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root development

93686 relationships annotated with this phrase. Showing first 500 of 93686.
Source entity Relationship Target entity Species
PIN2-like and pseudo-response regulator seven cytokinins activated may control root meristem activity likely through auxin–cytokinin crosstalk Populus trichocarpa
low N (LN) conditions leads to significantly increased trait values for root morphological traits Triticum aestivum
high N (HN) conditions leads to significant decrease in anatomical traits Triticum aestivum
LN supply showed decreasing trends for root surface area (RSA), root average diameter (RAD), and root volume (RV) Hordeum vulgare
fibrous root system of monocotyledons develops additional seminal roots (SRs)
broader understanding of lateral root (LR) development is still limited across plant species
crown rootless genes (CRLs) did not respond to submergence in (AR2, ATR2, AT4G30210)
late adventitious roots (LAR) have increased cortex-to-stele ratio Oryza sativa
LOC_Os04g50770 is negative regulator of root development Oryza sativa
(ATWRKY52, RRS1, RRS1-R, SLH1, AT5G45260) T may have been caused by weakened activation on increased root length in accessions with (ATWRKY52, RRS1, RRS1-R, SLH1, AT5G45260) T
GhMYC3 downstream genes are significantly enriched in pathways associated with oxidative stress responses, flowering time, signal transduction, metabolic process, JA, root development, and embryo development Gossypium hirsutum
ontogenetic root developmental program is executed as usual in strongest suberin phenotype mutants Populus trichocarpa
dir19 mutants display significantly increased root length Solanum lycopersicum
anatomical characteristics of Type III were confirmed in Arabidopsis thaliana Arabidopsis thaliana
LN supply significantly increased root morphological attributes Hordeum vulgare
significant upregulation of vacuolar H+-pyrophosphatase, tonoplast intrinsic protein and plasma membrane intrinsic protein indicates possible involvement of these genes in AR growth
LOC_Os04g50770 might play an important role in root development Oryza sativa
root phenotypes showed no significant differences in the two genotypes Nicotiana attenuata
soil P availability determines benefits and carbon costs of changes in root morphology and physiology
pi4kβ1,2 displays aberrant root hair morphology Arabidopsis thaliana
GA metabolic enzymes predominantly expressed in endodermis facilitate cell elongation Arabidopsis thaliana
plant MADS-box transcription factors (plant MADS-box TFs) play crucial roles in root growth
cell wall extensibility is major factor in regulation of root cell growth
μ2-1 roots in 4- to 8-d-old light-grown seedlings approximately 20% longer than wild-type seedling roots Arabidopsis thaliana
POPTR_0002s23090 overexpression results in high density of root hairs Arabidopsis thaliana
auxin signaling is central feature of root development
AZG1-YFP expression shares expression domain with (ATPIN1, PIN1, AT1G73590) Arabidopsis thaliana
convergently selected genes between wheat and barley were associated with root morphological traits under LN/HN conditions Triticum aestivum; Hordeum vulgare
average (TRL, AT5G53770) of genotypes carrying (GCS1, HAP2, AT4G11720) was significantly higher than average (TRL, AT5G53770) of inbreeds carrying (HAP1, MAGO, MEE63, AT1G02140) Hordeum vulgare
parent roots ( (PRS, PRS1, WOX3, AT2G28610) (ATSRS, OVA7, SRS, AT1G11870) and ARs) develop lateral roots (LRs)
adventitious roots and crown roots have in common their origin from aerial nodes Oryza sativa
root diameter is also linked to their specific initiation site
NSC allocated to roots may trigger changes in root morphology and physiology
phosphorus addition increases adventitious-root mass ratio of Leymus chinensis Leymus chinensis
(SCR, SGR1, AT3G54220) promoter is active in quiescent center (QC) and endodermis as well as cortex/endodermis initials of RAM Arabidopsis thaliana
division of different initials results in predictably ordered tissue organization of root Arabidopsis thaliana
Analysis of root weight showed reduction in SL-deficient slg1-1, slg1-2, psy1-2, and cdd7 plants compared with WT controls Solanum lycopersicum
(ASG6, CRK2, AT1G70520) mutant is consistent with slow root growth Zea mays
plant species coordinate root growth based on nutrient status and signals
synthesized tetraploid wheat showed increased root hair length Triticum aestivum
endodermal complementation restoring root phenotype suggests that gibberellin (GA) is required in inner root tissues for normal root development Pisum sativum
(ATHSFA2, HSFA2, AT2G26150) expression restored at least partially root length Arabidopsis thaliana
auxin is not essentially required in lateral root (LR) branching
(AR1, AtCPR1, ATR1, AT4G24520) emerges several days before (AR2, ATR2, AT4G30210)
Robust Root System 1 (RRS1) knockout plants show longer lateral root length
OE lines had fewer cells than WT in the root meristem zone Oryza sativa
forward genetics identified negative regulator gene for rice robust root system
(AtTLP6, TLP6, AT1G47270) PI4Kβ1, and PI4Kβ2 seem to have role in root growth Arabidopsis thaliana
TaLBD41-RNAi lines had increased root dry weight Triticum aestivum
exodermis was not formed at any point during 5 wk of hydroponic cultivation Populus × canescens
(EEP1, MIR164, MIR164C, AT5G27807) (anac021, ANAC022, NAC1, AT1G56010) module in Arabidopsis roots is involved in lateral root initiation Arabidopsis thaliana
multiple cortical layers exist in many monocot plants such as barley, maize, and rice Hordeum vulgare; Zea mays; Oryza sativa
evolution of auxin signaling is likely intertwined with lateral root (LR) development
(AR2, ATR2, AT4G30210) emergence delay promotes higher elongation capacity
(ATCCC1, CCC1, HAP5, AT1G30450) might be potential elite haplotype for robust root system Oryza sativa
miR4407-OX transgenic roots show significantly increased root volume Glycine max
Leymus chinensis always has significantly higher root diameter Leymus chinensis; Cleistogenes squarrosa
imbalance between photosynthetic rate (P n ) and root morphological traits under high phosphorus addition might be due to changes in root anatomical traits under high phosphorus addition Leymus chinensis
pi4kβ1,2 mutant phenocopies (AtTLP6, TLP6, AT1G47270) OE lines with regard to root development Arabidopsis thaliana
