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gravitropism

11494 relationships annotated with this phrase. Showing first 500 of 11494.
Source entity Relationship Target entity Species
gravitropic response plays essential role in controlling plant growth direction and architecture
egt2 mutation results in enhanced gravitropic response in barley roots Hordeum vulgare
gravity changes lead to alterations in shape of endodermal cells
gravistimulation caused transcriptome adjustment Hordeum vulgare
modules with strong correlation with genotype were contrastingly correlated with gravitropic response of WT and egt2 Hordeum vulgare
interaction candidates that responded to gravistimulation was significantly higher than expected by chance Hordeum vulgare
Mp (ATPIN1, PIN1, AT1G73590) is required for orthotropic growth of gametangiophore stalks Marchantia polymorpha
gravity vectors influence directional growth of gametophore stalks Marchantia polymorpha
study results highlight transcriptomic reprogramming of gravitropic response of barley roots Hordeum vulgare
homolog of ZmCIPK15 was significantly downregulated in root cap after 12 h of gravistimulation root cap Hordeum vulgare
gravity changes lead to alterations in transcript levels of genes associated with cell wall modifications
seedlings pretreated with 10 µm NPPB show no auxin reporter asymmetry between upper and lower flanks of root Arabidopsis thaliana
gravitropic bending is subject to more extensive transcriptomic regulation in elongation zone Hordeum vulgare
EGT2 mediates gravity signal transduction at protein level Hordeum vulgare
gain-of-function mutant of OsIAA3 lost gravitropism
(AtMYB1, MYB1, SRM1, AT3G09230) mutant shows severely impaired responses to gravity Oryza sativa
WT barley roots angle adjustment reached 30° (> 60% of the total adjusted angle) after 12 h of rotation Hordeum vulgare
signal transduction in meristem involves less transcriptomic regulation than gravitropic bending in elongation zone Hordeum vulgare
gravity affects morphology and functions of organisms
caulonema filaments in Δ ftsZ3 mutants grew in different directions directional growth Physcomitrella patens
EGT2 plays a critical role in regulating root gravitropic bending Hordeum vulgare
RRS1-KO mutants had stronger gravitropic response in roots
phosphate (Pi) has no significant effect on gravitropic response of Arabidopsis roots Arabidopsis thaliana
root gravitropism allows plants to penetrate deeply into soil
RNA-seq performed at time points before gravistimulation and 3, 6, and 12 h after reorientation of roots by 90° Hordeum vulgare
hypergravistimulation achieved by reorienting specimens 90° under hypergravity conditions (e.g. 5 g) enhances root gravitropic curvature Arabidopsis thaliana
WEEP function in shoot gravitropism shows similarities to EGT2 function in roots
EGT2 might induce expression of gravity-responsive genes that negatively regulate root gravitropism Hordeum vulgare
gravitropism regulation of EGT2 might be similar to gravitropism regulation of EGT1 Hordeum vulgare
RRS1-OE lines is consistent with gain-of-function mutant of OsIAA3
homolog of AtLZY2 and AtLZY3 was significantly downregulated in root cap after 12 h of gravistimulation root cap Hordeum vulgare
NAKED PINS IN YUCCA 2 controls root gravitropic response Arabidopsis thaliana
gravistimulation induces asymmetric distribution of ROS in distal elongation zone of root
new dorsal tissue was facing upwards equally for all genotypes Marchantia polymorpha
dorsiventral polarity is determined by gravity vectors Marchantia polymorpha
EGT2-regulated genes in elongation zone were also regulated by gravistimulation in WT roots Hordeum vulgare
rapid gravity-sensing mechanism linearly transduces wide range of gravitational changes (0.5 g–2 g) into Ca2+ signals Arabidopsis thaliana
PABA suppresses root-coiling phenotype of (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) mutant Arabidopsis thaliana
re-orientation of the cytoskeleton initiates curvature of the growing cell Physcomitrella patens
EGT2 might play a positive role in regulating antigravitropic offset (AGO) Hordeum vulgare
modules correlated only with egt2 at some time point after gravistimulation might be involved in EGT2-dependent gravitropism Hordeum vulgare
ren1-D mutant roots exhibit enhanced gravitropic response Oryza sativa
gravity response involves asymmetric redistribution of auxin to lower side of root tip
PABA-promoted root gravitropism is due to PABA-promoted root asymmetric growth Arabidopsis thaliana
normal gravitropic growth orientation of the hypocotyl response is seemingly lost in phot1-deficient mutants in Arabidopsis Arabidopsis thaliana
(ATPIN3, PIN3, AT1G70940) and (ATPIN7, PIN7, AT1G23080) efflux facilitators are located in columella
five NPY genes all contribute to gravitropism Arabidopsis thaliana
auxin polar transport is essential for plants to properly respond to gravity stimuli Arabidopsis thaliana
gravitropism depends on auxin redistribution Arabidopsis thaliana
manipulation of endogenous free PABA levels impacts root graviresponse Arabidopsis thaliana
PABA suppresses root sinusoidal growth of wei8wei2 double mutant Arabidopsis thaliana
NPPB (5-nitro-2-(3-phenylpropylamino)-benzoic acid) pretreatment prevents creation of lateral asymmetry induced by gravity Arabidopsis thaliana
NPPB (5-nitro-2-(3-phenylpropylamino)-benzoic acid) pretreatment should impair gravitropism Arabidopsis thaliana
root curvature occurs in response to gravistimulus Arabidopsis thaliana
(ABI5, AtABI5, DPBF1, GIA1, AT2G36270) mutation partially rescues loss of hypocotyl negative gravitropism in pifq mutants Arabidopsis thaliana
Δ ftsZ3 mutants showed impaired gravitropic response Physcomitrella patens
gravistimulation at 3 h caused only little transcriptome adjustment Hordeum vulgare
AtLZY2 and AtLZY3 has role in root columella cells during gravitropic response Arabidopsis thaliana
number of observed interaction candidates that responded to gravistimulation highlights role of EGT2 in root gravitropic response Hordeum vulgare
hypergravistimulation achieved by reorienting specimens 90° under hypergravity conditions (e.g. 5 g) enhances gravitropic curvature Arabidopsis thaliana
ethylene inhibits cell elongation on lower side of gravistimulated root
transcriptional module of auxin response causes inhibition of cell elongation on lower side of root
