| (ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) |
did not affect |
(MED8, AT2G03070) protein expression |
Phaeodactylum tricornutum |
| BZR1-YFP protein level |
is reduced in |
(ARP6, ATARP6, ESD1, SUF3, AT3G33520) er-119 (ATXR3, SDG2, AT4G15180) mutant |
Arabidopsis thaliana |
| C05 and C14 proteins |
accumulated in |
inclusion bodies after IPTG induction under standard conditions |
Escherichia coli |
| GFP-CER-ZA construct |
was expressed in |
Nicotiana benthamiana leaves |
Nicotiana benthamiana |
| YN-TGB3 construction with HA tag |
co-delivered with |
bZIP60U-YC and CMV 2b |
Nicotiana benthamiana |
| YFP-SDE2 AA |
is detected at |
molecular weight c. 72 kDa |
Arabidopsis thaliana |
| oastlAB C +/− mutant |
shows 50% decrease in |
O-acetylserine(thiol)lyase isoform C protein amount |
Arabidopsis thaliana |
| zmbell10-1 mutants |
have substantially lower |
ZmBELL10 protein levels |
Zea mays L. |
| (MED8, AT2G03070) gene editing |
did not affect |
(ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) protein expression |
Phaeodactylum tricornutum |
| A2QK-7 transgenic line |
produced high levels of |
(ATHSFA2, HSFA2, AT2G26150) protein |
Arabidopsis thaliana |
| A2QK-10 transgenic line |
produced high levels of |
(ATHSFA2, HSFA2, AT2G26150) protein |
Arabidopsis thaliana |
| rNAD-ME2 |
had highest level of |
α-NAD-ME protein |
Kalanchoe fedtschenkoi |
| plant viruses |
are |
powerful tools in which to express heterologous proteins |
|
| level of (OHP, OHP1, PDE335, AT5G02120) |
is low in |
green leaves |
Arabidopsis thaliana |
| Row1::GFP |
is detected in |
total lysate |
Ustilago maydis |
| protein processing |
hampers |
production of recombinant proteins in plants |
Nicotiana benthamiana |
| WHY1-HA protein |
increases to peak at |
week 10 of plant development |
Arabidopsis thaliana |
| (BZR1, AT1G75080) protein content in (ARP6, ATARP6, ESD1, SUF3, AT3G33520) er-119 (ATXR3, SDG2, AT4G15180) SDG2pro -YFP |
is only slightly decreased in |
(ARP6, ATARP6, ESD1, SUF3, AT3G33520) er-119 (ATXR3, SDG2, AT4G15180) SDG2pro BZR1-YFP |
Arabidopsis thaliana |
| WHY1-HA protein |
is detected at |
week 6 of plant development |
Arabidopsis thaliana |
| Total proteomic analysis using tandem mass tags (TMT) |
revealed differential abundance of |
many proteins in (AtMYB1, MYB1, SRM1, AT3G09230) compared with HJ2 |
Oryza sativa |
| (MED8, AT2G03070) protein content in the mhsf3/ -GFP line |
was similar to |
MED8-GFP line |
Phaeodactylum tricornutum |
| ALMT-GFP fusion protein of 2,106 bp |
is |
larger size construct for viral vector testing |
Triticum aestivum |
| (AHA1, HA1, OST2, PMA, AT2G18960) and (AHA2, AtHA2, HA2, PMA2, AT4G30190) |
are |
two highly expressed proteins |
Arabidopsis thaliana |
| Agrobacterium-mediated transient gene expression system |
was applied to |
set out protein expression in cucumber |
Cucumis sativus |
| deletion of Slr1064 |
did not affect |
amount of Gap2 protein under autotrophic and mixotrophic conditions |
Synechocystis sp. PCC 6803 |
| YFP-SDE2 transgenic plants |
express |
SILENCING DEFECTIVE 2 (SDE2) |
Arabidopsis thaliana |
| deletion of Slr1064 |
does not affect total abundance of |
Gap2 protein |
Synechocystis sp. PCC 6803 |
| rhd3-8 mutant |
lacks detectable |
(GOM8, RHD3, AT3G13870) protein |
Arabidopsis thaliana |
| expression of full-length YFP-tagged (ATCNGC2, CNGC2, DND1, AT5G15410) (ATCNGC4, CNGC4, DND2, HLM1, AT5G54250) and (ATCNGC11, CNGC11, AT2G46440) /12 |
is very comparable |
across constructs |
Nicotiana benthamiana |
| oastlBC A +/− mutant |
shows gene dose effect on |
protein and activity levels |
Arabidopsis thaliana |
| cRNAs encoding the samples mentioned previously |
were co-injected in |
Xenopus oocytes |
Xenopus laevis |
| A2QK-12 transgenic line |
produced low levels of |
(ATHSFA2, HSFA2, AT2G26150) protein |
Arabidopsis thaliana |
| full length Bg_9562 |
is expressed in |
R. solanacearum (F1C1 + Bg_9562) |
Solanum lycopersicum |
| C06 and C15 proteins |
could be natively extracted as |
soluble proteins |
Escherichia coli |
| SRN1 H63A/H114A/ΔSP protein |
was isolated as |
catalytically dead control |
Pichia pastoris |
| synthetic OSC10 gene (SnOSC10) |
was created and expressed in |
yeast cells |
Pichia pastoris |
| A1AT expression |
indicates |
full-length A1AT |
|
| silencing NlVg |
decreased |
level of NlVgC |
|
| Strep A1AT |
was expressed in |
Nicotiana benthamiana wild type |
Nicotiana benthamiana |
| three transgenic lines |
had considerably greater |
(ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) protein levels |
Phaeodactylum tricornutum |
| (LIP2, LIP2p1, AT4G31050) RNAi plants |
show very low |
(LIP2, LIP2p1, AT4G31050) contents |
Arabidopsis thaliana |
| fluorescent marker proteins |
are expressed at high levels within |
1 week |
|
| Ory s 2 translated products |
abundance supported by |
proteome data |
Oryza sativa |
| Geminivirus vectors |
have been developed in recent years for |
heterologous protein expression |
|
| C-terminal YFP fusions of RPP1-like Ler R2, R3, R4, R8 genomic constructs, and ATR1-δ51 Hpa Gw |
were generated for |
Agrobacterium tumefaciens infiltration of tobacco leaves |
Arabidopsis thaliana; Hyaloperonospora arabidopsidis |
| (BAM1, AT5G65700) and (BAM3, AT4G20270) |
were expressed in |
Escherichia coli |
Escherichia coli |
| N. lugens-secreted mucin-like protein (NlMLP) |
is highly expressed in |
salivary glands |
Nilaparvata lugens |
| BSMV system |
has been used for |
virus-mediated overexpression (VOX) of a small protein such as a fungal toxin (ToxA, 534-bp cDNA, encoding a protein of 19.7 kD) |
|
| (AHA1, HA1, OST2, PMA, AT2G18960) YCE and YNE (ATDDM1, CHA1, CHR01, CHR1, DDM1, SOM1, SOM4, AT5G66750) constructs |
were transiently expressed in |
Nicotiana benthamiana leaves |
Nicotiana benthamiana |
| TrxBC34S protein |
was detected in |
SBC34S cells |
Synechocystis |
| expression in Escherichia coli BL21(DE3) cells |
was induced by addition of |
isopropyl-β-D-thiogalactoside (IPTG) |
Escherichia coli |
| HXK family proteins |
were subcloned as |
C-terminal GFP fusion proteins |
|
| artificial AVR variants |
were more abundant compared to |
natural AVR |
Nicotiana benthamiana |
| YCE (ATSYP22, ATVAM3, SGR3, SYP22, VAM3, AT5G46860) and YNE (ATVAMP711, VAMP711, AT4G32150) constructs |
were transiently expressed in |
Nicotiana benthamiana leaves |
Nicotiana benthamiana |
| binary vector encoding full-length A1AT |
was used to stably transform |
wild-type (Columbia-0 [Col-0]), (ATHEX2, HEXO1, AT3G55260) (ATHEX1, HEXO3, AT1G65590) and plants |
Arabidopsis thaliana |
| wild-type Kalanchoe fedtschenkoi |
possessed |
clear band of (PPDK, AT4G15530) protein |
Kalanchoe fedtschenkoi |
| NlMLP protein |
was detected in leaves infected by strains in |
OD 0.01 or over |
Nicotiana benthamiana |
| barley HvCslJ gene |
was expressed in |
heterologous host N. benthamiana |
Nicotiana benthamiana |
| MSI1:GFP fusion protein |
expressed in |
MSI1:GFP transgenic plants |
|
| INP1-YFP expressed from the (ARLIM15, ATDMC1, DMC1, AT3G22880) promoter |