loss of RAPID ALKALINISATION FACTOR 2 (RALF2) and FERONIA (FER, AT3G51550) leads to inhibition of root growth Solanum lycopersicum
(AtMYB1, MYB1, SRM1, AT3G09230) is required for establishment of an auxin gradient for (CCT, CRP, MED12, AT4G00450) and LRP differentiation Oryza sativa
removal of one cotyledon does not cause a reduction in root growth Pisum sativum
root morphological traits ( (TRL, AT5G53770) RSA, RV) were significantly increased in (AtNPF2.12, NPF2.12, NRT1.6, AT1G27080) mutant at LN than WT Triticum aestivum
KAR pathway controls root hair elongation Arabidopsis thaliana; Oryza sativa; Lotus japonicus; Brachypodium distachyon
adventitious roots and crown roots may be regulated by common or overlapping gene networks Oryza sativa
late adventitious roots (LAR) have increased xylem-to-stele ratio Oryza sativa
genome-wide association analysis identified genomic regions controlling root length Oryza sativa
KO mutants had greater meristem length than WT Oryza sativa
Arabidopsis PI4Kβs have been implicated in root growth Arabidopsis thaliana
root stem cell niche consists of infrequently dividing cells of quiescent center (QC) surrounded by initials Arabidopsis thaliana
callus formation can impede formation of base-born roots
plant growth-promoting microbes support plant growth by promoting root development
DIR19-OE plants show decreased root length Solanum lycopersicum
suppression of GmHAD1-2 could inhibit lateral root growth Glycine max
arsenic-repressed genes are related to trichoblast formation
BpMADS11 overexpression lines (BpMADS11-OE1, BpMADS11-OE2, BpMADS11-OE3) show increased root length Betula pendula
μ2-1 seedlings had longer primary roots Arabidopsis thaliana
significant differences in global gene expression levels observed in primary roots of different maize inbred lines and hybrids Zea mays
cells in (ATAZG1, AZG1, AT3G10960) and wild-type root apical meristems were compared for dimensions and volumes Arabidopsis thaliana
poplar genes involved in control of root morphogenesis and meristem activity may be under epigenetic control Populus trichocarpa
PIN2-like (Potri.008G127700) is under epigenetic control Populus trichocarpa
S. parvula under control conditions has shorter fully suberized zone than Arabidopsis Schrenkiella parvula
three independent hsc70.1 hsp70.4 transgenic plant lines expressing the nonmobile YFP-HSC70.1M showed no significant root growth differences compared with hsc70.1 hsp70.4 double mutants Arabidopsis thaliana
S-type lateral roots (LRs) facilitates induced root plasticity
gross morphology of lateral root (LR) is similar to parent roots
OsWOX11 was significantly induced in absence of leaf sheath Oryza sativa
Robust Root System 1 (RRS1) encodes R2R3-type MYB family transcription factor
Robust Root System 1 (RRS1) represses root development
APC/C TE plays key role in regulating root growth
phosphorus addition shows no significant change in root tissue density of Leymus chinensis Leymus chinensis
(ADH, ADH1, ATADH, ATADH1, AT1G77120) control lines showed ordered tissue organization Arabidopsis thaliana
(SLG1, AT5G08490) mutant displays subtle developmental phenotypes in the roots Solanum lycopersicum
buzz mutant produces hairless roots with root bulges along epidermis root morphology Brachypodium distachyon
monoterpene mixture at 6.25 mM applied at 14 dpi shows less pronounced effect on lateral root number Populus tremula × alba
plant root system architecture (RSA) is net result of salinity
grapevine fine roots exhibit dramatic changes in structure and function along length Vitis berlandieri × Vitis rupestris
environmental stresses alter plant root development and function
jam1jam2jam3 triple mutant show shorter roots Arabidopsis thaliana
primary roots (PRs) develops from embryo
DEEPER ROOTING 1 (AtNGR2, DRO1, LAZY4, AT1G72490) controls root growth angle Oryza sativa
P addition impacts root morphology
nonstructural carbohydrate concentrations ([NSC]) appeared to drive modifications of root morphology
phosphorus addition at P12.5 causes significant decrease in root shallowness of Leymus chinensis Leymus chinensis
buzz mutant has twice the lateral root density compared with wild-type Bd21 Brachypodium distachyon
root hairs massively increase surface area of root systems
auxin maximum is fundamental to cell fate and patterned root development Arabidopsis thaliana
auxin gradient in crown root primordia and lateral root primordia maintains stem cell identity and cell differentiation Oryza sativa
secondary growth initiated at distances of more than 100 mm from the root apex Vitis species
maize LBD gene lbd34 (GRMZM2G075499_T01) is preferentially expressed in wild-type versus rtcs coleoptilar nodes at all three developmental stages Zea mays
ECM fungi colonization results in radial elongation of the epidermal cells
L-type lateral roots (LRs) facilitates induced root plasticity
root system is important for anchoring plants to soil
STTM-4407 transgenic roots exhibit negative effect on root growth Glycine max
phosphorus addition at P5 reaches peak specific root area of Leymus chinensis Leymus chinensis
TaLBD41-RNAi lines had increases in total root length Triticum aestivum
disruption of symplastic signaling in the endodermis alters radial patterning Arabidopsis thaliana
disruption of symplastic signaling in the endodermis causes increase in number of cell layers Arabidopsis thaliana
(ATMYB63, MYB63, AT1G79180) N-OE plants show significantly inhibited root growth Solanum lycopersicum
dir19 mutant showed increased root length Solanum lycopersicum
GmHAD1-2 overexpression significantly influences soybean lateral root number Glycine max
nutrient-limiting conditions in the soil triggers redesign of root architecture
cortical cell file number (CCFN) measured on young plants from greenhouse mesocosms 30 d after planting was accurate reflection of cortical cell file number (CCFN) measured on mature plants in the field 70 d after planting Zea mays
large cortical cell size (CCS) permits greater root growth Zea mays
abscisic acid (ABA) promotes lateral root emergence Medicago truncatula
differences in root morphology and root apical meristem activity of (ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) in early stages of development draw some parallels with (EAL1, SGR7, SHR, AT4G37650) mutant Arabidopsis thaliana
high levels of auxin causes increased lateral rooting Arabidopsis thaliana
