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endocytosis

9156 relationships annotated with this phrase. Showing first 500 of 9156.
Source entity Relationship Target entity Species
inhibition of clathrin-mediated endocytosis strongly reduced endocytosis of (ABCG25, ATABCG25, AT1G71960)
(AP1M2, HAP13, AT1G60780) associates with (ATRBOHD, DELT1, RBOHD, AT5G47910)
MoEnd3-mediated endocytosis is responsible for internalization of sensor MoSho1 Magnaporthe oryzae
internalization of FM4-64 is commonly used to visualize general endocytosis in plant cells
wild-type seedlings showed many bright intracellular FM4-64 puncta Arabidopsis thaliana
medium subunit of the tetrameric (AP2, AtAP2, FL1, FLO2, AT4G36920) concomitantly recruits cargo proteins
STRUBBELIG (SUB) undergoes clathrin-mediated endocytosis
(AP180, PICALM6, AT1G05020) is encoded by Arabidopsis genome Arabidopsis thaliana
PB1CP-mediated relocalization of (ATRBOHD, DELT1, RBOHD, AT5G47910) involves endocytosis
endocytosis defect of μ2-1 would be expected to affect distribution of CESAs at plasma membrane Arabidopsis thaliana
RADIAL SWELLING9 (ADL1, ADL1A, AG68, DL1, DRP1A, RSW9, AT5G42080) mutant results in defective endocytosis Arabidopsis thaliana
μ2-1 does not affect rate of YFP-CESA6 delivery to plasma membrane therefore elevated density of YFP-CESA6 particles in μ2-1 prc1-1 background likely results from reduction in endocytosis of CESAs Arabidopsis thaliana
PINs and ABCBs are regulated by endocytosis pathway
small colocalization ratio between μ2-YFP and mCherry-CESA6 consistent with transient and infrequent nature expected of CESA endocytosis Arabidopsis thaliana
clathrin light chain (CLC) is encoded by Arabidopsis genome Arabidopsis thaliana
μ2-1 seedlings showed fewer intracellular FM4-64 puncta that were of lower intensity FM4-64 puncta Arabidopsis thaliana
remorin associates with (ATRBOHD, DELT1, RBOHD, AT5G47910)
OsDRP2A has been proposed to function in clathrin-mediated endocytosis (CME) Oryza sativa
role of (AP2, AtAP2, FL1, FLO2, AT4G36920) in plants may differ from what has been shown in animals Arabidopsis thaliana
SYNTAXIN OF PLANTS 132 (ATSYP132, SYP132, AT5G08080) appears to play diverse biological roles in endocytosis of plasma membrane H+-ATPase Arabidopsis thaliana; Nicotiana benthamiana; Triticum aestivum; Medicago truncatula
pattern recognition receptors (PRRs) are endocytosed after ligand perception through clathrin-mediated pathway Arabidopsis thaliana
mammalian homolog of μ2 is medium subunit of the tetrameric (AP2, AtAP2, FL1, FLO2, AT4G36920)
decreased FM4-64 internalization in μ2-1 cells supports role of μ2 in general endocytosis in Arabidopsis Arabidopsis thaliana
μ2-YFP and mCherry-CESA6 functionally associated at plasma membrane where CESAs can be endocytosed through μ2-mediated mechanism Arabidopsis thaliana
SPFH proteins associate with (ATRBOHD, DELT1, RBOHD, AT5G47910)
sterol endocytic pathway has been shown to interrupt polar recycling of (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) Arabidopsis thaliana
quantification of FM4-64 fluorescence in apical cytoplasm revealed significantly increased rate of membrane uptake in (LRX8, AT3G19020) /9/11 triple mutant Arabidopsis thaliana
ADAPTOR PROTEIN COMPLEX2 (AP2) complex is encoded by Arabidopsis genome Arabidopsis thaliana
μ2-YFP fully complemented FM4-64 internalization defect of μ2-1 mutant Arabidopsis thaliana
deletion of (AtPUB12, PUB12, AT2G28830) and (ATPUB13, PUB13, AT3G46510) leads to impeded internalization of FLAGELLIN-SENSITIVE2 (ATFLS2, FLS2, AT5G63580) Arabidopsis thaliana
filipin application reduces internalization of (ATPIN1, PIN1, AT1G73590)
sterol endocytic pathway has been shown to interrupt internalization of (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) Arabidopsis thaliana
ordered domains enriched with structural sterols on plasma membrane serve as internalization platforms for plasma membrane-associated molecules and cargo
plant sterols are distributed throughout endocytic pathway
(SUT1, AT5G63020) internalization is dependent on plasma membrane lipid composition
(ACR4, CR4, AT3G59420) and (ATDEK1, DEK1, EMB1275, EMB80, AT1G55350) activities can be increased by overaccumulation in multivesicular bodies Zea mays
increased rate of endocytosis observed in lrx mutant (ATPTS, PANC, PTS, AT5G48840) grown in presence of 5 µm LaCl3 was reduced to wild-type levels Arabidopsis thaliana
filipin has inhibitory role in internalization step of endocytosis
ergosterol- and lipid-dependent microdomains are functionally linked to endocytosis
XA21 endocytosis is observed only with BFA or wortmannin treatment Oryza sativa
(TPLATE, AT3G01780) is essential for clathrin-mediated endocytosis at plasma membrane Arabidopsis thaliana
lipophilic styryl dyes FM4-64 and FM1-43 were used to investigate rate of endocytosis Arabidopsis thaliana
SUPERNUMERARY ALEURONE LAYERS1 (SAL1) regulates formation of multivesicular bodies Zea mays
smooth (clathrin-independent) endocytosis leads to formation of coned-shaped zone of endocytic vesicles
sterols might be involved in endocytosis of LeEix2 receptor
(ADL1, ADL1A, AG68, DL1, DRP1A, RSW9, AT5G42080) plays significant role in endocytosis
CESAs are new set of clathrin-mediated endocytosis (CME) cargo proteins Arabidopsis thaliana
overexpression of FYVE-domain protein provokes formation of endosomal aggregates Arabidopsis thaliana
mechanism of endocytosis in plants is highly conserved in all eukaryotic cells
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) undergoes constitutive endocytic trafficking endocytosis Arabidopsis thaliana
association of FM 4-64 with dots depends on endocytotic uptake and membrane flux in living cells
VPS23A:RFP and (TOL6, AT2G38410) co-localize in early endosomal structures Arabidopsis thaliana
plant sterols are reported to be internalized into endosomes
(AtAUX1, AUX1, MAP1, PIR1, WAV5, AT2G38120) undergoes endocytosis in plants
lipid-enriched membrane rafts is functionally linked to endocytosis
cholesterol depletion alters endocytic structures
endocytosis occurs in at least two forms clathrin-dependent (clathrin-mediated endocytosis, CME) and independent (e.g. raft/caveloae endocytosis, RCE)
(ATIRT1, IRT1, AT4G19690) is endocytosed in monoubiquitylated state
syntaxin show increased levels of mRNA