2,3-butanedione 2-monoxime (BDM) affects amyloplast movement
plants orient their growth to ensure roots are anchored in soil and shoots grow upward Arabidopsis thaliana
gravitropism allows plants to anchor roots in soil for nutrient uptake
root curvature takes place at elongation zone Arabidopsis thaliana
(PIF1, PIL5, AT2G20180) mutation slightly rescues hypersensitive phenotypes of (AtHMAC6, AtHMP38, HMA6, PAA1, PCH1, AT4G33520) and pchl mutants Arabidopsis thaliana
calcium (Ca2+) play key roles in gravitropism
NPH3-like genes are hypothesized to be required for gravitropic responses Arabidopsis thaliana
NPY genes are expressed in right places for regulating gravitropism Arabidopsis thaliana
phytochromes suppress hypocotyl negative gravitropism by inhibiting PIFs Arabidopsis thaliana
plants can sense direction of gravity Arabidopsis thaliana
(ABR, PID, AT2G34650) regulates root gravitropic response Arabidopsis thaliana
(ABCB4, AtABCB4, ATPGP4, MDR4, PGP4, AT2G47000) and (ATCHS, CHS, TT4, AT5G13930) were shown to be epistatic in gravitropic bending
roots are anchored in soil Arabidopsis thaliana
(ARF7, BIP, IAA21, IAA23, IAA25, MSG1, NPH4, TIR5, AT5G20730) is required for gravitropism Arabidopsis thaliana
(HY3, OOP1, PHYB, AT2G18790) mutation completely rescues negative gravitropism phenotype Arabidopsis thaliana
(ABR, PID, AT2G34650) /WAG kinases have been implicated in gravitropism Arabidopsis thaliana
auxin signaling is essential for plants to properly respond to gravity stimuli Arabidopsis thaliana
polar streams of auxin regulate plastic growth responses to gravity
(ATXTH19, XTH19, AT4G30290) and (XTH23, XTR6, AT4G25810) expression is strongly induced by gravity stimulation Arabidopsis thaliana
plates with 4-day-old Arabidopsis seedlings photographed to measure angle between gravity and primary root Arabidopsis thaliana
Starch granules containing amyloplasts are responsible for gravity sensing Arabidopsis thaliana
JAZ4-mediated gravitropic response may play a role in unknown mechanisms of gravity sensing Arabidopsis thaliana
ammonium compromises PR gravitropism via attenuating asymmetric auxin reflow under gravistimulation
(ARF7, BIP, IAA21, IAA23, IAA25, MSG1, NPH4, TIR5, AT5G20730) (ARF11, ARF19, IAA22, AT1G19220) double mutants show agravitropic root growth Arabidopsis thaliana
NPY proteins direct partners are not known Arabidopsis thaliana
LZY4 is expressed in root tip Arabidopsis thaliana
LZY2 and LZY3 function in both shoot and root gravitropism Arabidopsis thaliana
(AtLAZY1, LAZY1, AT5G14090) family proteins localization in gravity-sensing cells is yet unknown gravity-sensing cells
(ATPIN3, PIN3, AT1G70940) and (ATPIN7, PIN7, AT1G23080) efflux facilitators initiate asymmetric auxin redistribution
LZY1, LZY2, LZY3, and LZY4 are expressed in gravity-sensing cells Arabidopsis thaliana
actin-mediated and PID-mediated mechanisms mediate (ATPIN3, PIN3, AT1G70940) symmetry re-establishment in endodermis Arabidopsis thaliana
OsYUC1 overexpression caused defective gravitropism Oryza sativa
Heatin did not interfere with gravitropism Arabidopsis thaliana
mechanosensitive channels have been implicated in perception of gravity
gravitropism ensures shoots grow upwards into air
silique (or fruit) might have fundamentally the same gravitropism as stem Arabidopsis thaliana
pedicel growth angle did not change in response to 3-D clinorotation growth conditions Arabidopsis thaliana
gravitropic responses allow plants to orient roots and shoots in the right directions
(AGC1-1, D6PK, AT5G55910) kinases have been implicated in gravitropism Arabidopsis thaliana
gravistimulation triggers (ATPIN3, PIN3, AT1G70940) relocation to basal side of endodermis cells Arabidopsis thaliana
root columella cells are involved in gravitropism in root organs Arabidopsis thaliana
LZY2 is expressed in shoot endodermal cells Arabidopsis thaliana
restoration of AUX1- and PIN3-mediated lateral auxin gradient protects root gravitropism under ammonium
Col-0 roots corrected significantly further than jaz4-1 roots Arabidopsis thaliana
diversity of characters involved in gravitropic reaction may contribute to differentiation of height growth strategies among young tropical trees
biomechanical model was used to separate effects of increasing self-weight and balancing gravitropic reaction
gravitropism is directional control of plant organ growth in response to gravity
NPY genes are hypothesized to be important for gravitropism Arabidopsis thaliana
(ABR, PID, AT2G34650) overexpression results in decrease in gravitropic response
diversity in gravitropic efficiency may contribute to differentiation of height growth strategies among young tropical trees
autotropic straightening movement is revealed by very non-uniform change in curvature along the stem
actin–myosin XI interactions act as sensor for plant posture Arabidopsis thaliana
LZY1 is located in nucleus
auxin maximum in lower hypocotyl stimulates differential growth and bending of hypocotyl against gravity vector Arabidopsis thaliana
myosin XI knockout exhibit hyperbending of stems in response to gravity Arabidopsis thaliana
(ATPIN3, PIN3, AT1G70940) displays uniform distribution in root columella cells
pldζ1 mutant displays exaggerated gravitropic response induced by salt
high-affinity auxin influx carrier is involved in root gravitropism Arabidopsis thaliana
plates rotated 90° and returned to darkness for additional 24 h
(AtLAZY1, LAZY1, AT5G14090) family proteins have conserved localization Arabidopsis thaliana
(AtLAZY1, LAZY1, AT5G14090) family proteins have conserved functional domain Arabidopsis thaliana
inositol 1,4,5-trisphosphate (InsP 3) is generated rapidly upon gravistimulation in plant tissues
PIN proteins are essential for root gravitropism
overexpressed (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) results in enhanced tropistic response Arabidopsis thaliana
growth response of plants to altered gravity conditions is plant specific
inositol 1,4,5-trisphosphate (InsP3) production is required for indole-3-acetic acid (IAA)-dependent asymmetric growth of the pulvini and gravitropic curvature Zea mays; Avena sativa
inhibitors of NOS and NR did not completely abolish fluorescent signal from DAF in gravitropic bending of root Glycine max
flavonoid mutant's altered gravitational response was eventually corrected in roots or aerial tissues Arabidopsis thaliana
