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The circadian clock contributes to the long-term water use efficiency of Arabidopsis

https://doi.org/10.1101/583526
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What this work says

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

inferredcites →https://doi.org/10.1002/pld3.35openalex-snapshot
Natural variation of life‐history traits, water use, and drought responses in Arabidopsis
inferredcites →https://doi.org/10.1007/s00425-003-1106-4openalex-snapshot
Response regulator homologues have complementary, light-dependent functions in the Arabidopsis circadian clock
inferredcites →https://doi.org/10.1007/s10529-014-1553-yopenalex-snapshot
Chimeric promoter mediates guard cell-specific gene expression in tobacco under water deficit
inferredcites →https://doi.org/10.1007/s11103-008-9407-4openalex-snapshot
Interactions between circadian and hormonal signalling in plants
inferredcites →https://doi.org/10.1016/j.cj.2015.04.002openalex-snapshot
From leaf to whole-plant water use efficiency (WUE) in complex canopies: Limitations of leaf WUE as a selection target
inferredcites →https://doi.org/10.1016/j.cub.2004.12.067openalex-snapshot
Overlapping and Distinct Roles of PRR7 and PRR9 in the Arabidopsis Circadian Clock
inferredcites →https://doi.org/10.1016/j.cub.2005.05.048openalex-snapshot
A Guard-Cell-Specific MYB Transcription Factor Regulates Stomatal Movements and Plant Drought Tolerance
inferredcites →https://doi.org/10.1016/j.cub.2010.12.013openalex-snapshot
Temporal Repression of Core Circadian Genes Is Mediated through EARLY FLOWERING 3 in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2011.06.025openalex-snapshot
FLOWERING LOCUS T Regulates Stomatal Opening
inferredcites →https://doi.org/10.1016/j.cub.2012.11.022openalex-snapshot
The Stomatal Response to Reduced Relative Humidity Requires Guard Cell-Autonomous ABA Synthesis
inferredcites →https://doi.org/10.1016/j.cub.2016.01.019openalex-snapshot
The Breakdown of Stored Triacylglycerols Is Required during Light-Induced Stomatal Opening
inferredcites →https://doi.org/10.1016/j.cub.2018.05.092openalex-snapshot
Circadian Entrainment in Arabidopsis by the Sugar-Responsive Transcription Factor bZIP63
inferredcites →https://doi.org/10.1016/j.cub.2018.07.027openalex-snapshot
Photosynthesis and circadian rhythms regulate the buoyancy of marimo lake balls
inferredcites →https://doi.org/10.1016/j.envexpbot.2013.09.003openalex-snapshot
Variability of water use efficiency in grapevines
inferredcites →https://doi.org/10.1016/j.fcr.2009.03.009openalex-snapshot
Effective use of water (EUW) and not water-use efficiency (WUE) is the target of crop yield improvement under drought stress
inferredcites →https://doi.org/10.1016/j.plantsci.2016.06.016openalex-snapshot
Modelling water use efficiency in a dynamic environment: An example using Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.tig.2016.08.002openalex-snapshot
Into the Evening: Complex Interactions in the Arabidopsis Circadian Clock
inferredcites →https://doi.org/10.1016/j.tplants.2013.11.007openalex-snapshot
Wheels within wheels: the plant circadian system
inferredcites →https://doi.org/10.1016/s0092-8674(00)80841-7openalex-snapshot
ZEITLUPE Encodes a Novel Clock-Associated PAS Protein from Arabidopsis
inferredcites →https://doi.org/10.1016/s0092-8674(00)81464-6openalex-snapshot
Constitutive Expression of the CIRCADIAN CLOCK ASSOCIATED 1 (CCA1) Gene Disrupts Circadian Rhythms and Suppresses Its Own Expression
inferredcites →https://doi.org/10.1016/s0092-8674(00)81465-8openalex-snapshot
The late elongated hypocotyl Mutation of Arabidopsis Disrupts Circadian Rhythms and the Photoperiodic Control of Flowering
inferredcites →https://doi.org/10.1016/s0092-8674(01)00460-3openalex-snapshot
An mRNA Cap Binding Protein, ABH1, Modulates Early Abscisic Acid Signal Transduction in Arabidopsis
inferredcites →https://doi.org/10.1016/s1534-5807(02)00200-9openalex-snapshot
tej Defines a Role for Poly(ADP-Ribosyl)ation in Establishing Period Length of the Arabidopsis Circadian Oscillator
inferredcites →https://doi.org/10.1023/a:1006496308160openalex-snapshot
pGreen: a versatile and flexible binary Ti vector for Agrobacterium-mediated plant transformation
inferredcites →https://doi.org/10.1038/emboj.2009.297openalex-snapshot
TOC1 functions as a molecular switch connecting the circadian clock with plant responses to drought
