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Maize tubulin folding cofactor B is required for cell division and cell growth through modulating microtubule homeostasis

https://doi.org/10.1111/nph.18839
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/jsbi.2001.4386openalex-snapshot
Review: Postchaperonin Tubulin Folding Cofactors and Their Role in Microtubule Dynamics
inferredcites →https://doi.org/10.1007/s00018-012-1114-2openalex-snapshot
Autoinhibition of TBCB regulates EB1-mediated microtubule dynamics
inferredcites →https://doi.org/10.1016/0022-2836(74)90381-7openalex-snapshot
Structural polarity and directional growth of microtubules of Chlamydomonas flagella
inferredcites →https://doi.org/10.1016/0305-0491(88)90320-3openalex-snapshot
Comparative analysis of tubulin sequences
inferredcites →https://doi.org/10.1016/b978-0-12-407757-7.00011-6openalex-snapshot
Tubulin-Specific Chaperones
inferredcites →https://doi.org/10.1016/j.molp.2022.08.001openalex-snapshot
An MCIA-like complex is required for mitochondrial complex I assembly and seed development in maize
inferredcites →https://doi.org/10.1016/j.pbi.2013.10.001openalex-snapshot
Modelling the role of microtubules in plant cell morphology
inferredcites →https://doi.org/10.1016/j.pbi.2018.07.002openalex-snapshot
Getting into shape: the mechanics behind plant morphogenesis
inferredcites →https://doi.org/10.1016/j.pep.2006.03.005openalex-snapshot
Native tubulin-folding cofactor E purified from baculovirus-infected Sf9 cells dissociates tubulin dimers
inferredcites →https://doi.org/10.1016/j.tcb.2012.10.003openalex-snapshot
End-binding proteins and Ase1/PRC1 define local functionality of structurally distinct parts of the microtubule cytoskeleton
inferredcites →https://doi.org/10.1016/j.tplants.2019.01.003openalex-snapshot
Copy Number Variation in Domestication
inferredcites →https://doi.org/10.1016/j.yexcr.2006.09.002openalex-snapshot
Role of cofactors B (TBCB) and E (TBCE) in tubulin heterodimer dissociation
inferredcites →https://doi.org/10.1016/s0171-9335(99)80011-9openalex-snapshot
Mutations in the PILZ group genes disrupt the microtubule cytoskeleton and uncouple cell cycle progression from cell division in Arabidopsis embryo and endosperm
inferredcites →https://doi.org/10.1016/s0960-9822(02)01109-0openalex-snapshot
Functional Analysis of the Tubulin-Folding Cofactor C in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/s0960-9822(02)01288-5openalex-snapshot
Tubulin Folding Cofactors: Half a Dozen for a Dimer
inferredcites →https://doi.org/10.1016/s0962-8924(97)01168-9openalex-snapshot
The α- and β-tubulin folding pathways
inferredcites →https://doi.org/10.1038/2171053a0openalex-snapshot
Amino-acid Composition of “Tubulin” constituting Microtubules of Sperm Flagella
inferredcites →https://doi.org/10.1038/34465openalex-snapshot
Structure of the αβ tubulin dimer by electron crystallography
inferredcites →https://doi.org/10.1038/nature13889openalex-snapshot
Inhibition of cell expansion by rapid ABP1-mediated auxin effect on microtubules
inferredcites →https://doi.org/10.1038/nprot.2007.199openalex-snapshot
Arabidopsis mesophyll protoplasts: a versatile cell system for transient gene expression analysis
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1083/jcb.138.4.821openalex-snapshot
Tubulin Subunits Exist in an Activated Conformational State Generated and Maintained by Protein Cofactors
inferredcites →https://doi.org/10.1083/jcb.144.1.113openalex-snapshot
Alf1p, a CLIP-170 Domain-containing Protein, Is Functionally and Physically Associated with α-Tubulin
inferredcites →https://doi.org/10.1083/jcb.200509150openalex-snapshot
TIP maker and TIP marker; EB1 as a master controller of microtubule plus ends
inferredcites →https://doi.org/10.1091/mbc.10.9.2987openalex-snapshot
Functional Dissection and Hierarchy of Tubulin-folding Cofactor Homologues in Fission Yeast
inferredcites →https://doi.org/10.1091/mbc.e01-10-0089openalex-snapshot
Dissociation of the Tubulin Dimer Is Extremely Slow, Thermodynamically Very Unfavorable, and Reversible in the Absence of an Energy Source
inferredcites →https://doi.org/10.1091/mbc.e11-07-0633openalex-snapshot
Drosophilatubulin-binding cofactor B is required for microtubule network formation and for cell polarity