roots show positive gravitropism
jaz4-1 roots show gravitropic effect Arabidopsis thaliana
gravity-sensing cells contain high-density starch-accumulating amyloplasts Arabidopsis thaliana
35S::MPID overexpression line did not alter root gravitropism
seedlings rotated 90° and grown for 24 hours in darkness gravitropic response assay
shoots grow against direction of gravity
xyloglucanase (AaXEG2) overexpression results in less gravitropism Populus trichocarpa
(ATCNGC11, CNGC11, AT2G46440) and (ATCNGC12, CNGC12, AT2G46450) null mutants exhibit attenuations in gravitropic responses Arabidopsis thaliana
statolith position affects local changes in [Ca2+]i
enhanced auxin redistribution in bending regions is mainly due to root gravitropism and anti-gravitropism of hypocotyl
microgravity environment of space altered angle of lateral organ growth with respect to the main stem
stem curvature depends on diameter growth
gravitropic movements occur in woody stems
NPA application or saturation of tissues with picloram disturbs coordinated gravity-directed growth (gravitropic response) Arabidopsis thaliana
LZY1 is located in plasma membrane
Cholodney–Went hypothesis is hypothesis on mechanism of gravitropism
lateral organs are maintained at particular angles with respect to the gravity vector during different stages of growth
SCAR complex subunit mutants do not have significantly altered root gravitropic responses
embryos reached the heart stage of development at ∼5 DAF corresponded to most pronounced response of siliques (e.g. P5 and P6) to 3-D clinorotation Arabidopsis thaliana
pedicels of pro35S::KNAT1 plants were insensitive to 3-D clinorotation Arabidopsis thaliana
gravitropic response was reduced in D132 and RNAi-CLA4 transgenic seedlings compared with D132-NIL and sibling control seedlings Zea mays
35S::PID overexpression line altered hypocotyl gravitropism
gravitropism ensures roots grow down into soil
gravi-stimulation induces asymmetric (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) distribution
plants grown in microgravity environment of space exhibited automorphogensis
most plant organs remain at particular angle with respect to the vertical growth axis
RAP2.4-ox seedlings exhibit enhanced negative gravitropic growth under continuous red light Arabidopsis thaliana
DAF-2DA probe has revealed detection of asymmetric intracellular NO during gravitropic bending of soybean roots Glycine max
statoliths sedimentation and membrane deformation affects cell expansion and growth
root gravitropism is not under the exclusive control of auxin
direction of lateral organ growth might reflect balance between the forces of negative and positive gravitropism
Arabidopsis siliques formed upward angles on inflorescence Arabidopsis thaliana
normal siliques (with developing seeds) showed no difference in angles compared to empty siliques under 1 g control growth condition Arabidopsis thaliana
lazy (la) mutant in rice is agravitropic mutant Oryza sativa
MSBP1-overexpressing seedlings show reduced sensitivity to NPA inhibition of root gravity response Arabidopsis thaliana
presence of developing seeds in the siliques is essential for pedicel response to altered gravity Arabidopsis thaliana
microtubule elimination blocks redistribution of auxin flow by gravitropic stimulation
vertical germination and growth assays are performed with plates placed vertically on a rack
reduced sensitivity to indole-3-acetic acid (IAA) in the absence of inositolpolyphosphates is in line with reduced gravitropic curvature responses in InsP5-ptase plants Arabidopsis thaliana
3-D clinorotated growth condition significantly increased angle between inflorescent stem and pedicels Arabidopsis thaliana
pedicels of siliques containing unfertilized, aborted seeds did not respond to 3-D clinorotation Arabidopsis thaliana
suppression of microtubule dynamics blocks redistribution of auxin flow by gravitropic stimulation Oryza sativa
mutations in (ATSYP22, ATVAM3, SGR3, SYP22, VAM3, AT5G46860) (= (AtGDPD1, GDPD1, SRG3, AT3G02040) ) suppress gravitropism Arabidopsis thaliana
elongated branch point cells might contribute to pedicel response to altered gravity
plants overexpressing (ABR, PID, AT2G34650) reduce relocalization of (ATPIN3, PIN3, AT1G70940) upon gravistimulation in root and shoot Arabidopsis thaliana
nph4map1 mutant seedlings exhibit alterations in root gravitropism Arabidopsis thaliana
RAP2.4-ox seedlings exhibit enhanced negative gravitropic growth under continuous far-red light Arabidopsis thaliana
starch–statolith hypothesis is hypothesis on mechanism of gravitropism
gravitropic reaction in woody stems is achieved by induction of asymmetric maturation stress in newly formed growth ring
auxin transporter (AtAUX1, AUX1, MAP1, PIR1, WAV5, AT2G38120) is required for correct gravitropic response in the roots
growth angles of pedicels under the 2-D horizontal rotation condition were apparently larger than growth angles in both the vertical and stationary condition Arabidopsis thaliana
gravitropic efficiency is expected to be larger in species producing large amount of tension wood located on upper side of tilted stem
(AtLAZY1, LAZY1, AT5G14090) family genes share common molecular function in plant gravitropism Arabidopsis thaliana
(ARAC4, ATRAC4, ATROP2, ROP2, AT1G20090) overexpression increases gravity responsiveness
Arabidopsis plants with two siliques grew for 5 d under simulated microgravity condition on a 3-D clinostat Arabidopsis thaliana
pedicels of plants grown on a rotating 3-D clinostat pedicel positioning is affected by altered gravity
stem re-orientations are costly in woody plants
shade-tolerant species have smaller efficiency of gravitropic reaction
autotropic movement seems to be designed to maintain a constant tilt angle in the distal parts while the stem straightens
LZY6 appears not to be expressed in gravity-sensing cells Arabidopsis thaliana
3 d old etiolated F3 progeny were scored for hypocotyl gravitropism Arabidopsis thaliana
plants grown on a 3-D clinostat displayed architecture similar to that of space-grown plants
clinorotated plants showed stem–pedicel angles ranging from 40° to 100° Arabidopsis thaliana
auxin triggers mechanism of gravitropic bending with concomitant asymmetric NO accumulation in the root Glycine max