inferredcites →https://doi.org/10.1038/hdy.2010.103openalex-snapshot
The quantitative-genetic and QTL architecture of trait integration and modularity in Brassica rapa across simulated seasonal settings
inferredcites →https://doi.org/10.1038/nature00954openalex-snapshot
The ELF4 gene controls circadian rhythms and flowering time in Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/nature00996openalex-snapshot
Molecular basis of seasonal time measurement in Arabidopsis
inferredcites →https://doi.org/10.1038/nature01843openalex-snapshot
The role of stomata in sensing and driving environmental change
inferredcites →https://doi.org/10.1038/nature02090openalex-snapshot
FKF1 is essential for photoperiodic-specific light signalling in Arabidopsis
inferredcites →https://doi.org/10.1038/nature02163openalex-snapshot
Targeted degradation of TOC1 by ZTL modulates circadian function in Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/nature03835openalex-snapshot
The ERECTA gene regulates plant transpiration efficiency in Arabidopsis
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/nature06132openalex-snapshot
ZEITLUPE is a circadian photoreceptor stabilized by GIGANTEA in blue light
inferredcites →https://doi.org/10.1038/nature12603openalex-snapshot
Photosynthetic entrainment of the Arabidopsis thaliana circadian clock
inferredcites →https://doi.org/10.1038/nature13919openalex-snapshot
Tissue-specific clocks in Arabidopsis show asymmetric coupling
inferredcites →https://doi.org/10.1038/nplants.2015.163openalex-snapshot
Decentralized circadian clocks process thermal and photoperiodic cues in specific tissues
inferredcites →https://doi.org/10.1038/nplants.2017.87openalex-snapshot
The evening complex coordinates environmental and endogenous signals in Arabidopsis
inferredcites →https://doi.org/10.1038/s41467-019-08398-5openalex-snapshot
Continuous dynamic adjustment of the plant circadian oscillator
inferredcites →https://doi.org/10.1046/j.0028-646x.2001.00338.xopenalex-snapshot
Stomatal development and CO2: ecological consequences
inferredcites →https://doi.org/10.1071/pp9920411openalex-snapshot
Early-Flowering Mutants of Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.0503029102openalex-snapshot
LUX ARRHYTHMO encodes a Myb domain protein essential for circadian rhythms
inferredcites →https://doi.org/10.1073/pnas.0707294104openalex-snapshot
Improvement of water use efficiency in rice by expression of HARDY , an Arabidopsis drought and salt tolerance gene
inferredcites →https://doi.org/10.1073/pnas.0914299107openalex-snapshot
Circadian control of carbohydrate availability for growth in Arabidopsis plants at night
inferredcites →https://doi.org/10.1073/pnas.1600826113openalex-snapshot
Reduced nighttime transpiration is a relevant breeding target for high water-use efficiency in grapevine
inferredcites →https://doi.org/10.1074/jbc.m109.030247openalex-snapshot
The Arabidopsis ATP-binding Cassette Protein AtMRP5/AtABCC5 Is a High Affinity Inositol Hexakisphosphate Transporter Involved in Guard Cell Signaling and Phytate Storage
inferredcites →https://doi.org/10.1080/00031305.1980.10483031openalex-snapshot
Population Marginal Means in the Linear Model: An Alternative to Least Squares Means
inferredcites →https://doi.org/10.1080/07352680903173175openalex-snapshot
Regulation of Transpiration to Improve Crop Water Use
inferredcites →https://doi.org/10.1080/15592324.2018.1457913openalex-snapshot
Involvement of the SnRK1 subunit KIN10 in sucrose-induced hypocotyl elongation
inferredcites →https://doi.org/10.1093/emboj/18.17.4679openalex-snapshot
GIGANTEA: a circadian clock‐controlled gene that regulates photoperiodic flowering in Arabidopsis and encodes a protein with several possible membrane‐spanning domains
inferredcites →https://doi.org/10.1093/jxb/erh034openalex-snapshot
Input signals to the plant circadian clock
inferredcites →https://doi.org/10.1093/jxb/erh277openalex-snapshot
Breeding for high water-use efficiency
inferredcites →https://doi.org/10.1093/jxb/ert180openalex-snapshot
The Arabidopsis thaliana MYB60 promoter provides a tool for the spatio-temporal control of gene expression in stomatal guard cells
inferredcites →https://doi.org/10.1093/mp/sss004openalex-snapshot
Quantitative Variation in Water-Use Efficiency across Water Regimes and Its Relationship with Circadian, Vegetative, Reproductive, and Leaf Gas-Exchange Traits
inferredcites →https://doi.org/10.1093/pcp/pcg148openalex-snapshot