three anatomical types of lateral roots were identified in pearl millet Pennisetum glaucum
diameter and growth rate change in parallel in oak and rubber tree
root growth induces root branching in the search for water
OsFBK1 knockdown lines showed no differences in root length Oryza sativa
sHSP22 OX seedlings transferred to medium containing 1 μM NPA had 57.2% reduced primary root length primary root growth Arabidopsis thaliana
(AtMYB62, BW62B, BW62C, MYB62, AT1G68320) overexpression does not influence localized Pi deficiency-induced inhibition of primary root growth Arabidopsis thaliana
positional cue from cortical cell layer triggers root epidermal hair/non-hair cell fate Arabidopsis thaliana
Mutation in (ATLSD1, ATSWP1, KDM1C, LDL1, LSD1, SWP1, AT1G62830) -LIKE1 ( also named ) induces activation of expression of LATERAL ROOT PRIMORDIUM1 (LRP1, AT5G12330) Arabidopsis thaliana
root tips hold root meristem Oryza sativa
(At-SCL28, SCL28, AT5G18810) promotes cell cycle exit in transition zone Arabidopsis thaliana
excess auxin accumulating in callus tissue induces ectopic rhizoids Marchantia polymorpha
removal of leaf sheath partially restored root anatomical features Oryza sativa
DEEPER ROOTING 1 (AtNGR2, DRO1, LAZY4, AT1G72490) controls deep rooting Oryza sativa
phosphorus addition at P5 and P12.5 decreases root tissue density of Cleistogenes squarrosa Cleistogenes squarrosa
(AT.EIF4E1, CUM1, EIF4E, eIF4E1, AT4G18040) mutants display shorter primary root length Arabidopsis thaliana
root area in shallow root zone (0–11 cm) was greater in S1 and S2 than in S4
HISTIDINE PHOSPHOTRANSFER PROTEIN 6 ( (AHP6, HP6, AT1G80100) ) is involved in root specification of protoxylem cell identity Arabidopsis thaliana
buzz mutant exhibits increased root growth rate Brachypodium distachyon
subgenome-divergent expression and histone modifications between TaRSL4-A and TaRSL4-B were observed in roots at 9 d DAG in hexaploid wheat Chinese Spring Triticum aestivum
same four functional zones could be identified in mutant cyp86a1_1,2;b1_1 roots Populus × canescens
Pi-deficient conditions resulted in higher root to shoot ratio Glycine max
GmHAD1-2 influences lateral root development Glycine max
SYNTAXIN OF PLANTS 132 (ATSYP132, SYP132, AT5G08080) appears to play diverse biological roles in root hair elongation Arabidopsis thaliana; Nicotiana benthamiana; Triticum aestivum; Medicago truncatula
endodermis is root cell type Arabidopsis thaliana
alterations of suberized apoplastic barriers would manifest over longer developmental time frames
sugar serves as a direct signal for root growth Arabidopsis thaliana
reduced root growth rate in RePRP2.1-overexpressing [RePRP2.1(ox)] lines similar to root growth rate in abscisic acid (ABA)-treated wild type Oryza sativa
vigor of the adult root systems predetermines plant development Zea mays
seed plants have lateral roots primarily derived from pericycle
late adventitious roots (LAR) have aerenchyma Oryza sativa
synthesized hexaploid wheat showed increased lateral root numbers Triticum aestivum
GmHAD1-2 regulates lateral root length Glycine max
phosphate (Pi) availability strongly affects root growth and development Arabidopsis thaliana
increased root surface contributes to recovery of main root growth
suppressor of (AtMAX2, MAX2, ORE9, PPS, AT2G42620) 1 (SMAX1, AT5G57710) mutant does not affect lateral root formation phenotype of (AtMAX2, MAX2, ORE9, PPS, AT2G42620) Arabidopsis thaliana
length-wise cell expansion inhibition causes shorter roots Oryza sativa
late adventitious roots (LAR) showed increased number of cortex cell layers Oryza sativa
leaf sheath likely provides mechanical barrier that delays outgrowth and promotes radial growth Oryza sativa
KO mutants had significant increase in EdU labeling level Oryza sativa
Rudbeckia hirta root system revealed high plasticity Rudbeckia hirta
eQTL regulatory network suggests that PtrXB38 participates in regulating root development Populus
number of seminal roots is quite variable between different genotypes Zea mays
difference in distribution of cytokinin-dependent signaling maxima did not result in significant difference in cellular structures of azg1-1 and wild-type root apical meristems Arabidopsis thaliana
pseudo-response regulator seven cytokinins activated (Potri.008G046200) may control root meristem activity Populus trichocarpa
fully suberized zone in S. parvula increases around three times in length under 125 mM NaCl and even further under 175 mM NaCl salt stress Schrenkiella parvula
YFP-HSC70.1 protein produced by the nonmobile YFP-HSC70.1M transcript failed to rescue primary root growth Arabidopsis thaliana
other genes related to crown root initiation and emergence did not respond to submergence in (AR2, ATR2, AT4G30210)
KO lines had significantly increased root dry weight compared to WT at booting stage Oryza sativa
GmIPT3-KD (GmIPT3 knockdown) promotes root development Glycine max
phosphorus limitation may induce thinner steles
root system is required for plant establishment Populus trichocarpa
callus formation delays formation of adventitious roots
7-wk-long hydroponic cultivation was carried out to obtain more mature roots with full endodermal suberization and periderm formation Populus × canescens
root angle is closely related to OsPINs Oryza sativa
bperf61 knockout lines (bperf61#-2, bperf61#-4, bperf61#-9) show significantly reduced root length Betula pendula
rtcs mutant forms primary root Zea mays
lack of (XXT5, AT1G74380) alone results in shorter root hair Arabidopsis thaliana
(ABCG14, AtABCG14, AT1G31770) mutant shows contrasting root elongation phenotypes Arabidopsis thaliana
PIN2-like (Potri.008G127700) may control root meristem activity Populus trichocarpa
mechanical impedance exerted by the leaf sheath significantly influenced timing of emergence and key morphological traits of the aquatic adventitious roots
OE lines showed opposite phenotypes to KO mutants Oryza sativa
(ATWRKY52, RRS1, RRS1-R, SLH1, AT5G45260) expression is consistent with its function in regulating root development Oryza sativa
NaAGO7 silencing by RNAi (ir (AGO7, ZIP, AT1G69440) ) does not change root development Nicotiana attenuata
(KAI2, AT4G37470) mutant shows altered root system architecture Arabidopsis thaliana
ETHYLENE INSENSITIVE 2-like 1 loss-of-function alleles exhibit increased root growth rate Brachypodium distachyon
(ASG6, CRK2, AT1G70520) mutants exhibit impeded root growth Zea mays
