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CRK2 enhances salt tolerance in Arabidopsis thaliana by regulating endocytosis and callose deposition in connection with PLDα1

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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/abbi.1998.0640openalex-snapshot

Substrate Selectivities and Lipid Modulation of Plant Phospholipase Dα, -β, and -γ

inferredcites →https://doi.org/10.1006/abio.1997.2299openalex-snapshot

Measurement of Phospholipase D Activity

inferredcites →https://doi.org/10.1007/s00425-013-1999-5openalex-snapshot

Phosphatidic acid integrates calcium signaling and microtubule dynamics into regulating ABA-induced stomatal closure in Arabidopsis

inferredcites →https://doi.org/10.1007/s10265-016-0870-8openalex-snapshot

Arabidopsis phospholipase D alpha 1-derived phosphatidic acid regulates microtubule organization and cell development under microtubule-interacting drugs treatment

inferredcites →https://doi.org/10.1016/j.bbalip.2009.02.017openalex-snapshot

Phospholipase D- and phosphatidic acid-mediated signaling in plants

inferredcites →https://doi.org/10.1016/j.bbrc.2014.02.013openalex-snapshot

The Arabidopsis thaliana cysteine-rich receptor-like kinases CRK6 and CRK7 protect against apoplastic oxidative stress

inferredcites →https://doi.org/10.1016/j.bbrc.2016.05.028openalex-snapshot

Salt stress induces internalization of plasma membrane aquaporin into the vacuole in Arabidopsis thaliana

inferredcites →https://doi.org/10.1016/j.devcel.2012.12.013openalex-snapshot

A bHLH Complex Controls Embryonic Vascular Tissue Establishment and Indeterminate Growth in Arabidopsis

inferredcites →https://doi.org/10.1016/j.phytochem.2004.06.021openalex-snapshot

Salt-induced lipid changes in Catharanthus roseus cultured cell suspensions

inferredcites →https://doi.org/10.1016/j.phytochem.2009.01.014openalex-snapshot

Changes in plasma membrane lipids, aquaporins and proton pump of broccoli roots, as an adaptation mechanism to salinity

inferredcites →https://doi.org/10.1016/j.plantsci.2011.10.015openalex-snapshot

Expression of Arabidopsis callose synthase 5 results in callose accumulation and cell wall permeability alteration

inferredcites →https://doi.org/10.1016/j.plaphy.2013.03.013openalex-snapshot

Arabidopsis cysteine-rich receptor-like kinase 45 functions in the responses to abscisic acid and abiotic stresses

inferredcites →https://doi.org/10.1016/j.plipres.2016.01.002openalex-snapshot

Plant phospholipases D and C and their diverse functions in stress responses

inferredcites →https://doi.org/10.1016/j.sjbs.2014.12.001openalex-snapshot

Soil salinity: A serious environmental issue and plant growth promoting bacteria as one of the tools for its alleviation

inferredcites →https://doi.org/10.1016/j.tplants.2005.06.002openalex-snapshot

Phosphatidic acid: a multifunctional stress signaling lipid in plants

inferredcites →https://doi.org/10.1016/s1097-2765(00)80265-8openalex-snapshot

FLS2

inferredcites →https://doi.org/10.1034/j.1399-3054.1998.1020219.xopenalex-snapshot

Stress tolerance in the marsh plant Spartina patens: Impact of NaCl on growth and root plasma membrane lipid composition

inferredcites →https://doi.org/10.1034/j.1600-0854.2003.00086.xopenalex-snapshot

Modulation of Membrane Curvature by Phosphatidic Acid and Lysophosphatidic Acid

inferredcites →https://doi.org/10.1038/ncb1401openalex-snapshot

The phox homology domain of phospholipase D activates dynamin GTPase activity and accelerates EGFR endocytosis

inferredcites →https://doi.org/10.1038/nmeth.1488openalex-snapshot

Spontaneous network activity visualized by ultrasensitive Ca2+ indicators, yellow Cameleon-Nano

inferredcites →https://doi.org/10.1038/nnano.2017.98openalex-snapshot

Nanoscale manipulation of membrane curvature for probing endocytosis in live cells

inferredcites →https://doi.org/10.1038/nplants.2016.34openalex-snapshot

Arabidopsis callose synthases CalS1/8 regulate plasmodesmal permeability during stress

inferredcites →https://doi.org/10.1046/j.1365-313x.1997.12051067.xopenalex-snapshot

