsis thaliana |
| expression dominance |
could be observed in |
a given tissue in allotetraploid cotton |
|
| G235 line |
shows H2B-GFP beginning to accumulate at |
transition domain |
Arabidopsis thaliana |
| anthocyanin fluorescence |
is exclusively localised to |
cells with yellow fluorescent nuclei |
Arabidopsis thaliana |
| some glossy genes |
was detected beyond |
tissues where (GL3, MYC6.2, AT5G41315) is expressed |
|
| V241 line |
shows H2B-Venus fluorescence in |
one–two immediate progeny of lateral root cap stem cells |
Arabidopsis thaliana |
| QC46 and mAGL42 promoters |
failed to produce |
expression specific to QC cells beyond 4 days after germination |
Arabidopsis thaliana |
| maize Glossy genes |
are largely inactive in |
seeds and roots |
Zea mays |
| 2-week-old plants |
showed no GUS signals in |
hypocotyl and upper part of primary root |
Arabidopsis thaliana |
| DOF proteins |
contribute to control of |
tissue-specific gene expression |
|
| OsNRAMP5 |
is highly expressed in |
roots |
Oryza sativa |
| OsNRAMP5 |
shows GUS activity in |
all cell types in maturation region of root |
Oryza sativa |
| Ghd7 expression |
is virtually absent in |
other tissues and preemerged immature leaf blade |
Oryza sativa |
| (ATNCED6, NCED6, AT3G24220) |
is highly expressed in |
testa |
Arabidopsis thaliana |
| TcADH1, TcADH2, TcALDH1, TcCDS, and TcGLIP transcripts |
are significantly more abundant in |
floral tissues |
Tanacetum cinerariifolium |
| pBdTHX1::GUS |
shows strong GUS staining throughout |
endosperm tissue |
Brachypodium distachyon |
| (AQC1, HPS7, TPST, AT1G08030) promoter |
directs expression in |
quiescent centre cells |
Arabidopsis thaliana |
| (GL3, MYC6.2, AT5G41315) |
was silenced in |
roots |
|
| (MIR400, AT1G32582) and (AT1G32583) expression |
is strongest in |
siliques |
Arabidopsis thaliana |
| Tsh |
demonstrates |
genotype- and tissue-specific effects on allelic expression |
Zea mays |
| apical meristem (AM) |
had more different transcripts and genes expressed only in |
this tissue |
Pinus pinaster |
| miR4407pro-GUS signal |
is localized in |
pericycle and inner cortex |
Glycine max |
| OsHMGB1 expression |
is relatively higher in |
leaves of 4-wk-old seedlings |
Oryza sativa |
| OsMTP1 |
is primarily expressed in |
root tip and lateral roots |
Oryza sativa |
| ZmRCAα transcripts |
accumulate to higher levels in |
leaves than in other tissues |
Zea mays |
| pBdTHX1::GUS |
shows GUS staining in |
immature vascular bundles |
Brachypodium distachyon |
| (ATMSRA2, MRSA2, PMSR2, AT5G07460) |
is more specifically expressed in |
roots |
Arabidopsis thaliana |
| GhnsLTPsA10 |
which was predominantly expressed in |
pathogen-infected roots |
Gossypium hirsutum |
| OsMTP1 level in roots |
is significantly higher in |
(HAP1, MAGO, MEE63, AT1G02140) accessions |
Oryza sativa |
| OsHMA5 |
is detected only in |
central cylinder of roots (pericycle and inner tissues) |
Oryza sativa |
| (CLEL 9, GLV2, RGF9, AT5G64770) promoter |
drives |
expression of (MIR399, MIR399F, AT2G34208) |
Arabidopsis thaliana |
| (PIP2;5, PIP2D, AT3G54820) |
exhibited high and specific expression in |
epidermal (L1) cells |
Arabidopsis thaliana |
| GUS signals |
are detected uniquely in |
leaf vascular bundles |
Oryza sativa |
| (AtNPF1.2, NPF1.2, NRT1.11, AT1G52190) pro:GUS transgenic plants |
showed GUS staining mainly in |
major veins |
