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Plastid Osmotic Stress influences cell differentiation at the Plant Shoot Apex

https://doi.org/10.1101/039115
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Antioxidant protection during ageing and senescence in chloroplasts of tobacco with modulated life span
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Methods for Determination of Proline in Plants
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The shooty callus induced by suppression of tobacco CHRK1 receptor-like kinase is a phenocopy of the tobacco genetic tumor
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Zeatin accumulation and misexpression of a class I knox gene are intimately linked in the epiphyllous response of the interspecific hybrid EMB-2 (Helianthus annuus × H. tuberosus)
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Interactions between abscisic acid and cytokinins during water stress and subsequent rehydration
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Modulation of intracellular proline levels affects flowering time and inflorescence architecture in Arabidopsis
inferredcites →https://doi.org/10.1007/s11103-009-9546-2openalex-snapshot
Developmental consequences of the tumorous shoot development1 mutation, a novel allele of the cellulose-synthesizing KORRIGAN1 gene
inferredcites →https://doi.org/10.1007/s11103-013-0023-6openalex-snapshot
dhm1, an Arabidopsis mutant with increased sensitivity to alkamides shows tumorous shoot development and enhanced lateral root formation
inferredcites →https://doi.org/10.1007/s11103-013-0102-8openalex-snapshot
The roles of two transcription factors, ABI4 and CBFA, in ABA and plastid signalling and stress responses
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A liquid chromatography–tandem mass spectrometry-based assay for indole-3-acetic acid–amido synthetase
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Retrograde Signaling by the Plastidial Metabolite MEcPP Regulates Expression of Nuclear Stress-Response Genes
inferredcites →https://doi.org/10.1016/j.cub.2005.11.044openalex-snapshot
MscS-like Proteins Control Plastid Size and Shape in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.cub.2011.02.020openalex-snapshot
The AP2/ERF Transcription Factor WIND1 Controls Cell Dedifferentiation in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2011.04.004openalex-snapshot
Heme Synthesis by Plastid Ferrochelatase I Regulates Nuclear Gene Expression in Plants
inferredcites →https://doi.org/10.1016/j.cub.2012.01.027openalex-snapshot
Mechanosensitive Channels Protect Plastids from Hypoosmotic Stress During Normal Plant Growth
inferredcites →https://doi.org/10.1016/j.cub.2012.07.028openalex-snapshot
Organelle Signaling: How Stressed Chloroplasts Communicate with the Nucleus
inferredcites →https://doi.org/10.1016/j.devcel.2011.11.011openalex-snapshot
Exit from Proliferation during Leaf Development in Arabidopsis thaliana: A Not-So-Gradual Process
inferredcites →https://doi.org/10.1016/j.devcel.2014.01.013openalex-snapshot
A Regulatory Framework for Shoot Stem Cell Control Integrating Metabolic, Transcriptional, and Phytohormone Signals
inferredcites →https://doi.org/10.1016/j.ejcb.2009.11.016openalex-snapshot
Role of A-type ARABIDOPSIS RESPONSE REGULATORS in meristem maintenance and regeneration
inferredcites →https://doi.org/10.1016/j.jplph.2010.05.013openalex-snapshot
Comparison of hormonal responses to heat, drought and combined stress in tobacco plants with elevated proline content
inferredcites →https://doi.org/10.1016/j.pbi.2008.06.002openalex-snapshot
Retrograde signaling and plant stress: plastid signals initiate cellular stress responses
inferredcites →https://doi.org/10.1016/j.pbi.2014.11.002openalex-snapshot
O Cell, Where Art Thou? The mechanisms of shoot meristem patterning
inferredcites →https://doi.org/10.1016/j.tcb.2010.12.004openalex-snapshot
Regeneration in plants and animals: dedifferentiation, transdifferentiation, or just differentiation?