exhibited much stronger fluorescence and had a very similar pattern of protein localization at the tetrad stage compared to |
(INP1, AT4G22600) -YFP driven by the native promoter |
|
| TrxB mutant version |
was properly expressed in |
SBC34S cells |
Synechocystis |
| pTaNAC69–CELD plasmid |
contains |
TaNAC69-1 coding region |
|
| CP106 AVR |
was allowed to accumulate prior to |
Rx1 expression |
Nicotiana benthamiana |
| plant viral-based transient expression system |
was used for |
recombinant expression of human A1AT |
|
| T-DNA insertion studies (136 reporting protein abundance) |
80% showed |
no protein expression |
Arabidopsis thaliana |
| 6xHis tag |
was detected in |
TrxBC34S protein |
Synechocystis |
| ZmRCAα and ZmRCAβ |
do encode |
(RCA, AT2G39730) proteins |
Zea mays |
| FLAG-tagged full-length (ADO1, FKL2, LKP1, ZTL, AT5G57360) |
can be expressed in |
HEK293T cells |
Homo sapiens |
| recombinant protein encoded by (ATCAD7, CAD7, CHR, ELI3, ELI3-1, AT4G37980) |
expressed as |
C-terminal His-tagged protein |
Escherichia coli |
| H3-H4 construct |
accumulated to |
lower levels in the cell than the complete CC |
Nicotiana benthamiana |
| (ATCCS, AtHMP03, CCS, AT1G12520) mutant line |
was the only line where |
(AtSOD1, CSD1, SOD1, AT1G08830) and (AtSOD2, CSD2, CZSOD2, SOD2, AT2G28190) expression affected |
Arabidopsis thaliana |
| (ATPUB9, PUB9, AT3G07360) |
is expressed in |
nearly all tissue types except leaves |
Arabidopsis thaliana |
| (ADG1, APS1, AT5G48300) protein |
was confirmed to be present in |
lines carrying the (ADG1, APS1, AT5G48300) construct |
Arabidopsis thaliana |
| T-DNA insertion studies (136 reporting protein abundance) |
one in five showed |
no effect on or reduced protein abundance or truncated protein product |
Arabidopsis thaliana |
| Trx-2-pET23b plasmid |
was transformed into |
Escherichia coli (BLH9, BLR, HB-6, LSN, PNY, RPL, VAN, AT5G02030) (DE3)pLysS |
Escherichia coli |
| two rNAD-ME lines |
displayed |
substantial reductions in the α-subunit |
Kalanchoë fedtschenkoi |
| four-RNA system |
allows |
expression of two different proteins in planta |
|
| AS2-YFP accumulation |
continues to rise during |
48 h incubation |
Arabidopsis thaliana |
| (FAD4, FADA, AT4G27030) |
rapidly diminished after being highly abundant at |
8 h post-induction |
Saccharomyces cerevisiae |
| pMRR13 plants |
have |
the highest level GFP accumulation (42% TSP) in leaves |
|
| Diffuse INP1-YFP fluorescence |
first appears in |
MMC |
|
| MMC prior to cytokinesis |
shows |
low levels of diffuse YFP fluorescence |
|
| reduced incidence of pollen tube phenotypes upon co-expression of PI4Kβ1:EYFP and PIP5K5:CFP K497A |
was not due to |
low expression of either construct |
|
| dCRY of Drosophila |
co-expressed in |
HEK293 cells |
Drosophila melanogaster |
| PrrnLT7g10 |
yields |
high levels of NPTII (23%, pHK40) |
|
| protein levels of PM3A HR -β, -γ, and -δ |
were similar to |
original PM3A HR |
Nicotiana benthamiana |
| gfp-PEL3 fusion protein |
is expressed in |
pel3-11 trichomes |
Arabidopsis thaliana |
| 6xHis tag |
was detected exclusively in |
SBC34S strain |
Synechocystis |
| Western blot analysis |
showed |
efficient heterologous expression of all proteins |
Saccharomyces cerevisiae |
| Arabidopsis thaliana hypocotyl cells |
accumulate |
eGFP fusion of (LTI6b, RCI2B, AT3G05890) ( –eGFP) |
Arabidopsis thaliana |
| ELONGATED HYPOCOTYL 5 (HY5, TED 5, AT5G11260) |
coding sequence was PCR-amplified and cloned into |
pDEST15 vector |
|
| cell-free expression |
can be |
automated |
|
| (ATCBL1, CBL1, SCABP5, AT4G17615) |
cloned into |
pGEX4T-1 vector |
|
| transplastomic pMRR20 and pMRR21 leaves |
accumulated |
relatively low (1% total soluble protein [TSP]) and high levels (9.1% TSP) of NPTII |
|
| GFP in the roots accumulated to very low levels, 0.14% TSP |
is similar to |
root expression of the pAI4 construct (0.13% TSP) |
|
| pYES2-BRI1:HA |
is used for expressing |
BRASSINOSTEROID INSENSITIVE 1 (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) |
|
| Arabidopsis |
has |
five cytoplasmic (HSP70, AT4G16660) forms |
Arabidopsis thaliana |
| CP106 AVR |
is less abundant in |
plants without Rx1 |
Nicotiana benthamiana |
| myxothiazol (Myxo) treatment |
slightly decreased |
chloroplast AtpC amount |
|
| transplastomic pMRR20 and pMRR21 leaves |
accumulated |
comparably high levels of GFP accumulation from the second ORF, 24% and 31% TSP, respectively |
|
| recombinant Arabidopsis farnesylcysteine lyase (FCLY, AT5G63910) |
is expressed in |
Spodoptera frugiperda (Sf9) cells |
Spodoptera frugiperda |
| all constructs |
accumulated |
ZED1-HA protein |
Arabidopsis thaliana |
| Agrobacterium-based in planta expression |
often results in |
uncontrolled overproduction of proteins |
|
| GFP in the roots |
accumulated to |
very low levels, 0.14% TSP |
|
| E. coli BL21(DE3)RIL culture |
induced with |
1 mM IPTG |
Escherichia coli |
| NLR protein (RPP7, AT1G58602) |
co-expressed with |
immune activating allele of RPW8 protein |
|
| protein accumulation from the second ORF |
is independent from |
the first ORF |
|
| myxothiazol (Myxo) treatment |
did not consistently change |
(ATPUMP1, ATUCP1, PUMP1, UCP, UCP1, AT3G54110) amount |
|
| pYFP::MYC1 vector |
allows expression of |
VvMYC1 and Yellow Fluorescent Protein (YFP) fusion protein |
|
| neo gene expressed from L T7g10 leader |
yields |
high levels of recombinant protein |
|
| acs2-2 RR fruits |
show fourfold lower |
(ACS2, AT-ACC2, AT1G01480) protein level |
Solanum lycopersicum |
| expression of marker proteins |
increases over |
time |
Nicotiana tabacum; Lilium |
| expression of membrane proteins in their native environment |
should lead to |
active transporters |
|
| pONAC131–CELD plasmid |
contains |
ONAC131 coding region |
|
| reduced incidence of pollen tube phenotypes upon co-expression of PI4Kβ1:EYFP K864A and PIP5K5:mCherry |
was not due to |
low expression of either construct |
Nicotiana tabacum |
| CP106 AVR protein |
remained undetected in |
Rx1 plants |
Nicotiana benthamiana |
| Nicotiana benthamiana |
is used for |
transient co-expression assays |
Nicotiana benthamiana |
| exchange of resistance-increasing and resistance-reducing residues |
did not affect |
protein abundance |
Nicotiana benthamiana |
| Strep-tagged (AtCPK21, CPK21, AT4G04720) |
is expressed in |
Arabidopsis thaliana |
Arabidopsis thaliana |
| (anac021, ANAC022, NAC1, AT1G56010) protein levels |
were increased in |
NAC1-OE hairy roots |
Salvia miltiorrhiza |
| full-length PSRP7 polyprotein |
appears to be a major species in |
Setaria |
Setaria viridis |
| shared property of five AVRPM3 A2/F2 variants |
is |
overabundance |
Nicotiana benthamiana |
| myc:PDX proteins |
are confirmed to be expressed in |
respective transgenic backgrounds |
Arabidopsis thaliana |
| co-expression experiment |
was repeated in |
onion epidermal cells by transient particle bombardment assays |
Allium cepa |
| full-length PSRP7 polyprotein in Setaria |
differs from that reported for |
Chlamydomonas |
Setaria viridis; Chlamydomonas |