endodermal CASP::NA expression in na mutant roots resulted in significant increase in cell length and lateral root length Pisum sativum
BpERF61 overexpression lines (BpERF61-OE5, BpERF61-OE6, BpERF61-OE7) show significantly higher root length Betula pendula
meristematic and elongation zone extends to distances of 10 to 30 mm from the root apex Vitis species
(EEP1, MIR164, MIR164C, AT5G27807) targeting (anac021, ANAC022, NAC1, AT1G56010) in Arabidopsis roots consequently inhibits lateral root initiation Arabidopsis thaliana
maize recombinant inbred lines (RILs) show phenotypic variation in cortical cell file number (CCFN) Zea mays
increase in (EAL1, SGR7, SHR, AT4G37650) expression in (ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) at 10 days after germination (DAG) reflects developmental time point when rate of root growth accelerates to approach wild-type levels Arabidopsis thaliana
impaired auxin distribution impairs primary root formation Arabidopsis thaliana
root apical meristem is impaired in (ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) mutant Arabidopsis thaliana
dissipation of auxin gradient in root tip leads to reduced cell division and expansion Arabidopsis thaliana
transcription factors have been shown to be directly involved in maintenance of stem cell niche Arabidopsis thaliana
(AQC1, HPS7, TPST, AT1G08030) (TYROSYLPROTEIN SULFOTRANSFERASE) has targets that are Tyr-sulfated peptides called root growth factors (RGFs) Arabidopsis thaliana
increased primary root length was rescued by application of low levels of auxin Arabidopsis thaliana
mutants that do not form obvious PPBs manage to produce relatively orderly roots
phenotyping pipeline was used to characterize early developmental patterns of root systems in two cereals Pennisetum glaucum; Zea mays
results in pearl millet confirm that types are well related to types obtained from model-based clustering of growth rate profiles Pennisetum glaucum
meristem length variation was associated with variation of the length of the elongation zone Zea mays
examination of single and multiple gain-of-function and loss-of-function receptor mutants revealed (AtETR1, EIN1, ETR, ETR1, RDO3, AT1G66340) controls lateral root and root hair initiation and elongation Arabidopsis thaliana
etr1-6 and etr1-7 null mutants formed statistically significantly fewer numbers of lateral roots relative to Col-0 Arabidopsis thaliana
transcriptomes that span the root tip developmental zone were used to cluster ACC-regulated transcripts by common developmental response Arabidopsis thaliana
sHSP22 OX lines initiated more lateral roots after auxin application Arabidopsis thaliana
gh1-hmga1-1 homozygous mutants exhibit short roots Arabidopsis thaliana
maize root system contains nodal roots Zea mays
(ATL5, OLI5, PGY3, RPL5A, uL18z, AT3G25520) mutant shows developmental defects in lateral root initiation Arabidopsis thaliana
SCARECROW (SCR, SGR1, AT3G54220) is specifically expressed in endodermis Arabidopsis thaliana
pht4;6 mutant exhibits abnormal cell expansion at the root tip Arabidopsis thaliana
impact of cell wall structural alterations resulting in weak cell walls affect root hair growth Arabidopsis thaliana
MC presence in Arabidopsis under salt stress is delayed rather than induced by salt Arabidopsis thaliana
(AR2, ATR2, AT4G30210) obtaining maximum length of 35 cm
OE lines had lesser meristem size than WT Oryza sativa
KO mutants had larger lateral root density than WT Oryza sativa
increase in lateral root number contributed to rise in total root length and root surface area Glycine max
root hair length of Sl Sl AA is consistent with previous study Triticum aestivum; Aegilops longissima; Triticum urartu
(ATBZIP60, BZIP60, AT1G42990) is crucial for primary root growth in response to chemically induced ER stress and root colonizing microbes Arabidopsis thaliana
BpMADS11 overexpression lines (BpMADS11-OE1, BpMADS11-OE2, BpMADS11-OE3) display increased root weight Betula pendula
Ectopic expression of RePRP2.1 led to shorter and thicker root phenotypes Oryza sativa
auxin plays important role in integrating various endogenous and exogenous cues
OE lines led to shorter roots than WT Oryza sativa
cell expansion rates in the elongation zone are not tied closely to cell production rates Arabidopsis thaliana
epidermal-derived GA have little influence on root development Pisum sativum
different brown planthopper (BPH) infestation times on rice plants causes different root growth among rice plants Oryza sativa
ralf2 dir19 double mutants exhibit longer roots compared to ralf2 mutants Solanum lycopersicum
root plasticity involves modulating root hairs
abscisic acid (ABA) application on rice root results in swelling of young root tips Oryza sativa
maize LBD gene asl2 (GRMZM2G154320_T01) was preferentially expressed in wild-type versus rtcs coleoptilar nodes at all three developmental stages Zea mays
higher expression of (XXT5, AT1G74380) in roots and root hairs compared with (XXT3, AT5G07720) and (XXT4, AT1G18690) correlates with dominant role of (XXT5, AT1G74380) in affecting cell wall strength and impacting root development Arabidopsis thaliana
ECM fungi colonization results in intense short root formation
KAR pathway controls root skewing Arabidopsis thaliana; Oryza sativa; Lotus japonicus; Brachypodium distachyon
lateral roots (LRs) is crucial feature of root system structure
reduction in mechanical stress by removal of the leaf sheath revealed gene network involved in crown root/adventitious root development
late adventitious roots (LAR) have increased cortex cell layers Oryza sativa
(ATWRKY52, RRS1, RRS1-R, SLH1, AT5G45260) (IAA3, SHY2, AT1G04240) had longer root than WT Oryza sativa
japonica accessions showed difference among haplotypes root length Oryza sativa
X-ray μCT imaging before and after the experiment enabled investigation of how new roots explored different pore structures Rudbeckia hirta; Panicum virgatum
(FER, AT3G51550) mutants show stunted root growth Solanum lycopersicum
increased distribution of lateral roots in top soils forms shallow root architecture
BpMADS11 overexpression lines (BpMADS11-OE1, BpMADS11-OE2, BpMADS11-OE3) show increased root fresh weight Betula pendula
maturation zone contains suberized exodermis and endodermis Vitis berlandieri × Vitis rupestris
developmental anatomy along the length of the fine root includes localization of suberized structures Vitis spp.