Arabidopsis thaliana |
| (NRT1.12, AT3G16180) expression levels in petiole and midrib |
are approximately 4 times higher than |
(NRT1.12, AT3G16180) expression levels in lamina |
Arabidopsis thaliana |
| parsley UBI (ubiquitin) promoter |
allows the expression of transgenes in |
buds, roots, stems, flowers, and seeds |
Arabidopsis thaliana |
| BpMADS11 |
is expressed at lowest level in |
mature stems |
Betula pendula |
| (AtNPF1.2, NPF1.2, NRT1.11, AT1G52190) expression levels in petiole and midrib |
are approximately 30 times higher than |
(AtNPF1.2, NPF1.2, NRT1.11, AT1G52190) expression levels in lamina |
Arabidopsis thaliana |
| tissue-specific expression of DT-A in GLABRA2-positive cells |
was used to test |
specificity in atrichoblast file of epidermis |
Arabidopsis thaliana |
| OsOSC10 |
exhibited high-expression level in |
lemma and palea |
Oryza sativa |
| BpMADS11 |
is expressed in |
young leaves |
Betula pendula |
| OsMTP1 |
is primarily expressed in |
roots, aleurone and embryo |
Oryza sativa |
| OsGlb-1 |
is primarily expressed in |
endosperm |
Oryza sativa |
| genes involved in various biological processes |
were found to be specifically expressed in |
different tissues |
Cicer arietinum |
| single gene representing B (nucleotide-binding) subunit of V-ATPase (Aco015226.1) |
was among |
most highly expressed transcripts in green CAM-performing sections of pineapple leaf |
Ananas comosus |
| group of genes with ubiquitous expression |
have |
high expression in at least one tissue |
Pinus pinaster |
| XhABI5A |
was expressed at very low levels in |
leaf desiccation series |
Xerophyta humilis |
| (RAE1, AT5G01720) homolog 1 (RAH1, AT5G27920) |
is preferentially expressed in |
root caps and vascular tissues |
Arabidopsis thaliana |
| XhFUS3 and XhLEC2 transcripts |
had normalised read counts in leaves |
extremely low (mean count < 6) across all RWCs |
Xerophyta humilis |
| SlSKOR |
is preferentially expressed in |
root stele |
Solanum lycopersicum |
| Aco005379.1 |
is |
highly expressed in green tissue |
Ananas comosus |
| GUS staining in fully unfolded leaves |
was mainly restricted to |
petiolule and major veins of each leaflet |
Lotus japonicus |
| (DHFR-TS3, DRTS3, AT2G21550) |
is specifically expressed in |
meristematic cells of the shoot apex |
Arabidopsis thaliana |
| guard cell data set produced by Wang et al. |
shared |
only 359 guard cell-enriched transcripts with Yang et al. |
Arabidopsis thaliana |
| CHS7 and CHS8 genes |
show overall expression pattern that varied in |
different tissues |
|
| (B73, CHL6, CNX, CNX1, SIR4, AT5G20990) Ptf allele |
is always higher in |
leaves |
Zea mays |
| GRMZM2G104789 (AtMYB36, MYB36, AT5G57620) |
was induced in |
roots |
|
| StPPI1 expression |
is higher in |
proliferative regions (shoot apex and flower buds) |
Solanum tuberosum L. |
| several laccases |
show apparent redundancy of gene expression patterns across |
wide variety of tissues, lignified and non-lignified |
Arabidopsis thaliana |
| regulatory genes |
usually have |
localized expression |
Pinus pinaster |
| 343 lncRNAs with fourfold or greater transcription levels in endosperm compared with embryo |
identified |
endosperm-preferred lncRNAs |
Ricinus communis |
| V311 line expression |
is expressed in |
pericycle layer |
Arabidopsis thaliana |
| ChCCR1 |
has |
high expression in the seed coat |
Cleome |
