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cell division

14319 relationships annotated with this phrase. Showing first 500 of 14319.
Source entity Relationship Target entity Species
unifacial stem cells provides new cells on one side of division plane
MC-LR prevents FtsZ polymerization Synechococcus 7942
resting cell formation does not necessarily involve mitosis
calculation of cell divisions has not been tested within developing ovaries of LA1589 tomatoes Solanum pimpinellifolium
approximately nine continuous cell divisions occur in both WT and mutants irrespective of division plane Solanum lycopersicum
maize (ASG6, CRK2, AT1G70520) mutant gives rise to abnormal and impaired mitosis Zea mays
centromeres play a pivotal role in chromosome segregation
cell number in RAM is inhibited under 125 and 175 mM NaCl in both species salt stress Schrenkiella parvula; Arabidopsis thaliana
ZipN interacts with FtsZ and other central divisome components Synechococcus 7942
microcystin-LR (MC-LR) can replace all GTPs located on FtsZ if the reaction time is sufficient Synechococcus 7942
diatom frustule must be produced before daughter cells separate upon mitosis
MC-LR-producing mutant strain 7942M shows filamentous cell morphology Synechococcus 7942
ZCN4 (Zm00001d003804) plays a role in mediating husk leaf width through affecting cell division Zea mays
cytokinin (CK) signalling initiates cell division in the cortex Pisum sativum
Z-ring was correctly localized in midcell in WT cells Synechococcus 7942
disruption of Z-ring assembly results in downregulated expression of min system Synechococcus 7942
(EMB2804, TFCB, AT3G10220) is required for microtubule-dependent cell division
outer nucellus comprises cells with highly active cell division Hordeum vulgare
kinetochore forms the link between chromosomes and spindle fibres
large genome size (GS) species have slowed cell division rates
R2R3 MYBs have been implicated in the regulation of cell division
FtsZ starts polymerization immediately with addition of GTP Synechococcus 7942
FtsZ protein is tubulin-like GTPase protein
FtsZ starts polymerization when combined with GTP
(HTB4, AT5G59910) is preferentially expressed in dividing/replicating cells Arabidopsis thaliana
tapetum cells in (DYT1, AT4G21330) ortholog mutants show periclinal divisional ability periclinal division Oryza sativa; Zea mays
microcystin-LR (MC-LR) inhibits assembly of FtsZ Synechococcus 7942
loss of pSCR-positive meristematic cells resulted in formative cell division of inner-lying pericycle cells Arabidopsis thaliana
smaller genomes have faster rates of cell division
ANP subfamily of MAP3K (mitogen-activated protein kinase kinase kinase) is implicated in regulation of cytokinesis Arabidopsis thaliana
Mob-1-like protein/phocein family is involved in cell proliferation Medicago truncatula
bacteria encode one single FtsZ protein
FtsZ mediates cell division
the core motif is required for interactions with ZipA and FtsA
callose is transiently deposited in cell plate
7942M cells show abnormal cell division throughout the culturing period Synechococcus 7942
inhibited growth of primary root in (ASG6, CRK2, AT1G70520) mutant was also caused by impaired mitotic cell division Zea mays
chromosome segregation occurs during mitosis and meiosis
calculation of cell divisions assumes all cells divide synchronously and continuously within ovary throughout development Solanum lycopersicum
null mutations of TFCs commonly result in cell-division defects Arabidopsis thaliana
(EMB2804, TFCB, AT3G10220) gene knockdowns do not affect cell division Drosophila
RhNAC100 might be involved in cell proliferation Rosa sp.
total cell number count in ovary from initial cell is used to estimate number of cell divisions and orientation of cell divisions Solanum lycopersicum
(At-SCL28, SCL28, AT5G18810) modulates selection of cell division planes Arabidopsis thaliana
overexpression line OE#1 has more epidermal cells Zea mays
crumpled kernel mutant (crk2) exhibits reductions in endosperm cell number Zea mays
FtsZ protein assembles Z-ring structure
Min system negatively regulates assembly of Z-ring Synechococcus 7942
restraint of FtsZ from polymerization makes daughter cells unable to separate normally Synechococcus 7942
ZmTFCB affects organization of phragmoplast microtubule (MT) array Zea mays
SIRT2 is involved in mitosis
secreted AGPs participate in cell division
(ANP2, MAPKKK2, NP2, AT1G54960) (ANP3, AtANP3, MAPKKK12, NP3, AT3G06030) regulate cytokinesis Arabidopsis thaliana
(H2A.Z, HTA11, AT3G54560) variant is essential for chromatin segregation mouse
effect of o/s on cell division is partially restored in t3/t5 Solanum lycopersicum
FtsZ expression level was detected in 7942M and WT cells Synechococcus 7942
production of microcystin-LR (MC-LR) is speculated to disrupt assembly of Z-ring in Synechococcus 7942 Synechococcus 7942
MC-LR-producing mutant strain 7942M fails to assemble Z-ring Synechococcus 7942
cytokinin (CK) regulates asymmetric cell division in root meristem zone
cell division is tightly linked to formation of spindle and phragmoplast microtubule array
lincRNA expression from centromeric regions suggests possible roles in cell division Glycine max
cell filamentation of 7942M may be caused by recombination of the mcy cluster on the genome of Synechococcus 7942 or by malfunctioned cell division Synechococcus 7942
FtsZ polymerization reaches plateau of 65.80 units within 65 min Synechococcus 7942
microcystins (MCs) disrupted cell division in nontoxic cyanobacteria Synechococcus 7942
(ATN, ATTAN, TAN1, AT3G05330) (AIR9, AT2G34680) expressing -YFP PPB angles were not completely restored to (AIR9, AT2G34680) single mutant PPB angles Arabidopsis thaliana
mitotic defect of ∆rei1 mutant may indicate moonlighting function of non-ribosome-bound Rei1 Saccharomyces cerevisiae
noise in vegetative cells is 2-fold greater than in heterocysts, indicating possibility of cellular division Anabaena sp. PCC 7120
PAN1 is expressed in wide variety of tissues where cells are actively dividing
(ANP2, MAPKKK2, NP2, AT1G54960) (ANP3, AtANP3, MAPKKK12, NP3, AT3G06030) double mutant displays developmental defects related to cytokinesis Arabidopsis thaliana
(ATN, ATTAN, TAN1, AT3G05330) single mutants had PPB angles within 80° to 100° in more than 90% of cells Arabidopsis thaliana
osers1 anthers show accelerated L2-d cell division Oryza sativa