(RWA2, AT3G06550) (RWA3, AT2G34410) (RWA4, AT1G29890) triple mutant was most affected mutant in root length Arabidopsis thaliana
RePRP2.1(ox) transgenic rice plants display shorter and wider root morphology Oryza sativa
PLETHORA2 and PLETHORA1 requirement for root development implies similar RTCS-dependent role of these genes in shoot-borne root formation Zea mays
fully suberized zone in Arabidopsis increases less than two times under 125 mM NaCl and does not increase under 175 mM NaCl salt stress Arabidopsis thaliana
barley mutant egt2 (enhanced root gravitropism 2) displays narrower root system Hordeum vulgare
lateral root (LR) has apically constricted conical shape tip
lateral roots (LRs) branching is sensitive to many stimuli
auxin signaling has distinct responses and downstream regulatory modules in different root types and plant groups
root diameter is not only determined by mechanical stress
epiphytes on bare bark cannot develop deep root system for anchorage
MicroRNA 4407 (miR4407) positively regulates root structures Glycine max
drip-irrigated wheat produces greater number of longer roots at surface compared to flood irrigation
loss of pSCR-positive cells retards primary root growth Arabidopsis thaliana
(APP1, AT5G53540) expression domain covers entire root meristematic zone
shoot infestation by gravid brown planthopper (BPH) decreases root growth Oryza sativa
hydraulic conductivity is critical for root growth
auxin modulates root system architecture (RSA) Arabidopsis thaliana
atgatl5-1 and wild-type seeds show no significant differences in root growth Arabidopsis thaliana
complex root system consists of embryonic primary and seminal roots Zea mays
mutations in Lateral Organ Boundaries (LOB) genes affect shoot-borne root formation Oryza sativa; Zea mays
knockout of (XXT3, AT5G07720) and (XXT4, AT1G18690) together with (XXT5, AT1G74380) further reduced length of root hair Arabidopsis thaliana
suberization zone in S. parvula and Arabidopsis roots starts from differentiation zone and ends close to the root tip Schrenkiella parvula; Arabidopsis thaliana
outer cortex layers in rice and barley roots exhibit rounder shape and more air-containing cavities between cells Oryza sativa; Hordeum vulgare
(AR2, ATR2, AT4G30210) emergence delay promotes thicker roots
removal of the mechanical barrier presented by the leaf sheath resulted in (AR2, ATR2, AT4G30210) became longer during short-term submergence
NIL-12 grew more (AR2, ATR2, AT4G30210) compared with paddy rice
salicylic acid (SA) plays important roles in root growth
miR4407-OX transgenic roots show significantly increased total root length Glycine max
Cleistogenes squarrosa has generally higher plasticity values for number of root tips, specific root area, and root tissue density Leymus chinensis; Cleistogenes squarrosa
root system of dicot Rhizobium hirta is known for substantial quantities of lateral roots Rhizobium hirta
substantial quantities of lateral roots demonstrated when growing into intact soil cores Rhizobium hirta
homozygous app1D plants exhibit defective SE differentiation and root growth
GmEXLB1/2 play a role in regulating root growth and Pi signaling network Glycine max
OsSYP132 RNAi lines showed retarded root growth Oryza sativa
(ATAZG1, AZG1, AT3G10960) mutant grown under high nitrate but short photoperiod (low C N balance) develops longer and more complex root systems compared to wild-type (WT) plants Arabidopsis thaliana
(ATAZG2, AZG2, AT5G50300) mutant shows differential phenotype under low carbon : nitrogen (C : N) regime after cytokinin (CK) application Arabidopsis thaliana
auxin seems to influence root tip bifurcation
regulation of CK biosynthesis by miR4407 controls root development Glycine max
(ADH, ADH1, ATADH, ATADH1, AT1G77120) control lines showed no significant change in lateral root number and primary root length with increasing inducer concentration Arabidopsis thaliana
transcriptional differences promote root hair elongation in SlSlAA Triticum aestivum
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) OE lines show differences in adventitious root numbers Populus tremula × alba
disruption of symplastic signaling in the endodermis causes misspecification of stele cells Arabidopsis thaliana
phosphate (Pi) availability regulates plant root growth
flavonoids regulate root growth
(AHDP, ANL2, AT4G00730) mutants exhibit irregular (GL2, AT1G79840) expression pattern
root hair morphology in xxt3xxt4xxt5 triple mutant plants is reminiscent of morphology of the root hairs of (ATXT1, AtXXT1, XT1, XXT1, AT3G62720) (ATXT2, AtXXT2, TXT2, XT2, XXT2, AT4G02500) double mutant plants Arabidopsis thaliana
Arabidopsis accessions showing relatively high HKT expression bore fewer lateral roots (LRs) Arabidopsis thaliana
(AtNPF2.12, NPF2.12, NRT1.6, AT1G27080) mutant plants demonstrated increased root growth performances under LN conditions than WT after both 7- and 14 d of NO3− treatments Triticum aestivum
ethylene signalling involvement in regulating root thickness remains unknown
root thickness showed no changes in KO and OE lines compared to WT Oryza sativa
root tissue density of Leymus chinensis is significantly negatively correlated with phosphorus addition Leymus chinensis
local variations in structural properties of soil greatly affects root growth patterns and architecture
length of primary root remained unaffected Arabidopsis thaliana
gibberellins (GA) have profound influence on lateral root organ formation
(At-SCL28, SCL28, AT5G18810) functions in transition and elongation zone Arabidopsis thaliana
(AR2, ATR2, AT4G30210) did not develop lateral roots Oryza sativa
CRLs are key regulators for crown root de novo formation in rice, rather than the main molecular signal for adventitious root development during flood events
OE lines had slower root growth rates than WT Oryza sativa
KO mutants had larger root volume than WT Oryza sativa
TAR2-LIKE loss-of-function alleles exhibit increased root growth rate Brachypodium distachyon
absence of gibberellin (GA) has significant impact on development of lateral roots Pisum sativum
DIR19 (dirigent protein 19) is required for regulation of root growth by RALF2-FER signaling Solanum lycopersicum
DIR19-OE plants showed inhibited root growth Solanum lycopersicum
transparent testa 4 mutant shows greatly accelerated lateral root growth Arabidopsis thaliana
Secondary root production impairment in (ANN1, ANNAT1, AtANN1, ATOXY5, OXY5, AT1G35720) confirms this annexin's involvement in adaptive root growth Arabidopsis thaliana