inferredcites →https://doi.org/10.1093/emboj/19.22.5971openalex-snapshot
Eukaryotic chaperonin CCT stabilizes actin and tubulin folding intermediates in open quasi‐native conformations
inferredcites →https://doi.org/10.1093/pcp/pcl001openalex-snapshot
Arabidopsis Tubulin Folding Cofactor B Interacts with α-Tubulin In Vivo
inferredcites →https://doi.org/10.1101/cshperspect.a023218openalex-snapshot
Mitosis
inferredcites →https://doi.org/10.1101/cshperspect.a025817openalex-snapshot
Microtubule-Based Transport and the Distribution, Tethering, and Organization of Organelles
inferredcites →https://doi.org/10.1101/gad.221702openalex-snapshot
The Arabidopsis PILZ group genes encode tubulin-folding cofactor orthologs required for cell division but not cell growth
inferredcites →https://doi.org/10.1104/pp.010911openalex-snapshot
Diversity of TITAN Functions in Arabidopsis Seed Development
inferredcites →https://doi.org/10.1104/pp.114.240689openalex-snapshot
Dynamic Transcriptome Landscape of Maize Embryo and Endosperm Development
inferredcites →https://doi.org/10.1104/pp.17.01329openalex-snapshot
Update: Plant Cortical Microtubule Arrays
inferredcites →https://doi.org/10.1104/pp.19.01336openalex-snapshot
ZmEHD1 Is Required for Kernel Development and Vegetative Growth through Regulating Auxin Homeostasis
inferredcites →https://doi.org/10.1105/tpc.1.10.1011openalex-snapshot
Changes in the Zein Composition of Protein Bodies during Maize Endosperm Development
inferredcites →https://doi.org/10.1105/tpc.106.048579openalex-snapshot
Arabidopsis MICROTUBULE-ASSOCIATED PROTEIN18 Functions in Directional Cell Growth by Destabilizing Cortical Microtubules
inferredcites →https://doi.org/10.1105/tpc.107.056846openalex-snapshot
The Microtubule Plus-End Binding Protein EB1 Functions in Root Responses to Touch and Gravity Signals in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.111.092684openalex-snapshot
MDP25, A Novel Calcium Regulatory Protein, Mediates Hypocotyl Cell Elongation by Destabilizing Cortical Microtubules inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.101360openalex-snapshot
Opaque1 Encodes a Myosin XI Motor Protein That Is Required for Endoplasmic Reticulum Motility and Protein Body Formation in Maize Endosperm
inferredcites →https://doi.org/10.1105/tpc.112.106781openalex-snapshot
Empty Pericarp5 Encodes a Pentatricopeptide Repeat Protein That Is Required for Mitochondrial RNA Editing and Seed Development in Maize
inferredcites →https://doi.org/10.1105/tpc.114.131482openalex-snapshot
The Microtubule Plus-End Tracking Proteins SPR1 and EB1b Interact to Maintain Polar Cell Elongation and Directional Organ Growth in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.18.00921openalex-snapshot
Maize Dek15 Encodes the Cohesin-Loading Complex Subunit SCC4 and Is Essential for Chromosome Segregation and Kernel Development
inferredcites →https://doi.org/10.1111/j.1471-4159.2006.04328.xopenalex-snapshot
Tubulin cofactor B plays a role in the neuronal growth cone
inferredcites →https://doi.org/10.1111/nph.14507openalex-snapshot
E+ subgroup PPR protein defective kernel 36 is required for multiple mitochondrial transcripts editing and seed development in maize and Arabidopsis
inferredcites →https://doi.org/10.1111/nph.15705openalex-snapshot
Microtubule nucleation for the assembly of acentrosomal microtubule arrays in plant cells
inferredcites →https://doi.org/10.1111/pbi.13292openalex-snapshot
Maize ZmRPH1 encodes a microtubule‐associated protein that controls plant and ear height
inferredcites →https://doi.org/10.1126/science.144.3620.872openalex-snapshot
Morphology of Microtubules of Plant Cell
inferredcites →https://doi.org/10.1128/mcb.25.9.3726-3736.2005openalex-snapshot
p21-Activated Kinase 1 Regulates Microtubule Dynamics by Phosphorylating Tubulin Cofactor B
inferredcites →https://doi.org/10.1186/1746-4811-6-5openalex-snapshot
A rapid and robust assay for detection of S-phase cell cycle progression in plant cells and tissues by using ethynyl deoxyuridine
inferredcites →https://doi.org/10.1186/s12870-014-0327-yopenalex-snapshot
A CRISPR/Cas9 toolkit for multiplex genome editing in plants
inferredcites →https://doi.org/10.1242/jcs.167387openalex-snapshot
The structure of the TBCE/TBCB chaperones and α-tubulin complex shows a tubulin dimer dissociation mechanism