| Arabidopsis thaliana Acyl-CoA-Binding Protein 1 (ACBP, ACBP1, AtACBP1, AT5G53470) |
is highly expressed in |
top and bottom of stems |
Arabidopsis thaliana |
| (AGP4, ATAGP4, JAGGER, AT5G10430) |
was selected for further analysis based on |
presence of transcripts in pistil tissues and absence in stamen tissues |
Arabidopsis thaliana |
| (AGP26, ATAGP26, AT2G47930) |
is upregulated in |
pistils compared with pollen |
Arabidopsis thaliana |
| (AtRABA1e, RABA1e, AT4G18430) |
is mainly expressed in |
roots |
Arabidopsis thaliana |
| (LAC7, AT3G09220) |
is uniquely expressed in |
hydathodes and root hairs |
Arabidopsis thaliana |
| each subunit of membrane-integral sector of V-ATPase |
has |
higher expression in green tissues than white leaf base |
Ananas comosus |
| (FLZ10, AT5G11460) promoter:GUS reporter line |
shows most activity in |
stelar region of the shoot and root |
Arabidopsis thaliana |
| GUS activity |
was detected in |
root epidermis, cortex, stele, root cap |
Oryza sativa |
| OsMTP1 |
is expressed in |
basal stem |
Oryza sativa |
| OsMTP1 |
is expressed in |
leaf blade |
Oryza sativa |
| ARABIDOPSIS PROFILIN 2 (AtPRF2, PFN2, PRF2, PRO2, AT4G29350) |
is expressed in |
vegetative tissues |
Arabidopsis thaliana |
| tissue type |
is more important to |
allelic variability |
Zea mays |
| ZmNF-YC17 |
was not expressed in |
different maize tissues |
Zea mays |
| highest expressed copy of nine glycolysis and gluconeogenesis enzymes |
shows |
stronger expression in photosynthetic green tissue (segments 4–6) than non-photosynthetic white base (segments 1–3) |
Ananas comosus |
| highest expressed copy of glucose-6-phosphate 1-epimerase, phosphoglucomutase, and UTP-glucose-1-phosphate uridylyltransferase |
shows |
strong diurnal expression with expression mainly in green leaf segments (segment 4–6) |
Ananas comosus |
| actualization of the database |
comprises |
gene expression localization |
Pinus pinaster |
| all three TaNAC77 homoeologs |
were preferentially expressed in |
endosperm of Chinese Spring |
Triticum aestivum |
| genetic background |
may influence |
tissue specificity of expression bias |
Zea mays |
| increasing (AtSWEET17, SWEET17, AT4G15920) expression towards leaf tip |
is also observed in |
rice and maize leaves based on leaf segment RNA-seq data |
Oryza sativa; Zea mays |
| expression of these kinds of transcripts |
is not generalized |
across tissues |
Pinus pinaster |
| (ATNCED6, NCED6, AT3G24220) |
is highly expressed in |
endosperm |
Arabidopsis thaliana |
| BdTHX1 and BdCSLF6 |
have nearly equal expression in |
elongating internodes and endosperm tissues |
Brachypodium distachyon |
| (AXS2, AT1G08200) |
shows higher expression in |
roots and dark-grown seedlings |
Arabidopsis thaliana |
| endosperm samples |
had the lowest number of |
genes expressed (17,323 on average) |
Zea mays |
| (MIR395, MIR395F, AT1G69797) levels |
are lower in |
leaves, panicles, and culms |
Oryza sativa |
| Q-5A |
predominantly expressed in |
developing spikes |
Triticum aestivum |
| V251 line |
shows H2B-Venus accumulation in |
cortical layer of root apical meristem |
Arabidopsis thaliana |
| V151 line |
shows fluorescent protein accumulation in |
pericycle layer |
Arabidopsis thaliana |
| glossy genes and photosynthesis-related genes |
were typically expressed at higher levels in |
young or newly emerged leaves across vegetative stages, leaf bases, silks, meiotic tassels, and anthers |
