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α -tubulin acetylation and detyrosination correlate with starvation-induced autophagy in tobacco cells

https://doi.org/10.1101/111484
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1097-4644(19971101)67:2<231::aid-jcb8>3.0.co;2-yopenalex-snapshot
Apoptosis in C3H-10T1/2 cells: Roles of intracellular pH, protein kinase C, and the Na+/H+ antiporter
inferredcites →https://doi.org/10.1002/cm.21020openalex-snapshot
Formation of an endoplasmic reticulum ring associated with acetylated microtubules in the angiosperm preprophase band
inferredcites →https://doi.org/10.1002/cm.970080309openalex-snapshot
Acetylated and detyrosinated α‐tubulins are co‐localized in stable microtubules in rat meningeal fibroblasts
inferredcites →https://doi.org/10.1006/abio.1976.9999openalex-snapshot
A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye Binding
inferredcites →https://doi.org/10.1007/bf01928191openalex-snapshot
Einige Versuche über die Wirkung von Heteroauxin auf die Symmetrieentwicklung der Brutkörperkeimlinge vonMarchantia polymorpha L.
inferredcites →https://doi.org/10.1007/s00425-003-1122-4openalex-snapshot
Post-translational modifications of ?-tubulin in Zea mays L. are highly tissue specific
inferredcites →https://doi.org/10.1007/s00709-010-0190-0openalex-snapshot
From signal transduction to autophagy of plant cell organelles: lessons from yeast and mammals and plant-specific features
inferredcites →https://doi.org/10.1007/s00709-011-0296-zopenalex-snapshot
Variations on a theme: plant autophagy in comparison to yeast and mammals
inferredcites →https://doi.org/10.1007/s10265-006-0057-9openalex-snapshot
Microtubule-associated proteins in higher plants
inferredcites →https://doi.org/10.1007/s13238-011-1104-4openalex-snapshot
Role of plant autophagy in stress response
inferredcites →https://doi.org/10.1016/j.ceb.2007.11.010openalex-snapshot
Tubulin modifications and their cellular functions
inferredcites →https://doi.org/10.1016/j.cell.2005.03.007openalex-snapshot
Autophagy Regulates Programmed Cell Death during the Plant Innate Immune Response
inferredcites →https://doi.org/10.1016/j.cub.2006.09.014openalex-snapshot
Microtubule Acetylation Promotes Kinesin-1 Binding and Transport
inferredcites →https://doi.org/10.1016/j.envexpbot.2009.11.004openalex-snapshot
UV-B overexposure induces programmed cell death in a BY-2 tobacco cell line
inferredcites →https://doi.org/10.1016/j.pbi.2004.09.008openalex-snapshot
Progress in understanding the role of microtubules in plant cells
inferredcites →https://doi.org/10.1016/j.pbi.2004.09.017openalex-snapshot
MAPs in plant cells: delineating microtubule growth dynamics and organization
inferredcites →https://doi.org/10.1016/j.pbi.2006.05.007openalex-snapshot
Autophagy in the control of programmed cell death
inferredcites →https://doi.org/10.1016/j.plantsci.2011.04.017openalex-snapshot
Nitric oxide signalling via cytoskeleton in plants
inferredcites →https://doi.org/10.1016/j.tplants.2008.08.006openalex-snapshot
Timing is everything: regulatory overlap in plant cell death
inferredcites →https://doi.org/10.1016/j.tplants.2009.02.008openalex-snapshot
Is the autophagy machinery an executioner of programmed cell death in plants?