| Rx1 plants constitutively expressing Rx1 agroinfiltrated with Dex::CP106 AVR construct |
only trace levels of CP were detected upon |
Dex/estradiol application |
Nicotiana benthamiana |
| Gh_A10G2048 overexpression in Arabidopsis |
significantly increases |
nsLTP protein content |
Arabidopsis thaliana |
| coding region of ZmMYB138 |
was subcloned into |
pGADT7 vector |
Zea mays |
| 12 h of 4°C treatment |
drastically inhibits |
(112A-2A, EMB30, GN, GNOM, MIZ2, VAN7, AT1G13980) expression |
Arabidopsis thaliana |
| antimycin A (AA) treatment |
resulted in variable changes in |
(ATPUMP1, ATUCP1, PUMP1, UCP, UCP1, AT3G54110) amount |
|
| CP106 AVR |
did accumulate in presence of |
Rx1-NES or Rx1-NLS or in combination with Rx1-NES + Rx1-NLS |
Nicotiana benthamiana |
| BnaNAC60 and BnaNAC60ΔTM |
were transiently expressed in |
oilseed rape protoplasts |
Brassica napus |
| oligomycin (OLIGO) treatment for 12 h |
dramatically increased |
chloroplast AtpC subunit amount |
|
| DpCRYs of Monarch butterfly |
co-expressed in |
HEK293 cells |
Danaus plexippus |
| casein kinase 2 (CK2) |
is |
ubiquitous kinase |
|
| L116Y variant |
had |
highest protein level |
Nicotiana benthamiana |
| PM3A HR -α |
was less abundant |
protein abundance |
Nicotiana benthamiana |
| Nicotiana benthamiana |
remains an excellent heterologous expression system to study proteins from |
various organisms (plants, microbes and animals) |
Nicotiana benthamiana |
| proteomic approach in plants |
has been employed to study |
alterations in cellular protein content |
|
| different sensitivity to heat stress |
explains |
different proteomes in roots versus leaves, grains, or fruits |
|
| (ATVHA-C, DET3, AT1G12840) protein tagged with 3× HA |
was transiently expressed in |
Nicotiana benthamiana leaves by agroinfiltration |
Nicotiana benthamiana |
| OsMTD2-MYC and SPL11-HA fusion proteins |
were transiently co-expressed in |
tobacco leaves by agroinfiltration |
Nicotiana tabacum |
| entire FLU protein |
could not be expressed in |
soluble form |
|
| cell-free expression of plastidic transporters |
in the presence of added detergents and lipids yields |
highly active transporter proteins |
|
| EGFP and EGFP-OsPIP1;3 fusion protein |
was properly expressed within |
cells |
Homo sapiens |
| abundance of amino acid biosynthetic enzymes |
is dynamically altered |
(PCK2, PEPCK, AT5G65690) mutant |
|
| GFP in the leaves of plants in this study |
was |
>10% of TSP |
|
| region α |
contributes to |
protein abundance |
Nicotiana benthamiana |
| chimeric phS:yfp gene |
allows for expression of |
fusion protein with C terminus of pherophorin-S fused to yellow fluorescent protein (YFP, mVenus) |
Volvox carteri |
| 40 independent transgenic rice lines |
were selected for expression of |
GluA2 or mGluA2 |
Oryza sativa |
| BFA res. line |
retains |
both expression and subcellular localization of (112A-2A, EMB30, GN, GNOM, MIZ2, VAN7, AT1G13980) after cold treatment |
Arabidopsis thaliana |
| transient transformation of plant tissues |
generates |
recombinant proteins |
|
| SlDXS1 and SlDXS2 sequences without transit peptide |
cloned into |
pQE60 expression vector |
|
| mislocalized Rx1 variants alone and in combination |
permit |
CP accumulation |
Nicotiana benthamiana |
| fluorescence protein-tagged ethylene receptors |
is detectable in |
Agrobacterium-infiltrated tobacco leaf cells |
Nicotiana tabacum |
| YFP–FIS1B Δ166–167 |
was expressed via |
35S promoter-driven construct |
Nicotiana tabacum |
| myxothiazol (MYXO) treatment in three independent experiments |
consistently reduced |
(ATPUMP1, ATUCP1, PUMP1, UCP, UCP1, AT3G54110) amount in alternative oxidase (AOX) overexpressor and knockdown plants |
|
| pGEX–5X-1 with Sal I – Not I fragments of PX-1 |
yields |
GST–PX-1 |
|
| (ATHAK5, HAK5, AT4G13420) |
was not functionally expressed in |
yeast |
Arabidopsis thaliana |
| 24 peach genes |
encode |
small GTPases |
Prunus persica |
| SCP1:gfp plants |
have strikingly low GFP protein levels of |
0.02–0.06% of total soluble proteins |
Oryza sativa |
| (ABA1, ATABA1, ATZEP, IBS3, LOS6, NPQ2, ZEP, AT5G67030) protein from SO |
was detected by |
SDS-PAGE and immunoblot assay |
Escherichia coli |
| rice U-box proteins |
were expressed with GST-tags in |
Escherichia coli |
Oryza sativa; Escherichia coli |
| C323S mutant of Arabidopsis (FHY2, FRE1, HY8, PHYA, AT1G09570) |
coexpressed with |
wild-type (FHY2, FRE1, HY8, PHYA, AT1G09570) |
Arabidopsis thaliana |
| Suppressed hybrids A3-2, A5-1, A10-1, A14-1, A16-1 |
do not contain detectable |
HT-M polypeptides |
Nicotiana plumbaginifolia; Nicotiana alata |
| (ATUCP2, PUMP2, UCP2, AT5G58970) protein |
reaches only |
0.02% of the mitochondrial proteins |
|
| SlTPR1-CFP and NR-YFP fusion proteins |
transiently expressed in |
onion epidermal cells |
Allium cepa |
| (AGC2, AGC2-1, AtOXI1, OXI1, AT3G25250) overexpression lines |
may have lower or higher OXI1 protein levels compared to |
wild type |
Arabidopsis thaliana |
| SGC-3xMYC and TLP-SmRSGFP |
were co-expressed transiently in |
Nicotiana benthamiana leaves |
Nicotiana benthamiana |
| Western blot analysis |
was used to compare |
protein amount of (ATPUMP1, ATUCP1, PUMP1, UCP, UCP1, AT3G54110) |
|
| YFP fusion proteins |
were expressed at |
expected molecular masses |
Nicotiana tabacum |
| marker proteins |
will have obtained |
steady-state level |
plant cells |
| PGD1:gfp plants |
have high GFP protein levels comparable to |
OsCc1:gfp, Act1:gfp, and ZmUbi1:gfp plants |
Oryza sativa |
| pEG202 and pJG4.5 plasmids |
generate |
AD-TF construct |
|
| GST-HY5 constructs |
generated as described previously |
protein construct |
|
| (ARA8, ATPCS1, CAD1, PCS1, AT5G44070) and (ATPCS2, PCS2, AT1G03980) proteins |
were expressed with |
C-terminal HA tag |
Arabidopsis thaliana |
| mutation of Complex I |
associates with |
increase in alternative oxidase (AOX) amount |
|
| marker protein expression |
examined at |
3 hours after bombardment |
Nicotiana tabacum; Lilium |
| N- and C-terminal split-YFP fusion proteins |
were properly expressed in |
tobacco cells |
Nicotiana tabacum |
| fusion of intact (ATRH1, RH1, AT4G15850) to GFP |
able to obtain |
fluorescent transformants |
Chlamydomonas reinhardtii |
| GFP- (ICR1, RIP1, AT1G17140) |
produces |
major band about 70-kD |
Arabidopsis thaliana |
| transformed onion epidermal cells |
were incubated in dark at |
28°C |
Oryza sativa |
| transgenic strain expressing recombinant His-tagged FcpA protein |
was created |
recombinant His-tagged FcpA protein expression |
Phaeodactylum tricornutum |
| three chimeric proteins, K50-C, R95-C and K124-C |
were stably expressed in transgenic |
Arabidopsis |
Arabidopsis thaliana |
| nYFP- and cYFP-fusion proteins |
were detected at similar levels in protoplasts transfected with |
AvrPto-nYFP and AvrPto Y89D-nYFP |
Arabidopsis thaliana |
| (AtSOD1, CSD1, SOD1, AT1G08830) and (AtSOD2, CSD2, CZSOD2, SOD2, AT2G28190) protein levels |
are reduced in |
ga1-3 quadruple-DELLA mutant |
Arabidopsis thaliana |
| cells |
harvested |
4 h after induction |
Escherichia coli |