single knockout mutants of all Physcomitrella patens ftsZ genes were generated to investigate function of five moss ftsZ genes Physcomitrella patens
reducing (TAP46, AT5G53000) expression by RNAi leads to anomaly in mitosis Arabidopsis thaliana
bacterial FtsZ assembles into Z-ring
oblique orientation of cross walls in wild-type moss is mediated by microtubules Physcomitrella patens
loss of FtsZ in Synechocystis sp. PCC 6803 causes lethality Synechocystis sp. PCC 6803
type of callose synthase complex active in plant cytokinesis is not shared with yeast
TAN1-YFP driven by its native promoter localized to division site Arabidopsis thaliana
(POK1, AT3G17360) and (POK2, AT3G19050) localize PHGAP1 and PHGAP2 only after PPB disassembles Arabidopsis thaliana
ANPs-MKK6-MPK4 cascade plays an essential role in cytokinesis Arabidopsis thaliana
cytosolic Rei1 protein was discovered through mitotic proliferation defect of the ∆rei1 mutant Saccharomyces cerevisiae
(AtSEC24A, ERMO2, SEC24A, AT3G07100) does not affect cytokinesis Arabidopsis thaliana
stele cells are morphologically normal except that meristem exhibits cessation or reduction in cell division activity Arabidopsis thaliana
(H2A.Z, HTA11, AT3G54560) variant is essential for chromatin segregation Drosophila melanogaster
(GNR1, NIA1, NR1, AT1G77760) (ATNR2, B29, CHL3, NIA2, NIA2-1, NR, NR2, AT1G37130) (ATNOA1, ATNOS1, NOA1, NOS1, RIF1, SVR10, AT3G47450) mutant roots display abnormal divisions Arabidopsis thaliana
ANPs-MKK6-MPK4 cascade regulates cytokinesis Arabidopsis thaliana
pan1 and pan2 single mutants have misoriented subsidiary mother cell (SMC) walls
centromeric lincRNAs showed higher transcriptional activity in actively dividing tissues Glycine max
important role for polarized membrane trafficking in polarization of plant cell division is plausible
mitotic index in miROE8 was about 9.4%, significantly lower than mitotic index in ZH10 (16.4%) Oryza sativa
(ANQ1, ATMKK6, MKK6, SUMM4, AT5G56580) has functions in cytokinesis Arabidopsis thaliana
PPB angles of (ATN, ATTAN, TAN1, AT3G05330) -YFP (AIR9, AT2G34680) were indistinguishable from (ATN, ATTAN, TAN1, AT3G05330) -∆II-YFP (AIR9, AT2G34680) Arabidopsis thaliana
AI cells developing in positions spatially removed from the MMC and megaspores remain undivided Hieracium spp.
Cyclin (AtNPF6.3, ATNRT1, B-1, CHL1, CHL1-1, NPF6.3, NRT1, NRT1.1, AT1G12110) ,2 is mitotic cyclin Medicago truncatula
ES7 (endosidin 7) hinders somatic cytokinesis Arabidopsis thaliana
bacterial cells divide by binary fission
(ATN, ATTAN, TAN1, AT3G05330) (AIR9, AT2G34680) double mutants expressing full-length -YFP still had occasional division plane defects Arabidopsis thaliana
fluorescence-labeled XXXG is diffused throughout dividing cell Nicotiana tabacum
fluorescence-labeled XXXG is clearly incorporated into new walls Nicotiana tabacum
soluble phenylpropanoids such as dehydrodiconiferyl alcohol glycosides have cell division-promoting effect
CHT7 affects proliferation Chlamydomonas reinhardtii
t17a/t19 double mutant increased in periclinal and decreased anticlinal divisions enhancing effect of o/s Solanum lycopersicum
Microcystin-LR (MC-LR) expression led to abnormal cell division Synechococcus 7942
elimination of pAHP6-positive pericycle cells resulted in ectopic cell division of endodermis Arabidopsis thaliana
(EMB2804, TFCB, AT3G10220) is required for cell division
(AS2, AT1G65620) bodies were distributed to daughter cells during progression of the M phase from anaphase to telophase Arabidopsis thaliana
peroxisome distribution is vital for proper cell division in mice skin cells Mus musculus
type I formins in moss Physcomitrella patens is needed for efficient cytokinesis Physcomitrella patens
AUXIN-INDUCED-IN-ROOTS9 (AIR9, AT2G34680) localizes to division site Arabidopsis thaliana
tobacco cells cultured in presence of 1 mM XXXG expand transversely and divide transversely into two daughter cells Nicotiana tabacum
mutation of (AtELP3, EAST1, ELO3, ELP3, HAC8, HAG3, AT5G50320) results in decreased cell division rate Arabidopsis thaliana
callose occurs in cell plates
LEM-2 exerts critical functions in chromosome segregation and cell division Caenorhabditis elegans
histone modifications maintenance during continuous cell division needs to be addressed maintenance of histone modifications during cell division
cell number was stable within each genotype across different time points ref8* and ref8* gir1-1 plants Arabidopsis thaliana
(ATMED14, MED14, SWP, AT3G04740) regulates cell number Arabidopsis thaliana
root initials produce daughter cells
fluorescent XXXG is sometimes incorporated into interface walls during mitosis Nicotiana tabacum
microtubules mark division plane in preprophase band Arabidopsis thaliana
nuclear envelope (NE) components play important roles during plant cell division
buds undergo series of oblique cell divisions Physcomitrium patens
(ATTPS1, TPS1, AT1G78580) mutant embryos show significantly reduced cell division rate Arabidopsis thaliana
cell numbers are decreased in CK2B1-silenced expression plant Brassica juncea
multi-polar spindles in polyspermic zygotes followed by abnormal cytokinesis Fucus distichus
plane of cell division is determined by preprophase band (PPB)
nuclear division is always complete in (GEM1, MOR1, AT2G35630) mutant spores Arabidopsis thaliana
cell expansion measurement performed by tracing single cells in process of dividing Nicotiana tabacum
(ATFH8, FH8, FORMIN 8, AT1G70140) was involved in cell division Arabidopsis thaliana
small RNAs activity maintenance in cell divisions is still to be unveiled maintenance of small RNA activity during cell divisions
wild-type plants have more dividing cells in Arabidopsis root tips Arabidopsis thaliana
lateral-axis expansion is regulated by cell proliferation Oryza sativa
alternative division planes correspond to local minimal areas
eccDNA segregation can be heterogenic resulting in progeny cells containing different eccDNA copy numbers
(CYP98A3, REF8, AT2G40890) mutant is severely defective in cell division Arabidopsis thaliana
asymmetric cell division is breakthrough in cell biology Physcomitrella patens
AIL/PLT protein gradient forms by distribution of AIL/PLT protein to daughter cells during cell division
AINTEGUMENTA (ANT) was proposed to regulate cell division via direct regulation of (CYCD3, CYCD3;1, AT4G34160)