Zea mays |
| S. foetida homolog |
showed preferential expression in |
seed tissue |
Steculia foetida |
| (AST68, SULTR2;1, AT5G10180) |
was expressed at similar levels in |
VN and VS |
|
| KINASE-INDEPENDENT 17 (AtKIN17, KIN17, AT1G55460) |
is not expressed in |
main part of the root |
Arabidopsis thaliana |
| xylem parenchyma |
is one of the sites of |
SULTR2;1 expression |
|
| pEPP : CKX2-72 line |
shows no expression in |
shoot tissue |
Hordeum vulgare |
| pBdTHX1::GUS |
is expressed in |
young leaves |
Brachypodium distachyon |
| HvTDF1 expression |
was rarely detected in later stages and not in |
other organs assessed |
Hordeum vulgare |
| (ATMSRB8, MSRB8, AT4G21840) |
is more specifically expressed in |
roots |
Arabidopsis thaliana |
| Ghd7 expression |
is mainly detected in |
emerged leaf blade |
Oryza sativa |
| 28 gene co-expression clusters with positive co-expression in green tissue |
show |
no correlated expression in white tissue |
Ananas comosus |
| two of these genes |
were also expressed in |
rm |
Pinus pinaster |
| (FLZ6, AT1G78020) promoter:GUS reporter line |
shows no activity in |
roots |
Arabidopsis thaliana |
| (ACP4, AtACP4, AT4G25050) |
is specifically present in |
leaf tissue |
Arabidopsis thaliana |
| ZmRCAα and ZmRCAβ transcripts |
accumulated to lesser extent in |
stems, tassel spikelets, and immature ears |
Zea mays |
| BdCSLF6 |
is highly expressed in |
elongating leaves |
Brachypodium distachyon |
| GUS product |
shows no accumulation in |
pavement cells |
Arabidopsis thaliana |
| BdCSLF6 |
is expressed at low levels in |
older stem tissues |
Brachypodium distachyon |
| BdXTH8 and BdTHX2 |
have higher expression in |
elongating internodes and elongating leaf tissue |
Brachypodium distachyon |
| duplicated genes |
appeared to be expressed in |
different tissues |
Oryza sativa |
| genes altered in expression in young and mature (MEX1, RCP1, AT5G17520) leaves |
were |
only a small proportion |
|
| expression of three aquaporin genes in Physcomitrella patens |
is restricted to |
gametophore tissue |
Physcomitrella patens |
| LOC_Os04g45180 |
suggests |
wide sporophytic expression |
Oryza sativa |
| (ATMSRB5, MSRB5, AT4G04830) |
is more specifically expressed in |
roots |
Arabidopsis thaliana |
| mesophyll marker gene expression |
indicated that mesophyll/epidermis mRNA constituted a major part of |
total mRNA in MN and VN |
|
| (ATMSRB9, MSRB9, AT4G21850) |
is more specifically expressed in |
roots |
Arabidopsis thaliana |
| OsABCG18 |
is expressed in |
phloem and xylem cells of stems and leaf midribs |
Oryza sativa |
| (DHFR-TS3, DRTS3, AT2G21550) |
is specifically expressed in |
columella and lateral root cap |
Arabidopsis thaliana |
| bHLH6 expression |
is higher in |
leaves |
Oryza sativa |
| S. foetida homolog |
had |
27 occurrences in leaf tissue |
Steculia foetida |
| ProOsMTP1:GFP transgenic line |
shows strong GFP signal in |
primary root tip |
Oryza sativa |
| V241 line |
marks |
most of stem cells surrounding stem cell niche |
Arabidopsis thaliana |
| PHS9 gene |
is specifically expressed in |
embryo |
Oryza sativa |
| BnaA09.GSL5 and BnaC09.GSL5 |
had |
highest expression levels in the root tissues |
Brassica napus |
| GUS signals |
were restricted to |
phloem side of vascular tissues |
Arabidopsis thaliana |
| WPRP1 transcripts |
were detected in |