XA21 K736E–GFP localizes to plasma membrane Oryza sativa
mRFP–SCAMP1 localizes to plasma membrane Oryza sativa
clathrin was recently identified in plant cells
sterols play a role in internalization of (SUT1, AT5G63020) from the PM Nicotiana tabacum
tyrphostin A23 argues for clathrin-independent endocytosis of (SUT1, AT5G63020)
(ATFLS2, FLS2, AT5G63580) can undergo endocytosis Arabidopsis thaliana
XA21–GFP localizes to plasma membrane Oryza sativa
MβCD treatment prevented formation of (SUT1, AT5G63020) vesicles Nicotiana tabacum
Tyrphostin treatment did not alter effect of BFA Nicotiana tabacum
internalization of StSUT1 (SOLANUM TUBEROSUM SUCROSE TRANSPORTER 1) depends on formation of raft-like structures Solanum tuberosum
(ATFLS2, FLS2, AT5G63580) undergoes endocytosis and degradation only upon stimulation with flagellin epitope flg22 Arabidopsis thaliana
multivesicular body (MVB) morphology dependent on the Rab-F family
clathrin-mediated endocytosis is regulated by PI(4,5)P2
brefeldin A (BFA) does not inhibit endocytosis
mβCD (methyl-beta-cyclodextrin) application results in no detection of vesicles in infiltrated tobacco leaves Nicotiana tabacum
clathrin-dependent endocytosis is highly conserved pathway
FM4-64 is endocytic tracer
StSUT1–GFP fusion protein is targeted to intracellular vesicles Nicotiana benthamiana
SlSUT1–GFP accumulates at internalization sites Saccharomyces cerevisiae
accumulation of various proton symporters at sites of endocytosis is dependent on lipid and ergosterol composition Saccharomyces cerevisiae
(AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) and (AtAUX1, AUX1, MAP1, PIR1, WAV5, AT2G38120) are subject to endocytic regulation Arabidopsis thaliana
(AtAUX1, AUX1, MAP1, PIR1, WAV5, AT2G38120) undergo endocytosis Arabidopsis thaliana
AtFlot1 functions in endocytic pathway independent from clathrins Arabidopsis thaliana
punctate signals in (TOL2, AT1G06210) (TOL3, AT1G21380) (TOL5, AT5G63640) localization potentially represent accumulations in endosomal structures Arabidopsis thaliana
(FER, AT3G51550) modulates endocytosis Arabidopsis thaliana
eisosomes are characterized as static sites for internalization of membrane proteins and lipids Saccharomyces cerevisiae
wortmannin treatment increases cytosolic vesicles containing XA21 K736E–GFP Oryza sativa
SUT localization to sterol-enriched membrane rafts promotes actin-dependent endocytosis
vacuole membrane staining was observed after 1.5 h in all treatments Arabidopsis thaliana
(AtBOR1, BOR1, AT2G47160) polarity relies on DRP1A-dependent, clathrin-mediated endocytosis Arabidopsis thaliana
tyrphostin A23 does not block endocytic events
StSUT1 is internalized from plasma membrane Solanum tuberosum; Nicotiana tabacum
(AtSCAMP1, SC3, SCAMP1, AT1G61250) labels early endosome (EE) or recycling endosome (RE) Oryza sativa
phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2) has been shown to modulate endocytosis
perception of external stimuli leads to selective internalization of membrane proteins via endocytosis
(AtBOR1, BOR1, AT2G47160) undergoes endocytosis in plants
(AtBOR1, BOR1, AT2G47160) is trafficked from plasma membrane to vacuole via endocytic pathway Arabidopsis thaliana
cholesterol depletion causes flattening of clathrin-coated endocytic structures
(ATPPME1, PPME1, AT1G69940) localization is unaffected by BFA treatment Arabidopsis thaliana
genes involved in endocytosis such as vesicle transport v-SNARE and syntaxin family genes are up-regulated upon ToxA treatment
endocytic vesicles co-localize with K63-linked ubiquitin cargo
BFA inhibition of endosomal cycling leads to formation of endosomal aggregates called BFA bodies
excess membrane labelled with both FM 1-43 and FM 4-64 is internalized via smooth vesicle endocytosis Nicotiana tabacum
brefeldin A (BFA) treatment does not inhibit endocytosis
root infection system provides reliable system for further investigation of XA21 endocytosis during interaction with Xoo Oryza sativa
stress-induced (PIP2, prePIP2, AT4G37290) responses at the plasma membrane may have a role in clathrin-mediated endocytosis
Rab-D1 is also found on endosomes
lipophilic FM dyes are internalized via endocytosis
DYM root tissue after 30 min FM4-64 treatment showed increased relative FM4-64 signal associated with internal membranes of cytoplasm Sorghum bicolor
DDYM root cells after 1 h BFA treatment contained fewer BFA bodies Sorghum bicolor
polar outer localization of NIP5;1 is maintained by threonine phosphorylation-dependent clathrin-mediated endocytosis Arabidopsis thaliana
StSUT1 undergoes constant recycling rather than protein degradation Solanum tuberosum; Nicotiana tabacum
plasma membrane TOLs could bind ubiquitylated cargos before completion of endocytosis Arabidopsis thaliana
(TOL5, AT5G63640) functions at MVBs Arabidopsis thaliana
(AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) localizes in endosomes
FM4-64 distributes to tonoplast
novel markers have been used to map endocytic pathways
FER-LLG1 receptor complex clustering triggers endocytosis
DYM root cells after 1 h BFA treatment contained approximately eight BFA bodies per cell Sorghum bicolor
(112A-2A, EMB30, GN, GNOM, MIZ2, VAN7, AT1G13980) localizes to components of endocytic pathway Arabidopsis thaliana
inhibition of (AtAVP1, ATAVP3, AtVHP1;1, AVP-3, AVP1, FUGU5, VHP1, AT1G15690) expression will affect endocytosis Arabidopsis thaliana
endosidin 1 (ES1) does not affect internalization of FM4-64 dye
disruption of sterol-enriched membrane domains prevents (SUT1, AT5G63020) internalization
FM4-64 signal in PM and cytosol after 30 min treatment showed higher PM/cytosol ratio in DDYM compared to DYM Sorghum bicolor
cellulose synthase (CESA) activity is regulated by removal from the plasma membrane (endocytosis)
DYM root hairs exposed to FM4-64 for 15 min resulted in more dye internalization Sorghum bicolor
Brownian motion of FM4-64 vesicles and aggregates was recorded by confocal microscopy Arabidopsis thaliana
plant sterols have mechanistic role during endocytosis
(AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) contains Tyrosine-based signals of NP X Y or Y XX Ø sequence
capacitance changes are consistent with imaging studies using fluorescent styryl dyes to label internalized membrane
MSBP1-overexpressing roots show inhibited BFA compartment formation Arabidopsis thaliana
(AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) protein sequence contains multiple endocytosis signals Arabidopsis thaliana
stomatal closure should produce large number of endocytotic vesicles
endocytotic structures can occasionally be found in present study
NOAs (1-NOA being more effective) can induce formation of endosomes containing auxin carriers Nicotiana tabacum
wortmannin suppresses internalization of proteins from plasma membrane
defense receptor may contain motif for endocytosis
(AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) traffics through TGN/endosome compartment
Membrane Steroid Binding Protein 1 (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) contains endocytosis signal Y XX Ø motif
endocytosis in plants has been proposed to be important for removal of excess membrane at sites of cell growth Arabidopsis thaliana
(ARF1, AT1G59750) mediates endocytosis in Arabidopsis Arabidopsis thaliana
glucose (Glc) treatment led to enhanced accumulation of (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) protein in early endocytic vesicles Arabidopsis thaliana
tyrphostin A23 nevertheless allowed endocytic vesicles formation and internalization Arabidopsis thaliana
(AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) in BFA compartments colocalized with FM4-64 Arabidopsis thaliana
clathrin-mediated pathway can be inhibited by auxin Arabidopsis thaliana
salt stress induces increase in intracellular accumulation of (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090)
(JK224, NPH1, PHOT1, RPT1, AT3G45780) internalization from plasma membrane occurs upon blue-light irradiation Arabidopsis thaliana
product (encoded by PP_LEa0009I13f) with dynamin GTPase domain is highly homologous to (ADL1, ADL1A, AG68, DL1, DRP1A, RSW9, AT5G42080) (Arabidopsis dynamin-like protein 1A) and Glycine max phragmoplastin Arabidopsis thaliana; Glycine max
cells undergoing either division or rapid growth internalize large amounts of pectins and GPI-anchored arabinogalactan proteins
(ABCB23, ATATM1, ATM1, AT4G28630) is co-localized with vesicles decorated with GFP-tagged (ARA-6, ARA6, AtARA6, ATRAB5C, ATRABF1, RABF1, AT3G54840) Arabidopsis thaliana
pharmacological inhibition of ARF–GEF by brefeldin A (BFA) results in internalization of PIN cargoes from basal plasma membrane domain into BFA compartments Arabidopsis thaliana
endocytosis of coated vesicles occurs in distal region of the growth zone and along the shank of the pollen tube Nicotiana tabacum
plant β-adaptins may function analogously to mammalian β-adaptins
endocytic vesicles can invaginate into coated pits
four genes encoding putative proteins with roles in endocytosis were identified as differentially expressed between juicy and woolly peaches Prunus persica
clathrin heavy chain is significantly upregulated at 15 days after anthesis (DAA) Triticum aestivum
FM4-64 labels plasma membrane
fusion site disappeared through putative endocytosis-dependent membrane metabolism and/or recycling
SCA produced in the pistil enters pollen tube tip
constitutive active mutants of (ARA-7, ARA7, atARA7, ATRAB-F2B, ATRAB5B, ATRABF2B, RAB-F2B, RABF2B, AT4G19640) form aggregates of deformed endosomes Arabidopsis thaliana
condensates in yeast and animals initiate endocytosis rather than being involved throughout the process condensates in plants
MSBP1-deficient plants show decreased internalization of FM4-64 Arabidopsis thaliana
defects in endocytosis could explain SCAR and (ARP2, ATARP2, WRM, AT3G27000) /3 complex mutant phenotypes Arabidopsis thaliana
decreased membrane tension stimulates endocytosis Nicotiana tabacum; Mammalia
roles of plant β-adaptins in clathrin binding to AP-2 complexes have not been experimentally demonstrated
endocytosis in plants has been proposed to be important for wall assembly Arabidopsis thaliana
(AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) was detected in intracellular compartments Arabidopsis thaliana
pectins that are cross-linked with boron and calcium are internalized and apparently recycled via early endosomes
smooth vesicles have been shown to accumulate as discrete class of endosome that mediates traffic to the Golgi complex
electron microscopy on cryo-fixed serial sections showed density of clathrin-coated pits was highest in a region from 6 μm to 18 μm distal to the tip Nicotiana tabacum
tyrphostin A23 (TyrA23) inhibits clathrin-coated vesicle (CCV) formation Arabidopsis thaliana
endocytic pathway occurs along shank region of the pollen tube Nicotiana tabacum
(RAB, RBE, AT5G06070) proteins are implicated in a multitude of biological functions such as in the regulation of early and late endocytic pathways
present study did not observe expected number of endocytotic vesicles
Shope et al. (2003) observed endocytosis in intact guard cells
endocytosis in guard cells must occur against high turgor pressures in guard cells
(ABCB23, ATATM1, ATM1, AT4G28630) tail–green fluorescent protein fusion protein co-localization implies a role of ATM1 in endocytosis Nicotiana tabacum
cell shrinking increases endocytic membrane retrieval at the apex Nicotiana tabacum
plant SCAMPs have not been functionally characterized
(ARA-6, ARA6, AtARA6, ATRAB5C, ATRABF1, RABF1, AT3G54840) regulates endocytosis Arabidopsis thaliana
results from protoplasts may not be possible to extrapolate to intact guard cells
Diekmann et al. (1993) demonstrated endocytosis in shrunken protoplasts but found that endocytotic vesicles could not be retrieved to plasmalemma in response to protoplast swelling
NaSBP1 may be relevant to transportation of products by endocytosis Nicotiana tabacum
FM 4-64 internalization along the shank of the pollen tube occurs second mechanism for FM 4-64 internalization Nicotiana tabacum
smooth vesicle endocytosis is known to be important in mammalian cells
NOA-induced vesicles of EYFP:AUX1 partially colocalized with membrane-selective endocytic tracer FM 4-64 Nicotiana tabacum
MSBP1-overexpressing plants show clearly increased internalization of FM4-64 Arabidopsis thaliana
first membrane progesterone receptor complex 1 (PGRMC1) contains endocytosis signal Y XX Ø motif
SCAR and (ARP2, ATARP2, WRM, AT3G27000) /3 complex-dependent actin polymerization requires further work to directly investigate possible roles in endocytosis or exocytosis in plant cells Arabidopsis thaliana