plant-specific protein MACERATOR 4 (CORD4, MACET4, AT1G23790) /CORTICAL MICROTUBULE DISORDERING 4 tethers AtAUG7 to the phragmoplast
Arabidopsis GCP6 mutants display aberrations in spindle organization Arabidopsis thaliana
large cell repeats division step unequal periclinal cell division Dictyota
pan1;pan2 double mutants have considerably more misoriented subsidiary mother cell (SMC) walls
double knockout mutants for (ATFTSZ1-1, CPFTSZ, FtsZ1, FTSZ1-1, AT5G55280) and ftsZ2 gene families were generated to investigate function of five moss ftsZ genes Physcomitrella patens
bacterial FtsZ is capable by itself and without the use of any interaction partner to generate force that is sufficient to constrict liposomes
microtubules contribute to formation of phragmoplast during cytokinesis Arabidopsis thaliana
nuclear pore components play important roles during plant cell division
sex relates to cell size restoration
Physcomitrella patens possesses expanded complement of FtsZ genes Physcomitrella patens
loss of FtsZ in E. coli causes lethality Escherichia coli
sub-cellular localization of (ATFH8, FH8, FORMIN 8, AT1G70140) in root tip cells suggests that AtFH8 is involved in cell division in the root tip Arabidopsis thaliana
DNA repair in the presence of oxidative stress may put this candidate gene in relation to cell division efficiency Zea mays
phosphate or nitrogen limitation blocks cell division Synechocystis sp. PCC 6803
application of ST on Populus tremula leaf buds showed that captured information was specific for gene ontology terms related to translation, photosynthesis, and several categories involved in cell division, differentiation, and genome organization, including cell morphogenesis Populus tremula
tetrahedral apical cell can self-renew self-renewal Physcomitrium patens
Loss-of-function cle mutants have aberrant cell division planes Physcomitrium; Marchantia
immuno-affinity isolation of (POK1, AT3G17360) results in co-purification of (ATMYA1, MYA1, XI-1, AT1G17580)
microtubule-associated protein MAP65 cross-bridges microtubules at particular stages of plant cell division
preprophase bands in KCH1 overexpressor cells only starts to develop when the nucleus reaches its position
TMBP200 has novel requirement in control of spindle orientation tobacco
UV-B-reduced leaf expansion is exclusively due to UV-B-mediated inhibition of cell division Lactuca sativa
thickened hypocotyls is not result of additional cell layers
cells produced in (AtHSPR, SMXL4, AT4G29920) (SMXL5, AT5G57130) mutants potentially maintained ability to divide for a longer time
shoot apical meristem (SAM) serves as site of cell division
cytoskeleton response to mechanical stress in animal systems is consistent with cytoskeleton response to mechanical stress in plant systems
cell cycle is connected to oriented growth through placement of cell division planes
cuneate thallus apical cells produce derivatives in four planes (two lateral, dorsal and ventral) Marchantia polymorpha
expressed genes classified based on methylation level within gene body were enriched for biological process term cell division Solanum lycopersicum
n-butanol treatment of DDYM did not alter length of cells in ZoD Sorghum bicolor
normal plant growth requires proper orientation of cell divisions
small leaves and flowers in rcd1-3; sro1-1 plants suggests that cell proliferation may be defective in these areas Arabidopsis thaliana
Brefeldin A alone induced slight labelling of newly formed cell plates Zea mays
Arabidopsis ESCRT components have essential role in cytokinesis Arabidopsis thaliana
female gametophyte provides traceable model system to study mechanisms controlling cell growth, cell division, cell fate, pattern formation Arabidopsis thaliana
imprecision of cell divisions combined with variable cellular growth rates would be expected to increase variability in cell sizes
L2 cell layer divide exclusively with cell division plane perpendicular to surface angiosperms
actin microfilaments form cortical network flanking the cortical division zone
Arabidopsis myosin (ATXIK, XI-17, XI-K, XIK, AT5G20490) have been detected in phragmoplast midzone and/or cortical division zone Arabidopsis thaliana
mutants with narrower leaves and slender organs lead to fewer cells
cell divisions are oriented
U/ (ACD, ALATS, AT1G50200) (unequal and asymmetrical cell division) is observed in many examples in land plants
Kinesin-12 motor (ATVPS52, POK, TTD8, VPS52, AT1G71270) is required for localization of myosins and other CAMP proteins like (ATRANGAP1, RANGAP1, AT3G63130) at the cell cortex
disruption of cell plate formation is caused by defects in plasma membrane Nicotiana tabacum
cell divisions are classified as asymmetric or symmetric
symmetric (proliferative) cell divisions give rise to two identical daughter cells
KCH2 motor is associated with preprophase band (PPB) Oryza sativa
actin microfilament depolymerization leads to diffusion of protein localization in all directions
Solyc03g114520.3 (Kinetochore protein) is example of expressed gene enriched in cell division Solanum lycopersicum
cell wall biogenesis is involved in cytokinesis
diatoms exhibit centrifugal cell wall neosynthesis
polygalacturonases (PGs) can regulate cell proliferation Arabidopsis thaliana
cell-division arises from intrinsic properties and hierarchical organization of plant system components
cell division patterns can be compared to Errera's rule Arabidopsis thaliana
plasma membrane-associated polarity domains control division orientation in plant cells
fluorescent linear wrinkles during anaphase increases fluorescence intensity in interface walls during telophase and G1 phase Nicotiana tabacum
Kinesin-12 motor (POK1, AT3G17360) co-localizes with (ATN, ATTAN, TAN1, AT3G05330)
(POK1, AT3G17360) localization at the cortical division zone is dependent on redundant functions of (ATN, ATTAN, TAN1, AT3G05330) and (AIR9, AT2G34680)
location of the nucleus within the PPB plane is more variable
(GEM1, MOR1, AT2G35630) mutants may exhibit allele-specific defects on interphase cortical MT Arabidopsis thaliana
UV-B does not affect cell division Lactuca sativa
plant cells divide by default along smallest possible plane that produces equally-sized daughter cells
polarized cell-division regulators instruct divisional behaviors Arabidopsis thaliana
sub-apical cell in Sphacelaria spp. divides equally transversely daughter cells Sphacelaria spp.