gravitropism is associated with statoliths
(ARP2, ATARP2, WRM, AT3G27000) /3 complex subunit mutants do not have significantly altered root gravitropic responses
shift of the motor process is usually termed automorphogenesis
control of gravitropic reaction is expected to be influenced by plagiotropic or orthotropic habit of stem
autotropic straightening is achieved by production of reaction wood on the opposite side of the stem before it overshoots the vertical
change in tangent angle for C. obtusa and T. melinonii is non-negligible contribution to the up-righting movement Cecropia obtusa; Tachigali melinonii
seedlings allowed to grow along agar surface
MSBP1-deficient seedlings show reduced hypocotyl anti-gravitropism Arabidopsis thaliana
MSBP1-deficient plants show almost undetectable asymmetric auxin distribution after 4 h gravi-stimulation Arabidopsis thaliana
Pedicels at early development stage did not respond to 3-D clinorotation Arabidopsis thaliana
genetic or pharmacological interference with the late (ATPIN3, PIN3, AT1G70940) polarization prevents termination of the response
xiao mutant had enhanced gravitropism of roots Oryza sativa
gravitropic efficiency quantifies intrinsic efficiency of the gravitropic mechanism
other species started up-righting mainly by distal parts
curvature analysis was used to analyse up-righting response along the stems
gravitropic reaction in woody stems is necessarily related to diameter growth increments
trajectory parallel to the diagonal indicates changes in curvature occurring in the middle and distal parts of the stem compensate each other
autotropic counter-curving process takes place for all species before stem is close to the vertical
stem curvature in distal parts decreases strongly until reaching values close to 0 during autotropic straightening
change in proximal angle is due to large changes in curvature occurring in the basal part of the stem
cortical arrays change during tropic responses to gravity
gravity-mediated redirection of PIN3-mediated auxin flow redirects auxin fluxes at different time points of gravity response
(AtLAZY1, LAZY1, AT5G14090) mutant shows nearly prostrate growth habit Arabidopsis thaliana
(AtLAZY1, LAZY1, AT5G14090) mutant shows slower response than wild-type inflorescence stem gravitropism Arabidopsis thaliana
tree orientation in angiosperms is based on production of high tensile stress on the upper side of the inclined axis
efficiency of gravitropic reaction differed between species
gravitropic movements are based on common mechanism associated with similar dynamic patterns
functional diversity of gravitropic reaction has possible relationship with ecological or developmental traits
basal part of the stem still rights-up during the third phase species with stabilized distal angle
(AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) polarity changes in response to gravity stimulation
DR5-GUS control plants show extending auxin distribution basipetally along lower side in ~47% of plants after 6 h gravi-stimulation asymmetric auxin distribution Arabidopsis thaliana
MSBP1-deficient plants show small proportion with asymmetric auxin distribution after 6 h gravi-stimulation asymmetric auxin distribution Arabidopsis thaliana
Arabidopsis plants exposed to 3-D clinorotation exhibited altered architecture characterized by orthogonal or downward-oriented siliques Arabidopsis thaliana
plants grown in a 2-D vertical clinorotation condition pedicel angles were not statistically different from stationary control Arabidopsis thaliana
up-righting movement was measured over three months
efficient gravitropic reaction corrects mechanical perturbations
trajectories during the third phase for D. guianensis are almost horizontal distal part of the stem is stabilized at a non-zero angle from vertical Dicorynia guianensis
gravity perception and signal transduction is followed by differential growth
glucose (Glc) application caused a significant decrease in bending of roots upon gravistimulation Arabidopsis thaliana
gravitropic response was compared with D132-NIL and sibling control seedlings
efficient gravitropic reaction is essential for successful height growth and light interception
phytohormones mediates differential growth response with respect to gravity
stem curvature depends on efficiency of the gravitropic reaction
heliophilic species have equilibrium angle closer to vertical
(AtLAZY1, LAZY1, AT5G14090) mutant in Arabidopsis is agravitropic mutant Arabidopsis thaliana
up-righting movement in stems that stabilize at a non-zero angle is followed by decrease in curvature mainly located in the distal part during the last period
mutations in (ATVTI11, ATVTI1A, ITT3, SGR4, VTI11, VTI1A, ZIG, ZIG1, AT5G39510) (= ) exhibit abnormal distribution of endodermal statoliths Arabidopsis thaliana
(ATPIN3, PIN3, AT1G70940) localization to lower membrane of root cap columella contributes to establishment of lateral auxin gradient across root cap
aux1-201 allele exhibits response intermediate between aux1-113 and aux1-7 and aux1-105 alleles Arabidopsis thaliana
(BP, BP1, KNAT1, AT4G08150) expression has relationship with pedicel gravity response Arabidopsis thaliana
downward-oriented siliques of bp mutant is similar to morphology of wild-type plants grown on clinostat Arabidopsis thaliana
auxin redistribution during gravitropic responses is affected by auxin distribution Arabidopsis thaliana
variations in TOL6:mCherry distribution are reminiscent of variable (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) distribution upon gravistimulation Arabidopsis thaliana
auxin influx carrier AUXIN RESISTANT 1 (AtAUX1, AUX1, MAP1, PIR1, WAV5, AT2G38120) plays important roles in auxin transport from the root tip to differentiated tissues during the gravitropic response
curvature analysis was used to study dynamics and kinematics of up-righting movement
all species are decreasing both proximal and distal angles during the second phase
trajectories during the third phase for C. obtusa are almost horizontal distal part of the stem is stabilized at a non-zero angle from vertical Cecropia obtusa
maturation shrinkage of fibre secondary wall is induced by induction of asymmetric maturation stress in newly formed growth ring
angle of equilibrium of stems have been analysed to provide first evaluation of functional diversity of gravitropic reaction