endocytosis is poorly defined in plants
interference with clathrin-dependent endocytosis inhibits endocytosis in general Arabidopsis thaliana
(ARA-7, ARA7, atARA7, ATRAB-F2B, ATRAB5B, ATRABF2B, RAB-F2B, RABF2B, AT4G19640) like its animal counterpart acts as regulator of endosome membrane fusion Arabidopsis thaliana
FM 4-64 rapidly labels pool of small vesicles located in the apical dome Nicotiana tabacum
NO-dependent actin rearrangements have consequences for endocytosis Zea mays
internalization of noncanonical (GCR2, GPCR, AT1G52920) Pth11 and sensor MoSho1 affects plasma membrane localization Magnaporthe oryzae
medium subunit of the tetrameric (AP2, AtAP2, FL1, FLO2, AT4G36920) docks to plasma membrane
Mammalian μ2 believed to be exclusively involved in endocytosis at plasma membrane
FM4-64 endocytosis in (ARAC3, ATROP6, RAC3, RHO1PS, ROP6, AT4G35020) CA root hairs was completely blocked endocytosis Arabidopsis thaliana
(AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) accumulation in BFA bodies increased in (SPK1, AT4G16340) mutants Arabidopsis thaliana
Mp SRI2 (Mp SHORT RHIZOIDS2) encodes EF-hand-containing protein similar to S. cerevisiae PAN1 Marchantia polymorpha
phosphorylation of MAPK and production of ROS are unimpaired in mutants affecting (ATFLS2, FLS2, AT5G63580) endocytosis
excess plasma membrane was retrieved by endocytosis at the apex Nicotiana tabacum
constitutive endocytic membrane retrieval from the apical plasma membrane generates pool of small vesicles in the apical dome Nicotiana tabacum
indole-3-acetic acid (IAA), 1-naphthaleneacetic acid (NAA), 2,4-dichlorophenoxyacetic acid (2,4-D), and α-(phenylethyl-2-oxo)-IAA (PEO-IAA) inhibit clathrin-mediated endocytosis (CME) Arabidopsis thaliana
various plant plasma-membrane proteins are internalized from cell surface
actin microfilaments mediates endocytosis
glucose (Glc) significantly increased ratio between intracellular versus plasma-membrane-localized (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) signal Arabidopsis thaliana
clathrin-dependent endocytosis is prominent endocytic pathway
plant β-adaptins have been identified in zucchini Cucurbita pepo
transporters, receptors, and extracellular-peptide ligands internalization occurs at plant plasma membrane
rop6-1 and ric1-1 roots show more association of clathrin with the plasma membrane compared to wild-type (WT) roots Arabidopsis thaliana
PAN1 is required for association of ARP-actin polymerization complex with clathrin-coated vesicles during endocytosis Saccharomyces cerevisiae
Pit develops into bud
cytoplasmic clumps are formed by endocytosis of the tonoplast
(ATM2, ATM4, ATMYOS1, AT5G54280) could mediate transportation through the endocytic pathway in concert with (ABCB23, ATATM1, ATM1, AT4G28630)
photoconverted red PIN2-EosFP internalizes from and accumulates in intracellular endosomal aggregates (BFA compartments) Arabidopsis thaliana
fluorescence imaging-based screen identifies Arabidopsis thaliana mutants defective in internalization of proteins including PINs Arabidopsis thaliana
tyrphostin A23 treatment affected DR5::GUS expression notably around quiescent center Arabidopsis thaliana
ARF-GTPase involvement in clathrin-mediated endocytosis prompted inquiry into whether uptake of the fluorescent endocytic tracer FM 1-43 is impaired in (AGD1, VAL1, AT5G61980) root hairs
FM4-64 colocalizes with BEN1-GFP-positive structures at very early stages of its internalization Nicotiana tabacum
meristematic and transition zones show highest endocytosis activity in developing protophloem Arabidopsis thaliana
(ARAC7, ATRAC7, ATROP9, RAC7, ROP9, AT4G28950) and (ARAC10, ATRAC10, ATROP11, RAC10, ROP11, AT5G62880) confirmed that ROP6 is not the only regulator of PIN endocytosis Arabidopsis thaliana
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) internalization shows significant reduction in (UBC13A, UBC35, AT1G78870) (AtUBC36, UBC13B, UBC36, AT1G16890) background Arabidopsis thaliana
FM 1-43 uptake in growing wild type root hairs was similar to that of (AGD1, VAL1, AT5G61980) root hairs
three genes have not been functionally characterized in green plants to date
PVC is pre-vacuolar compartment
coated-like pits have been detected at plant plasma membrane
protoplasts showing observable amount of cytoplasm are easier to follow endocytosis Arabidopsis thaliana
BRASSINOSTEROID INSENSITIVE1 (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) endocytosis occurs to early endosomes Arabidopsis thaliana
full appreciation of diverse functions of endocytosis in plants is important topic for future studies Arabidopsis thaliana
(ATRABA1B, BEX5, RAB11, RABA1b, AT1G16920) mutant does not affect endocytosis of FM4-64 dye Nicotiana benthamiana
FM4-64 dye is widely used as tracer to study pollen tube endocytosis Nicotiana tabacum
(CLC2, AT2G40060) co-localizes with sterols Arabidopsis thaliana
Lucifer Yellow (LY) was used to detect uptake of the dye in hyperosmotically treated guard cell protoplasts
okadaic acid and cantharidin treatment could enhance (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) endocytosis Arabidopsis thaliana
presence of glucose along with latrunculin B (Lat-b) could cause formation of large intracellular bodies Arabidopsis thaliana
FM1-43 was used to observe diffuse distribution of FM1-43 label throughout the cytoplasm
AtCLCd–green fluorescent protein (GFP) co-localized with endocytosed FM4-64 Arabidopsis thaliana
Ca2+ in (ATPTS, PANC, PTS, AT5G48840) is hypothesized to promote endocytosis Arabidopsis thaliana
disruption of the spatial organization of apical F-actin by wortmannin directly arrests tip-focused endocytosis Nicotiana tabacum
intracellular PIN2-GFP localizes to endocytic pathway Arabidopsis thaliana
glucose-stimulated fission of vesicles was not affected by ikarugamycin
accumulated Agrobacterium-delivered GFP 11−VirE2 are subsequently internalized through clathrin-mediated endocytosis Nicotiana benthamiana
3-D reconstruction revealed observed change in (ATRGS1, RGS1, AT3G26090) was due to internalization as opposed to clustering on the plasma membrane Arabidopsis thaliana
(ABP, ABP1, AT4G02980) (AUXIN BINDING PROTEIN 1) is required for PIN internalization Arabidopsis thaliana
AUXIN BINDING PROTEIN 1 (ABP, ABP1, AT4G02980) gain of function induces (ATPIN1, PIN1, AT1G73590) internalization Arabidopsis thaliana