actin microfilaments are highly dynamic during mitosis
transition from loose and wide preprophase band (PPB) to condensed and narrow one involves microtubule-based motor kinesins
immuno-affinity isolation of (POK1, AT3G17360) results in co-purification of (ATN, ATTAN, TAN1, AT3G05330)
(PHGAP1, REN2, AT5G12150) /ROPGAP shares similar localization at cortical division zone
(POK1, AT3G17360) and (POK2, AT3G19050) are required for (ATRANGAP1, RANGAP1, AT3G63130) localization
consolidation of Myosin XI, (POK1, AT3G17360) and other proteins into concrete patches requires actin microfilaments
preprophase band (PPB) encircles cell in the position at which the new cross-wall will insert after mitosis
other kinesins are required for spindle organization Arabidopsis thaliana
distribution of bridge microtubules is typically fairly uniform
TMBP200 has novel role in spindle orientation Nicotiana tabacum
microtubules (MTs) function during all types of cell division
control cells show callose mainly present in newly formed cross-walls Arabidopsis thaliana
pyrenoid reproduces by fission during cell division Chlamydomonas reinhardtii
(ATN, ATTAN, TAN1, AT3G05330) (TANGLED1) is not localized to PPB sites in (ATVPS52, POK, TTD8, VPS52, AT1G71270) background Arabidopsis thaliana
gamete fusion sites have no relation to position of the first division plane Oryza sativa
RNAi SlARF7 lines show de-regulated cell division activity Solanum lycopersicum
SUP Curly tissue proliferation was more rapid than wild-type tissue proliferation Nicotiana tabacum
Tobacco homolog of PLDδ localizes to mitotic spindle Nicotiana tabacum
(CORD4, MACET4, AT1G23790) functions in proper recruitment of (AAA1, ATKTN1, BOT1, ERH3, FRA2, FRC2, FRC4, FTR, KATANIN, KTN1, LUE1, AT1G80350) to phragmoplasts Arabidopsis thaliana
polarised cell organisation of the mother cell occurs before asymmetrical or unequal cell divisions
somatic plant cells present mature preprophase band (PPB) array with condensed microtubule bundles at prophase
proper maturation of the central cell prevents unwanted premature division
Arabidopsis (GEM1, MOR1, AT2G35630) mutant microspores appear to undergo relatively normal division planes Arabidopsis thaliana
UV-B-reduced leaf expansion is exclusively due to UV-B-mediated inhibition of cell division Pisum sativum
short-root phenotype in main-2 and mail1-1 mutants is associated with reduced cell division in the RAM Arabidopsis thaliana
ectopically expressed moss Myosin VIII persists at site at later stages of mitosis Nicotiana tabacum
motor proteins (kinesins) deliver new cell-wall material to the growing cell plate
plant phragmoplast opens out into centrifugally growing ring
(ATVPS52, POK, TTD8, VPS52, AT1G71270) kinesins function upstream of (ATN, ATTAN, TAN1, AT3G05330) (TANGLED1) Arabidopsis thaliana
nucleus typically resides within plane of the preprophase band (PPB)
rcd1-3; sro1-1 double mutant roots display abnormal cell divisions Arabidopsis thaliana
plant CRT is highly expressed during mitosis in tobacco Nicotiana tabacum
tubulin abundance is regulated by cytokinin (CK) Arabidopsis thaliana
Arabidopsis PLDα1 was enriched in phragmoplasts of meristematic cells Arabidopsis thaliana
Arabidopsis PLDα1 was enriched in mitotic spindles Arabidopsis thaliana
endocytosis is involved in cytokinesis
stochastic component may reflect underlying molecular mechanism
asymmetric (formative) cell divisions give rise to cells with two distinct fates
male-derived (MIR159, MIR159A, AT1G73687) acts in endosperm promoting nuclear division Arabidopsis thaliana
(ARK3, RK3, AT4G21380) (Armadillo repeat kinesin 3)/KINUa function in PPB dynamics is unclear preprophase band (PPB) dynamics Arabidopsis thaliana
other forms of cytokinesis are not always associated with nuclear division
tobacco BY-2 cells have strong cycling activity Nicotiana tabacum
Kinesin-12 motor (ATVPS52, POK, TTD8, VPS52, AT1G71270) motor activity may be expressed when encountering or capturing microtubules emanating from the edge of the expanding phragmoplast
synchrony of cell division results in higher frequency of cell files with even cell numbers Nicotiana tabacum
asymmetry can emerge as the direct result of cell division
cells with expressing GhADF7 gene were binucleate, even four- and eight-nucleate at 20 hours after induction Schizosaccharomyces pombe
(GEM1, MOR1, AT2G35630) mutants have disturbed cytokinesis Arabidopsis thaliana
ARABIDOPSIS HOMOLOG of TRITHORAX1 ( (ATX1, SDG27, AT2G31650) ) regulates cell production Arabidopsis thaliana
seed phenotype correlates with cell division alteration Arabidopsis thaliana
plant-specific KCH kinesins are required for pre-mitotic nuclear positioning
trifluralin is inhibited by tubulin
Augmin complex in human cells enhances spindle formation and functionality
synchrony of cell division in VBI-3 is not significantly altered when comparing dark-cultivated files versus white light-cultivated files
temperature-sensitive (ts) mor1-1 mutants disturb cortical MT arrays in root cells Arabidopsis thaliana
Al 3+ can induce rapid change in the position of cell division activity Zea mays
temperature-sensitive (ts) mor1-2 mutants disturb cortical MT arrays in root cells Arabidopsis thaliana
(GEM1, MOR1, AT2G35630) mutants may not exhibit defects on spindle Arabidopsis thaliana
centromere scattering occurs between anaphase and telophase
CBP70-containing plastids are absent from sites of cell division within apex Zea mays
delayed onset of division in KCH1 overexpressor was observed in the KCH1 overexpressor
(GEM1, MOR1, AT2G35630) is required for various microtubule arrays in somatic cells Arabidopsis thaliana
UV-B reduces cell division Trifolium repens
excess Fe in combination with AVG reduces extent and area of GUS-stained region more than Fe alone treatment Arabidopsis thaliana