inferredcites →https://doi.org/10.1016/j.tplants.2008.08.008openalex-snapshot
Plastid signalling to the nucleus and beyond
inferredcites →https://doi.org/10.1016/j.tplants.2009.11.009openalex-snapshot
Proline: a multifunctional amino acid
inferredcites →https://doi.org/10.1016/j.ydbio.2009.11.029openalex-snapshot
Twenty years on: The inner workings of the shoot apical meristem, a developmental dynamo
inferredcites →https://doi.org/10.1016/s0092-8674(00)80700-xopenalex-snapshot
The Stem Cell Population of Arabidopsis Shoot Meristems Is Maintained by a Regulatory Loop between the CLAVATA and WUSCHEL Genes
inferredcites →https://doi.org/10.1038/379066a0openalex-snapshot
A member of the KNOTTED class of homeodomain proteins encoded by the STM gene of Arabidopsis
inferredcites →https://doi.org/10.1038/nature04270openalex-snapshot
WUSCHEL controls meristem function by direct regulation of cytokinin-inducible response regulators
inferredcites →https://doi.org/10.1038/nature09126openalex-snapshot
Hormonal control of the shoot stem-cell niche
inferredcites →https://doi.org/10.1038/ncomms1486openalex-snapshot
A chloroplast envelope-bound PHD transcription factor mediates chloroplast signals to the nucleus
inferredcites →https://doi.org/10.1046/j.1365-313x.1996.10060967.xopenalex-snapshot
The SHOOT MERISTEMLESS gene is required for maintenance of undifferentiated cells in Arabidopsis shoot and floral meristems and acts at a different regulatory level than the meristem genes WUSCHEL and ZWILLE
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00124.xopenalex-snapshot
dCAPS, a simple technique for the genetic analysis of single nucleotide polymorphisms: experimental applications in Arabidopsis thaliana genetics
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01197.xopenalex-snapshot
TUMOROUS SHOOT DEVELOPMENT (TSD) genes are required for co‐ordinated plant shoot development
inferredcites →https://doi.org/10.1073/pnas.0402887101openalex-snapshot
In planta functions of the Arabidopsis cytokinin receptor family
inferredcites →https://doi.org/10.1073/pnas.0803054105openalex-snapshot
Tetrapyrrole profiling in Arabidopsis seedlings reveals that retrograde plastid nuclear signaling is not due to Mg-protoporphyrin IX accumulation
inferredcites →https://doi.org/10.1073/pnas.0908122106openalex-snapshot
Multiple feedback loops through cytokinin signaling control stem cell number within the Arabidopsis shoot meristem
inferredcites →https://doi.org/10.1073/pnas.0913918107openalex-snapshot
Putative Arabidopsis Transcriptional Adaptor Protein (PROPORZ1) is required to modulate histone acetylation in response to auxin
inferredcites →https://doi.org/10.1073/pnas.1115982109openalex-snapshot
Carotenoid oxidation products are stress signals that mediate gene responses to singlet oxygen in plants
inferredcites →https://doi.org/10.1073/pnas.1200636109openalex-snapshot
Cytokinin signaling as a positional cue for patterning the apical–basal axis of the growing Arabidopsis shoot meristem
inferredcites →https://doi.org/10.1073/pnas.1320457111openalex-snapshot
Arabidopsis JAGGED links floral organ patterning to tissue growth by repressing Kip-related cell cycle inhibitors
inferredcites →https://doi.org/10.1073/pnas.98.4.2053openalex-snapshot
Arabidopsis genomes uncoupled 5 ( GUN5 ) mutant reveals the involvement of Mg-chelatase H subunit in plastid-to-nucleus signal transduction
inferredcites →https://doi.org/10.1093/emboj/18.7.1730openalex-snapshot