(ATRGS1, RGS1, AT3G26090) phosphorylation mediates endocytosis
ZmEA1 most likely becomes internalized as shown by occurrence of internal granules containing DyLight-labeled ZmEA1 at pollen tube tip Zea mays
ZmEA1 might be internalized as signal molecule by receptor-mediated endocytosis Zea mays
(ATDEK1, DEK1, EMB1275, EMB80, AT1G55350) colocalizes with SUPERNUMERARY ALEURONE LAYERS1 (SAL1) Zea mays
plant sterols are distributed within endocytic pathway
EIX triggers internalization of LeEix2 receptor Nicotiana tabacum; Solanum lycopersicum
(DRP5A, AT1G53140) encodes dynamin-related protein Arabidopsis thaliana
PIN2-GFP in (FREE1, FYVE1, PDE330, AT1G20110) mutant showed apparent signal colocalized with endocytic tracker FM4-64 on the vacuolar membrane at 6 hr after uptake Arabidopsis thaliana
(ATMIN7, BEN1, BIG5, MIN7, AT3G43300) localizes to early endocytic compartments Arabidopsis thaliana
CLAVATA1 (ATCLV1, CLV1, FAS3, FLO5, AT1G75820) undergoes endocytosis from plasma membrane Arabidopsis thaliana
FM4-64 uptake is monitored to test effect on endocytosis Arabidopsis thaliana
(ARAC3, ATROP6, RAC3, RHO1PS, ROP6, AT4G35020) CA overexpression caused inhibition of FM4-64 endocytic uptake Arabidopsis thaliana
(RIC1, AT2G33460) overexpression inhibited (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) aggregation into BFA bodies Arabidopsis thaliana
endocytic activity occurs at subapical membrane domain
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) is absent from brefeldin A (BFA) bodies Arabidopsis thaliana
(ADL1, ADL1A, AG68, DL1, DRP1A, RSW9, AT5G42080) function in endocytosis may occur through feedback modulation of membrane lipid order by (ADL1, ADL1A, AG68, DL1, DRP1A, RSW9, AT5G42080)
endocytic tracer FM4–64 labels endosomes
intracellular PIN2-GFP colocalizes with FM4-64 Arabidopsis thaliana
(ATFLS2, FLS2, AT5G63580) S-acylation does not require (AtCHC2, CHC2, AT3G08530) function
prolonged hypertonic treatment revealed distinct zone with significantly decreased labelling on the plasma membrane Nicotiana tabacum
double-mutant lines SS12S6 (ARAC3, ATROP6, RAC3, RHO1PS, ROP6, AT4G35020) SS12S6 (RIC1, AT2G33460) SS12K9 or SS12K9 showed increased PIN1 and PIN2 internalization phenotypes similar to rop6-1 and ric1-1 mutants Arabidopsis thaliana
reserve hexose is transported in bulk into vacuole
accessory protein recruitment results in CLAVATA1 (ATCLV1, CLV1, FAS3, FLO5, AT1G75820) internalization Arabidopsis thaliana
BFA at 10 μM induced hardly any PIN2 internalization in wild-type (WT) roots Arabidopsis thaliana
ABP1-mediated signaling pathway targets clathrin-mediated endocytosis at the plasma membrane
intracellular PIN1-GFP punctae colocalize with FM4-64 Arabidopsis thaliana
tyrphostin A23 still allowed detectable FM4-64 uptake Arabidopsis thaliana
(AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) internalization inhibition by Tyrphostin A23 was even more apparent in presence of BFA Arabidopsis thaliana
jasplakinolide (Jasp) treatment suppressed increase in (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) accumulation in BFA bodies Arabidopsis thaliana
salt treatment induces FM1-43 uptake Arabidopsis thaliana
saline stress activates after 24-h period endocytosis of biotinylated bovine serum albumin Oryza sativa
FM 1-43 at 10 min after washing was internalized by the root hair cell and distinct labeling at the extreme apex of both wild type and (AGD1, VAL1, AT5G61980) root hairs was observed
(SUT1, AT5G63020) might not be internalized via clathrin-dependent pathway Nicotiana tabacum
endocytosis is possible in mature phloem sieve elements Solanum tuberosum; Nicotiana tabacum
end3p is essential for endocytosis
XA21 compartment resembles early endosome or recycling endosome Oryza sativa
vesicle formation is related to protein turnover or recycling of (SUT1, AT5G63020) protein Nicotiana tabacum
BFA treatment causes formation of vesicles in sieve elements Solanum tuberosum
XA21K736E can be internalized in presence of BFA or wortmannin Oryza sativa
actin-related protein (Arp)2/3 complex controls endocytic internalization of plasma membrane
PIN2-EosFP internalizes in response to and is photoconverted in BFA and BFA-compartment-localized Arabidopsis thaliana
regulation of endocytosis is essential in plant cells under challenging biotic or abiotic environmental conditions
ARF-GTPases are involved in clathrin-mediated endocytosis
medium subunit of the tetrameric (AP2, AtAP2, FL1, FLO2, AT4G36920) acts as core of clathrin-mediated endocytosis (CME) machinery
small bright intracellular FM4-64 puncta with TGN/EE localization visible after short exposure of root cells to FM4-64 Arabidopsis thaliana
CPI is required for endocytosis Arabidopsis thaliana
BFA treatment resulted in formation of typical compartments containing (SUT1, AT5G63020) Nicotiana tabacum
elevated density of YFP-CESA6 particles in μ2-1 prc1-1 background likely results from reduction in endocytosis of CESAs due to lack of μ2 function Arabidopsis thaliana
tonic cycling is suggested by calyculin A-accelerated endocytosis without glucose Arabidopsis thaliana
2% D-glucose treatment for 3 days results in over 60% (ATRGS1, RGS1, AT3G26090) internalization Arabidopsis thaliana
(ADL1, ADL1A, AG68, DL1, DRP1A, RSW9, AT5G42080) colocalizes with clathrin light chain (CLC)
GFP–RSL1 and (ATVTI12, VTI12, VTI1B, AT1G26670) /WAVE13 co-localization suggests GFP–RSL1 can recycle from the plasma membrane via the endocytic pathway Nicotiana benthamiana
(ADL1, ADL1A, AG68, DL1, DRP1A, RSW9, AT5G42080) function in endocytosis is required to restrict lateral diffusion of KNOLLE to the plane of cell division Arabidopsis thaliana
uptake of FM4-64 can be quantified under short exposure conditions Arabidopsis thaliana
transient formation and disappearance of μ2-YFP particles synchronized with disappearance of mCherry-CESA6 fluorescence suggest that μ2-YFP and mCherry-CESA6 are functionally associated at plasma membrane Arabidopsis thaliana
ToxA uptake occurs via receptor-mediated-like endocytosis
SNARE family proteins show increased levels of mRNA
endocytosis of membrane-intrinsic proteins is followed by degradation or recycling to the PM
clathrin-dependent endocytosis is well characterized in plants
plant RLKs display diverse endocytosis behavior