plant annexins are expressed during differential growth during gravitropism
detailed function of OMT, GXM, and HMT in determination of setpoint angle of barley seminal roots by interacting with EGT2 remains to be investigated in future studies Hordeum vulgare
gravistimulation regulates growth direction
D132-NIL seedlings recovered vertical growth in less than 8 hours after being positioned horizontally in dark
spk1-1 mutant seedlings showed altered (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) levels after gravistimulation Arabidopsis thaliana
(AtLAZY1, LAZY1, AT5G14090) mutant shows slower bending during initial hour of gravitropic response Arabidopsis thaliana
pAtLAZY1:AtLAZY1-eGFP rescues (AtLAZY1, LAZY1, AT5G14090) branch angle phenotype Arabidopsis thaliana
lack of auxin transport inhibition during oscillations from positive to negative gravitropic responses possibly caused root looping phenotype in (ATCHS, CHS, TT4, AT5G13930) Arabidopsis thaliana
gravitropic efficiency have been analysed to provide first evaluation of functional diversity of gravitropic reaction
WT barley roots angle adjustment of 10° after 3 h of rotation Hordeum vulgare
Mp (ATPIN1, PIN1, AT1G73590) pro Mp Mp -Citrine /Mp and wild-type thalli positioned dorsal side down showed re-orientation of new thallus growth Marchantia polymorpha
(AtLAZY1, LAZY1, AT5G14090) affects magnitude of growth differential across hypocotyl Arabidopsis thaliana
pif quadruple mutant (pifQ) displays disrupted negative gravitropism of hypocotyls Arabidopsis thaliana
plant roots need to overcome the signal from gravity
pks1pks2pks4 mutant showed gravitropism with same kinetics irrespective of cotyledon position
ROS-related processes supports hypothesis of critical role of EGT2 in regulating root gravitropic bending Hordeum vulgare
gravitropic response was reduced in D132 and RNAi-CLA4 transgenic seedlings
shoot gravitropism leads to alteration in leaf angle (LA) Zea mays
Arabidopsis wild-type (Col-0) inflorescence stems bend upward when gravistimulated by horizontal placement Arabidopsis thaliana
root bending results from differential lateral auxin fluxes due to gravitropism Arabidopsis thaliana
plant organs guide their growth at a specified angle from gravity vector
lazy mutant in maize is agravitropic mutant Zea mays
spk1-4 mutant showed reduced sensitivity to gravistimulation Arabidopsis thaliana
shoot gravitropism of Arabidopsis is physiological phenotype that most sensitively indicates state of TGN to PVC/vacuole vesicle trafficking Arabidopsis thaliana
zig-1 mutant of Arabidopsis shows little shoot gravitropism Arabidopsis thaliana
seedling roots subjected to root bending assay Arabidopsis thaliana
(ATCESA3, ATH-B, CESA3, CEV1, ELI1, IXR1, MRE1, AT5G05170) je5; (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) ::PIN1-HA showed partial restoration of gravitropic response and growth Arabidopsis thaliana
TOL accumulation at PM of lower epidermis cells might promote resetting of (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) levels during later stages of gravitropic root growth Arabidopsis thaliana
(ATPIN3, PIN3, AT1G70940) polarization to the opposite cell side depletes auxin maximum
loss of geotropism causes tiller-spreading phenotype in leaf blade Oryza sativa
disruption of the PAT regulator ZmLA1 resulted in prostrate growth phenotypes with reduced shoot gravitropism Zea mays
(AtZIP1, ZIP1, AT3G12750) zig-1 double mutant had gravitropic response similar to wild-type Arabidopsis thaliana
pks1pks2pks4 mutant shows normal negative hypocotyl gravitropism in darkness
NO and cGMP are implicated in gravitropism
PABA promotes root gravitropism Arabidopsis thaliana
D132 seedlings required 12 hours to recover vertical growth
ZmCLA4 regulates shoot gravitropism Zea mays
auxin is responsible for gravity responses
Arabidopsis wild-type (Col-0) inflorescence stems become nearly perpendicular in approximately 90 min Arabidopsis thaliana
auxin-ethylene cross talk is necessary for root gravitropism Arabidopsis thaliana
caulonema filaments in Δ ftsZ3 mutants had lost gravitropic response Physcomitrella patens
br2 mutant roots have reduced gravitropic growth responses Zea mays
(SPK1, AT4G16340) is required for PIN2-mediated root gravitropic responses Arabidopsis thaliana
elongation zone displayed by far the most differentially expressed genes (DEGs) Hordeum vulgare
ZmCIPK15 functions in regulating maize root angles Zea mays
(VPS26A, AT5G53530) and (VPS35A, ZIP3, AT2G17790) mutations were identified in suppressor screen of (ATVTI11, ATVTI1A, ITT3, SGR4, VTI11, VTI1A, ZIG, ZIG1, AT5G39510) shoot gravitropic phenotype Arabidopsis thaliana
xerotropism indicates enhanced root downward growth guided by gravity upon water stress
repp mutants showed positive gravitropic response Arabidopsis thaliana
differential growth in apical elongation zone pushes subapical root region upward against resistance of surrounding agar Arabidopsis thaliana
depletion of auxin maximum ends bending
(AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) is implicated in gravitropism response Arabidopsis thaliana
PABA-promoted root gravitropism is dependent on ethylene Arabidopsis thaliana
PIN3-mediated auxin flow toward the lower hypocotyl side causes auxin to gradually accumulate and promote growth
pAtLAZY1:AtLAZY1 K252A/K253A rescues (AtLAZY1, LAZY1, AT5G14090) branch angle phenotype Arabidopsis thaliana
pAtLAZY1:AtLAZY1-eGFP K252A/K253A rescues (AtLAZY1, LAZY1, AT5G14090) branch angle phenotype Arabidopsis thaliana
gravitropism involves asymmetric growth response
nuclear localization of (AtLAZY1, LAZY1, AT5G14090) is not required for (AtLAZY1, LAZY1, AT5G14090) function in control of gravitropic branch orientation Arabidopsis thaliana
NR23 exhibited normal gravitropism Arabidopsis thaliana
(FER, AT3G51550) mutants encountering barrier form similar initial slippage bend but show little-to-no subsequent raising of subapical root regions Arabidopsis thaliana
pks1pks2pks4 mutant shows enhanced gravi-reorientation
(ATPIN3, PIN3, AT1G70940) repolarizes to the cellular side facing the ground in response to gravity Populus trichocarpa
dynamic changes in (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) protein redistribution are important for (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) function in root gravitropism Arabidopsis thaliana