(ATMAP65-3, MAP65-3, PLE, AT5G51600) although present may not be active in metaphase spindle Arabidopsis thaliana
cells underexpressing (CESA6, E112, IXR2, PRC1, AT5G64740) have mid-body not formed Homo sapiens
control cells show callose around dividing cells Arabidopsis thaliana
plant cells divide by assembling new cross-wall (cell plate)
preprophase band (PPB) marks future division site
imaging of GFP-α-TUBULIN-decorated MT arrays demonstrates requirement for TMBP200 in organization of spindle and phragmoplast MT arrays tobacco
random spindle orientation and division planes in both polarized and unpolarized microspores suggests that division plane control may be linked to taxa-specific nuclear migration Nicotiana tabacum
wild-type fruits show cell division planes in mesocarp at 3–4 mm and 5–6 mm stages Solanum lycopersicum
plant-specific microtubule-associated protein (ATN, ATTAN, TAN1, AT3G05330) (Tangled1) is detected at cortical division zone after preprophase band (PPB) disassembly Arabidopsis thaliana
microtubules in spindle midzone can bridge spindle and phragmoplast midzones and cortical division zone
new cross-wall (cell plate) grows out centrifugally from remnants of the anaphase spindle
kiesel mutants show defects in cytokinesis Arabidopsis thaliana
myosin (ATXIK, XI-17, XI-K, XIK, AT5G20490) shares similar localization at cortical division zone
actin microfilaments and myosin motors provide positional cues for microtubules to act in spatially regulated manner
asymmetric cell division is a research field in plant stem cell biology
centromere enables fidelity in chromosome segregation during cell division
enlarged cell divides in particular direction
Kinesin-like calmodulin-binding protein (KCBP, PKCBP, ZWI, AT5G65930) is associated with preprophase band (PPB) Arabidopsis thaliana
Arabidopsis mutants lacking (KCBP, PKCBP, ZWI, AT5G65930) do not exhibit noticeable phenotype in cell division Arabidopsis thaliana
(ATMYA1, MYA1, XI-1, AT1G17580) (also known as Myo11F or Myosin ) shows even more prominent association with cortical division zone than Myosin (ATXIK, XI-17, XI-K, XIK, AT5G20490) Arabidopsis thaliana
Arabidopsis mutants uncovered multiple functions for kinesins in cells undergoing division Arabidopsis thaliana
(ATVPS52, POK, TTD8, VPS52, AT1G71270) kinesins are specifically required for establishment of the PPB memory Arabidopsis thaliana
intense mitotic activity leads to increase in cell number Solanum lycopersicum
loss of LjINV activity maintains correct cell proliferation Lotus japonicus
Cytoskeleton-Associated Motor assemblies at the PPB site (CAMPs) are competent to mediate interaction between microtubules and actin microfilaments
preprophase band has a guiding function for the correct orientation of the cell plate
depletion of TMBP200 caused random spindle orientation and division planes Nicotiana tabacum
UV-B-reduced leaf expansion is exclusively due to UV-B-mediated inhibition of cell division Arabidopsis thaliana
principal directions of growth (PDGs) are postulated to affect orientation of cell divisions
secondary meristems generate source of new cells
central SAM part in decussate vegetative SAM of Anagallis has infrequent cell divisions Anagallis arvensis
microtubule-associated protein MAP65 is related to (SPD1, AT3G10420)
inhibition of cell division is specific to NO2 Tyr Nicotiana tabacum
RADICAL-INDUCED CELL DEATH1 (ATP8, AtRCD1, CEO, CEO1, RCD1, RIMB1, AT1G32230) and SIMILAR TO RCD (ONE1, AT3G21140) (SRO1, AT2G35510) are necessary to regulate division plane placement Arabidopsis thaliana
Solyc02g071590.2 and Solyc02g071593.1 (Trehalose-6-phosphate synthase) are examples of expressed genes enriched in cell division Solanum lycopersicum
lipids play crucial roles in membrane fusion events
individual cells often deviate from general rule of division along smallest possible plane
differences between somatic and gametophytic cells in requirement for preprophase band (PPB) may imply additional cofactors that enable plant MAP215/ (ARP3, ATARP3, DIS1, AT1G13180) proteins to promote organization of cell type-specific microtubule arrays
UV-B does not affect cell division Solanum lycopersicum
33% of Ph[H] signalling clones are implicated in cell division and polarity Solanum tuberosum
improved root growth of scr-1 (ABA2, ATABA2, ATSDR1, GIN1, ISI4, SDR1, SIS4, SRE1, AT1G52340) and shr-2 mutants can be attributed to higher mitotic activity in root apical meristem Arabidopsis thaliana
silent chromatin state is heritable through multiple cell division cycles
total cell number along the style was higher in (MIR167A, AT3G22886) transgenic lines than in wild-type control lines Solanum lycopersicum
parthenolide causes alteration of microtubule-dependent cell plate alignment Nicotiana tabacum
polar preference in cell division and anisotropy of mitotic expansion may be related to change in orientation of plane of cell division
sub-apical smaller cell tilts its cell division plane along longitudinal axis Dictyota
myosin motors may be involved in maturation stage of preprophase band (PPB) development
(ATN, ATTAN, TAN1, AT3G05330) shares similar localization at cortical division zone
(POK1, AT3G17360) and (POK2, AT3G19050) are required for (ATMYA1, MYA1, XI-1, AT1G17580) localization at the cortical division zone
overexpression of (PNET1, AT1G07970) increases cell division event in mitotically inducible tobacco pavement cells Nicotiana tabacum
uninduced and control cells were binucleate at approximately 1% Schizosaccharomyces pombe
first cell division is usually geometrically unequal Sphacelaria
(ATN, ATTAN, TAN1, AT3G05330) mutants have phenotype comparable to (ATVPS52, POK, TTD8, VPS52, AT1G71270) mutants Arabidopsis thaliana
[3H]thymidine incorporation used as measure for cell division Nicotiana tabacum
CAM can accelerate cell proliferation Angelica
LOB (Lateral organ boundaries) is required for asymmetric cell division in meristems Solanum tuberosum