Comparative Genetic Studies on the APRR5 and APRR7 Genes Belonging to the APRR1/TOC1 Quintet Implicated in Circadian Rhythm, Control of Flowering Time, and Early Photomorphogenesis
inferredcites →https://doi.org/10.1093/pcp/pch065openalex-snapshot
Characterization of Circadian-Associated APRR3 Pseudo-Response Regulator Belonging to the APRR1/TOC1 Quintet in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcm067openalex-snapshot
Genetic Linkages of the Circadian Clock-Associated Genes, TOC1, CCA1 and LHY, in the Photoperiodic Control of Flowering Time in Arabidopsis thaliana
inferredcites →https://doi.org/10.1098/rsif.2013.0326openalex-snapshot
Impact of plant shoot architecture on leaf cooling: a coupled heat and mass transfer model
inferredcites →https://doi.org/10.1104/pp.103.030007openalex-snapshot
EARLY FLOWERING 4Functions in Phytochrome B-Regulated Seedling De-Etiolation
inferredcites →https://doi.org/10.1104/pp.111.180422openalex-snapshot
Growth Arrest by Trehalose-6-Phosphate: An Astonishing Case of Primary Metabolite Control over Growth by Way of the SnRK1 Signaling Pathway
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.114.237107openalex-snapshot
Stomatal Size, Speed, and Responsiveness Impact on Photosynthesis and Water Use Efficiency
inferredcites →https://doi.org/10.1104/pp.114.253369openalex-snapshot
OPEN ALL NIGHT LONG: The Dark Side of Stomatal Control
inferredcites →https://doi.org/10.1104/pp.17.01214openalex-snapshot
CIRCADIAN CLOCK ASSOCIATED1 (CCA1) and the Circadian Control of Stomatal Aperture
inferredcites →https://doi.org/10.1104/pp.17.01395openalex-snapshot
The Energy-Signaling Hub SnRK1 Is Important for Sucrose-Induced Hypocotyl Elongation
inferredcites →https://doi.org/10.1104/pp.17.01461openalex-snapshot
STOREKEEPER RELATED1/G-Element Binding Protein (STKR1) Interacts with Protein Kinase SnRK1
inferredcites →https://doi.org/10.1104/pp.90.4.1329openalex-snapshot
Circadian Stomatal Rhythms in Epidermal Peels from Vicia faba
inferredcites →https://doi.org/10.1104/pp.96.3.831openalex-snapshot
Circadian Rhythms in Photosynthesis
inferredcites →https://doi.org/10.1105/tpc.010332openalex-snapshot
A Role for LKP2 in the Circadian Clock of Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.013730openalex-snapshot
TheTIME FOR COFFEEGene Maintains the Amplitude and Timing of Arabidopsis Circadian Clocks[W]
inferredcites →https://doi.org/10.1105/tpc.104.029504openalex-snapshot
PSEUDO-RESPONSE REGULATOR 7 and 9 Are Partially Redundant Genes Essential for the Temperature Responsiveness of the Arabidopsis Circadian Clock
inferredcites →https://doi.org/10.1105/tpc.106.047241openalex-snapshot
TIME FOR COFFEE Encodes a Nuclear Regulator in the Arabidopsis thaliana Circadian Clock
inferredcites →https://doi.org/10.1105/tpc.109.072843openalex-snapshot
F-Box Proteins FKF1 and LKP2 Act in Concert with ZEITLUPE to Control Arabidopsis Clock Progression
inferredcites →https://doi.org/10.1105/tpc.109.072892openalex-snapshot
PSEUDO-RESPONSE REGULATORS 9, 7, and 5 Are Transcriptional Repressors in the Arabidopsis Circadian Clock
inferredcites →https://doi.org/10.1105/tpc.110.078691openalex-snapshot
The Arabidopsis GTL1 Transcription Factor Regulates Water Use Efficiency and Drought Tolerance by Modulating Stomatal Density via Transrepression of SDD1
inferredcites →https://doi.org/10.1105/tpc.111.093807openalex-snapshot
EARLY FLOWERING4 Recruitment of EARLY FLOWERING3 in the Nucleus Sustains the Arabidopsis Circadian Clock
inferredcites →https://doi.org/10.1105/tpc.13.6.1305openalex-snapshot
ELF3 Modulates Resetting of the Circadian Clock in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02531.xopenalex-snapshot
ELF4 is a phytochrome‐regulated component of a negative‐feedback loop involving the central oscillator components CCA1 and LHY
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02933.xopenalex-snapshot
Time of day modulates low‐temperature Ca2+ signals in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03371.xopenalex-snapshot
Gene trap lines identify Arabidopsis genes expressed in stomatal guard cells
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03591.xopenalex-snapshot
The small glycine‐rich RNA binding protein AtGRP7 promotes floral transition in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04302.xopenalex-snapshot
AtALMT12 represents an R-type anion channel required for stomatal movement in Arabidopsis guard cells