gravitropic responses relies on dynamic changes of auxin distribution
mel1234 loss-of-function mutants exhibit agravitropic pin2-like root phenotypes
pks1pks2pks4 triple mutant shows no influence of cotyledon position on gravitropic response
(AtLAZY1, LAZY1, AT5G14090) primary inflorescence stems show significantly reduced bending rate during first hour of gravitropism response Arabidopsis thaliana
auxin efflux carrier PIN-FORMED 2 (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) plays important roles in auxin transport from the root tip to differentiated tissues during the gravitropic response
anatomical characters associated with efficiency of gravitropic reaction differed between species
traits determining gravitropic reaction may contribute to differentiation of ecological strategies
bending moment from asymmetric maturation shrinkage curves up stem
rate of change in curvature is inversely proportional to stem cross-sectional area
light-demanding species seedlings are expected to have gravitropic reaction that reorients stem quickly and efficiently towards vertical
resetting of (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) levels during later stages of gravitropic root growth avoids excess root bending Arabidopsis thaliana
asymmetric growth response results in organ bending
stabilized SAUR fusion proteins expression alters tropic responses Arabidopsis thaliana
(AtLAZY1, LAZY1, AT5G14090) mutants show reduced gravitropic response Oryza sativa
repp3 roots showed positive gravitropic response Arabidopsis thaliana
mutations that impair responses to gravity commonly affect angle at which lateral organs are held Arabidopsis thaliana; Oryza sativa
large retromer complex consisting of (VPS26A, AT5G53530) and (VPS35A, ZIP3, AT2G17790) is critical for shoot gravitropism Arabidopsis thaliana
(ATVTI11, ATVTI1A, ITT3, SGR4, VTI11, VTI1A, ZIG, ZIG1, AT5G39510) is essential for shoot gravitropism Arabidopsis thaliana
EXO70A3ox and pin4-3 cross shows variance phenotype of pin4-3 mutant Arabidopsis thaliana
(ATEXO70A3, EXO70A3, EXOCYST70A3, AT5G52350) overexpression and mutant lines exert control of gravitropism less precisely in pin4-3 mutants Arabidopsis thaliana
horizontal reorientation of control seedlings caused preferential DR5::GFP expression along lower side of root Arabidopsis thaliana
spk1-1 seedlings showed less pronounced asymmetric DR5::GFP expression at lower side of lateral root cap Arabidopsis thaliana
variations in TOL6:mCherry distribution point to dynamic adjustments in TOL-controlled endocytic sorting processes Arabidopsis thaliana
gravitropic response was explored in D132, D132-NIL, RNAi transgenic lines, and sibling control plants
transgenic (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) ::PIN1-HA into mutant background does not rescue agravitropic root growth of (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) mutant Arabidopsis thaliana
gravity stimulation polarizes PIN-FORMED3 (ATPIN3, PIN3, AT1G70940)
four-day-old seedlings grown in half-strength MS media containing 1% sucrose are turned 90° and incubated for 24 h Arabidopsis thaliana
phytochromes suppress hypocotyl negative gravitropism Arabidopsis thaliana
spk1-1 mutant showed reduced sensitivity to gravistimulation Arabidopsis thaliana
vacuolar targeting of (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) at upper epidermis of horizontally positioned root tips reinforces establishment of lateral auxin gradients Arabidopsis thaliana
gravistimulation in egt2 elongation zone induced differential expression of thousands of EGT2-regulated genes Hordeum vulgare
control root tips achieved 90° root tip angle by 4 h Arabidopsis thaliana
gravity (vertical rotation) is one of 12 specific treatments Arabidopsis thaliana
gravitropism uses two ARFs Arabidopsis thaliana
OsIAA3 is involved in response to gravity
Arabidopsis seedlings germinated and grown in space showed little gravitropic growth under continuous microgravity conditions Arabidopsis thaliana
cytoplasmic pH increased from pH 7.2 to pH 7.6 during gravistimulation
genes in modules with genotype correlation are potential components involved in regulating gravitropic response and AGO Hordeum vulgare
Arabidopsis seedlings possess rapid gravity-sensing mechanism Arabidopsis thaliana
dark-grown wild-type seedlings grown on 5 μM BFA display strong negative gravitropism defect
depletion of Arabidopsis Separase (AtESP) inhibits gravitropic response Arabidopsis thaliana
Depletion of either AtESP or AtESP-interacting Kin7.3-clade proteins induces perturbed root gravitropic response
gravity affects angle between the inflorescence stem and fruit pedicel Arabidopsis thaliana
EGT2 mediates root gravitropism through regulation of AGO Hordeum vulgare
embryos placed in horizontal position or upside-down in vertical position were stimulated with gravity for 6 h Arabidopsis thaliana
(AtMYB1, MYB1, SRM1, AT3G09230) mutant shows significantly retarded root gravitropic response Oryza sativa
EGT2 might not play an important role in gravity perception in root cap Hordeum vulgare
protein phosphorylation plays a critical role in root gravitropism
plant cell wall organization supports hypothesis of critical role of EGT2 in regulating root gravitropic bending Hordeum vulgare
tolQ shows significant delay in reorientation of root growth in response to gravity Arabidopsis thaliana
loss of (ABCB4, AtABCB4, ATPGP4, MDR4, PGP4, AT2G47000) function alters timing and spatial pattern of gravitropic curvature development Arabidopsis thaliana
transition zone roots initiate responses to gravity Arabidopsis thaliana
EGT1 mediates AGO Hordeum vulgare
pifq mutant seedlings display disrupted negative gravitropism in the dark Arabidopsis thaliana
gravity-responsive genes showed no overlap with genes regulated by EGT2 in meristem Hordeum vulgare
antigravitropic offset (AGO) counteracts gravitropism
(ATPIN3, PIN3, AT1G70940) is required for gravitropic responses Arabidopsis thaliana
(AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) is required for gravitropic responses Arabidopsis thaliana
gravitropism has no significant effect on phosphate (Pi) dependency Arabidopsis thaliana
Arabidopsis CNGC s have been implicated in gravitropism Arabidopsis thaliana
stabilized 3×GFP:bdl protein interfered with gravitropic growth of inflorescence branches