spindle midzone microtubules eventually give rise to phragmoplast microtubule array upon remodeling Nicotiana tabacum
(POK1, AT3G17360) and (ATMYA1, MYA1, XI-1, AT1G17580) and other proteins form Cytoskeleton-Associated Motor assemblies at the PPB site (CAMPs)
spindle array segregates duplicated chromosomes
1-NOA results in decreased cell division activity Nicotiana tabacum
first subset of kinesin KCH is important for pre-mitotic nuclear migration and mitosis plants
pre-mitotic nuclear migration defines symmetry of cell division
KCH overexpression delays pre-mitotic nuclear migration
(ATMAP65-3, MAP65-3, PLE, AT5G51600) protein is present at prophase, metaphase, and early anaphase stages Arabidopsis thaliana
(ATMAP65-3, MAP65-3, PLE, AT5G51600) does not stain early anaphase spindle microtubules Arabidopsis thaliana
BB-GUS and BB C197S,C200S-GUS expression patterns are compared to pCycB1;1::CDBGUS mitotic marker Arabidopsis thaliana
protoxylem cell divides once per cell in wild-type Arabidopsis thaliana
aurora1 aurora2 (aur1-2 ; 2-2) double mutant lacks key AURORA kinases required to correctly position cell plate in asymmetric formative cell divisions Arabidopsis thaliana
altered MT nucleation in ede1-1 mutant albeit being not so robust was sufficient to drive cell division forward Arabidopsis thaliana
number of dividing cells in (AGL8, FUL, AT5G60910) SAM and meristem-primordia boundaries augmented 6 wab in non-pruned (AGL8, FUL, AT5G60910) plants
divisions along the plane of minimal surface area leads to daughter cells of same size
cell divisions defined division planes through center of dividing cell where direction of division was determined depending on division rule applied
in planta results very much in accordance with anticlinal cell divisions in radially stressed regions Arabidopsis thaliana
spindle misorientation caused phragmoplast misorientation Marchantia polymorpha; Arabidopsis thaliana
MsRBR protein shows lack of accumulation in non-dividing cells cultured in hormone-free medium for a prolonged time Medicago sativa
trafficking is implicated in control of cytokinesis
enlargement of procambial strands indicates more cell divisions Arabidopsis thaliana
F-actin commonly assembled at cleavage site prior to cell division Porphyra yezoensis
(EDE1, EMB3116, QWRF5, AT2G44190) is essential gene Arabidopsis thaliana
Errera's rule does not capture division pattern in elongated cambium stem cells Arabidopsis thaliana
presence of (ATRBR1, RB, RB1, RBR, RBR1, AT3G12280) proteins is linked to plant cell division activity Medicago sativa
histone H4 might mark cells undergoing mitotic cell division Arabidopsis thaliana
cytokinins act as endogenous mitogens
determinate meristems produce new cells
simultaneous knockouts of three genes encoding Myosin XI that are actively expressed in meristematic cells lead to mild phenotypes of distorted division plane orientation Arabidopsis thaliana
(ATMYA1, MYA1, XI-1, AT1G17580) shares similar localization at cortical division zone
(EMB2789, MOS7, AT5G05680) mutant shows irregular cell plate formation Arabidopsis thaliana
microtubule-associated protein MAP65 is related to Feo
atk5-1-null mutant plants exhibit diminished structural integrity in spindles Arabidopsis thaliana
attractive forces between PPB and prophase spindle cause prophase spindle lateral migration and deformation Arabidopsis thaliana
orientation of the ensuing cell plate in KCH1 overexpressor cells would not be structurally altered in these cells
(ARF1-BP, ARF2, AtARF2, HSS, ORE14, AT5G62000) /mnt1 mutation causes more cell divisions Arabidopsis thaliana
subsequent propagation of the cells showing silencing would contribute to expansion of the silenced area
ANX11 translocates to spindle midzone in anaphase
exocyst is important participant in plant cytokinesis regulation Arabidopsis thaliana
endosperm at 3 daf is undergoing rapid cell division Arabidopsis thaliana
PHRAGMOPLAST ORIENTING KINESIN 1 and 2 ( (POK1, AT3G17360) and (POK2, AT3G19050) ) are involved in phragmoplast guidance Arabidopsis thaliana
division plane orientations were altered in Arabidopsis thaliana seedling root meristems upon long-term, low concentration NO2-Tyr treatment Arabidopsis thaliana
dynamin-related proteins have role in cytokinesis and cell expansion including cell wall formation Arabidopsis thaliana
(ATP8, AtRCD1, CEO, CEO1, RCD1, RIMB1, AT1G32230) and (SRO1, AT2G35510) support population of dividing cells
mesophyll (M) cells in Cleome angustifolia and Cleome gynandra continue to have active anticlinal divisions up to Stage 2 Cleome angustifolia; Cleome gynandra
cohesin is required to hold sister chromatids
AtTAN::YFP colocalizes with preprophase band (PPB) Arabidopsis thaliana
AtTAN::YFP and CFP::TUA1 analysis observed similar results in tissues where other patterns of division occur Arabidopsis thaliana
defects in the polarity of cell division result from changes in subcellular distribution of auxin transporters Nicotiana tabacum
1 mM ancymidol does not arrest nuclear division Nicotiana tabacum
tobacco cell culture cells treated with NO2-Tyr exhibited mitotic inhibition Nicotiana tabacum
transient DNA–topoisomerase covalent complexes are implicated in chromosome segregation
basal stem cells in embryos with decreased transcript levels of PaWOX8/9 divide inclined cell division Picea abies
AtCSPs expression is enriched in shoot apices Arabidopsis thaliana
apical stem cell of Fucus divides unequally and asymmetrically daughter cells Fucus
myosin XI is required for organization of other CAMP proteins into discrete patches
Kinesin-12 motor (ATVPS52, POK, TTD8, VPS52, AT1G71270) is not required for localization of CAMP proteins at the phragmoplast
mitotic and cytokinetic phenotypes may be linked with each other in context of dynamic microtubules present in spindle midzone Arabidopsis thaliana