K63-polyubiquitylation does not seem to be a prerequisite for endocytosis per se
CME proteins has been extensively characterized in mammals
phosphatidylinositol-4,5-bisphosphate (PI(4,5)P2) modulates endocytosis of PIN-FORMED (PIN) proteins Arabidopsis thaliana
increased number of YFP-CESA6 particles at plasma membrane in μ2-1 prc1-1 background could result from reduced endocytosis of CESAs Arabidopsis thaliana
brittle culm3 (bc3) mutant was mapped to OsDRP2A Oryza sativa
(AP4M, AT4G24550) associates with (ATRBOHD, DELT1, RBOHD, AT5G47910)
medium subunit of the tetrameric (AP2, AtAP2, FL1, FLO2, AT4G36920) concomitantly recruits accessory proteins
medium subunit of the tetrameric (AP2, AtAP2, FL1, FLO2, AT4G36920) concomitantly recruits clathrin triskelia
clathrin-mediated endocytosis (CME) is best-characterized type of endocytosis in eukaryotic cells
clathrin-independent endocytosis mechanisms exist in Arabidopsis Arabidopsis thaliana
dynamin-related proteins is encoded by Arabidopsis genome Arabidopsis thaliana
clathrin-independent pathways are less well investigated understanding of endocytosis
(ATPIN1, PIN1, AT1G73590) undergo endocytosis Arabidopsis thaliana
control strain SUSY7 shows internalization of SUT1–GFP in response to BFA treatment Saccharomyces cerevisiae
end3p interacts with DRM structures
K63-polyubiquitylation does not seem to be a prerequisite for endocytosis
(112A-2A, EMB30, GN, GNOM, MIZ2, VAN7, AT1G13980) localizes to elements of the endocytic pathway Arabidopsis thaliana; Nicotiana benthamiana
GFP–RABA1b Q72L or GFP–RABA1b S27N expression was examined for effect on FM4-64 uptake Arabidopsis thaliana
GTP-fixed (ATRABA1B, BEX5, RAB11, RABA1b, AT1G16920) mutant does not affect endocytosis of FM4-64 dye
(AtKAT1, KAT1, AT5G46240) puncta dissolution is marked by substantial increase in mobility and endocytosis of channels Arabidopsis thaliana
green-to-red photoconvertible fluorescent reporter EosFP demonstrates constitutive endocytosis of PIN auxin efflux carriers Arabidopsis thaliana
Tyrphostin A23 presence only FM4-64 accumulated in BFA compartments while (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) retained at plasma membrane Arabidopsis thaliana
S. cerevisiae (RIC1, AT2G33460) is guanine exchange factor involved in activating Ypt6p GTPase Saccharomyces cerevisiae
animal dynamin has no direct interaction with cargo proteins, such as receptors or transporters
endocytosis appeared to be particularly active in quiescent center Arabidopsis thaliana
different other ROP homologs perform distinct functions in PIN endocytosis Arabidopsis thaliana
FLS2-GFP internalization is significantly reduced in (UBC13A, UBC35, AT1G78870) (AtUBC36, UBC13B, UBC36, AT1G16890) background Arabidopsis thaliana
BY-2 cells is used as model for plant endocytosis
ROS production has been associated with triggering endocytotic events Arabidopsis thaliana
(HUB1, RDO4, AT2G44950) (C-terminal part of clathrin heavy chain) exerts dominant negative effect on clathrin function Arabidopsis thaliana
disruption of spatial organization and proper function of apical F-actin results in inhibition of apical endocytosis
(ATFLS2, FLS2, AT5G63580) becomes specifically internalized into highly mobile vesicles upon addition of flg22 Arabidopsis thaliana
TE is trafficking and endocytosis inhibitor
(AGC1-1, D6PK, AT5G55910) becomes visible in cytosol
cell-plate formation relies on sterol-dependent endocytosis Arabidopsis thaliana
GN has a role in control of endocytosis at the plasma membrane
1-naphthaleneacetic acid (1-NAA) treatment inhibits FM4-64 uptake
meristematic cells other than protophloem have low endocytosis rate Arabidopsis thaliana
latrunculin B treatment induced (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) accumulation in BFA bodies Arabidopsis thaliana
cell-plate formation relies on DYNAMIN-RELATED PROTEIN1A (ADL1, ADL1A, AG68, DL1, DRP1A, RSW9, AT5G42080) -dependent endocytosis Arabidopsis thaliana
low concentrations of wortmannin (10–25 nM) does not affect Vps34p endocytosis in yeast
AtPMEI-2 is trapped in BFA-induced endosomal aggregates Arabidopsis thaliana
clathrin- and microdomain-dependent endocytic pathways cooperatively regulate (ATRBOHD, DELT1, RBOHD, AT5G47910) dynamics
effectors may induce endocytosis
clathrin-mediated endocytosis (CME) is major endocytic pathway in Arabidopsis Arabidopsis thaliana
clathrin H chain is encoded by Arabidopsis genome Arabidopsis thaliana
μ2-1 cells exhibited approximately 45% decrease in FM4-64 internalization compared with wild type Arabidopsis thaliana
μ2 mediates internalization of CESAs would be expected to affect distribution of CESAs at plasma membrane Arabidopsis thaliana
sterols have role in internalization of membrane structures
filipin application reduces internalization of FM4-64
Wortmannin (Wm) interferes with maturation of late endosomes and multivesicular bodies
StSUT1 undergoes endocytosis in sieve elements Solanum tuberosum; Nicotiana tabacum
(ACR4, CR4, AT3G59420) and (ATDEK1, DEK1, EMB1275, EMB80, AT1G55350) are regulated by ligand-induced endocytosis Zea mays
non-elongating root hairs did not internalize and accumulate FM4-64
PIN auxin transporters activity is regulated by constitutive cycling between plasma membrane and endosomes Arabidopsis thaliana
clathrin-independent mechanisms may occur via lipid rafts
changes in cellular sterol composition by filipin reduce LeEix2 internalization
sterols might be involved in nonclathrin endocytosis
general endocytic efficiency of μ2-1 and wild-type seedlings quantified in root epidermal cells after 8.5-min exposure to 2 μM FM4-64 Arabidopsis thaliana
temporal behavior of colocalized μ2-YFP and mCherry-CESA6 particles observed transient formation and disappearance of μ2-YFP particles synchronized with disappearance or depletion of mCherry-CESA6 fluorescence Arabidopsis thaliana
filipin application reduces internalization of (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090)
PIRE facilitates endocytosis of (ATRBOHD, DELT1, RBOHD, AT5G47910)
higher density of YFP-CESA6 at plasma membrane in μ2-1 mutant seedlings may result from endocytosis defect of μ2-1 Arabidopsis thaliana
CRINKLY4 (ACR4, CR4, AT3G59420) colocalizes with SUPERNUMERARY ALEURONE LAYERS1 (ALX8, AtFRY1, ATSAL1, FRY1, HOS2, OLD101, RON1, SAL1, SUPO1, AT5G63980) Zea mays