strong agravitropic root growth phenotypes are hallmark feature of (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) alleles
WEEP has role in shoot gravitropism Prunus persica
EGT2-regulated gravity-responsive genes were regulated in opposite direction in WT gravistimulation time-course experiment and pairwise comparisons of egt2 and WT roots Hordeum vulgare
modules correlated only with WT at some time point after gravistimulation might be involved in EGT2-independent gravitropism Hordeum vulgare
hub genes of significantly correlated modules in elongation zone were regulated by gravity and/or EGT2 Hordeum vulgare
plant cell wall and ROS-related processes might be involved in EGT2-controlled root gravitropic response Hordeum vulgare
EGT2 might suppress expression of gravity-responsive genes that play a positive role in root gravitropism Hordeum vulgare
asymmetrical elongation of cells on two sides of gravistimulated root leads to gravitropic root bending in direction of gravity
PIN-mediated auxin redistribution is critical for gravitropic growth
kin7.1kin7.3kin7.5 triple mutant shows reduced root tip curvature in gravitropism assay
(PIF1, PIL5, AT2G20180) is epistatic to pch mutants Arabidopsis thaliana
gravitropism allows plants to grow stems straight in air
phosphorylation of PIN proteins by AGC kinases is still an open question whether it is part of mechanism for converting gravity signals to auxin flow Arabidopsis thaliana
NO and auxin have been linked in root gravitrophic bending
asymmetric auxin translocation following gravistimulation is required for gravitropic root growth Arabidopsis thaliana
(FHY2, FRE1, HY8, PHYA, AT1G09570) mutants show diminished ability to reorient hypocotyl upon gravitropism in darkness
lateral roots of pgm-1 mutants demonstrate wild-type rates of gravitropism Arabidopsis thaliana
phosphoglucomutase (ATPGMP, PGM, PGM1, STF1, AT5G51820) mutant was gravitropic Arabidopsis thaliana
pAtLAZY1:AtLAZY1-eGFP construct rescues (AtLAZY1, LAZY1, AT5G14090) aberrant branch angle phenotype Arabidopsis thaliana
gravitropism is more effective when cotyledons face downwards
pin3pin4pin7 hypocotyl does not grow against the gravity vector in darkness
lateral roots is subject of analysis of gravitropic responses Arabidopsis thaliana
perturbation of (ATPIN1, PIN1, AT1G73590) and (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) cycling in (ATEXO70A1, EXO70A1, AT5G03540) mutants is not so severe to alter gravitropic root responses Arabidopsis thaliana
hypocotyls with cotyledons that face downwards show more rapid gravitropic response
(AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) is required for root gravitropism
abnormal localization of (ATPIN4, PIN4, AT2G01420) is required for pronounced disturbance of quick root gravitropism Arabidopsis thaliana
(AESP, AESP1, ESP, RSW4, AT4G22970) mutant shows delayed gravitropic response
sensory microtubules participate in alignment with gravity-dependent load
Arabidopsis thaliana (ATEXO70A1, EXO70A1, AT5G03540) mutant exhibits reduced level of statolite starch Arabidopsis thaliana
pks1pks2pks4 mutant displayed smaller bending difference dependent upon cotyledon position during gravitropism
gravitropic signal is perceived by columella cells in root tip Arabidopsis thaliana
(ABR, PID, AT2G34650) /WAG proteins regulates gravitropism in both shoots and roots
root gravitropism enables plants to adjust root growth direction
egt2 mutant shows enhanced root gravitropism Hordeum vulgare
auxin feedback on PIN-FORMED3 (ATPIN3, PIN3, AT1G70940) polarization restores symmetry of PIN3-dependent auxin flow
jaz4-1 root curvature angle was recorded near 50° correction point Arabidopsis thaliana
(AP-3 beta, PAT2, WAT1, AT3G55480) loss-of-function mutant has defect in shoot gravitropic response Arabidopsis thaliana
PKS genes role in hypocotyl gravi-reorientation is independent of photoreceptors Arabidopsis
(ATPIN3, PIN3, AT1G70940) phosphorylation is relevant to plant gravitropism Arabidopsis thaliana
Arabidopsis thaliana (ATEXO70A1, EXO70A1, AT5G03540) mutant shows 25% of primary roots with disorientation greater than 45 degrees from gravity vector Arabidopsis thaliana
pks1pks2pks4 hypocotyl grows against the gravity vector in darkness
impaired root gravitropism is expected result of reduced auxin differential in gravistimulated roots caused by NPPB blockage of ABCB channel function Arabidopsis thaliana
(AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) loss of function mutant results in agravitropic root growth
gravity perception in root cap involves less transcriptomic regulation than gravitropic bending in elongation zone Hordeum vulgare
rhizoid growth had no observed gravitropic component Marchantia polymorpha
LZY5 appears not to be expressed in gravity-sensing cells Arabidopsis thaliana
(ATPIN3, PIN3, AT1G70940) relocation to basal side of endodermis cells in upper hypocotyl redirects flow of auxin towards lower hypocotyl side Arabidopsis thaliana
asymmetric expression of (HOS9, PFS2, WOX6, AT2G01500) and (WOX11, AT3G03660) modulates tiller angle
strigolactones (SLs) regulate rice tiller angle
multifaceted approach and interdisciplinary research will help unravel intricate mechanisms of how plants sense and respond to gravity
LjLAZY3 deficiency does not influence amyloplast sedimentation Lotus japonicus
mutant and wild-type seedlings showed nearly similar time course of geotropic curvature Solanum lycopersicum
sec24a-2 mutant roots are able to properly respond to gravity Arabidopsis thaliana
(CKRC1, SAV3, TAA1, TIR2, WEI8, AT1G70560) roots failed to properly orient growth with respect to gravity vector Arabidopsis thaliana
asymmetric auxin gradient is instrumental in signal transduction from columella to elongation zone
cell wall-related processes is closely related to asymmetric cell elongation in distal elongation zone of gravistimulated roots
EGT2 regulates targets in elongation zone to control root gravitropism Hordeum vulgare
caulonema grows negatively gravitropic in absence of light Physcomitrella patens
jasmonic acid (JA) and auxin interaction regulates coleoptile gravitropism
auxin gradient leads to asymmetric growth
Arabidopsis AGCVIII kinases provide insight into auxin transport in plant gravitropism Arabidopsis thaliana
control seedlings display high GFP signal indicative of auxin levels along lower flank of root Arabidopsis thaliana