rapidly dividing tissues in shoots |
Triticum aestivum |
| pollen-expressed pectate lyase loci |
share sequences that distinguish them from |
predominantly sporophytically expressed loci |
Oryza sativa |
| (FLZ6, AT1G78020) promoter:GUS reporter line |
shows GUS activity in |
cotyledons |
Arabidopsis thaliana |
| V431 line |
shows H2B-Venus fluorescence localised to |
root cap |
Arabidopsis thaliana |
| mAGL42 promoter |
was tested for |
stem cell niche-specific expression |
Arabidopsis thaliana |
| lncRNAs in cluster II |
specifically expressed in |
endosperm |
Ricinus communis |
| OSR flowering time genes |
show significantly different pattern of tissue-specific expression from |
genome-wide level |
Brassica napus |
| (AtMYB6, MYB6, AT4G09460) |
shows higher expression in |
young leaves |
Populus tomentosa |
| expression dominance |
is not observed at |
genome-wide level among 35 different tissues in allotetraploid cotton |
|
| XP_010522015.1 (ChC4H1) transcript levels |
were much the highest in |
stem (fiber) and developing seeds |
Cleome |
| TcGDS transcripts |
are trace in |
ray florets |
Tanacetum cinerariifolium |
| (AtNPF1.2, NPF1.2, NRT1.11, AT1G52190) |
is mainly expressed in |
shoot |
Arabidopsis thaliana |
| SlSKOR |
transcript levels were checked in |
other plant tissues |
Solanum lycopersicum |
| (PGA6, WUS, WUS1, AT2G17950) response genes with reduced expression |
are mainly expressed in |
leaves |
Arabidopsis thaliana |
| lncRNAs in cluster I |
lowly expressed in |
endosperm tissue |
Ricinus communis |
| 11 NLR(-like) genes in the 857-kb MH-I region |
had lower expression levels in |
other tissues |
Oryza sativa |
| AtHSFA7b |
is detected in |
sepals |
Arabidopsis thaliana |
| regulatory genes |
may be activated only in |
specific tissues |
Hordeum vulgare |
| V111 line |
shows Venus accumulation absent in |
apical meristem |
Arabidopsis thaliana |
| PtrMYB6 |
is expressed preferentially in |
leaves and roots |
Populus trichocarpa |
| 76.69% of the transcribed non-TE genes |
were expressed throughout |
the plant, including panicle, leaf, and root |
Oryza sativa |
| Co2::SCM-GFP construct |
produces SCM-GFP in |
cortex |
Arabidopsis thaliana |
| (ACAM-3, CAM3, AT3G56800) |
could not be detected in |
floral stocks |
Arabidopsis thaliana |
| V251 line |
shows fluorescence stopping before or at |
transition domain |
Arabidopsis thaliana |
| V431 line |
shows Venus accumulation in |
columella cells |
Arabidopsis thaliana |
| V201 line |
shows H2B-Venus accumulation in |
nuclei of vascular initial cells |
Arabidopsis thaliana |
| (DEL1, E2FE, E2L3, AT3G48160) and (APC11, ZGY1, ZYG1, AT3G05870) promoters |
failed to produce |
meristem-specific reporter line |
Arabidopsis thaliana |
| (COBL9, DER9, MRH4, SHV2, AT5G49270) promoter |
directs expression in |
elongating trichoblast cells |
Arabidopsis thaliana |
| OSR flowering time genes |
show leaf-specific expression |
leaf tissue |
Brassica napus |
| VvRabGDI1 |
was expressed in |
buds or berries at pre-véraison |
Vitis vinifera |
| OsKCH1 expression |
was found highest in |
young roots, young leaves, young flowers, and flowers post-pollination |
Oryza sativa |
| patterns in young (MEX1, RCP1, AT5G17520) leaves transcriptome |
were not consistent with |
patterns in mature (MEX1, RCP1, AT5G17520) leaves transcriptome |
|
| VvK1.2 signal |
was mainly located in |
nucellus |
Vitis vinifera |