rate of mitosis during the first days of the culture cycle in BY-2 KCH1 was clearly reduced in BY-2 KCH1 Nicotiana tabacum
tetrahedral apical cell divides to form distinct merophytes Physcomitrium patens
nucleoporins (Nups) and LINC complex interaction regulates centromere scattering
fluctuations in bridge microtubule distributions are transient
(ATMAP65-3, MAP65-3, PLE, AT5G51600) stains preprophase band Arabidopsis thaliana
microtubules are required for initial recruitment of Arabidopsis TANGLED fused to YFP (AtTAN::YFP) Arabidopsis thaliana
cortical guidance cue remains behind when PPB is disassembled Arabidopsis thaliana
(ARC11, ATMIND1, MIND, AT5G24020) and (MCD1, AT1G20830) localization at chloroplast division site is similar to MinCD and DivIVA localization in Gram-positive bacteria Arabidopsis thaliana; Bacillus subtilis
PPB and cell plate orientation may show variability between PPB and cell plate orientation Arabidopsis thaliana
new walls do not bear stress right after division
cell division keeps the wall stress from homogenizing
(CYC1, CYCB1, CYCB1;1, AT4G37490) ;2:Dbox-GUS cell-division marker shows cell division activity in root meristem Arabidopsis thaliana
(HB-3, STIP, WOX9, WOX9A, AT2G33880) is required for maintaining cell division activity during embryonic and post-embryonic development Petunia hybrida
genes associated with mitosis and cytokinesis expression peaks at or before 2 DAF Hordeum vulgare
splicing factors are divided between newly formed sperm cells Hyacinthus orientalis
ANX11 translocates from nucleus to spindle poles
sexual phase in diatoms involves marked changes from coupling of nuclear division, cell division, and frustule formation exhibited by the vegetative stage
dwarf phenotype in A2Wt lines is associated with reduced cell number, but not cell size, in expanded leaves Arabidopsis thaliana
wild-type leaves were actively producing new cells Arabidopsis thaliana
daughter cells unable to separate normally results in cell filamentation Synechococcus 7942
myosin VIII proteins are associated with cytokinesis
pre-mitotic nuclear movement defines symmetry of division
cell divisions in (AGL8, FUL, AT5G60910) were not completely repressed in (AGL8, FUL, AT5G60910)
Errera's rule derives from observation that cells often behave similar to surface-minimizing soap bubbles
short-axis divisions anticlinal divisions were clearly most prominent category anticlinal divisions Arabidopsis thaliana
cultivation of cells in 1 mM ancymidol results in bi-nuclear cells Nicotiana tabacum
F-actin pre-positioning was observed during third and fourth cell divisions Porphyra yezoensis
cells in Lotus mutant remained in division for much greater distance from the root tip Lotus japonicus
hexoses delivered by acid invertases support mitotic activity
three divisions in periclinal direction and six in anticlinal are estimated for WT as well as single and double t3/t5 Solanum lycopersicum
lack of cell proliferation in inner nucellus does not appear to be directly dependent upon PME activity or HG accumulation Hordeum vulgare
Min system expression level was detected in 7942M and WT cells Synechococcus 7942
Epidermal cell number in zmbell10-1 is significantly decreased in zmbell10-1 compared to WT Zea mays L.
zcn4-1 mutant plants have reduced number of epidermal cells Zea mays
ZmTFCB affects organization of spindle microtubule (MT) array Zea mays
centromeres is responsible for accurate chromosome segregation during cell division
Microcystin-LR (MC-LR) expression led to cellular filamentation Synechococcus 7942
MinE is part of Min system Synechococcus 7942
chromosomal duplications might arise from nondisjunction during mitosis or meiosis Fusarium oxysporum
OsSYP132 is required for root cell division Oryza sativa
increased elongation in 35S::EXPA5 transgenic lines was not caused by increased cell number Arabidopsis thaliana
specialized generations require differing suites of microtubule-associated proteins (MAPs)
inner nucellus cells exhibit low cell division activity Hordeum vulgare
pericycle cells re-enter cell cycle Arabidopsis thaliana
RHW1 (Zm00001d018482) mediates husk leaf width by affecting cell division Zea mays
null mutations of TFCs severely inhibit mitosis Arabidopsis thaliana
(EMB2804, TFCB, AT3G10220) appears to have conserved function in cell division
stem cells at basal part of embryonal mass in normal control embryos divide anticlinally to give rise to one cell which remains in embryonal mass Picea abies
kinesin KCH conveys architectural functions plants
(ATMAP65-3, MAP65-3, PLE, AT5G51600) is essential for cytokinesis Arabidopsis thaliana
live-cell microscopy of ase1-deleted cells demonstrated Ase1p is essential for slow phase of spindle elongation in anaphase B Saccharomyces cerevisiae
determinate root growth phenotype in (AHK4, ATCRE1, CRE1, WOL, WOL1, AT2G01830) plants results from reduced number of cell divisions in the procambium
Arabidopsis TANGLED fused to YFP (AtTAN::YFP) maintenance is microtubule independent cortical AtTAN::YFP rings Arabidopsis thaliana
Arabidopsis TANGLED homolog (ATN, ATTAN, TAN1, AT3G05330) is investigated to advance understanding of TAN localization and function Arabidopsis thaliana
cortical ring after PPB disassembly persists throughout mitosis and cytokinesis Arabidopsis thaliana
NO2-Tyr treatment did not produce more pronounced defects in (ATVPS52, POK, TTD8, VPS52, AT1G71270) single and double mutants Arabidopsis thaliana
mechanism of phragmoplast guidance was not specifically affected upon NO2-Tyr treatment Arabidopsis thaliana
nucleus undergoes mitosis at apical pole Arabidopsis thaliana
cytoskeletal pre-prophase band is indicative of future site of cell division
stem cells continuously produce daughter cells Picea abies
pre-mitotic nuclear migration is controlled by actin filaments and microtubules around nucleus forming perinuclear cage linked by KCH