| (ATKTI1, AtKTI4, KTI1, AT1G73260) overexpression lines S8, S13, and S16 |
express |
functional, detectable proteins |
Arabidopsis thaliana |
| GFP–AtCASP or GFP–GC1 |
expressed with ST–mRFP and inducible Sar1-GTP–YFP |
NII tobacco plants |
Nicotiana tabacum |
| GsCRCK1a/1b/1c/1d-Cub fusion proteins |
were normally expressed |
yeast cells |
|
| Synechocystis PCC6803 strain |
was used as |
heterologous expression system for functional definition of Phat3_J9316 acyl-ACP Δ9-desaturase |
Synechocystis PCC6803 |
| nodular-compact and fast-growing oil palm calli |
show significant differences in |
protein patterns and content |
Elaeis guineensis |
| fluorescence protein-tagged ethylene receptors |
failed to express in |
Arabidopsis cell culture protoplasts |
Arabidopsis thaliana |
| version 2 of RH1–GFP construct |
produced |
eight fluorescent transformants |
Chlamydomonas reinhardtii |
| ubiquitin–S subunit fusion |
approximately 10% of |
soluble |
Escherichia coli |
| recombinant cryptochrome proteins |
were produced in |
insect cell cultures |
|
| vector pET16b |
purchased from |
Novagen (Madison, USA) |
|
| Escherichia coli strain BL21(DE3)/pLysS containing pMM1311 |
was grown for 48 h at room temperature in |
ZY autoinduction medium |
Escherichia coli |
| recombinant (ATPAO2, PAO2, AT2G43020) and (ATPAO4, PAO4, AT1G65840) proteins |
have apparent molecular weight of |
∼54 500 Da |
Arabidopsis thaliana |
| LexA-HY5 protein |
could not be stably expressed |
stable expression |
|
| YFP–FIS1A Δ167–170 |
was expressed via |
35S promoter-driven construct |
Nicotiana tabacum |
| R1G1B:gfp plants |
have GFP protein levels ranging from |
0.11% to 0.34% of total soluble proteins |
Oryza sativa |
| (ATTSPO, TSPO, AT2G47770) |
was heterologously expressed in |
Saccharomyces cerevisiae |
Arabidopsis thaliana; Saccharomyces cerevisiae |
| two genetically encoded inhibitors |
affect organelle movement several days after |
expression |
higher plants |
| HvDRF1:GFP fusion construct |
resulted in |
no detectable GFP fluorescence |
Hordeum vulgare |
| (HSP60, HSP60-3B, AT3G23990) SrUCPA, and SrAOX |
are highly expressed in |
stamens |
|
| FPN3-FLAG |
is expressed in |
yeast cells |
Saccharomyces cerevisiae |
| pET16b-ETR1 |
was transformed into |
Escherichia coli strain C43 (DE3) |
Escherichia coli |
| Ntann12 |
is not expressed in |
aerial part |
tobacco |
| E. coli transformed with pLEV1, pL335V, and pLEVUbS |
produced large amounts of |
tobacco L subunits |
Escherichia coli; Nicotiana tabacum |
| unique functions of roots |
explains |
different proteomes in roots versus leaves, grains, or fruits |
|
| (ATXTH14, XTH14, XTR9, AT4G25820) and (ATXTH26, XTH26, AT4G28850) |
were recombinantly produced in |
yeast Pichia pastoris |
Pichia pastoris |
| VvGST1, VvGST2, VvGST3, VvGST4, and VvGST5 |
were expressed in |
Escherichia coli |
Vitis vinifera; Escherichia coli |
| pEG202 and pJG4.5 plasmids |
generate |
LexA-HY5 construct |
|
| YFP–FIS1A/B TMD+CE (C-terminus including TMD and the adjacent C-terminal end) |
was expressed via |
35S promoter-driven construct |
Nicotiana tabacum |
| NbDER:GFP |
was expressed in |
N. benthamiana leaves by agroinfiltration |
Nicotiana benthamiana |
| γ-secretase subunits and marker proteins |
were introduced simultaneously into |
Arabidopsis thaliana protoplasts |
Arabidopsis thaliana |
| ACD6-Col-0 |
was transiently expressed in |
human embryonic kidney 293 (HEK293) cells |
Homo sapiens |
| pUbi-HK5 |
is |
expression construct |
|
| (SPPA, SPPA1, AT1G73990) mutants |
are not constitutively expressing |
(ELIP, ELIP1, AT3G22840) |
Arabidopsis thaliana |
| wild type and MINELESS seeds |
showed no clear differences in |
myrosinase-binding protein (MBP) expression |
Brassica napus |
| pAct-HK5 |
is |
expression construct |
|
| Isopropyl β-D-1-thiogalactopyranoside (IPTG) |
is added to |
culture |
Escherichia coli |
| different bands in AOX immunoblots |
correlate with |
expression of different isoforms of AOX protein |
|
| amount of Rubisco activase in Δ43 and rwt46 plants |
is reduced compared with |
wild type |
Arabidopsis thaliana |
| sandwich construct with engineered HvDRF1 cDNA between two GFP open reading frames |
yielded |
green-fluorescing fusion product |
Hordeum vulgare |
| three different patterns of ZmCKX10 variants |
were overexpressed in |
Pichia pastoris |
Zea mays; Pichia pastoris |
| perturbations to translational processing |
significantly constrain |
production of foreign Rubiscos in tobacco plastids |
Nicotiana tabacum |
| ER–marker–RFP fusion |
co-expressed with |
ΔTM-ETR2:GFP |
Nicotiana tabacum |
| phage T7 promoter vector pETMCSI |
is |
described in Neylon et al., 2000 |
|
| (AVB1, IFL, IFL1, REV, AT5G60690) protein |
has abundance that is |
increased in (AtDRB1, DRB1, HYL1, AT1G09700) seedlings |
|
| full-length open reading frame (813 bp) of kiwifruit LCY-β |
was cloned in |
translational fusion into pET30b expression vector with c-terminal HIS 6 tag |
Actinidia chinensis |
| observed aggregation of IPT1::GFP protein |
could also be interpreted as |
overexpression artefact of the maize ubiquitin promoter |
Physcomitrella patens |
| cDNA clone encoding 6-SFT from L. perenne stubble |
was isolated and characterized by |
heterologous expression in Pichia pastoris |
Lolium perenne; Pichia pastoris |
| BjCHI1 protein |
is present in |
transplastomic tobacco lines HisBjCHI1-3 and HisBjCHI1-4 |
Nicotiana tabacum |
| (HSP60, HSP60-3B, AT3G23990) SrUCPA, and SrAOX |
are undetectable in |
other tissues |
|
| recombinant cystatins |
successfully expressed in |
E. coli |
Escherichia coli |
| removal of N-terminal 60 amino acids from Solanum lycopersicum GABA transaminase 3 (Sl GABA-T3) |
facilitates |
soluble expression |
Solanum lycopersicum |
| GSTs recovered after transient expression in N. benthamiana |
were shown to be |
intact |
Nicotiana benthamiana |
| protein levels in (AGC2, AGC2-1, AtOXI1, OXI1, AT3G25250) overexpression lines |
are higher in |
wild type |
Arabidopsis thaliana |
| 35S::OXI1-YFP lines |
show |
low levels of YFP protein |
Arabidopsis thaliana |
| overexpression of gliadin in the tobacco system |
is |
good way to get closer to the native expression of prolamins |
Nicotiana tabacum |
| Arabidopsis plants stably transformed with 35SCaMV :: AtPAO5-6His /pK2GW7 construct |
show no detectable accumulation of |
recombinant (AtPAO5, PAO5, AT4G29720) protein |
Arabidopsis thaliana |
| ectopic (BASL, AT5G60880) induction at later stages |
showed |
co-expression with epidermal (ATPIN1, PIN1, AT1G73590) expression only in developing serrations |
|
| pGST-CNGC20C T560A |
is used for |
bacterial protein expression |
|
| Resultant plasmids |
are transformed into |
Escherichia coli strain BL21 (DE3) |
Escherichia coli |
| CST-BIN2 |
is |
tagged (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) protein |
|
| pET-28M |
is |
protein expression vector |
|
| embryo axes |
exhibited only one band corresponding to |
α isoform of GDH |
Medicago truncatula |
| LjINV1 |
is |
the major isoform in the plant |
Lotus japonicus |