Protection of Escherichia coli cells against extreme turgor by activation of MscS and MscL mechanosensitive channels: identification of genes required for MscS activity
inferredcites →https://doi.org/10.1093/jxb/erl116openalex-snapshot
Effect of partial rootzone drying on the concentration of zeatin-type cytokinins in tomato (Solanum lycopersicum L.) xylem sap and leaves
inferredcites →https://doi.org/10.1093/jxb/erq186openalex-snapshot
The Arabidopsis plastid-signalling mutant gun1 (genomes uncoupled1) shows altered sensitivity to sucrose and abscisic acid and alterations in early seedling development
inferredcites →https://doi.org/10.1093/jxb/ers184openalex-snapshot
The Arabidopsis organelle-localized glycyl-tRNA synthetase encoded by EMBRYO DEFECTIVE DEVELOPMENT1 is required for organ patterning
inferredcites →https://doi.org/10.1093/jxb/erv132openalex-snapshot
Regulation of chloroplast development and function by cytokinin
inferredcites →https://doi.org/10.1093/mp/ssr106openalex-snapshot
Coordination of Plastid and Light Signaling Pathways upon Development of Arabidopsis Leaves under Various Photoperiods
inferredcites →https://doi.org/10.1093/mp/sst133openalex-snapshot
Plastid Signals and the Bundle Sheath: Mesophyll Development in Reticulate Mutants
inferredcites →https://doi.org/10.1093/pcp/pce015openalex-snapshot
Novel Family of Sensor Histidine Kinase Genes in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pce127openalex-snapshot
The Arabidopsis AHK4 Histidine Kinase is a Cytokinin-Binding Receptor that Transduces Cytokinin Signals Across the Membrane
inferredcites →https://doi.org/10.1093/pcp/pcq147openalex-snapshot
Versatile Roles of Plastids in Plant Growth and Development
inferredcites →https://doi.org/10.1098/rstb.2013.0232openalex-snapshot
Influence of plastids on light signalling and development
inferredcites →https://doi.org/10.1104/pp.102.019026openalex-snapshot
Hormonal Control of Cell Proliferation Requires PASTICCINO Genes
inferredcites →https://doi.org/10.1104/pp.106.082040openalex-snapshot
Production and Scavenging of Reactive Oxygen Species in Chloroplasts and Their Functions
inferredcites →https://doi.org/10.1104/pp.112.211763openalex-snapshot
A Robust and Sensitive Synthetic Sensor to Monitor the Transcriptional Output of the Cytokinin Signaling Network in Planta
inferredcites →https://doi.org/10.1104/pp.113.224667openalex-snapshot
A Novel Protective Function for Cytokinin in the Light Stress Response Is Mediated by the ARABIDOPSIS HISTIDINE KINASE2 and ARABIDOPSIS HISTIDINE KINASE3 Receptors
inferredcites →https://doi.org/10.1104/pp.114.1.161openalex-snapshot
Biochemical Characterization of the aba2 and aba3 Mutants in Arabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.114.236620openalex-snapshot
Plastid Osmotic Stress Activates Cellular Stress Responses in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.118.2.637openalex-snapshot
Superoxide Dismutase in Arabidopsis: An Eclectic Enzyme Family with Disparate Regulation and Protein Localization
inferredcites →https://doi.org/10.1104/pp.122.3.721openalex-snapshot
Hormone Autotrophic Growth and Differentiation Identifies Mutant Lines of Arabidopsis with Altered Cytokinin and Auxin Content or Signaling
inferredcites →https://doi.org/10.1104/pp.15.01464openalex-snapshot
The Arabidopsis thaliana Class III Peroxidase AtPRX71 Negatively Regulates Growth under Physiological Conditions and in Response to Cell Wall Damage.