down-regulated genes in Scfrk1-S1 are associated with GO terms for cell cycle control Solanum chacoense
Al 3+ cations can induce rapid change in cell division Zea mays
(ATMAP65-3, MAP65-3, PLE, AT5G51600) has essential role in cytokinesis in plant cells Arabidopsis thaliana
structural reorganization of the SAM affects mitotic activity
blocking of membrane dynamics by 1-NOA and 2-NOA has detrimental effects on cell division Nicotiana tabacum
NO₂-Tyr treatment altered division planes in BY-2 cells Nicotiana tabicum
defects in phragmoplast expansion and vesicle transport typically result in incomplete cell walls and multinucleated cells
(ATMAP65-3, MAP65-3, PLE, AT5G51600) does not stain prophase spindle microtubules Arabidopsis thaliana
proximal stem cells daughters form transitory-amplifying cell population
Stage 1 of C4 development is distinguished by M and BS cells performing anticlinal/radial divisions Cleome angustifolia; Cleome gynandra
regulation of multiple fission is expected to attract future research attention
nuclear genomes of land plants encode homologues of MinE
disorientation of cross walls is heralded by disturbed geometry of metaphase plate plants
actin filaments are essential components of machinery required for nuclear division and cytokinesis
numerous vesicles could be found throughout the cytoplasm of (GGP, VTC2, AT4G26850) cells Arabidopsis thaliana
faint staining of metaphase spindle and clear staining in late anaphase may explain why karyokinesis is not affected in (ATMAP65-3, MAP65-3, PLE, AT5G51600) mutants Arabidopsis thaliana
anaphase spindle in (ATMAP65-3, MAP65-3, PLE, AT5G51600) mutants appears normal Arabidopsis thaliana
primary plasmodesmata (PD) form during cell division Arabidopsis thaliana
dynamic microtubule (MT) arrays play pivotal roles in regulation of mitosis
endodermis was set to not proliferate Arabidopsis thaliana
one division event per step ensured tissue growth in addition to divisions and allowed tissue to integrate effects of one division before possibly undergoing another one in nearest neighbors Arabidopsis thaliana
compressed regions exhibit periclinal divisions
mitotic cells are located in root, shoot and intercalary meristems
plant and animal (AKIN10, KIN10, SnRK1, SnRK1α1, SNRK1.1, AT3G01090) /AMPK coordinate cell division
significance of (ARC11, ATMIND1, MIND, AT5G24020) localization at division site is still not clear even in bacterial models Escherichia coli; Bacillus subtilis
parallel arrays of cortical MTs affect spatial pattern of cell division
early embryo lethality of null ede1-3 mutant is due to failures in cell division Arabidopsis thaliana
orientation of cortical microtubule (CMT) arrays influences selection of division plane Arabidopsis thaliana
pif4-101 mutant exhibits decrease in cell numbers Arabidopsis thaliana
established cell division models often consider surface cells of shoots or roots that are typically under tension
geometry affects division plane orientation
H_A function penalizes increase of interface between two daughter cells Arabidopsis thaliana
Arabidopsis seedling cells divide at high frequency Arabidopsis thaliana
cytokinin and ethylene could potentially additively influence cell division in the QC
cell plate is formed at final step of cytokinesis
emergence of extra spikelets in flo.a may be related to ectopic cell division Hordeum vulgare
mechanism of phragmoplast guidance is disturbed in (ATVPS52, POK, TTD8, VPS52, AT1G71270) mutants Arabidopsis thaliana
root-supplied Fe significantly reduces mitotically active zone Arabidopsis thaliana
(ATMAP65-3, MAP65-3, PLE, AT5G51600) localization suggests role in cell division but not in cell expansion Arabidopsis thaliana
cells underexpressing (CESA6, E112, IXR2, PRC1, AT5G64740) have microtubules at midzone of anaphase spindle not inter-digitated Homo sapiens
GO terms including Golgi apparatus, nuclear envelope, and cell division were statistically enriched within differential patterns (DP5, DP6, and DP7) Arabidopsis thaliana
midzone MAPs family includes mammalian (CESA6, E112, IXR2, PRC1, AT5G64740) Homo sapiens
MinE constrains (ARC11, ATMIND1, MIND, AT5G24020)
tubulin participates in chromosome separation
critical MC size is required to undergo at least one round of cytokinesis Chlamydomonas
Flb somatic variant shows impaired cell division Vitis vinifera
actin cytoskeleton participates in cytokinesis
metabolites associated with the developing embryo control rate of cell division in surrounding fruit tissue
cells treated with 1-NOA and 2-NOA at 50 μM after 48 h were not dividing Nicotiana tabacum
RAN GTPase-activating protein (ATRANGAP1, RANGAP1, AT3G63130) has conserved function in cell division
(ATMAPK6, ATMPK6, MAPK6, MPK6, AT2G43790) controls cell division plane specification Arabidopsis thaliana
nuclear genomes of land plants encode homologues of Filamenting temperature-sensitive Z (FtsZ)
apum23-3 mutant shows reduced cell division activity in roots Arabidopsis thaliana
shorter stem phenotype of ABI1oe might be primarily result of decreased levels of longitudinal cell-division activity Arabidopsis thaliana
(AIR9, AT2G34680) single mutants had PPB angles within 80° to 100° in more than 90% of cells Arabidopsis thaliana
GSH affects initiation and maintenance of cell division Arabidopsis thaliana
Z-ring acts as scaffold for assembly of other division components
long-term treatment with NOAs causes changes in polarity of cell division Nicotiana tabacum
(ATVPS52, POK, TTD8, VPS52, AT1G71270) single mutants are phenotypically wild type Arabidopsis thaliana
cell wall positioning defects in (ATVPS52, POK, TTD8, VPS52, AT1G71270) mutants are comparable with those of wild-type plants Arabidopsis thaliana
NO2-Tyr treatment might become useful tool to induce oblique division planes Arabidopsis thaliana