cytokinin signaling cascades are prominent among morphogenic signaling cascades Arabidopsis thaliana
middle cortex (MC) in roots of 3-d-old seedlings of S. parvula fully presents in roots of 3-d-old seedlings of S. parvula Schrenkiella parvula
number of cells in single row of cortex from QC to root-hypocotyl junction in 4-d-old wild-type plants is 58 ± 4 cells Arabidopsis thaliana
parent roots ( (PRS, PRS1, WOX3, AT2G28610) (ATSRS, OVA7, SRS, AT1G11870) and ARs) develop lateral roots postembryonically postembryonic development
ethylene signalling suggests involvement of molecular control on the root growth
root growing into dense soil matrix overcomes penetration resistance
XPP promoter (AT4G30450) is active in xylem pole pericycle (XPP) cells Arabidopsis thaliana
AMF inoculation has no effect on root system development in domesticated rice Oryza sativa
PvPS2:1 overexpression enhanced root growth Phaseolus vulgaris
plant root system architecture (RSA) is net result of gravity
Arabidopsis ecotype Wassilewskija (Ws-4) is notorious for root skewing phenotype Arabidopsis thaliana
(SMXL3, AT3G52490) is candidate for having role in root growth Arabidopsis thaliana
double RNAi lines targeting the RePRPs maintain long cell shape Oryza sativa
treatment with 0.1 and 1 µm naphthylacetic acid (NAA) resulted in significant increase in number of lateral roots (LRs) Arabidopsis thaliana
root cortical aerenchyma (RCA) is enlarged air space in the root cortex
(AtSWEET16, SWEET16, AT3G16690) mutants show reduced root growth under (ATBHLH029, ATBHLH29, ATFIT1, BHLH029, FIT, FIT1, FRU, AT2G28160) excess Arabidopsis thaliana
(ATPDX1.1, PDX1.1, AT2G38230) mutant shows benefit to growth in presence of sucrose (Suc) Arabidopsis thaliana
gradient of auxin distribution is important for establishment and maintenance of root apical meristem Arabidopsis thaliana
root growth impairment in (ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) draws parallels with (EAL1, SGR7, SHR, AT4G37650) mutant Arabidopsis thaliana
vitamin B6 deficiency is consequence of differential cascade of events in (ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) Arabidopsis thaliana
root apical meristem (RAM) activity is impaired in (ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) mutant Arabidopsis thaliana
ROOT GROWTH FACTORs (RGFs) affect expression of stem cell transcription factor PLTs Arabidopsis thaliana
NPA treatment causes more significant reduction of root length in ren1-D mutants Oryza sativa
auxin and cytokinin play roles in regulation of root development
Auxin application to wild-type Arabidopsis thaliana roots decreases primary root length Arabidopsis thaliana
(ATIRE1-2, AtIRE1A, IRE1-2, IRE1A, AT2G17520) (ATIRE1-1, AtIRE1b, IRE1, IRE1-1, IRE1B, AT5G24360) mutant exhibits less defective phenotype than (BZIP17, AT2G40950) and (BZIP28, AT3G10800) double mutant
auxin causes root inhibition
production of large number of crown roots can promote development of root length Zea mays
P availability, phenotype, and their interactions significantly affects crown number (CN)
large-CN phenotypes have significantly greater crown number (CN) under high P
Leu-rich-repeat receptor-like kinase regulated plant root architecture
CHD-type ATPase (CHD3, CHR6, CKH2, EPP1, GYM, HRB2, LWR1, PKL, SSL2, AT2G25170) is involved in root elongation Arabidopsis thaliana
arabinan epitope persists at external surface of distal root cap cells Arabidopsis thaliana
poplar genes involved in root initiation participate in ectomycorrhizal formation Populus tremula × Populus alba
inner cortex layers in rice and barley roots have flattened shape similar to endodermis and thicker cell walls Oryza sativa; Hordeum vulgare
AtSAM5 has role in regulating lateral root angle in Arabidopsis Arabidopsis thaliana
seminal roots (SRs) and/or adventitious roots (ARs) develops from shoot
miR4407-OX transgenic roots show significantly increased average root diameter Glycine max
XBAT35-OE plants showed no differences in root development Arabidopsis thaliana
DNA methylomes and transcriptomes were constructed in roots Triticum aestivum
GA metabolic enzymes predominantly expressed in endodermis maintain appropriate meristem size Arabidopsis thaliana
cell-cell communication between different cell layers in root tip plays essential role in determining cell fate and differentiation
adventitious roots in their primary developmental stage were complemented with data from older roots exhibiting secondary periderm formation Populus trichocarpa
phosphate (Pi) effect on root growth was investigated in soil Arabidopsis thaliana
maize rum1 gene is required for seminal and lateral root initiation Zea mays
autophagy has role in regulating lateral root (LR) development under phosphate starvation Arabidopsis thaliana
nitric oxide (NO) accumulates in elongation/differentiation zone
pPDX1.3:PDX1.3 control construct complements (ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) short-root phenotype Arabidopsis thaliana
sugar produced by photosynthesis is sufficient for regulation of root elongation in light Arabidopsis thaliana
disruption of (ATPDX1.1, PDX1.1, AT2G38230) results in differential cascade of events Arabidopsis thaliana
remodeling of root system architecture (RSA) results in increased root surface area for Pi absorption Arabidopsis thaliana
anthocyanin-producing plants displayed changes in root epithelial cell morphology Solanum lycopersicum
(AtROS1, DML1, ROS1, AT2G36490) /DEL lines 4, 8, and 11 developed significantly more (up to 2-fold) lateral roots on DEX Solanum lycopersicum
wild-type root growth suppressed in dim light condition Arabidopsis thaliana
faster growth of fer-4 mutant roots caused by absence of FERONIA kinase suppressing intracellular accumulation of mCitAHA2 protein under dim light condition Arabidopsis thaliana
TAN1-∆II-YFP functioned as well as TAN1-YFP Arabidopsis thaliana
ectopic expression of a single CKX gene generates barley plants with enhanced root system Hordeum vulgare
Al 3+ ion inhibits root growth
LRX proteins have been shown to modulate lateral root development Arabidopsis thaliana
removal of a specific root class induced increase in the growth of the remaining root classes Phaseolus vulgaris
(ATECS1, AtGSH1, CAD2, GSH1, GSHA, PAD2, RAX1, RML1, AT4G23100) mutant is characterized by drastically reduced root system Arabidopsis thaliana