seedlings treated with 10 µm NPPB achieved only 48° root tip angle by 4 h Arabidopsis thaliana
empty plastids may trigger residual gravitropic responses because of their mass
WUSCHEL-RELATED HOMEOBOX11 (WOX11, AT3G03660) regulates rice tiller angle
WUSCHEL-RELATED HOMEOBOX6 (HOS9, PFS2, WOX6, AT2G01500) and (WOX11, AT3G03660) are core components that act downstream of auxin
Mtpin2 mutant roots show less gravitropic response compared with wild-type roots Medicago truncatula
(ARF7, BIP, IAA21, IAA23, IAA25, MSG1, NPH4, TIR5, AT5G20730) (ARF11, ARF19, IAA22, AT1G19220) double mutant impairs root response to gravity
functional loss of AP-3 caused slight defects in gravitropic responses
NPPB (5-nitro-2-(3-phenylpropylamino)-benzoic acid) treatment at 10 µm greatly slowed development of gravitropic bending Arabidopsis thaliana
(AtIAMT1, IAMT1, AT5G55250) overexpression disrupts gravitropic responses Arabidopsis thaliana
roots of the three zmpgp1 mutant seedlings showed less gravitropic responses Zea mays
(AtAUX1, AUX1, MAP1, PIR1, WAV5, AT2G38120) loss of function mutant results in agravitropic root growth
gravity sensing in moss protonema is restricted to growing tip cells Physcomitrella patens
GO enrichment analysis identified gravitropism functions Zea mays
gravitropism is directional control of growth in response to gravity
expression level of (AtLAZY1, LAZY1, AT5G14090) family genes determines magnitude of gravitropism Arabidopsis thaliana
specialized cells in plant organs can sense direction of gravity
gravity-induced auxin gradient across the root is less rapidly dissipated by normal shootward (basipetal) transport of the hormone through the elongation zone gravitropic curvature development Arabidopsis thaliana
(ATEXO70A3, EXO70A3, EXOCYST70A3, AT5G52350) mutant lines do not alter number of gravity perceiving statocytes and statoliths Arabidopsis thaliana
pin4-3 knockout mutants show dynamic root gravitropic response similar to Col-0 Arabidopsis thaliana
(ATWRKY52, RRS1, RRS1-R, SLH1, AT5G45260) partially affected gravitropism
continuous hypergravity conditions applied parallel to growth axis caused morphological changes (e.g. alterations in hypocotyl length and diameter) Arabidopsis thaliana
OsPIN1-RNAi plants showed wider tiller angle Oryza sativa
K252A/K253A mutations do not significantly affect rescue of (AtLAZY1, LAZY1, AT5G14090) phenotype Arabidopsis thaliana
mpk1-1, mkk3-1, rbk1-2, mpk1-1 rbk1-2, and rop2i rop4-1 seedlings displayed response similar to wild-type Arabidopsis thaliana
PIN is fundamentally linked to orthotropism
asymmetric distribution of ROS in distal elongation zone promotes root gravitropic bending
gravistimulation less than 1 g (e.g. 0.39 g–0.93 g) created by centrifugation in space induces reduced gravitropic curvature Lens culinaris
OsHOX28 positively regulates rice tiller angle
AtLAZY3/LZY4 is responsible for root gravitropism Arabidopsis thaliana
(AtLAZY2, AtNGR1, DRO3, LAZY2, AT1G17400) /LZY2 is involved in shoot and root gravitropism Arabidopsis thaliana
snx1-1 mutants exhibited normal root gravitropism
higher order (AGC1-1, D6PK, AT5G55910) mutants exhibit defects in negatively gravitropic hypocotyl bending Arabidopsis thaliana
(EMB173, FIS1, MEA, SDG5, AT1G02580) homozygous seedlings exhibit severe agravitropic growth Arabidopsis thaliana
(AtLAZY1, LAZY1, AT5G14090) (LZY1) is component acting in the transmission of signals triggered by gravity-sensing statolith relocation Oryza sativa L.
OsHOX1 positively regulates rice tiller angle
AtLAZY5 / LZY5 roles in gravitropism remain unexplored gravitropism Arabidopsis thaliana
apical polar localization of (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) in root epidermal cells is required for asymmetric auxin translocation following gravistimulation Arabidopsis thaliana
vacuolar accumulation of PIN2:VENUS in upper epidermis of gravistimulated tolQ is markedly less than in controls Arabidopsis thaliana
(FER, AT3G51550) mutants encountering barrier eventually grow flat along barrier surface Arabidopsis thaliana
formin family proteins have been implicated in regulation of gravitropic response
(TNO1, AT1G24460) mutant has delayed gravitropic responses
altered auxin activity is trademark of reduced response to gravity Arabidopsis thaliana
Mtpin2 mutant formed lateral roots that emerged at shallower angle (gravitropic set point angle) Medicago truncatula
Membrane Steroid Binding Protein 1 (AtMAPR5, ATMP1, MAPR5, MSBP1, AT5G52240) overexpression stimulates root gravitropism
transcriptional responses to gravi-stimulation suggest existence of inositol 1,4,5-trisphospate (IP3)-dependent regulatory pathways
empty siliques did not change significantly in comparison with those of both normal and empty siliques under 1 g control condition Arabidopsis thaliana
PABA does not suppress root-coiling phenotype of pin2wei8wei2 triple mutant Arabidopsis thaliana
(AtLAZY1, LAZY1, AT5G14090) mutant lacks transient overshooting of final angle Arabidopsis thaliana
gravitropic response of primary roots of pgm-1 mutants is indistinguishable from gravitropic response of lateral roots of wild-type Arabidopsis thaliana
(GGP, VTC2, AT4G26850) mutant shows aberrant gravitropic response of primary root and lateral roots Arabidopsis thaliana
(WAG2, AT3G14370) regulates root gravitropic response Arabidopsis thaliana
RRS1-OE lines were insensitive to gravity
(ABR, PID, AT2G34650) /WAG kinases are involved in gravitropic responses Arabidopsis thaliana
sp2l-4 mutants exhibit similar root curvature to wild-type seedlings
columella cells sense gravity Arabidopsis thaliana
weight of the seeds influenced pedicel response Arabidopsis thaliana
(AtAUX1, AUX1, MAP1, PIR1, WAV5, AT2G38120) influx and (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) efflux carriers catalyze auxin transport from columella cells to epidermal cells of elongation zone
starch-rich plastids trigger re-orientation of the cytoskeleton Physcomitrella patens
cellulase (AtCel1) overexpression results in normal gravitropism Populus trichocarpa
quadruple mutants of Arabidopsis 5PTase family members display enhanced gravitropic response Arabidopsis thaliana
rib1 mutant shows gravity response defects Arabidopsis thaliana
PCH1OE and PCHLOE seedlings do not respond to changes in direction of gravity Arabidopsis thaliana