Calcium signalling in Arabidopsis thaliana responding to drought and salinity

inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00265.xopenalex-snapshot

Plants have a sensitive perception system for the most conserved domain of bacterial flagellin

inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01060.xopenalex-snapshot

Involvement of a novel Arabidopsis phospholipase D, AtPLDδ, in dehydration‐inducible accumulation of phosphatidic acid in stress signalling

inferredcites →https://doi.org/10.1046/j.1471-4159.2003.02189.xopenalex-snapshot

Phospholipase D2 modulates agonist‐induced µ‐opioid receptor desensitization and resensitization

inferredcites →https://doi.org/10.1073/pnas.0607656103openalex-snapshot

Surface comparison of active and inactive protein kinases identifies a conserved activation mechanism

inferredcites →https://doi.org/10.1073/pnas.1319955111openalex-snapshot

Salt stress-induced Ca 2+ waves are associated with rapid, long-distance root-to-shoot signaling in plants

inferredcites →https://doi.org/10.1074/jbc.272.11.7048openalex-snapshot

Identification and Characterization of a Novel Plant Phospholipase D That Requires Polyphosphoinositides and Submicromolar Calcium for Activity in Arabidopsis

inferredcites →https://doi.org/10.1074/jbc.272.11.7055openalex-snapshot

Molecular Cloning and Functional Analysis of Polyphosphoinositide-dependent Phospholipase D, PLDβ, from Arabidopsis

inferredcites →https://doi.org/10.1074/jbc.272.45.28267openalex-snapshot

Molecular Heterogeneity of Phospholipase D (PLD)

inferredcites →https://doi.org/10.1074/jbc.m405771200openalex-snapshot

Sphingosine Kinase 1 Is an Intracellular Effector of Phosphatidic Acid

inferredcites →https://doi.org/10.1093/jxb/err280openalex-snapshot

NADPH oxidase AtrbohD and AtrbohF function in ROS-dependent regulation of Na+/K+ homeostasis in Arabidopsis under salt stress

inferredcites →https://doi.org/10.1093/jxb/erv143openalex-snapshot

Cysteine-rich receptor-like kinase CRK5 as a regulator of growth, development, and ultraviolet radiation responses in Arabidopsis thaliana

inferredcites →https://doi.org/10.1093/jxb/erx225openalex-snapshot

Shaping intercellular channels of plasmodesmata: the structure-to-function missing link

inferredcites →https://doi.org/10.1093/jxb/ery171openalex-snapshot

Exposure to heavy metal stress triggers changes in plasmodesmatal permeability via deposition and breakdown of callose

inferredcites →https://doi.org/10.1093/mp/sst072openalex-snapshot

Inositol Polyphosphate Phosphatidylinositol 5-Phosphatase9 (At5PTase9) Controls Plant Salt Tolerance by Regulating Endocytosis

inferredcites →https://doi.org/10.1093/nar/gkm812openalex-snapshot

PhosPhAt: a database of phosphorylation sites in Arabidopsis thaliana and a plant-specific phosphorylation site predictor

inferredcites →https://doi.org/10.1093/nar/gkp810openalex-snapshot

PhosPhAt: the Arabidopsis thaliana phosphorylation site database. An update

inferredcites →https://doi.org/10.1093/nar/gks1081openalex-snapshot

PhosPhAt goes kinases—searchable protein kinase target information in the plant phosphorylation site database PhosPhAt

inferredcites →https://doi.org/10.1093/pcp/pcg095openalex-snapshot

The Effects of the Phospholipase D-Antagonist 1-Butanol on Seedling Development and Microtubule Organisation in Arabidopsis

inferredcites →https://doi.org/10.1093/pcp/pcn173openalex-snapshot

Multiple PLDs Required for High Salinity and Water Deficit Tolerance in Plants

inferredcites →https://doi.org/10.1101/gad.366506openalex-snapshot

Ligand-induced endocytosis of the pattern recognition receptor FLS2 in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.010444openalex-snapshot

A Novel Phospholipase D of Arabidopsis That Is Activated by Oleic Acid and Associated with the Plasma Membrane

inferredcites →https://doi.org/10.1104/pp.010928openalex-snapshot

The Arabidopsis Phospholipase D Family. Characterization of a Calcium-Independent and Phosphatidylcholine-Selective PLDζ1 with Distinct Regulatory Domains

inferredcites →https://doi.org/10.1104/pp.103.021964openalex-snapshot

Expansion of the Receptor-Like Kinase/Pelle Gene Family and Receptor-Like Proteins in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.103.025379openalex-snapshot

Induction of Salt and Osmotic Stress Tolerance by Overexpression of an Intracellular Vesicle Trafficking Protein AtRab7 (AtRabG3e)

inferredcites →https://doi.org/10.1104/pp.108.120287openalex-snapshot

Plant Receptors Go Endosomal: A Moving View on Signal Transduction

inferredcites →https://doi.org/10.1104/pp.108.2.451openalex-snapshot

Plant Protein Kinase Families and Signal Transduction

inferredcites →https://doi.org/10.1104/pp.126.2.473openalex-snapshot

A Superfamily of Proteins with Novel Cysteine-Rich Repeats

inferredcites →https://doi.org/10.1104/pp.16.01404openalex-snapshot

A Cysteine-Rich Protein Kinase Associates with a Membrane Immune Complex and the Cysteine Residues Are Required for Cell Death

inferredcites →https://doi.org/10.1105/tpc.016097openalex-snapshot

An Arabidopsis Callose Synthase, GSL5, Is Required for Wound and Papillary Callose Formation

inferredcites →https://doi.org/10.1105/tpc.107.056390openalex-snapshot

Phospholipase Dα3 Is Involved in the Hyperosmotic Response in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.111.087742openalex-snapshot