cells in azg1-1 and wild-type root apical meristems showed no significant difference in cellular structures Arabidopsis thaliana
primary roots of Cardamine hirsuta have prepatterned middle cortex during embryogenesis Cardamine hirsuta
(WOX11, AT3G03660) expressed in crown roots activating the meristem
(AtMAX2, MAX2, ORE9, PPS, AT2G42620) ∆CTH mutant exhibits changes in root hair development Arabidopsis thaliana
GWAS study discovered developmental regulators Populus trichocarpa
phytohormone signaling contributes to shaping plant root system architecture
CK application in pea leads to excessive root swelling Pisum sativum
ralf2 mutant had shorter root lengths than WT
Phosphate-Dependent Skewing (PDS) is exciting addition to understanding phosphate (Pi) importance for plants Arabidopsis thaliana
root tip lacks suberization Vitis berlandieri × Vitis rupestris
abscisic acid (ABA) is involved in root development under water deficit conditions
215 down-regulated genes are associated with root hair cell differentiation Arabidopsis thaliana
pub9-1, ark2-1, and ark2-1/pub9-1 lines expressing GUS under control of auxin-responsive DR5 promoter (DR5::uidA) generated for investigation of auxin role in ARK2-PUB9-mediated regulation of LR development Arabidopsis thaliana
algorithm considers developmental constraint on branch emergence
(ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) mutant develops anchor roots (adventitious roots emerging from hypophysis) at 5 days after germination (DAG) Arabidopsis thaliana
removal of bottom 2 to 3 millimeters (mm) of root apical meristem at 3 days after germination (DAG) dramatically increased anchor root development Arabidopsis thaliana
mutated ERE lines show increased root growth compared with (ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) mutant Arabidopsis thaliana
low auxin levels causes changes in root hair growth Arabidopsis thaliana
P-stressed root apices in reduced genotypes maintain same amount of vasculature necessary for axial transport
(AHA2, AtHA2, HA2, PMA2, AT4G30190) localization profile is specific to transition zone Arabidopsis thaliana
(AtG3Pp2, G3Pp2, RHS15, AT4G25220) is downregulated in (ATNRAMP3, NRAMP3, AT2G23150) (ATNRAMP4, NRAMP4, AT5G67330) mutant Arabidopsis thaliana
three anatomical types of lateral roots were identified in maize Zea mays
identification of three lateral root types raises questions about their origin during development
pPER : CKX fusion construct yielded transgenic plants with enhanced root system Hordeum vulgare
root cortical senescence reduces root metabolic costs
HOS3 inhibits maintenance of primary root growth Arabidopsis thaliana
(AtMYB62, BW62B, BW62C, MYB62, AT1G68320) overexpressing plants show significantly altered root system architecture (RSA) Arabidopsis thaliana
(AtMYB62, BW62B, BW62C, MYB62, AT1G68320) overexpressing plants show altered root system architecture (RSA)
cortical cell size (CCS) varies across root cortex Zea mays
(ATPDX1.1, PDX1.1, AT2G38230) mutant in presence of sucrose (Suc) shows lateral root growth impairment less pronounced than (ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) Arabidopsis thaliana
StCLV2 is preferentially expressed in root apical meristem (RAM) and base of emerged lateral roots Solanum tuberosum
auxin and cytokinin cross talk mediates root development Oryza sativa
RCc3:OsCKX4 transgenic plants showed no obvious effects in lateral root development Oryza sativa
(AtIAMT1, IAMT1, AT5G55250) overexpression disrupts root elongation Arabidopsis thaliana
lateral root sections 2.5 to 5 mm represents elongation zone Pisum sativum
(ATS1P, ATSBT6.1, S1P, AT5G19660) /2p roots were still longer than 17/28 roots Arabidopsis thaliana
(AtETR1, EIN1, ETR, ETR1, RDO3, AT1G66340) (ETHYLENE RECEPTOR 1) controls root hair initiation Arabidopsis thaliana
auxin and ethylene both stimulate root hair proliferation Arabidopsis thaliana
m123-1 mutant seedlings exhibited inhibition of root growth Arabidopsis thaliana
SCARECROW (SCR, SGR1, AT3G54220) is required for radial patterning Arabidopsis thaliana
(FAS2, MUB3.9, NFB01, NFB1, AT5G64630) mutants have defects in root apical meristem (RAM) Arabidopsis thaliana
epi-regulators that only repress LUC gene cassette in roots of CCT431 and CCT396 may be specifically directed to LUC gene during root development
LBD genes are involved in lateral root formation in Arabidopsis Arabidopsis thaliana
addition of 0.001 µm naphthylacetic acid (NAA) was sufficient to rescue ark2-1/pub9-1 lateral root (LR) defect in −Pi/−Suc medium Arabidopsis thaliana
reduction of root metabolic costs permits more internal resources to be allocated to greater root growth
reduced root respiration would permit greater rooting depth
maize breeding program lines from Lilongwe University of Agriculture and Natural Resources shows range of cortical cell file number (CCFN) Zea mays
genetic and physiological mechanisms of cortical cell file number (CCFN) variation in maize are not yet known understanding of cortical cell file number (CCFN) variation Zea mays
maize genotypes with greater cortical cell size have greater rooting depth Zea mays
Malawian landraces in MW2012-1 show variation in cortical cell size (CCS) Zea mays
root architectural development includes physiological traits
(ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) mutant exhibits reduced meristem activity Arabidopsis thaliana
asymmetric divisions in the endodermis lead to formation of a middle cortex
extensin-like proteins have a role in root hair formation Arabidopsis thaliana
OsFBK1 knockdown line has increased root proliferation Oryza sativa
etr1-6 and etr1-7 root elongation was still sensitive to ACC Arabidopsis thaliana
large-CN phenotype had 32% shallower rooting depth Zea mays
cpc-1 mutant exhibits fewer numbers of root hairs
exogenous auxin is sufficient to rescue lateral root (LR) developmental defects in ark2-1/pub9-1 lines Arabidopsis thaliana
genotypes with less costly root tissue could develop extensive, deep root systems required to fully utilize soil water resources in drying soil without as much yield penalty Zea mays
(GNR1, NIA1, NR1, AT1G77760) (ATNR2, B29, CHL3, NIA2, NIA2-1, NR, NR2, AT1G37130) double mutation has marginal effect in root growth inhibition Arabidopsis thaliana
high Pi supply prevents cluster-root production Hypoxis prostrata
(AtSWEET17, SWEET17, AT4G15920) ectopic expression leads to decreased root growth in the presence of (ATBHLH029, ATBHLH29, ATFIT1, BHLH029, FIT, FIT1, FRU, AT2G28160) Arabidopsis thaliana