| native and chimeric constructs |
were inserted into |
pINIII vector |
Escherichia coli |
| line P310 (Pγzein-BSP-LT-B::GFP) |
compared to |
line P308c (P35S-BSP-LT-B::GFP) |
Zea mays |
| consequence of promoter specificity |
results in |
TAEP of P310 from the endosperm of transgenic seed |
Zea mays |
| Ntann12 |
is highly expressed in |
root system |
tobacco |
| (MED8, AT2G03070) and (ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) protein levels in double-gene-edited algae |
were not affected by |
gene editing of the other protein |
Phaeodactylum tricornutum |
| GFP protein |
accumulated in |
C. sativus |
Cucumis sativus |
| QK mutant |
did not contain detectable |
(ATHSFA2, HSFA2, AT2G26150) protein |
Arabidopsis thaliana |
| ORFs of cystatin genes |
cloned into |
pRS300 fused to eGFP and driven by 35S promoter |
Nicotiana tabacum |
| (EBS, AT4G22140) Y155A |
is expressed at levels similar to |
fully functional EBS:FLAG |
|
| (SHL, AT4G39100) W63L/Y65A |
is expressed at levels similar to |
fully functional HA:SHL |
|
| Arabidopsis thaliana (Col-0) 35S::Lti6b-GFP |
is |
fluorescent protein expression line |
Arabidopsis thaliana |
| Escherichia coli strain BL21 (DE3) |
carrying |
pET32a-SIE141, pET32a-AtCDSP32, pET32a-NbCDSP32, pET32a-StCDSP32, or pET32a-ATH5 |
Escherichia coli |
| Ntann12 |
is more abundant in |
roots |
tobacco |
| mature pea leaves |
could express other isoforms of |
AOX protein |
Pisum sativum |
| high-throughput proteomic analysis |
is used to study |
changes in protein accumulation levels |
|
| (NDHI, ATCG01090) protein reduction |
was approximately |
75% reduction |
Synechocystis 6803 |
| (AtLEA14, LEA1, LEA14, LSR3, AT1G01470) |
was expressed and purified from |
E. coli |
Escherichia coli |
| steady-state levels of various mitochondrial polypeptides |
were measured in |
wild-type and (nMAT4, AT1G74350) plants |
Arabidopsis thaliana |
| pEAQ-HT vector |
enables |
higher expression of proteins |
Nicotiana benthamiana |
| CRYs |
exhibit dark activity regulating |
proteome (174 genes) |
Arabidopsis thaliana |
| full-length complementary DNA (cDNA) represented by SGN-U575556 |
was expressed in E. coli with |
N-terminal Flag epitope tag |
Solanum lycopersicum |
| genetic constructs coding for γ-secretase subunits fused with GFP |
were introduced into |
Arabidopsis thaliana leaf mesophyll protoplasts |
Arabidopsis thaliana |
| proteomics data |
identified |
11.2% of TFs and TRs as differentially expressed |
Chlamydomonas |
| (AtPHOT2, NPL1, PHOT2, AT5G58140) |
is absent under |
non-inducing conditions |
Nicotiana benthamiana |
| native tobacco S subunit expressed in E. coli |
showed solubility similar to |
ubiquitin–S subunit fusion |
Escherichia coli; Nicotiana tabacum |
| (ATGSTF5, ATGSTF8, GST6, GSTF8, AT2G47730) splice variant without a plastidic targeting peptide |
is |
major form in vivo |
Arabidopsis thaliana |
| purified recombinant protein from Escherichia coli |
showed the presence of |
protein of molecular mass 57 kDa |
Escherichia coli |
| D1 protein level |
shows no obvious difference among |
tested lines under normal condition |
Solanum lycopersicum |
| pGEX4T1:PHT1;4-C terminus |
is |
protein expression vector |
|
| thalli of 3-week-old Mp pbla-1 /pro 35S ::Mp PBLa-cit |
were infiltrated with |
Agrobacterium tumefaciens carrying constructs |
Marchantia polymorpha |
| pB7FWG2.0 p35S::GLR3.3D 543G -eGFP |
encodes |
(ATGLR3.3, GLR3.3, AT1G42540) D543G-eGFP fusion protein |
|
| ASY1-FL construct |
generated previously |
(ASY1, ATASY1, AT1G67370) protein expression |
Arabidopsis thaliana |
| (AtPUB22, PUB22, AT3G52450) (AtPUB23, PUB23, AT2G35930) (PUB24, AT3G11840) triple mutant |
shows unchanged |
(ATMAPK3, ATMPK3, MPK3, AT3G45640) protein abundance |
Arabidopsis thaliana |
| pHBT-CNGC20-FLAG |
is used for |
protein expression |
|
| HisMBP-ASY1 1-300 construct |
generated previously |
(ASY1, ATASY1, AT1G67370) N-terminal domain expression |
Arabidopsis thaliana |
| clones |
were transformed into |
S. cerevisiae strain WΔ6 |
Saccharomyces cerevisiae |
| (AtSOD1, CSD1, SOD1, AT1G08830) and (AtSOD2, CSD2, CZSOD2, SOD2, AT2G28190) protein levels |
are increased in |
ga1-3 |
Arabidopsis thaliana |
| double mutant H330F/H454F |
showed similar expression intensities as |
WT (SLAH3, AT5G24030) or H330K/H454K double mutant |
Xenopus laevis |
| 33 proteins (root hair-specific proteins) |
are referred to as |
root hair-specific proteins |
Arabidopsis thaliana |
| 'omics' approaches |
investigated at |
protein expression level |
Citrus sinensis |
| RPX-GFP fusion protein |
expressed in |
transgenic Arabidopsis |
Arabidopsis thaliana |
| pER8-Gateway-3Flag |
is used for |
inducible expression of protein fusions to 3xFLAG tag |
|
| (PFU3, UBC26, AT1G53025) (a homolog of human hKIAA1734) |
was impossible to induce expression of |
under the various conditions tested |
Arabidopsis thaliana; Escherichia coli |
| E2 genes |
were cloned into |
plant expression vector |
Arabidopsis thaliana |
| all plant lines |
express |
NPTII protein to similar levels |
Nicotiana tabacum |
| re-introduced tobacco L 8 S 8 Rubiscos examined in this study |
were abundantly expressed |
|
Nicotiana tabacum |
| level of (ATPAP10, PAP10, PUP1, AT2G16430) protein in SR– and R– |
is much higher than |
level of (ATPAP10, PAP10, PUP1, AT2G16430) protein in SR+ or R+ |
Arabidopsis thaliana |
| MT FRET-based metal-binding sensor |
was expressed in |
cytoplasm of Chlamydomonas reinhardtii |
Chlamydomonas reinhardtii |
| immunoblot analysis |
confirmed expression of |
CsCCD2-thioredoxin and ALDH-thioredoxin fusion proteins |
Escherichia coli |
| (ATVAMP711, VAMP711, AT4G32150) |
was transferred into |
RS72 yeast strain expressing heterologous (AHA2, AtHA2, HA2, PMA2, AT4G30190) |
Saccharomyces cerevisiae |
| MINELESS seeds |
lacked |
35 kDa isoform of epithiospecifier protein (AESP, AESP1, ESP, RSW4, AT4G22970) |
Brassica napus |
| fusion protein |
is expressed in |
native genomic context |
Physcomitrella patens |
| maco2 knockout line |
shows |
significant decrease in mACO2 protein abundance |
Arabidopsis thaliana |
| four-component BSMV system |
demonstrates the ability of |
overexpress genes of larger size within 7 d post infection (dpi) |
|
| Trx-1-pET23b plasmid |
was transformed into |
Escherichia coli (BLH9, BLR, HB-6, LSN, PNY, RPL, VAN, AT5G02030) (DE3)pLysS |
Escherichia coli |
| CNF1-YFP and GFP-CNF1 fusion proteins |
were efficiently expressed |
in Nicotiana benthamiana |
Nicotiana benthamiana |
| maize Ac transposase (TPase) |
is expressed in |
cells |
Arabidopsis thaliana |
| A total of 17 Arabidopsis E2s |
were cloned into |
pET28a vector |
Arabidopsis thaliana |
| proteins expressed in plants via agroinfiltration |
are produced in |
large amounts |
Arabidopsis thaliana |
| pNB1YN-CNGC20 |
is used for |
oocyte expression |
|
| Xenopus oocytes |
injected with |
cRNAs or water |
Xenopus laevis |
| TPR and PPR proteins |
when expressed as recombinant protein in E. coli are often |
insoluble |
|
| levels of (ATPAP10, PAP10, PUP1, AT2G16430) protein on P+ medium |