inferredcites →https://doi.org/10.2741/e135openalex-snapshot
AtTFC B is involved in control of cell division
inferredcites →https://doi.org/10.3390/cells8040362openalex-snapshot
The Cytoskeleton—A Complex Interacting Meshwork

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4641581openalex-extracted
inferred← citeshttps://doi.org/10.1007/s00122-023-04434-7openalex-snapshot
The genetic architecture of prolificacy in maize revealed by association mapping and bulk segregant analysis
inferred← citeshttps://doi.org/10.1007/s00122-025-05038-zopenalex-snapshot
Genetic and histological characterization of a dwarf mutant in melon (Cucumis melo L.) reveals potential for breeding semi-dwarf cultivars
inferred← citeshttps://doi.org/10.1007/s00122-026-05239-0openalex-snapshot
TaGα knockout in wheat causes early heading and short organ length, with dose-dependent effects through various pathways
inferred← citeshttps://doi.org/10.1007/s11427-025-3022-6openalex-snapshot
Decades’ progress and prospects on maize functional genomics and molecular breeding
inferred← citeshttps://doi.org/10.1016/j.cj.2026.07.013openalex-snapshot
CLUMPED TASSAL1 controls maize plant height by modulating cell elongation
inferred← citeshttps://doi.org/10.1016/j.jgg.2026.03.021openalex-snapshot
Natural variation in Miniature5 determines mitochondrial nad1 splicing and seed development in maize
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110082openalex-snapshot
A DEAD-box RNA helicase encoded by DEK223 is essential for maize kernel development by affecting pre-rRNA processing
inferred← citeshttps://doi.org/10.1016/j.scienta.2024.113645openalex-snapshot
LpY3IP1 Enhances the drought and salt tolerance of perennial ryegrass by protecting the photosynthetic apparatus
inferred← citeshttps://doi.org/10.1111/jipb.13639openalex-snapshot
FKF1b controls reproductive transition associated with adaptation to geographical distribution in maize
inferred← citeshttps://doi.org/10.1111/jipb.13780openalex-snapshot
Regulation of maize growth and immunity by ZmSKI3‐mediated RNA decay and post‐transcriptional gene silencing
inferred← citeshttps://doi.org/10.1111/jipb.70296openalex-snapshot
Rice OsTUB1 interacts with OsEB1c and OsEB1a to separately modulate endosperm development and grain size
inferred← citeshttps://doi.org/10.1111/nph.19107openalex-snapshot
Tubulin folding cofactor B regulates microtubule homeostasis through an evolutionarily conserved pathway
inferred← citeshttps://doi.org/10.1111/pbi.14279openalex-snapshot
Genetic variation in ZmKW1 contributes to kernel weight and size in dent corn and popcorn
inferred← citeshttps://doi.org/10.1111/tpj.16900openalex-snapshot
Identification of anther thermotolerance genes by the integration of linkage and association analysis in maize
inferred← citeshttps://doi.org/10.1111/tpj.71029openalex-snapshot
The HD ‐Zip IV gene ZmHB118 is required for basal endosperm transfer layer formation and maternal‐to‐filial nutrient allocation during maize seed filling
inferred← citeshttps://doi.org/10.3389/fmicb.2024.1476738openalex-snapshot
Transcriptomic analysis reveals the mechanism underlying salinity-induced morphological changes in Skeletonema subsalsum
inferred← citeshttps://doi.org/10.3389/fpls.2023.1204889openalex-snapshot
Subcellular positioning during cell division and cell plate formation in maize
inferred← citeshttps://doi.org/10.3389/fpls.2025.1640284openalex-snapshot
Non-coding RNA-mediated regulation of seed endosperm development
inferred← citeshttps://doi.org/10.3390/genes15121606openalex-snapshot
Mechanisms, Machinery, and Dynamics of Chromosome Segregation in Zea mays
inferred← citeshttps://doi.org/10.3390/horticulturae12070837openalex-snapshot
Evolutionary Dynamics of the Tubulin Gene Family Across Plants and Identification of PaTUA1 as a Candidate Gene Associated with Apricot Kernel Development
inferred← citeshttps://doi.org/10.3390/ijms252212301openalex-snapshot
TBCC Domain-Containing Protein Regulates Sporulation and Virulence of Phytophthora capsici via Nutrient-Responsive Signaling
inferred← citeshttps://doi.org/10.48130/vegres-0024-0012openalex-snapshot
Genome-wide identification of Kip-related protein (KRP) gene family members in eggplant and the function of SmKRP3 under salt stress
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