relative root growth of wild type and mutants was similar when grown on media with or without 1% (w/v) Suc Arabidopsis thaliana
wild-type plants do not develop anchor roots at 5 days after germination (DAG) Arabidopsis thaliana
elevated auxin content in (ATPDX1.1, PDX1.1, AT2G38230) impairs root growth Arabidopsis thaliana
pyruvate rescues lateral root formation to levels observed in Landsberg erecta Arabidopsis thaliana
altered expression of transcription factors is consistent with observed defects in (AQC1, HPS7, TPST, AT1G08030) root development Arabidopsis thaliana
ACC (1-aminocyclopropane-1-carboxylic acid) interacts antagonistically with auxin in inhibiting polar auxin transport during lateral root development and hypocotyl elongation Arabidopsis thaliana
functional redundancy among CKX genes explains lack of significant difference in root architecture at mature stage Oryza sativa
reduction in SHORT-ROOT (EAL1, SGR7, SHR, AT4G37650) movement triggers asymmetric divisions in the endodermis
roots grown under bright condition sustain growth Arabidopsis thaliana
(ATN, ATTAN, TAN1, AT3G05330) (AIR9, AT2G34680) double mutants had elongation zones that were statistically significantly shorter Landsberg erecta controls Arabidopsis thaliana
genetic engineering of CK breakdown generates barley plants with enhanced root system Hordeum vulgare
shallow root system is comparable to OsFBK1 overexpression lines Oryza sativa
ACC (ethylene precursor) inhibits root elongation
axial roots in monocots are morphologically and developmentally distinct from axial roots in dicots
GLABRA2 (GL2, AT1G79840) is required for repression of root hair formation Arabidopsis thaliana
cobra-1 mutant exhibits short and swollen root phenotype Arabidopsis thaliana
root phenotype of pht4;6 under ionic stress shows similarity with monensin- or BFA-treated root tips Arabidopsis thaliana
(AtXTH31, ATXTR8, XTH31, XTR8, AT3G44990) is predominantly expressed in root tips, including elongation zone Arabidopsis thaliana
high- and low-NO concentrations with very similar developmental consequences in root growth Arabidopsis thaliana
(EAL1, SGR7, SHR, AT4G37650) mutant has severely shortened main root throughout its life cycle Arabidopsis thaliana
(EAL1, SGR7, SHR, AT4G37650) plays role in maintaining root apical meristem Arabidopsis thaliana
specific induction of auxin biosynthesis genes in root meristem does not rescue root growth in (ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) Arabidopsis thaliana
perturbations to root elongation and lateral root production are not accompanied by patterning defects Oryza sativa
root system architecture is complex trait
CK regulates the formation of passage cells in the Casparian strip
ectopic expression of GhPMEI3 modulates root elongation Gossypium hirsutum
mutant defective in the expression of (OTU5, AT3G62940) produce shorter primary roots Arabidopsis thaliana
both loss-of-function mutants had similar numbers of lateral roots in presence and absence of ACC treatment Arabidopsis thaliana
maize root system contains lateral roots Zea mays
dominant primary root and its laterals comprise basic architectural phenotype
increasing the density of the medium with low concentrations of agar alleviates root swelling symptoms Arabidopsis thaliana
Mutants of AtGCN5 show defects in root quiescent center specification Arabidopsis thaliana
wild-type tomato seedlings exhibit short root phenotype upon NO donor application Solanum lycopersicum
scl6-II scl6-III (ATHAM3, HAM3, LOM3, SCL6-IV, AT4G00150) mutant seedlings have significantly shorter primary roots Arabidopsis thaliana
disruption of a single NPY gene did not cause obvious defects in root development
incomplete rescue of (RGFR1, RGI1, AT3G24240) /2/3/4/5 phenotype by proRGI2:MKK4 DD or proRGI2:MKK5 DD could account for partially rescued primary root length Arabidopsis thaliana
(EMB71, MAPKKK4, YDA, AT1G63700) may be directly phosphorylated by RGI receptors Arabidopsis thaliana
reduction of stem diameter in (AtHSPR, SMXL4, AT4G29920) (SMXL5, AT5G57130) mutants is caused by root growth defects
acidic stress negatively regulates elongation of plant roots
root architecture redesign generates lateral roots (LRs)
3-d-old seedlings grown in medium lacking Pi and Suc (−Pi/−Suc) ark2-1/pub9-1 has severely reduced numbers of lateral roots (LRs) Arabidopsis thaliana
l-NMMA is not toxic to plant roots but inhibits root elongation Arabidopsis thaliana
depletion of NO reduces primary root growth Arabidopsis thaliana
pPDX1.3:GUS construct shows concentration of GUS activity in root tip and lateral root emergence areas Arabidopsis thaliana
(ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) seedlings in presence of sucrose (Suc) develop anchor roots Arabidopsis thaliana
inorganic phosphate (Pi) deficiency inhibits primary root growth Arabidopsis thaliana
root enhancer1 (ren1-D) mutant exhibits increased crown root number Oryza sativa
(ILL2, AT5G56660) (ILR1, AT3G02875) (IAR3, JR3, AT1G51760) triple mutants show increased primary root length Arabidopsis thaliana
misregulation due to compromising the intact amino terminus causes reduced ability of mCitAHA2 to rescue impaired root growth Arabidopsis thaliana
lateral root sections 5 to 10 mm represents mature zone Pisum sativum
(AtETR1, EIN1, ETR, ETR1, RDO3, AT1G66340) complemented line is longer than triple mutant Arabidopsis thaliana
previously published data sets that identify cell type-specific transcriptomes were used to cluster ACC-regulated transcripts by common developmental response Arabidopsis thaliana
reduction of internal resources available to individual basal root axes slowed root elongation into deeper soil domains Phaseolus vulgaris
root apical meristem (RAM) forms underground root system
lateral roots are initiated from anti-clinal cell divisions in pericycle Arabidopsis thaliana
(ATXTH17, XTH17, AT1G65310) mutant has moderately shorter roots Arabidopsis thaliana
specific root length (SRL) is influenced by root diameter as well as root anatomy, or tissue mass density Zea mays
cortical cell diameter is weakly correlated with cell length Zea mays
endodermis is rate-limiting tissue for root growth Arabidopsis thaliana
genetic (mutation in auxin signaling) and environmental (severe shading) variations translate into altered proportions of lateral root types, not into a redefinition of each type
root system architecture involves numerous genes