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Dual-targeted transcription factors are required for optimal photosynthesis and stress responses in Arabidopsis thaliana
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/4735_2007_0232openalex-snapshot
Transcription and transcriptional regulation in plastids
inferredcites →https://doi.org/10.1007/4735_2007_0235openalex-snapshot
Processing, degradation, and polyadenylation of chloroplast transcripts
inferredcites →https://doi.org/10.1007/978-1-4939-1136-3_2openalex-snapshot
Chloroplast Gene Expression—Translation
inferredcites →https://doi.org/10.1016/j.bbabio.2015.02.011openalex-snapshot
The TIC complex uncovered: The alternative view on the molecular mechanism of protein translocation across the inner envelope membrane of chloroplasts
inferredcites →https://doi.org/10.1016/j.bbamcr.2012.06.020openalex-snapshot
Plastid-to-nucleus communication, signals controlling the running of the plant cell
inferredcites →https://doi.org/10.1016/j.celrep.2018.01.054openalex-snapshot
Chloroplast Signaling Gates Thermotolerance in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2004.11.049openalex-snapshot
Mechanisms of Protein Import and Routing in Chloroplasts
inferredcites →https://doi.org/10.1016/j.devcel.2015.05.011openalex-snapshot
Chloroplast Stromules Function during Innate Immunity
inferredcites →https://doi.org/10.1016/j.gene.2006.06.022openalex-snapshot
Eukaryotic transcription factors in plastids — Bioinformatic assessment and implications for the evolution of gene expression machineries in plants
inferredcites →https://doi.org/10.1016/j.jmb.2014.08.016openalex-snapshot
New Insights into the Mechanism of Chloroplast Protein Import and Its Integration with Protein Quality Control, Organelle Biogenesis and Development
inferredcites →https://doi.org/10.1016/j.molp.2015.05.005openalex-snapshot
Regulation of Photosynthesis during Abiotic Stress-Induced Photoinhibition
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/s0304-3940(02)01423-4openalex-snapshot
Assumption-free analysis of quantitative real-time polymerase chain reaction (PCR) data
inferredcites →https://doi.org/10.1016/s0968-4328(01)00011-7openalex-snapshot
Effects of ultraviolet radiation on plant cells
inferredcites →https://doi.org/10.1038/cr.2008.297openalex-snapshot
Towards a comprehensive catalog of chloroplast proteins and their interactions
inferredcites →https://doi.org/10.1038/ncomms11388openalex-snapshot
Arabidopsis PROTEASOME REGULATOR1 is required for auxin-mediated suppression of proteasome activity and regulates auxin signalling
inferredcites →https://doi.org/10.1038/ncomms11654openalex-snapshot
A voltage-dependent chloride channel fine-tunes photosynthesis in plants
inferredcites →https://doi.org/10.1038/nmeth.4197openalex-snapshot
Salmon provides fast and bias-aware quantification of transcript expression
inferredcites →https://doi.org/10.1038/nrm3702openalex-snapshot
Biogenesis and homeostasis of chloroplasts and other plastids
inferredcites →https://doi.org/10.1038/s41467-017-00074-wopenalex-snapshot
Photosynthesis-dependent H2O2 transfer from chloroplasts to nuclei provides a high-light signalling mechanism
inferredcites →https://doi.org/10.1038/s41467-019-10760-6openalex-snapshot
Oxidative post-translational modification of EXECUTER1 is required for singlet oxygen sensing in plastids
inferredcites →https://doi.org/10.1038/s41477-019-0415-yopenalex-snapshot
Control of retrograde signalling by protein import and cytosolic folding stress
inferredcites →https://doi.org/10.1038/scientificamerican0762-109openalex-snapshot
Single-Stranded DNA
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01076.xopenalex-snapshot
Knock‐out of the plastid ribosomal protein L11 in Arabidopsis: effects on mRNA translation and photosynthesis
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01340.xopenalex-snapshot
Searching limiting steps in the expression of chloroplast‐encoded proteins: relations between gene copy number, transcription, transcript abundance and translation rate in the chloroplast of Chlamydomonas reinhardtii
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01476.xopenalex-snapshot
Thylakoid membrane‐bound ascorbate peroxidase is a limiting factor of antioxidative systems under photo‐oxidative stress
inferredcites →https://doi.org/10.1073/pnas.0702061104openalex-snapshot
EXECUTER1- and EXECUTER2-dependent transfer of stress-related signals from the plastid to the nucleus of Arabidopsis thaliana
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.1603562113openalex-snapshot
Singlet oxygen- and EXECUTER1-mediated signaling is initiated in grana margins and depends on the protease FtsH2
inferredcites →https://doi.org/10.1073/pnas.1604936113openalex-snapshot
Sensing and signaling of oxidative stress in chloroplasts by inactivation of the SAL1 phosphoadenosine phosphatase
inferredcites →https://doi.org/10.1093/jxb/eri056openalex-snapshot
Is PsbS the site of non-photochemical quenching in photosynthesis?