A Plasmodesmata-Localized Protein Mediates Crosstalk between Cell-to-Cell Communication and Innate Immunity in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.111.091454openalex-snapshot

Single-Molecule Analysis of PIP2;1 Dynamics and Partitioning Reveals Multiple Modes of Arabidopsis Plasma Membrane Aquaporin Regulation

inferredcites →https://doi.org/10.1105/tpc.112.104182openalex-snapshot

Phosphatidic Acid Regulates Microtubule Organization by Interacting with MAP65-1 in Response to Salt Stress in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.113.122358openalex-snapshot

Clathrin and Membrane Microdomains Cooperatively Regulate RbohD Dynamics and Activity in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.15.00154openalex-snapshot

Salt-Induced Remodeling of Spatially Restricted Clathrin-Independent Endocytic Pathways in Arabidopsis Root

inferredcites →https://doi.org/10.1105/tpc.16.00947openalex-snapshot

Bound by Fate: The Role of Reactive Oxygen Species in Receptor-Like Kinase Signaling

inferredcites →https://doi.org/10.1111/j.1365-3040.2008.01817.xopenalex-snapshot

NaCl‐induced changes in cytosolic free Ca2+ in Arabidopsis thaliana are heterogeneous and modified by external ionic composition

inferredcites →https://doi.org/10.1111/j.1365-3040.2009.02087.xopenalex-snapshot

Phospholipase D and phosphatidic acid signalling in plant response to drought and salinity

inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03134.xopenalex-snapshot

Induction of phosphatidylinositol 3‐kinase‐mediated endocytosis by salt stress leads to intracellular production of reactive oxygen species and salt tolerance

inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04841.xopenalex-snapshot

Fluorescence recovery after photobleaching reveals high cycling dynamics of plasma membrane aquaporins in Arabidopsis roots under salt stress

inferredcites →https://doi.org/10.1111/j.1365-313x.2012.04901.xopenalex-snapshot

Abiotic stress‐inducible receptor‐like kinases negatively control ABA signaling in Arabidopsis

inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03422.xopenalex-snapshot

Phosphatidic acid mediates salt stress response by regulation of MPK6 in Arabidopsis thaliana

inferredcites →https://doi.org/10.1111/nph.14754openalex-snapshot

Control of basal jasmonate signalling and defence through modulation of intracellular cation flux capacity

inferredcites →https://doi.org/10.1111/nph.14920openalex-snapshot

Elucidating the molecular mechanisms mediating plant salt‐stress responses

inferredcites →https://doi.org/10.1111/tra.12119openalex-snapshot

Building a Better Dynasore: The Dyngo Compounds Potently Inhibit Dynamin and Endocytosis

inferredcites →https://doi.org/10.1128/mcb.21.2.595-602.2001openalex-snapshot

Role for Phospholipase D in Receptor-Mediated Endocytosis

inferredcites →https://doi.org/10.1186/1471-2229-10-95openalex-snapshot

Transcriptional regulation of the CRK/DUF26 group of Receptor-like protein kinases by ozone and plant hormones in Arabidopsis

inferredcites →https://doi.org/10.1371/journal.pgen.1005373openalex-snapshot

Large-Scale Phenomics Identifies Primary and Fine-Tuning Roles for CRKs in Responses Related to Oxidative Stress

inferredcites →https://doi.org/10.1371/journal.pone.0054533openalex-snapshot

EHD1 Functions in Endosomal Recycling and Confers Salt Tolerance

inferredcites →https://doi.org/10.1529/biophysj.106.092015openalex-snapshot

Phosphatidic Acid Domains in Membranes: Effect of Divalent Counterions

inferredcites →https://doi.org/10.3389/fpls.2014.00771openalex-snapshot

Cell wall remodeling under abiotic stress

inferredcites →https://doi.org/10.3390/horticulturae3020030openalex-snapshot

Soil Salinity: Effect on Vegetable Crop Growth. Management Practices to Prevent and Mitigate Soil Salinization

inferredcites →https://doi.org/10.7554/elife.18515openalex-snapshot

Phospholipase D activity couples plasma membrane endocytosis with retromer dependent recycling

What points at this work

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

inferred← citeshttps://doi.org/10.1073/pnas.1907799117openalex-snapshot

Chitin perception in plasmodesmata characterizes submembrane immune-signaling specificity in plants

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