inferredcites →https://doi.org/10.1016/s0014-5793(98)01718-9openalex-snapshot
Gibberellic acid stabilises microtubules in maize suspension cells to cold and stimulates acetylation of α‐tubulin 1
inferredcites →https://doi.org/10.1016/s0021-9258(19)78150-2openalex-snapshot
Molecular characterization of light chain 3. A microtubule binding subunit of MAP1A and MAP1B
inferredcites →https://doi.org/10.1016/s0074-7696(08)62452-3openalex-snapshot
Tobacco BY-2 Cell Line as the “HeLa” Cell in the Cell Biology of Higher Plants
inferredcites →https://doi.org/10.1016/s0092-8674(02)00691-8openalex-snapshot
Expansion of the Cell Plate in Plant Cytokinesis Requires a Kinesin-like Protein/MAPKKK Complex
inferredcites →https://doi.org/10.1016/s1074-5521(99)89002-4openalex-snapshot
How Taxol® stabilises microtubule structure
inferredcites →https://doi.org/10.1016/s1360-1385(01)02090-8openalex-snapshot
Plant microtubule-associated proteins: the HEAT is off in temperature-sensitive mor1
inferredcites →https://doi.org/10.1023/a:1026501430422openalex-snapshot
The role of hexokinase in plant sugar signal transduction and growth and development
inferredcites →https://doi.org/10.1038/212425a0openalex-snapshot
Fluorescence Microscopy of Lysosomes and Related Structures in Living Cells
inferredcites →https://doi.org/10.1038/cdd.2009.79openalex-snapshot
Cell-autonomous requirement for DNaseII in nonapoptotic cell death
inferredcites →https://doi.org/10.1038/cdd.2011.39openalex-snapshot
Organisation and regulation of the cytoskeleton in plant programmed cell death
inferredcites →https://doi.org/10.1038/nature06069openalex-snapshot
A central integrator of transcription networks in plant stress and energy signalling
inferredcites →https://doi.org/10.1038/ncb2152openalex-snapshot
AMPK and mTOR regulate autophagy through direct phosphorylation of Ulk1
inferredcites →https://doi.org/10.1038/nn.2314openalex-snapshot
Tubulin tyrosination navigates the kinesin-1 motor domain to axons
inferredcites →https://doi.org/10.1038/onc.2009.487openalex-snapshot
Involvement of JNK in the regulation of autophagic cell death
inferredcites →https://doi.org/10.1038/sj.cdd.4401777openalex-snapshot
Another way to die: autophagic programmed cell death
inferredcites →https://doi.org/10.1042/bc20040516openalex-snapshot
Starvation‐induced expression of autophagy‐related genes in Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.1994.6050625.xopenalex-snapshot
Expression of α‐amylases, carbohydrate metabolism, and autophagy in cultured rice cells is coordinately regulated by sugar nutrient
inferredcites →https://doi.org/10.1073/pnas.85.16.5946openalex-snapshot
Selective stabilization of microtubules oriented toward the direction of cell migration.
inferredcites →https://doi.org/10.1073/pnas.92.13.5965openalex-snapshot
Cell acidification in apoptosis: granulocyte colony-stimulating factor delays programmed cell death in neutrophils by up-regulating the vacuolar H(+)-ATPase.
inferredcites →https://doi.org/10.1074/jbc.270.7.3203openalex-snapshot
Apoptosis in an Interleukin-2-dependent Cytotoxic T Lymphocyte Cell Line Is Associated with Intracellular Acidification
inferredcites →https://doi.org/10.1074/jbc.m109.091553openalex-snapshot
Starvation-induced Hyperacetylation of Tubulin Is Required for the Stimulation of Autophagy by Nutrient Deprivation
inferredcites →https://doi.org/10.1074/jbc.m110.206532openalex-snapshot
Microtubule-associated Protein 1S (MAP1S) Bridges Autophagic Components with Microtubules and Mitochondria to Affect Autophagosomal Biogenesis and Degradation
inferredcites →https://doi.org/10.1074/jbc.m111.300749openalex-snapshot
Rapamycin and Glucose-Target of Rapamycin (TOR) Protein Signaling in Plants
inferredcites →https://doi.org/10.1083/jcb.106.1.141openalex-snapshot
Enhanced stability of microtubules enriched in detyrosinated tubulin is not a direct function of detyrosination level.
inferredcites →https://doi.org/10.1083/jcb.126.6.1455openalex-snapshot
Microtubule dynamics in fish melanophores.
inferredcites →https://doi.org/10.1091/mbc.e09-01-0044openalex-snapshot
Posttranslational Modifications of Tubulin and the Polarized Transport of Kinesin-1 in Neurons
inferredcites →https://doi.org/10.1093/jxb/erg038openalex-snapshot
Metabolic signalling and carbon partitioning: role of Snf1-related (SnRK1) protein kinase
inferredcites →https://doi.org/10.1093/jxb/erp067openalex-snapshot
Sugars, senescence, and ageing in plants and heterotrophic organisms
inferredcites →https://doi.org/10.1093/pcp/pcl031openalex-snapshot
AtATG Genes, Homologs of Yeast Autophagy Genes, are Involved in Constitutive Autophagy in Arabidopsis Root Tip Cells
inferredcites →https://doi.org/10.1093/pcp/pcm123openalex-snapshot
Salt Tolerance Requires Cortical Microtubule Reorganization in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcs099openalex-snapshot