are similar between WT and ein2 but are higher in |
(AtCTR1, CTR1, SIS1, AT5G03730) mutant |
Arabidopsis thaliana |
| protoplasts |
were co-transformed with |
DNA constructs encoding fusion proteins of red fluorescent protein (RFP) with sulphite reductase (SiR:RFP) or RFP with a chloroplast transcription-stimulation factor (STF:RFP) |
Nicotiana benthamiana |
| altered LeCDJ1 expression |
affects |
D1 protein level |
Solanum lycopersicum |
| maize SPS B isoform |
was expressed in |
Escherichia coli |
Zea mays; Escherichia coli |
| Tobacco mosaic virus-based magnICON vector (pICHα26211) |
was used for |
transient expression |
|
| SDE2-GFP transgenic plants |
show |
63 kDa band |
Arabidopsis thaliana |
| WHY1-HA protein |
declines at |
week 8 of plant development |
Arabidopsis thaliana |
| full-length (ESV1, AT1G42430) |
encodes |
entire (ESV1, AT1G42430) sequence |
Arabidopsis thaliana |
| truncated version of the cDNA |
was expressed in |
Escherichia coli |
Escherichia coli |
| minovincine 19-O-acetyltransferase (MAT) |
is inactive when expressed in planta |
plant tissue |
Catharanthus roseus |
| minovincine 19-O-acetyltransferase (MAT) |
is inactive when expressed in |
yeast |
Catharanthus roseus; Saccharomyces cerevisiae |
| plastid proteome of Silene noctiflora |
was examined for |
divergent (CLPP1, PCLPP, ATCG00670) expression and function |
Silene noctiflora |
| mutated (ATRBOHA, RBOHA, AT5G07390) -B, -E and -G |
do not affect |
level of expression |
|
| HIS-MBP-PHGAP1 |
is |
tagged (PHGAP1, REN2, AT5G12150) protein |
|
| pAct-ARK-440-1148 |
is |
expression construct |
|
| ThrRS–dTP deletion constructs |
contains |
GFP fusion protein |
|
| NlMLP without the signal peptide |
was transiently expressed in |
rice protoplasts |
Oryza sativa |
| GST–ThrRS–dTP(2–60) fusion protein |
accumulated in |
inclusion bodies |
Escherichia coli |
| pHBT-CNGC19-nYFP |
is used for |
protein expression |
|
| pRI201-AN |
is |
expression vector |
|
| PIF4-GST fusion protein expression |
was induced by |
isopropyl β-D-1-thiogalactopyranoside (IPTG) |
Escherichia coli |
| mass spectrometric data on SPS protein abundance in leaves |
suggest |
(ATSPS2F, KNS2, SPS1, SPS2F, SPSA2, AT5G11110) is the dominant isoform in leaves with respect to protein levels |
Arabidopsis thaliana |
| pHBT-CNGC20N-FLAG |
is used for |
protein expression |
|
| HIS-MBP-PHGAP1(8A) |
is |
phosphorylation-deficient (PHGAP1, REN2, AT5G12150) mutant |
|
| pMAL-BAK1 CD-HA |
is used for |
protein expression |
|
| pGST-CNGC20C |
is used for |
bacterial protein expression |
|
| HIS-MBP-PHGAP2(1-420) |
is |
truncated (PHGAP2, REN3, AT5G19390) protein |
|
| NB-Bem and ND-Cdc proteins |
express at similar levels |
|
Arabidopsis thaliana |
| GFP1-10 |
is expressed inside |
recipient cells |
|
| AvrPto expression |
did not reduce |
MAPK protein accumulation |
Arabidopsis thaliana |
| pNB1YFP-CNGC19 |
is used for |
oocyte expression |
|
| pAct-HK5-1-631 |
is |
expression construct |
|
| all four phospho-dead mutations |
did not significantly alter |
(ABCG36, ATABCG36, ATPDR8, PDR8, PEN3, AT1G59870) expression or PM location |
Arabidopsis thaliana |
| (HCAR, AT1G04620) (Hydroxymethylchlorophyll a reductase) |
was expressed in |
Escherichia coli |
Escherichia coli |
| soluble protein of (UBC32, AT3G17000) |
was obtained when |
transmembrane domain was deleted |
Arabidopsis thaliana |
| transgenic protein |
was not detected by |
antibody-based analyses |
Solanum lycopersicum |
| eGFP |
is detected in |
pGW1 (PPR10-atpH), pGW8 (HCF152-petB), pGW9 (CRR2-ndhB) and pGW10 (RPL2, uL2Mz, ATMG00560) lines |
Nicotiana tabacum |
| pGW5 (PPR10-mutated (ATPH, ATCG00140) ) lines with mutated PPR10 binding site |
do not promote accumulation of |
eGFP |
Nicotiana tabacum |
| Both GFP-CNF1 and CNF1-YFP T2 seedlings |
were strongly fluorescent |
fluorescence |
Arabidopsis thaliana |
| large amounts of proteins expressed in plants |
is useful for |
subsequent experiments |
Arabidopsis thaliana |
| transient protein expression in plants |
may overcome |
problems with post-translational modifications |
Arabidopsis thaliana |
| heterologous (CaS, AT5G23060) expression in plants and yeast |
is |
first report |
|
| transformed protoplasts |
are incubated at |
18°C for 16 h in the dark |
Arabidopsis thaliana |
| QSK1C-AA and QSK1C-DD |
were cloned into |
Escherichia coli BL21(DE3) expressing plasmid pETGST1a |
Arabidopsis thaliana; Escherichia coli |
| (SCPL19, SNG2, AT5G09640) |
transiently expressed in |
Nicotiana benthamiana |
Nicotiana benthamiana |
| wild-type or E46K mutant protein |
mostly was expressed as |
soluble protein |
Escherichia coli |
| BRI1-CITRINE amounts |
are |
generally not limiting |
Arabidopsis thaliana |
| live-cell marker ( (AML1, ML1, AT5G61960) pro:RCI2A-mNeonGreen) |
was created for |
epidermal cell outlines |
Solanum lycopersicum |
| WT or mutated QSK1 co-expression in tobacco |
does not significantly alter |
(ABCG36, ATABCG36, ATPDR8, PDR8, PEN3, AT1G59870) expression or location |
Nicotiana benthamiana |
| part of Tab 1 containing the PPPEW/OPR repeats |
was insoluble when expressed as recombinant protein in |
E. coli |
Chlamydomonas reinhardtii |
| 2-Cys peroxiredoxin (BAS1, CYP72B1, CYP734A1, AT2G26710) |
was downregulated by |
high nitrogen availability at 21 days post-anthesis (DPA) |
|
| AtD14 G158E |
is not known if |
stably expressed in planta |
|
| ELONGATION FACTOR-Tu RECEPTOR (EFR, AT5G20480) C975 S-GFP |
was transiently expressed in |
Nicotiana benthamiana |
Nicotiana benthamiana |
| pGreen0179-pGLR3.3::gGLR3.3 |
encodes |
(ATGLR3.3, GLR3.3, AT1G42540) protein |
Arabidopsis thaliana |
| β-estradiol-inducible expression system |
is used to express |
fluorescently tagged fusion proteins |
Nicotiana tabacum |
| gain-of-function ACD6-1 variant |
was transiently expressed in |
human embryonic kidney 293 (HEK293) cells |
Homo sapiens |
| pHBT-CNGC20C T560/S617/S618/T619A-HA |
is used for |
protein expression |
|
| (ATGSTU24, GST, GSTU24, AT1G17170) fusion constructs |
transformed into |
Escherichia coli strain BL21(DE3) cells |
Escherichia coli |
| CP105 RB and CP106 AVR proteins |
can be first detected at |
3 and 2 h post-Dex application respectively |
Nicotiana benthamiana |
| transgenic lines ( (ZAR1, AT3G50950) background) carrying V544E, H597E, and W825A/F839A variants |
accumulate similar amounts of |
(ZAR1, AT3G50950) protein |
Arabidopsis thaliana |
| Col-0 cerk1-2 mutant |
does not accumulate |
CHITIN ELICITOR RECEPTOR KINASE 1 (AtCERK1, AtLYK1, CERK1, LYK1, LYSM RLK1, AT3G21630) protein |
Arabidopsis thaliana |
| (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) D105N protein expression |
is not lacking |
inability of (ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) D105N to confer 5-MT resistance |
Arabidopsis thaliana |
| wild type |
did not contain detectable |
(ATHSFA2, HSFA2, AT2G26150) protein |
Arabidopsis thaliana |
| rPPDK1 |
had complete absence of |
detectable (PPDK, AT4G15530) protein |
Kalanchoe fedtschenkoi |
| TrxB mutant version expression level |