inferredcites →https://doi.org/10.1093/jxb/err093openalex-snapshot
Accumulation of the transcription factor ABA-insensitive (ABI)4 is tightly regulated post-transcriptionally
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/mp/ssu060openalex-snapshot
Mitogen-Activated Protein Kinase 4 Is a Salicylic Acid-Independent Regulator of Growth But Not of Photosynthesis in Arabidopsis
inferredcites →https://doi.org/10.1093/nar/gki576openalex-snapshot
RNR1, a 3'-5' exoribonuclease belonging to the RNR superfamily, catalyzes 3' maturation of chloroplast ribosomal RNAs in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/nar/gkl635openalex-snapshot
Advancing uracil-excision based cloning towards an ideal technique for cloning PCR fragments
inferredcites →https://doi.org/10.1093/nar/gkn654openalex-snapshot
PPDB, the Plant Proteomics Database at Cornell
inferredcites →https://doi.org/10.1093/nar/gkp805openalex-snapshot
PlnTFDB: updated content and new features of the plant transcription factor database
inferredcites →https://doi.org/10.1093/nar/gkt1016openalex-snapshot
PlantTFDB 3.0: a portal for the functional and evolutionary study of plant transcription factors
inferredcites →https://doi.org/10.1093/pcp/pcs171openalex-snapshot
The Chloroplast Function Database II: A Comprehensive Collection of Homozygous Mutants and Their Phenotypic/Genotypic Traits for Nuclear-Encoded Chloroplast Proteins
inferredcites →https://doi.org/10.1093/pcp/pcs172openalex-snapshot
Diverse Responses to Blue Light via LOV Photoreceptors
inferredcites →https://doi.org/10.1093/pcp/pcv107openalex-snapshot
Rate Constants of PSII Photoinhibition and its Repair, and PSII Fluorescence Parameters in Field Plants in Relation to their Growth Light Environments
inferredcites →https://doi.org/10.1093/pcp/pcw083openalex-snapshot
Contribution of PsbS Function and Stomatal Conductance to Foliar Temperature in Higher Plants
inferredcites →https://doi.org/10.1093/pcp/pcw232openalex-snapshot
Evidence for the Involvement of Electrical, Calcium and ROS Signaling in the Systemic Regulation of Non-Photochemical Quenching and Photosynthesis
inferredcites →https://doi.org/10.1104/pp.011577openalex-snapshot
ARAMEMNON, a Novel Database for Arabidopsis Integral Membrane Proteins
inferredcites →https://doi.org/10.1104/pp.101.3.947openalex-snapshot
Ultraviolet-Induced Photodegradation of Cucumber (Cucumis sativus L.) Microsomal and Soluble Protein Tryptophanyl Residues in Vitro
inferredcites →https://doi.org/10.1104/pp.104.043646openalex-snapshot
LESION SIMULATING DISEASE 1 Is Required for Acclimation to Conditions That Promote Excess Excitation Energy
inferredcites →https://doi.org/10.1104/pp.104.047043openalex-snapshot
Crosslinking of Ribosomal Proteins to RNA in Maize Ribosomes by UV-B and Its Effects on Translation
inferredcites →https://doi.org/10.1104/pp.106.078162openalex-snapshot
Spatial Dependence for Hydrogen Peroxide-Directed Signaling in Light-Stressed Plants
inferredcites →https://doi.org/10.1104/pp.108.122796openalex-snapshot
Single-Stranded DNA-Binding Protein Whirly1 in Barley Leaves Is Located in Plastids and the Nucleus of the Same Cell
inferredcites →https://doi.org/10.1104/pp.109.137240openalex-snapshot
CIA2 Coordinately Up-Regulates Protein Import and Synthesis in Leaf Chloroplasts
inferredcites →https://doi.org/10.1104/pp.110.157057openalex-snapshot
Plant L10 Ribosomal Proteins Have Different Roles during Development and Translation under Ultraviolet-B Stress