inferredcites →https://doi.org/10.1105/tpc.018978openalex-snapshot
Type-A Arabidopsis Response Regulators Are Partially Redundant Negative Regulators of Cytokinin Signaling[W]
inferredcites →https://doi.org/10.1105/tpc.10.6.1043openalex-snapshot
The Arabidopsis Abscisic Acid Response Locus ABI4 Encodes an APETALA2 Domain Protein
inferredcites →https://doi.org/10.1105/tpc.106.041673openalex-snapshot
Posttranscriptional Induction of Two Cu/Zn Superoxide Dismutase Genes in Arabidopsis Is Mediated by Downregulation of miR398 and Important for Oxidative Stress Tolerance
inferredcites →https://doi.org/10.1105/tpc.107.052662openalex-snapshot
Cytokinin Regulates Type-A Arabidopsis Response Regulator Activity and Protein Stability via Two-Component Phosphorelay
inferredcites →https://doi.org/10.1105/tpc.108.061341openalex-snapshot
A Heterocomplex of Iron Superoxide Dismutases Defends Chloroplast Nucleoids against Oxidative Stress and Is Essential for Chloroplast Development inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.111.084160openalex-snapshot
Pause-and-Stop: The Effects of Osmotic Stress on Cell Proliferation during Early Leaf Development in Arabidopsis and a Role for Ethylene Signaling in Cell Cycle Arrest
inferredcites →https://doi.org/10.1105/tpc.111.087395openalex-snapshot
Analysis of Cytokinin Mutants and Regulation of Cytokinin Metabolic Genes Reveals Important Regulatory Roles of Cytokinins in Drought, Salt and Abscisic Acid Responses, and Abscisic Acid Biosynthesis
inferredcites →https://doi.org/10.1105/tpc.111.088112openalex-snapshot
Two Mechanosensitive Channel Homologs Influence Division Ring Placement in Arabidopsis Chloroplasts
inferredcites →https://doi.org/10.1105/tpc.111.090894openalex-snapshot
JUNGBRUNNEN1 , a Reactive Oxygen Species–Responsive NAC Transcription Factor, Regulates Longevity in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.111.091033openalex-snapshot
Evidence for a SAL1-PAP Chloroplast Retrograde Pathway That Functions in Drought and High Light Signaling in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.111.094458openalex-snapshot
Gain and Loss of Photosynthetic Membranes during Plastid Differentiation in the Shoot Apex of Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.116053openalex-snapshot
Plant Callus: Mechanisms of Induction and Repression
inferredcites →https://doi.org/10.1105/tpc.114.133595openalex-snapshot
The Yin-Yang of Hormones: Cytokinin and Auxin Interactions in Plant Development
inferredcites →https://doi.org/10.1111/j.1365-3040.2010.02188.xopenalex-snapshot
Mechanisms independent of abscisic acid (ABA) or proline feedback have a predominant role in transcriptional regulation of proline metabolism during low water potential and stress recovery
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03318.xopenalex-snapshot
Duplicated P5CS genes of Arabidopsis play distinct roles in stress regulation and developmental control of proline biosynthesis
inferredcites →https://doi.org/10.1111/j.1399-3054.2009.01331.xopenalex-snapshot
The role of reactive oxygen species in signalling from chloroplasts to the nucleus
inferredcites →https://doi.org/10.1111/tpj.12198openalex-snapshot
The A rabidopsis homeobox gene SHOOT MERISTEMLESS has cellular and meristem‐organisational roles with differential requirements for cytokinin and CYCD3 activity
inferredcites →https://doi.org/10.1111/tpj.12455openalex-snapshot
MAIN ‐ LIKE 1 is a crucial factor for correct cell division and differentiation in A rabidopsis thaliana
inferredcites →https://doi.org/10.1111/tpj.13211openalex-snapshot
Repression of callus initiation by the mi RNA ‐directed interaction of auxin–cytokinin in Arabidopsis thaliana
inferredcites →https://doi.org/10.1126/science.1103178openalex-snapshot
The Genetic Basis of Singlet OxygenInduced Stress Responses of Arabidopsis thaliana
inferredcites →https://doi.org/10.1126/science.1140516openalex-snapshot
Signals from chloroplasts converge to regulate nuclear gene expression.