was slightly higher than |
TrxB expression level in WT cells |
Synechocystis |
| OFP3-Flag fusion proteins |
were detected in |
transgenic plants |
Oryza sativa |
| S10-AtGONST1-3 × HA-S11 sandwich fusions |
were highly expressed and correctly targeted |
|
Arabidopsis thaliana |
| myc-AGO4 plant |
produces |
Myc-AGO4 protein at 110 kDa |
Arabidopsis thaliana |
| transcription factors |
can be expressed at levels as low as |
a single copy per cell |
|
| Most toxin B-expressing T1 and T2 seedlings |
showed only a weak fluorescent signal |
fluorescence |
Arabidopsis thaliana |
| recombinant full-length TBP |
is encoded by |
yeast |
Saccharomyces cerevisiae |
| MRK1-GFP, RAF26-GFP, and RAF39-GFP |
transiently expressed in |
Nicotiana benthamiana |
Nicotiana benthamiana |
| TaLBD41 protein |
was detectable under |
N-S conditions |
Triticum aestivum |
| A2QK-9 transgenic line |
produced undetectable levels of |
(ATHSFA2, HSFA2, AT2G26150) protein |
Arabidopsis thaliana |
| binary vectors |
were used to express |
A1AT |
|
| BZR1pro : BZR1-YFP and BES1pro : BES1-YFP |
show much lower protein levels in |
(ARP6, ATARP6, ESD1, SUF3, AT3G33520) er-119 (ATXR3, SDG2, AT4G15180) mutant ovules |
Arabidopsis thaliana |
| split mVenus fusion protein located at C-terminus of bZIP60U |
allows fluorescence visualization only when |
full-length bZIP60U-YC is expressed |
Nicotiana benthamiana |
| MAX1-1400 enzyme |
was expressed in |
yeast |
Oryza sativa |
| GFP::BRC1 protein |
accumulated at high levels |
5 h after beginning of oestradiol induction |
Arabidopsis thaliana |
| SRN1 ΔSP fused with α-factor |
was expressed by |
P. pastoris |
Pichia pastoris |
| mBRI1-FLAG |
accumulates in |
transgenic Ws-2 seedlings |
Arabidopsis thaliana |
| full-length (GOM8, RHD3, AT3G13870) or (RL2, AT5G45160) |
were expressed as |
glutathione S-transferase fusion proteins in Escherichia coli |
Escherichia coli |
| absence of YFP fluorescence |
could not be ascribed to |
an effect of the YFPc fusion on protein expression |
Xenopus laevis |
| oastlAC B +/− mutant |
shows gene dose effect on |
protein and activity levels |
Arabidopsis thaliana |
| SRN1 H63A/ΔSP protein |
was obtained in |
sufficient amounts for biochemical analyses |
Pichia pastoris |
| N-terminal transmembrane domain of (ATL5, AT3G62690) |
inhibited |
adequate expression and nuclear localization of (ATL5, AT3G62690) in yeast |
Saccharomyces cerevisiae |
| stable apple callus lines overexpressing MdNAC5 (OL-1, OL-3, and OL-4) |
have markedly increased |
protein expression of MdNAC5 |
Malus domestica |
| SlSKOR |
expressing in |
Xenopus oocytes |
Solanum lycopersicum; Xenopus laevis |
| Proenzymes of each legumain |
were expressed in |
E. coli |
Escherichia coli |
| PtaJAM1.1 |
could not be correctly expressed coupled to |
HALO tag in vitro |
Populus tremula × alba |
| cucumber mosaic virus 2b silencing suppressor protein |
used to boost |
fluorescence signal |
Nicotiana benthamiana |
| pPICZ α A vector containing synthesized OSCs |
were expressed in |
Pichia pastoris |
Pichia pastoris |
| proteins in (AtMYB1, MYB1, SRM1, AT3G09230) |
included |
672 downregulated and 660 upregulated proteins |
Oryza sativa |
| (BHLH039, bHLH39, ORG3, AT3G56980) and (ATPK10, CIPK15, PKS3, SIP2, SNRK3.1, AT5G01810) protein fusions |
were properly expressed |
plant cells |
Arabidopsis thaliana |
| recombinant full-length TBP |
is encoded by |
humans |
Homo sapiens |
| (AtCPK21, CPK21, AT4G04720) variants |
is transiently expressed in |
Nicotiana benthamiana |
Nicotiana benthamiana |
| CP106 AVR accumulation was not detectable on immunoblot following Dex application |
in plants co-expressing |
Rx1-nls or myr-Rx1 variants |
Nicotiana benthamiana |
| acs2-1 RR fruits |
show fourfold higher |
(ACS2, AT-ACC2, AT1G01480) protein level |
Solanum lycopersicum |
| (AtCPK21, CPK21, AT4G04720) wild-type and mutant enzymes |
were transiently expressed in |
Nicotiana benthamiana leaves |
Nicotiana benthamiana |
| each combination of AtCRL-GFP/AtCRL-Myc, AtCRLM5-GFP/AtCRLM5-Myc, or AtCRLM6-GFP/AtCRLM6-Myc |
were co-expressed in |
Nicotiana benthamiana leaves |
Nicotiana benthamiana |
| ZmDREB2A overexpression in maize protoplasts |
shows significantly greater |
ZmDREB2A protein accumulation |
Zea mays |
| Vectors pMRR13, pMRR18 and pMRR15 |
yielded |
6.6%, 2.9% and 0.5% AAD |
|
| (AtCSP1, CSDP1, CSP1, AT4G36020) levels |
were lower in |
atcsp1-1 rosettes at normal and low temperatures |
Arabidopsis thaliana |
| tagged fusion proteins |
were expressed in plants for |
further purification |
Nicotiana benthamiana |
| UBC21–GFP |
was properly expressed, determined by |
Comas-blue staining on its protein amount |
Arabidopsis thaliana; Nicotiana benthamiana |
| tobacco leaf epidermal cells |
were found to be better suited for the expression of CDS fusion proteins than |
previously used BY2 cells |
Nicotiana tabacum |
| ND-Cdc protein |
expressed well |
|
Arabidopsis thaliana |
| His6-tagged NB-GAL H, NB-Cdc, NB C357S-Cdc, ND-GAL H and ND-Cdc proteins |
present in transgenic lines at |
comparable steady-state levels |
Arabidopsis thaliana |
| steady-state levels of complex I (NAD9, ATMG00070) and (BETA CA2, CA18, CA2, DEG12, AT5G14740) subunits |
varied only little between |
wild-type and (nMAT4, AT1G74350) plants |
Arabidopsis thaliana |
| TOP1–GFP fusion |
expressed in |
Nicotiana benthamiana |
Nicotiana benthamiana |
| expression level of YFP-XI-i-Δmotor fusion protein in (WIT1, AT5G11390) (WIT2, AT1G68910) |
was the same as in |
wild-type |
Arabidopsis thaliana |
| pMAL-BAK1 CD KM-HA |
is used for |
protein expression |
|
| GFP-STF1 and GFP-STF2 proteins |
were clearly detected in |
leaves of scions |
Glycine max |
| pAct-ARK-295-1148 |
is |
expression construct |
|
| individual wells |
were transformed with |
expression constructs |
Homo sapiens |
| Protein expression of MpSERK Y418F -mTb-Myc |
was even higher compared with |
MpSERK-mTb-Myc |
Marchantia polymorpha |
| (ATFD1, FD1, AT1G10960) and (ATFD2, FD2, FED A, AT1G60950) |
accumulate at |
different abundances |
|
| level of (AtSERPIN1, SERPIN1, AT1G47710) in wild-type plants |
is |
low |
Arabidopsis thaliana |
| NC-Cdc protein |
present in extracts in very low amounts when |
expressed either alone or with NB-Bem |
Arabidopsis thaliana |
| pHBT-SERK4-FLAG |
is used for |
protein expression |
|
| MBP-RIC1 |
is |
tagged (RIC1, AT2G33460) protein |
|
| pAct-HK5-YFP |
is |
expression construct |
|
| pB7FWG2.0 p35S::GLR3.3 wt -eGFP |
encodes |
GLR3.3-eGFP fusion protein |
|
| truncated GmPT without predicted transit peptide |
cloned in |
yeast expression vector |
Saccharomyces cerevisiae |
| Western blot analyses |
confirmed an increase in |
(ATPUB14, PUB14, AT3G54850) protein levels following infection |
Arabidopsis thaliana |
| DRM2uba |
has |
similar protein level as that of wild-type (DMT7, DRM2, AT5G14620) |
|
| NB-Bem and NB-Cdc proteins |
despite being transcribed from the 35S promoter are present at steady-state levels similar to |
native (HY3, OOP1, PHYB, AT2G18790) |
Arabidopsis thaliana |
| single-site mutants |