inferredcites →https://doi.org/10.1104/pp.112.208116openalex-snapshot
LESION SIMULATING DISEASE1, ENHANCED DISEASE SUSCEPTIBILITY1, and PHYTOALEXIN DEFICIENT4 Conditionally Regulate Cellular Signaling Homeostasis, Photosynthesis, Water Use Efficiency, and Seed Yield in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.113.228338openalex-snapshot
RBF1, a Plant Homolog of the Bacterial Ribosome-Binding Factor RbfA, Acts in Processing of the Chloroplast 16S Ribosomal RNA
inferredcites →https://doi.org/10.1104/pp.114.249052openalex-snapshot
Natural Variation in Sensitivity to a Loss of Chloroplast Translation in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.15.02033openalex-snapshot
GUN1 Controls Accumulation of the Plastid Ribosomal Protein S1 at the Protein Level and Interacts with Proteins Involved in Plastid Protein Homeostasis
inferredcites →https://doi.org/10.1104/pp.16.00434openalex-snapshot
ROS, Calcium, and Electric Signals: Key Mediators of Rapid Systemic Signaling in Plants
inferredcites →https://doi.org/10.1104/pp.16.01930openalex-snapshot
Seedlings Lacking the PTM Protein Do Not Show a genomes uncoupled (gun) Mutant Phenotype
inferredcites →https://doi.org/10.1104/pp.18.00009openalex-snapshot
Control of Retrograde Signaling by Rapid Turnover of GENOMES UNCOUPLED1
inferredcites →https://doi.org/10.1104/pp.18.01047openalex-snapshot
Plastid-to-Nucleus Retrograde Signalling during Chloroplast Biogenesis Does Not Require ABI4
inferredcites →https://doi.org/10.1105/tpc.010148openalex-snapshot
Leaf-Specific Upregulation of Chloroplast Translocon Genes by a CCT Motif–Containing Protein, CIA 2
inferredcites →https://doi.org/10.1105/tpc.105.033191openalex-snapshot
A Conserved Transcription Factor Mediates Nuclear Control of Organelle Biogenesis in Anciently Diverged Land Plants
inferredcites →https://doi.org/10.1105/tpc.105.039073openalex-snapshot
Nuclear Photosynthetic Gene Expression Is Synergistically Modulated by Rates of Protein Synthesis in Chloroplasts and Mitochondria
inferredcites →https://doi.org/10.1105/tpc.108.059618openalex-snapshot
Chloroplast Signaling andLESION SIMULATING DISEASE1Regulate Crosstalk between Light Acclimation and Immunity inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.108.065250openalex-snapshot
GLK Transcription Factors Coordinate Expression of the Photosynthetic Apparatus 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.113.113985openalex-snapshot
A Membrane-Bound NAC Transcription Factor, ANAC017, Mediates Mitochondrial Retrograde Signaling in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.117168openalex-snapshot
The Membrane-Bound NAC Transcription Factor ANAC013 Functions in Mitochondrial Retrograde Regulation of the Oxidative Stress Response in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.13.9.2053openalex-snapshot
Leaf-Specific Upregulation of Chloroplast Translocon Genes by a CCT Motif-Containing Protein, CIA 2
inferredcites →https://doi.org/10.1105/tpc.18.00016openalex-snapshot
Chloroplast Translation: Structural and Functional Organization, Operational Control, and Regulation
inferredcites →https://doi.org/10.1105/tpc.19.00132openalex-snapshot
Leaf Variegation and Impaired Chloroplast Development Caused by a Truncated CCT Domain Gene in albostrians Barley
inferredcites →https://doi.org/10.1105/tpc.9.4.627openalex-snapshot
Photosynthetic electron transport regulates the expression of cytosolic ascorbate peroxidase genes in Arabidopsis during excess light stress.