Beginning to Understand Autophagy, an Intracellular Self-Degradation System in Plants
inferredcites →https://doi.org/10.1101/gad.436407openalex-snapshot
HDAC6 controls major cell response pathways to cytotoxic accumulation of protein aggregates
inferredcites →https://doi.org/10.1104/pp.104.044362openalex-snapshot
Transcriptome Profiling of the Response of Arabidopsis Suspension Culture Cells to Suc Starvation
inferredcites →https://doi.org/10.1104/pp.113.229948openalex-snapshot
The Role of Target of Rapamycin Signaling Networks in Plant Growth and Metabolism
inferredcites →https://doi.org/10.1105/tpc.111.093112openalex-snapshot
A New Type of Compartment, Defined by Plant-Specific Atg8-Interacting Proteins, Is Induced upon Exposure of Arabidopsis Plants to Carbon Starvation
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02397.xopenalex-snapshot
AtATG18a is required for the formation of autophagosomes during nutrient stress and senescence in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2012.04984.xopenalex-snapshot
Arabidopsis thaliana histone deacetylase 14 (HDA14) is an α‐tubulin deacetylase that associates with PP2A and enriches in the microtubule fraction with the putative histone acetyltransferase ELP3
inferredcites →https://doi.org/10.1111/j.1469-185x.2009.00082.xopenalex-snapshot
Multiple roles of the cytoskeleton in autophagy
inferredcites →https://doi.org/10.1111/j.1471-4159.2009.06102.xopenalex-snapshot
Tau – an inhibitor of deacetylase HDAC6 function
inferredcites →https://doi.org/10.1111/tpj.12102openalex-snapshot
Microtubules, signalling and abiotic stress
inferredcites →https://doi.org/10.1126/science.1113010openalex-snapshot
Tubulin Polyglutamylase Enzymes Are Members of the TTL Domain Protein Family
inferredcites →https://doi.org/10.1146/annurev-arplant-042811-105441openalex-snapshot
Autophagy: Pathways for Self-Eating in Plant Cells
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105441openalex-snapshot
SUGAR SENSING AND SIGNALING IN PLANTS: Conserved and Novel Mechanisms
inferredcites →https://doi.org/10.1186/1471-2121-11-89openalex-snapshot
Acetylated microtubules are required for fusion of autophagosomes with lysosomes
inferredcites →https://doi.org/10.1186/1471-2164-2-2openalex-snapshot
Kinesins in the Arabidopsis genome: A comparative analysis among eukaryotes
inferredcites →https://doi.org/10.1242/jcs.026492openalex-snapshot
Differential trafficking of Kif5c on tyrosinated and detyrosinated microtubules in live cells
inferredcites →https://doi.org/10.1242/jcs.107.8.2249openalex-snapshot
Isolation of polypeptides with microtubule-translocating activity from phragmoplasts of tobacco BY-2 cells
inferredcites →https://doi.org/10.1242/jcs.115626openalex-snapshot
Autophagy and microtubules – new story, old players
inferredcites →https://doi.org/10.1271/bbb.130261openalex-snapshot
Acetylation of α-Tubulin on Lys40Is a Widespread Post-Translational Modification in Angiosperms
inferredcites →https://doi.org/10.1271/bbb.130475openalex-snapshot
Regulated Changes in the Acetylation of α-Tubulin on Lys40during Growth and Organ Development in Fast Plants,Brassica rapaL.
inferredcites →https://doi.org/10.1371/journal.pone.0011883openalex-snapshot
TOR Is a Negative Regulator of Autophagy in Arabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pone.0042218openalex-snapshot
Tubulin Acetylation Alone Does Not Affect Kinesin-1 Velocity and Run Length In Vitro
inferredcites →https://doi.org/10.3103/s0095452712010112openalex-snapshot
Inhibitors of tyrosine kinases and phosphatases as a tool for the investigation of microtubule role in plant cold response
inferredcites →https://doi.org/10.3732/ajb.93.10.1466openalex-snapshot
A unified hypothesis of mechanoperception in plants
inferredcites →https://doi.org/10.4161/auto.2092openalex-snapshot
Autophagy in Development and Stress Responses of Plants
inferredcites →https://doi.org/10.4161/auto.4158openalex-snapshot
Constitutive Autophagy in Plant Root Cells
inferredcites →https://doi.org/10.4161/auto.5.7.9290openalex-snapshot
Autophagy is required for tolerance of drought and salt stress in plants
inferredcites →https://doi.org/10.4161/auto.6.8.13694openalex-snapshot
Autophagy as a trigger for cell death: Autophagic degradation of inhibitor of apoptosis dBruce controls DNA fragmentation during late oogenesis in Drosophila
inferredcites →https://doi.org/10.4161/cc.6.17.4633openalex-snapshot
The Tubulin Code
inferredcites →https://doi.org/10.4161/psb.6.1.14202openalex-snapshot
Cytoskeleton and plant salt stress tolerance

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inferred← citeshttps://doi.org/10.1038/s41526-024-00381-9openalex-snapshot
Autophagy formation, microtubule disorientation, and alteration of ATG8 and tubulin gene expression under simulated microgravity in Arabidopsis thaliana
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