inferredcites →https://doi.org/10.1126/science.283.5409.1911openalex-snapshot
Signaling of Cell Fate Decisions by CLAVATA3 in Arabidopsis Shoot Meristems
inferredcites →https://doi.org/10.1126/science.aac6014openalex-snapshot
Mechanosensitive channel MSL8 regulates osmotic forces during pollen hydration and germination
inferredcites →https://doi.org/10.1146/annurev-arplant-042811-105555openalex-snapshot
Plant Stem Cell Niches
inferredcites →https://doi.org/10.1146/annurev-arplant-043015-111854openalex-snapshot
Learning the Languages of the Chloroplast: Retrograde Signaling and Beyond
inferredcites →https://doi.org/10.1146/annurev.arplant.51.1.111openalex-snapshot
N ONPHOTOSYNTHETIC M ETABOLISM IN P LASTIDS
inferredcites →https://doi.org/10.1146/annurev.arplant.55.031903.141701openalex-snapshot
REACTIVE OXYGEN SPECIES: Metabolism, Oxidative Stress, and Signal Transduction
inferredcites →https://doi.org/10.1186/s13104-015-1010-6openalex-snapshot
Gateway-compatible tissue-specific vectors for plant transformation
inferredcites →https://doi.org/10.1199/tab.0140openalex-snapshot
Proline Metabolism and Its Implications for Plant-Environment Interaction
inferredcites →https://doi.org/10.1242/dev.117614openalex-snapshot
The never-ending story: from pluripotency to plant developmental plasticity
inferredcites →https://doi.org/10.1242/dev.125.5.909openalex-snapshot
The PASTICCINO genes of Arabidopsis thaliana are involved in the control of cell division and differentiation
inferredcites →https://doi.org/10.1242/dev.127.3.595openalex-snapshot
Molecular analysis of SCARECROW function reveals a radial patterning mechanism common to root and shoot
inferredcites →https://doi.org/10.1371/journal.pgen.1003655openalex-snapshot
Pattern Dynamics in Adaxial-Abaxial Specific Gene Expression Are Modulated by a Plastid Retrograde Signal during Arabidopsis thaliana Leaf Development
inferredcites →https://doi.org/10.1371/journal.pone.0040336openalex-snapshot
Functional Analysis of Conserved Motifs in the Mechanosensitive Channel Homolog MscS-Like2 from Arabidopsis thaliana
inferredcites →https://doi.org/10.3389/fpls.2012.00304openalex-snapshot
ABI4 and its role in chloroplast retrograde communication
inferredcites →https://doi.org/10.3389/fpls.2014.00219openalex-snapshot
Post-embryonic organogenesis and plant regeneration from tissues: two sides of the same coin?
inferredcites →https://doi.org/10.3389/fpls.2015.01028openalex-snapshot
Involvement of Plant Stem Cells or Stem Cell-Like Cells in Dedifferentiation
inferredcites →https://doi.org/10.3389/fpls.2015.01148openalex-snapshot
RNA Sequencing Analysis of the msl2msl3, crl, and ggps1 Mutants Indicates that Diverse Sources of Plastid Dysfunction Do Not Alter Leaf Morphology Through a Common Signaling Pathway

What points at this work

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

inferred← citeshttps://doi.org/10.1002/pld3.124openalex-snapshot
Genetic and physical interactions between the organellar mechanosensitive ion channel homologs MSL 1, MSL 2, and MSL 3 reveal a role for inter‐organellar communication in plant development
inferred← citeshttps://doi.org/10.1016/j.pbi.2017.07.002openalex-snapshot
Plant mechanosensitive ion channels: an ocean of possibilities
inferred← citeshttps://doi.org/10.1016/j.sajb.2024.07.029openalex-snapshot
Integrative analysis of transcriptome and phytohormones reveals new genes network involved in shoot apical meristem development in maize under blue and red light
inferred← citeshttps://doi.org/10.1093/jxb/erad044openalex-snapshot
Plastids: diving into their diversity, their functions, and their role in plant development
inferred← citeshttps://doi.org/10.1093/plcell/koab230openalex-snapshot
Plant cell mechanobiology: Greater than the sum of its parts
inferred← citeshttps://doi.org/10.1126/scisignal.abf0322openalex-snapshot
Plasmodesmata-localized proteins and ROS orchestrate light-induced rapid systemic signaling in Arabidopsis
inferred← citeshttps://doi.org/10.3390/antiox8120641openalex-snapshot
Assessment of Subcellular ROS and NO Metabolism in Higher Plants: Multifunctional Signaling Molecules
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