cholesterol has important role in internalization steps through clathrin-coated pits
sterols and sphingolipids are responsible for functionality in endocytic pathway
FM4-64 dye is thought to enter secretory pathway by endocytosis Arabidopsis thaliana
Wortmannin (Wm) interferes with formation of endocytic vesicles from the plasma membrane
raft-like microdomains were previously linked to endocytosis
StSUT1–GFP can be found at internalization sites
PM-bound XA21 can be internalized in presence of BFA or wortmannin Oryza sativa
(AtBOR1, BOR1, AT2G47160) is endocytosed in monoubiquitylated state
(ARA-7, ARA7, atARA7, ATRAB-F2B, ATRAB5B, ATRABF2B, RAB-F2B, RABF2B, AT4G19640) present on late endosomes in various cell types
clathrin-mediated endocytosis takes place in sub-apical region of pollen tube
endocytosis is required to bring activated receptors to endosome
EIX triggers localization of LeEix2 receptor to endosomes Nicotiana tabacum; Solanum lycopersicum
vesicle transport v-SNARE show increased levels of mRNA
plant sterols are internalized into endosomes
sterols might be involved in clathrin-mediated endocytosis
5-h treatment of roots in a solution containing β-estradiol caused apical cytoplasmic space of elongating root hairs contained FM4-64 fluorescence significantly less
(ATRGS1, RGS1, AT3G26090) co-trafficked with endosomal markers that reside in early to late endosomes Arabidopsis thaliana
substitution of the conserved Thr residues inhibits NIP5;1 endocytosis Arabidopsis thaliana
endocytic processes require membrane components that form transport vesicles
clathrin-coated pits serve as internalization platforms for plasma membrane-associated molecules and cargo
lack of B results in inhibition of endocytosis
MoEnd3-mediated endocytosis is responsible for internalization of noncanonical (GCR2, GPCR, AT1G52920) Pth11 Magnaporthe oryzae
(AP2, AtAP2, FL1, FLO2, AT4G36920) complex component is first to visualize in living plant cells Arabidopsis thaliana
GFP–RABA1b Q72L or GFP–RABA1b S27N expression had no significant effect on FM4-64 internalization kinetics Arabidopsis thaliana
SlCPI activity affects endocytosis Solanum lycopersicum
clathrin-dependent endocytic pathways is focus of endocytosis and plant trafficking research
inducibly overexpressed PCaP2–GFP suppressed FM4-64 internalization Arabidopsis thaliana
inducibly overexpressed (MAP18, PCAP2, AT5G44610) –GFP derivative lacking the N23 domain did not suppress FM4-64 internalization Arabidopsis thaliana
(MAP18, PCAP2, AT5G44610) ∆23 overexpression induction did not affect formation of PIN2–GFP-containing BFA bodies
wild-type AtRGS1-YFP was localized to the plasma membrane and endocytosed upon D-glucose treatment Arabidopsis thaliana
(MAP18, PCAP2, AT5G44610) overexpression was examined for effects on endocytic recycling of (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090)
PIN1-RFP coexpression with secreted AUXIN BINDING PROTEIN 1 (ABP, ABP1, AT4G02980) ΔKDEL-GFP results in strong internalization of PIN1-RFP Nicotiana tabacum
pPLAIIγ-YFP co-localizes with endocytic tracer FM4-64 Arabidopsis thaliana
μ2 plays role in clathrin-mediated endocytosis (CME) in Arabidopsis Arabidopsis thaliana
PtrXB38 localization in Golgi apparatus suggests that PtrXB38 may affect endocytosis pathway Populus tremula × Populus alba
1-naphthaleneacetic acid (1-NAA) treatment does not inhibit BFA-induced (AGC1-1, D6PK, AT5G55910) internalization
(ATWNK1, WNK1, ZIK4, AT3G04910) promotes clathrin-dependent endocytosis of potassium channels
AtWNK kinases phosphorylate (ATRGS1, RGS1, AT3G26090)
endosomes play a critical role in sorting the degradation or reutilization of membrane components
flg22-induced, BAK1-dependent (ATFLS2, FLS2, AT5G63580) S-acylation prevents premature internalization of activated (ATFLS2, FLS2, AT5G63580) complexes
FM1-43 is used as endocytic tracer
(ATWNK1, WNK1, ZIK4, AT3G04910) promotes clathrin-dependent endocytosis of renal ion transporters
reduced expression of AUXIN BINDING PROTEIN 1 (ABP, ABP1, AT4G02980) leads to reduced (ATPIN1, PIN1, AT1G73590) internalization Arabidopsis thaliana
AUXIN BINDING PROTEIN 1 (ABP, ABP1, AT4G02980) exported from ER regulates endocytosis Nicotiana tabacum
35S::ABP1 ΔKDEL-GFP expression in moderately expressing seedlings increased (ATPIN1, PIN1, AT1G73590) internalization Arabidopsis thaliana
PIN proteins are internalized by clathrin-based mechanism of endocytosis Arabidopsis thaliana
(ATGPA1, GP ALPHA 1, GPA1, AT2G26300) (Q222L) mutation combined with (ATRGS1, RGS1, AT3G26090) (E320K) mutation failed to trigger (ATRGS1, RGS1, AT3G26090) (E320K) internalization under any condition Arabidopsis thaliana
endocytosis has identified endocytic cargos
DN- (ARAC4, ATRAC4, ATROP2, ROP2, AT1G20090) (dominant negative ) coexpression increases endosome-like PIN1-GFP dots in cytoplasm Arabidopsis thaliana
dose-duration reciprocity operates above 1% D-glucose concentration Arabidopsis thaliana
cholesterol has important role in internalization steps through caveolae
wortmannin treatment for 30 min prior to adding FM dye could inhibit endocytosis in apex of the pollen tube but not in tube shank Nicotiana tabacum
DRP2 gene family exhibits redundancy Arabidopsis thaliana
FM4-64 binds to plasma membrane Arabidopsis thaliana
(ATRGS1, RGS1, AT3G26090) trafficking was measured in the absence of selected WNK kinases with and without 6% D-glucose Arabidopsis thaliana
C-terminal truncation mutant (AtRGS1-ΔCtSA) was assayed for D-glucose dependent endocytosis Arabidopsis thaliana
(ATWNK8, EIP1, WNK8, AT5G41990) associated with (ATRGS1, RGS1, AT3G26090) at endosomes occurred within 30 minutes of stimulation Arabidopsis thaliana
(MAP18, PCAP2, AT5G44610) binding to PtdIns(4,5)P2 on the plasma membrane may arrest clathrin-mediated endocytosis
(ATPIN1, PIN1, AT1G73590) internalization is not indirect result of lobing defect Arabidopsis thaliana
(SUT1, AT5G63020) raft localization is linked to capacity of (SUT1, AT5G63020) protein to be internalized by endocytosis Saccharomyces cerevisiae
smooth (clathrin-independent) endocytosis occurs at extreme apex of pollen tube
(AP2, AtAP2, FL1, FLO2, AT4G36920) complex component is first to show affect of endocytosis in plants Arabidopsis thaliana
VPS23A:RFP and (TOL6, AT2G38410) are found in early endosomal structures Arabidopsis thaliana