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03951.xopenalex-snapshot
Unequally redundant RCD1 and SRO1 mediate stress and developmental responses and interact with transcription factors
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04276.xopenalex-snapshot
A DEAD box protein is required for formation of a hidden break in Arabidopsis chloroplast 23S rRNA
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04791.xopenalex-snapshot
The plastid‐specific ribosomal proteins of Arabidopsis thaliana can be divided into non‐essential proteins and genuine ribosomal proteins
inferredcites →https://doi.org/10.1111/j.1438-8677.2012.00718.xopenalex-snapshot
Responses of antioxidant enzymes to cold and high light are not correlated to freezing tolerance in natural accessions of A rabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02452.xopenalex-snapshot
Targeting of nucleus‐encoded proteins to chloroplasts in plants
inferredcites →https://doi.org/10.1111/nph.15488openalex-snapshot
Hydrogen peroxide metabolism and functions in plants
inferredcites →https://doi.org/10.1111/pce.12288openalex-snapshot
LESION SIMULATING DISEASE 1 and ENHANCED DISEASE SUSCEPTIBILITY 1 differentially regulate UV ‐ C ‐induced photooxidative stress signalling and programmed cell death in A rabidopsis thaliana
inferredcites →https://doi.org/10.1111/tpj.12000openalex-snapshot
Versatile roles of Arabidopsis plastid ribosomal proteins in plant growth and development
inferredcites →https://doi.org/10.1126/science.284.5414.654openalex-snapshot
Systemic Signaling and Acclimation in Response to Excess Excitation Energy in Arabidopsis
inferredcites →https://doi.org/10.1126/science.289.5480.768openalex-snapshot
Cloning of the Arabidopsis Clock Gene TOC1 , an Autoregulatory Response Regulator Homolog
inferredcites →https://doi.org/10.1146/annurev-arplant-042916-041007openalex-snapshot
Retrograde Signals: Integrators of Interorganellar Communication and Orchestrators of Plant Development
inferredcites →https://doi.org/10.1146/annurev-arplant-050213-040159openalex-snapshot
Pentatricopeptide Repeat Proteins in Plants
inferredcites →https://doi.org/10.1146/annurev-arplant-050312-120147openalex-snapshot
Intracellular Signaling from Plastid to Nucleus
inferredcites →https://doi.org/10.1146/annurev.arplant.58.032806.103844openalex-snapshot
Sensing and Responding to Excess Light
inferredcites →https://doi.org/10.1186/1472-6750-10-21openalex-snapshot
A mutant Pfu DNA polymerase designed for advanced uracil-excision DNA engineering
inferredcites →https://doi.org/10.1186/1746-4811-10-7openalex-snapshot
Phenotypic analysis of the Arabidopsis heat stress response during germination and early seedling development
inferredcites →https://doi.org/10.1186/1746-4811-5-1openalex-snapshot
Simple allele-discriminating PCR for cost-effective and rapid genotyping and mapping
inferredcites →https://doi.org/10.1186/1746-4811-5-6openalex-snapshot
The FAST technique: a simplified Agrobacterium-based transformation method for transient gene expression analysis in seedlings of Arabidopsis and other plant species
inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
inferredcites →https://doi.org/10.1186/s13059-016-1004-2openalex-snapshot
Chloroplast genomes: diversity, evolution, and applications in genetic engineering
inferredcites →https://doi.org/10.1263/jbb.104.34openalex-snapshot
Development of series of gateway binary vectors, pGWBs, for realizing efficient construction of fusion genes for plant transformation
inferredcites →https://doi.org/10.12688/f1000research.7563.1openalex-snapshot
Differential analyses for RNA-seq: transcript-level estimates improve gene-level inferences
inferredcites →https://doi.org/10.12688/f1000research.7563.2openalex-snapshot
Differential analyses for RNA-seq: transcript-level estimates improve gene-level inferences
inferredcites →https://doi.org/10.1371/journal.pgen.1007555openalex-snapshot
Multilevel effects of light on ribosome dynamics in chloroplasts program genome-wide and psbA-specific changes in translation
inferredcites →https://doi.org/10.1371/journal.pone.0056429openalex-snapshot
Plant Sterol Metabolism. Δ7-Sterol-C5-Desaturase (STE1/DWARF7), Δ5,7-Sterol-Δ7-Reductase (DWARF5) and Δ24-Sterol-Δ24-Reductase (DIMINUTO/DWARF1) Show Multiple Subcellular Localizations in Arabidopsis thaliana (Heynh) L
inferredcites →https://doi.org/10.15252/embj.201695959openalex-snapshot
The complete structure of the chloroplast 70S ribosome in complex with translation factor pY
inferredcites →https://doi.org/10.3389/fpls.2012.00001openalex-snapshot
Protein Phylogenetic Analysis of Ca2+/cation Antiporters and Insights into their Evolution in Plants
inferredcites →https://doi.org/10.3389/fpls.2012.00300openalex-snapshot
Reconsidering the nature and mode of action of metabolite retrograde signals from the chloroplast
inferredcites →https://doi.org/10.3390/ijms130911085openalex-snapshot
Dual Targeting and Retrograde Translocation: Regulators of Plant Nuclear Gene Expression Can Be Sequestered by Plastids
inferredcites →https://doi.org/10.3390/plants8080290openalex-snapshot
Biotechnological Potential of LSD1, EDS1, and PAD4 in the Improvement of Crops and Industrial Plants
inferredcites →https://doi.org/10.7554/elife.39324openalex-snapshot
Consolidation alters motor sequence-specific distributed representations
inferredcites →https://doi.org/10.7554/elife.43284openalex-snapshot
Arabidopsis RCD1 coordinates chloroplast and mitochondrial functions through interaction with ANAC transcription factors
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/s00425-020-03537-5openalex-snapshot
Genome-wide characterization and analysis of the CCT motif family genes in soybean (Glycine max)
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