were individually expressed in |
yeast H1246 |
Saccharomyces cerevisiae |
| (FRO1, NDUFS4, AT5G67590) |
was notably reduced in |
(nMAT4, AT1G74350) mutants |
Arabidopsis thaliana |
| eGFP accumulation in pGW9 (CRR2-ndhB) plants |
is much more than in |
pGW1 plants (PPR10-atpH) |
Nicotiana tabacum |
| RAB-A5c[N125I] and RAB-A5c[WT] |
show relative abundance after |
3 days of incubation with 20 μM Dex |
Arabidopsis thaliana |
| ADF8p : NTF / ACT2p : BirA transgenic line |
expresses |
nuclear targeting fusion (NTF) protein |
Arabidopsis thaliana |
| TaAAED1: GFP and amiRNA1 co-expression |
accumulated much less |
GFP fusion protein |
Nicotiana benthamiana |
| mutant proteins |
were purified from |
E. coli |
Escherichia coli |
| (APEM7, PEX4, UBC21, AT5G25760) (a homolog of yeast (AtUBC10, UBC10, AT5G53300) ) |
was |
insoluble |
Arabidopsis thaliana |
| Proteins expressed in Nicotiana benthamiana by agroinfiltration |
were used |
for those proteins that could not be induced or are insoluble when expressed in bacteria |
Nicotiana benthamiana; Arabidopsis thaliana |
| crr2-2 and sig4-10 |
are defective in |
NdhB and (NDHF, ATCG01010) accumulation, respectively |
|
| nuclear targeting fusion (NTF) protein |
is expressed properly in |
each transgenic line |
Arabidopsis thaliana |
| transient expression in tobacco |
is |
protein expression technique |
Nicotiana benthamiana |
| pAct-ARK-472-1148 |
is |
expression construct |
|
| antimycin A (AA) treatment |
slightly increased |
chloroplast AtpC amount |
|
| Variant transporters |
were expressed in |
Xenopus oocytes |
Xenopus laevis |
| antimycin A (AA) and myxothiazol (MYXO) treatments |
increased |
relative protein amount of mitochondrial (AthCF1beta, ATPB, CF1beta, PB, ATCG00480) protein across plant lines |
|
| GFP protein accumulation in chromoplasts of ripe tomatoes |
represents |
highest expression level achieved in non-green plastids to date |
|
| cop1-4 mutant |
expresses |
N-terminal part of (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) protein |
Arabidopsis thaliana |
| transformant ZF37 |
expressed |
truncated Ble::Gfp::∆AphVIII fusion protein |
Chlamydomonas reinhardtii |
| α-subunit |
was less strongly down-regulated in |
line rNAD-ME2 |
Kalanchoë fedtschenkoi |
| mammalian tissue culture |
is |
rapid eukaryotic protein expression system |
Homo sapiens |
| Tobacco mosaic virus, Potato virus X, and Tobacco rattle virus |
have successfully been designed and developed as |
vectors to express foreign proteins in dicotyledonous plants |
|
| ZmBELL10 overexpression lines |
have highly increased |
ZmBELL10 protein abundance |
Zea mays L. |
| mutations in Osalkbh5-1 and Osalkbh5-2 |
caused |
complete disappearance of the protein |
Oryza sativa L. ssp. japonica |
| G103R substitution (pbs1-3) |
accumulated poorly |
|
Nicotiana benthamiana |
| PaACLB1-B2 silencing |
results in differential expression of |
345 up-regulated proteins |
Petunia hybrida |
| PaACLB1 protein abundance |
is significantly down-regulated |
in PaACLB1-B2-silenced plants |
Petunia hybrida |
| hierarchical clustering |
grouped |
proteins with similar expression patterns |
Oryza sativa |
| decreased activity in the dark in Elysia chlorotica |
is most likely due to |
lower levels of (PRK, AT1G32060) protein |
Elysia chlorotica |
| highest expressing proteins |
are often |
housekeeping or structural proteins |
|
| MtChit5 in pET28b vector |
was expressed as |
His-tagged recombinant protein |
Escherichia coli BL21 (DE3) |
| CSLF6 lines |
exhibit |
133 kDa band |
Brachypodium distachyon |
| other phiLOV2.1-tagged virulence proteins |
show |
very weak fluorescence signals |
Agrobacterium tumefaciens |
| (ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) abundance |
may be |
low in vivo |
Arabidopsis thaliana |
| (ATCDC48, AtCDC48A, CDC48, CDC48A, AT3G09840) variants |
were transiently expressed as |
YFP fusions in leaf mesophyll protoplasts |
Arabidopsis thaliana |
| maize |
contains |
β-form (RCA, AT2G39730) polypeptides |
Zea mays |
| (AAD6, FTM1, HUP7, SAD6, AT1G43800) gene |
was expressed in |
Escherichia coli |
Escherichia coli |
| low levels of diffuse YFP fluorescence in MMC |
are significantly higher than |
background level in untransformed plants |
|
| A2Wt transgenic line |
produced high levels of |
(ATHSFA2, HSFA2, AT2G26150) protein |
Arabidopsis thaliana |
| CsCCD2-thioredoxin and ALDH-thioredoxin fusion proteins |
were expressed at |
expected molecular masses of 81.9 and 69.8 to 76.9 kD |
Escherichia coli |
| GlgC-TM protein |
was confirmed to be present in |
lines carrying the GlgC-TM construct |
Arabidopsis thaliana |
| (AAD6, FTM1, HUP7, SAD6, AT1G43800) gene |
was expressed in |
Saccharomyces cerevisiae |
Saccharomyces cerevisiae |
| rNAD-ME1 |
had reduction in |
α-subunit protein level |
Kalanchoe fedtschenkoi |
| NIP7;1 protein |
is expressed preferentially at high levels in |
tapetum compared with other floral tissues |
Arabidopsis thaliana |
| Strep A1AT |
was expressed in |
glycosylation mutant ∆XT/FT |
Nicotiana benthamiana |
| GFP-tagged (AtTCP21, CHE, TCP21, AT5G08330) |
can be expressed in |
HEK293T cells |
Homo sapiens |
| (ATDDM1, CHA1, CHR01, CHR1, DDM1, SOM1, SOM4, AT5G66750) YCE and YNE (ATVAMP711, VAMP711, AT4G32150) constructs |
were transiently expressed in |
Nicotiana benthamiana leaves |
Nicotiana benthamiana |
| 13 E2 proteins belonging to nine E2 groups |
were successfully expressed in Escherichia coli and purified using |
Ni-NTA agarose |
Arabidopsis thaliana; Escherichia coli |
| cold stress |
alters |
protein expression profiles |
Arabidopsis thaliana |
| 35S promoter |
controls expression of |
PdGATL1.1-EYFP fusion construct |
|
| (AAD6, FTM1, HUP7, SAD6, AT1G43800) protein |
was not active in |
heterologous expression systems |
Saccharomyces cerevisiae; Escherichia coli |
| (ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) T-DNA KO lines |
show |
477 proteins significantly up- or down-regulated |
Arabidopsis thaliana |
| suitable virus vector for systemic expression of heterologous proteins in the recalcitrant monocotyledonous plants |
is currently |
not available |
|
| two proteins identified in (B73, CHL6, CNX, CNX1, SIR4, AT5G20990) shoot apices |
disappear in |
either kn1 or (AtSIP1, RS1, SIP1, AT1G55740) mutants |
Zea mays |
| TrxB protein |
was not detected in |
STXB mutant cells |
Synechocystis |
| constitutive promoter-driven expression of ZmSRO1d-S and ZmSRO1d-R |
results in |
low ZmSRO1d-S and ZmSRO1d-R protein levels |
Zea mays |
| 22 proteins |
accumulated to higher levels in |
yl mutant compared with WT |
Solanum lycopersicum |
| SlGDSL2 protein |
failed to be detected in |
epidermis from gdsl2-b fruit |
Solanum lycopersicum |
| fluorescent fusions of FtsZ from diverse photosynthetic organisms |
were expressed in |
heterologous system |
|
| FLAG-tagged (ADO1, FKL2, LKP1, ZTL, AT5G57360) decoy |
can be expressed in |
HEK293T cells |
Homo sapiens |
| Immunoblotting with anti-His-6 antibody |
revealed |
CsUGT74AD1-thioredoxin fusion protein |
Escherichia coli |