In root parenchymal cells the number of vesicles in the lumen of the MVBs was slightly higher in mutant than in WT cells Arabidopsis thaliana
phospholipase D induces increase in clathrin-mediated endocytosis
endocytosis in plants is actin-dependent Arabidopsis thaliana
C-terminal μ-homology domain of μ2 (μ2MHD) involved in specific interactions with endocytic cargo proteins
FYVE-domain protein binds to and sequesters phosphatidylinositol-3-phosphate enriched endosomal membranes Arabidopsis thaliana
membrane potential of yeast plasma membrane is linked to capacity of (SUT1, AT5G63020) protein to be internalized by endocytosis Saccharomyces cerevisiae
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) constitutively endocytoses
EXPO (exocyst-positive organelle) is distinct from multivesicular endosomes
(AGC1-1, D6PK, AT5G55910) becomes internalized into FM4-64-labeled endosomes
(ATIRT1, IRT1, AT4G19690) and (AtBOR1, BOR1, AT2G47160) are endocytosed in monoubiquitylated state without K63-linked polyubiquitylation Arabidopsis thaliana
endocytotic cycling provides necessary spatial and temporal dimensions to signaling
(ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) and (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) endocytose from membrane Arabidopsis thaliana
BFA pre-treatment of potato leaf tissue results in punctuate structures in sieve elements labeled with SUT1-specific antibody Solanum tuberosum
inhibitor studies affecting vesicle trafficking concluded that (SUT1, AT5G63020) can be internalized in an actin-dependent manner Nicotiana tabacum
XA21–GFP and XA21 K736E–GFP-containing organelles are likely the same as early endosomes containing mRFP–SCAMP1 Oryza sativa
sterol composition of yeast plasma membrane is linked to capacity of (SUT1, AT5G63020) protein to be internalized by endocytosis Saccharomyces cerevisiae
endocytic pathways differ in participation of different proteins
pLat52:TPLATE-GS yellow transgenic line shows dynamic recruitment of TPLATE-GS yellow at plasma membrane Arabidopsis thaliana
BFA (brefeldin A) treatment induces internalization of SUT1–GFP Saccharomyces cerevisiae
(SUT1, AT5G63020) internalization is actin-dependent actin Nicotiana tabacum
uptake and trafficking of FM4-64 dye occurs more slowly in DDYM mutant Sorghum bicolor
some aggregates of FM4-64 vesicles did not show Brownian motion Arabidopsis thaliana
XA21 can be internalized via SCAMP-positive early endosomal compartment Oryza sativa
(ATIRT1, IRT1, AT4G19690) and (AtBOR1, BOR1, AT2G47160) lack K63-linked polyubiquitylation
TGN is now considered to be independent and endocytic compartment of plant cells Arabidopsis thaliana
StSUT1 localizes to vesicles Solanum tuberosum
sieve elements demonstrate capability for endocytosis Solanum tuberosum; Nicotiana tabacum
BFA (brefeldin A) has no effect in yeast ergosterol mutant Δerg6 Saccharomyces cerevisiae
wortmannin treatment increases cytosolic vesicles containing XA21–GFP Oryza sativa
FER-mediated endocytosis mediates root growth Arabidopsis thaliana
brefeldin A (BFA) disrupts endocytosis
internalization signals are present in plasma membrane cargo proteins
(AtKAT1, KAT1, AT5G46240) undergoes endocytosis in plants
TOL6:Ven localization indicated by signal overlaps with endocytosed styryl dye FM4-64 Arabidopsis thaliana
BFA treatment induces accumulation of (SUT1, AT5G63020) in BFA compartments Solanum tuberosum
(SUT1, AT5G63020) association to raft-like structures is interdependent with capacity of (SUT1, AT5G63020) to be internalized Saccharomyces cerevisiae; Nicotiana tabacum
Δend3 mutant is defective in endocytosis Saccharomyces cerevisiae
endocytic processes occur in plants
StSUT1 is internalized in presence of brefeldin A (BFA) Saccharomyces cerevisiae; Nicotiana tabacum; Solanum tuberosum
(ATPIN1, PIN1, AT1G73590) undergoes endocytosis in plants
actin cytoskeleton is essential for internalization step of endocytosis
TOL6:mCherry is also found in endocytic membrane fractions Arabidopsis thaliana
FM4-64 internalization is inhibited in sos1-1 root meristematic cells under salt stress Arabidopsis thaliana
MSBP1-deficient plants show decreased vesicle trafficking Arabidopsis thaliana
K63-linked ubiquitin chains have been associated with endocytosis Saccharomyces cerevisiae; Mammalia; Arabidopsis thaliana
K63-linked ubiquitination fulfills important roles in endocytosis
SlCPI attenuates endocytosis Solanum lycopersicum
TyrA23 treatment leads to reduced internalization of endocytic vesicles from the plasma membrane
BFA effect in plants can affect endocytic processes Arabidopsis thaliana; Nicotiana benthamiana
alterations in sterol composition that induce accumulation of cyclopropylsterols affect the release of (ADL1, ADL1A, AG68, DL1, DRP1A, RSW9, AT5G42080) from the membrane during endocytosis
sterol endocytic pathway has been shown to interrupt trafficking of (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) Arabidopsis thaliana
endocytosis of SlSUT1 in yeast cells depends on cortical actin cytoskeleton Saccharomyces cerevisiae
cytoskeletal components are prerequisite for endocytic events
membrane rafts is suggested to be involved in endocytic process
2% D-glucose treatment for 4 days increases (ATRGS1, RGS1, AT3G26090) internalization to 70% Arabidopsis thaliana
BFA treatment causes endocytosed PINs to accumulate in BFA compartments Arabidopsis thaliana
(AGC1-1, D6PK, AT5G55910) removal from plasma membrane is much faster than PIN protein removal from plasma membrane Arabidopsis thaliana
(JK224, NPH1, PHOT1, RPT1, AT3G45780) is trafficking by clathrin-mediated endocytosis
FM4-64 can still be detected in BFA compartments
endocytic pathways differ in size, shape, and composition of endocytic vesicles
PMEI is internalized via clathrin-mediated endocytosis
PA probes colocalized with endocytic dye FM4-64 Arabidopsis thaliana
Pep1-PEPR complex on plasma membrane is internalized and transported to vacuole Arabidopsis
findings regarding GN and (AGC1-1, D6PK, AT5G55910) do not support role for GN in control of endocytosis in the case of (AGC1-1, D6PK, AT5G55910)
RAB-A5c compartments fail to accumulate non-specific membrane dye FM4-64
cytokinin perception might target endocytotic pathways
inhibition of apical endocytosis only results in swollen or balloon-like shape of pollen tube tip
wortmannin is used to inhibit endocytosis