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04312.xopenalex-snapshot
AtTPS1-mediated trehalose 6-phosphate synthesis is essential for embryogenic and vegetative growth and responsiveness to ABA in germinating seeds and stomatal guard cells
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04362.xopenalex-snapshot
Cell wall composition contributes to the control of transpiration efficiency in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2012.05073.xopenalex-snapshot
Aberrant temporal growth pattern and morphology of root and shoot caused by a defective circadian clock in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1438-8677.2008.00072.xopenalex-snapshot
The plant WNK gene family and regulation of flowering time in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1469-8137.2004.01005.xopenalex-snapshot
Independent circadian regulation of assimilation and stomatal conductance in the ztl‐1 mutant of Arabidopsis
inferredcites →https://doi.org/10.1111/j.2041-210x.2012.00261.xopenalex-snapshot
A general and simple method for obtaining R 2 from generalized linear mixed‐effects models
inferredcites →https://doi.org/10.1111/jipb.12547openalex-snapshot
Circadian clock component, LHY, tells a plant when to respond photosynthetically to light in nature
inferredcites →https://doi.org/10.1111/nph.12489openalex-snapshot
The circadian clock has transient plasticity of period and is required for timing of nocturnal processes in A rabidopsis
inferredcites →https://doi.org/10.1111/nph.13347openalex-snapshot
Increasing water‐use efficiency directly through genetic manipulation of stomatal density
inferredcites →https://doi.org/10.1111/nph.15162openalex-snapshot
Circadian rhythms are associated with shoot architecture in natural settings
inferredcites →https://doi.org/10.1111/nph.15344openalex-snapshot
Rice with reduced stomatal density conserves water and has improved drought tolerance under future climate conditions
inferredcites →https://doi.org/10.1111/pce.12903openalex-snapshot
The metabolic sensor AKIN10 modulates the Arabidopsis circadian clock in a light‐dependent manner
inferredcites →https://doi.org/10.1111/tpj.12947openalex-snapshot
Phototropins maintain robust circadian oscillation of PSII operating efficiency under blue light
inferredcites →https://doi.org/10.1126/science.1082971openalex-snapshot
Enhanced Fitness Conferred by Naturally Occurring Variation in the Circadian Clock
inferredcites →https://doi.org/10.1126/science.1086391openalex-snapshot
Genome-Wide Insertional Mutagenesis of Arabidopsis thaliana
inferredcites →https://doi.org/10.1126/science.1110586openalex-snapshot
FKF1 F-Box Protein Mediates Cyclic Degradation of a Repressor of CONSTANS in Arabidopsis
inferredcites →https://doi.org/10.1126/science.1115581openalex-snapshot
Plant Circadian Clocks Increase Photosynthesis, Growth, Survival, and Competitive Advantage
inferredcites →https://doi.org/10.1126/science.1167206openalex-snapshot
A Functional Genomics Approach Reveals CHE as a Component of the Arabidopsis Circadian Clock
inferredcites →https://doi.org/10.1126/science.1230397openalex-snapshot
Circadian Control of Chloroplast Transcription by a Nuclear-Encoded Timing Signal
inferredcites →https://doi.org/10.1126/science.1230406openalex-snapshot
Regulation of Flowering by Trehalose-6-Phosphate Signaling in Arabidopsis thaliana
inferredcites →https://doi.org/10.1126/science.274.5288.790openalex-snapshot
Conditional Circadian Dysfunction of the Arabidopsis early-flowering 3 Mutant
inferredcites →https://doi.org/10.1126/science.282.5387.287openalex-snapshot
Role of Farnesyltransferase in ABA Regulation of Guard Cell Anion Channels and Plant Water Loss
inferredcites →https://doi.org/10.1126/science.282.5393.1488openalex-snapshot
Phytochromes and Cryptochromes in the Entrainment of the Arabidopsis Circadian Clock
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/10.1126/science.290.5499.2110openalex-snapshot
Orchestrated Transcription of Key Pathways in Arabidopsis by the Circadian Clock
inferredcites →https://doi.org/10.1126/science.42.1074.161openalex-snapshot
The Proceedings of the National Academy of Sciences
inferredcites →https://doi.org/10.1126/science.7855595openalex-snapshot
Circadian Clock Mutants in Arabidopsis Identified by Luciferase Imaging
inferredcites →https://doi.org/10.1146/annurev-arplant-050213-040000openalex-snapshot
Genetic Engineering and Breeding of Drought-Resistant Crops
inferredcites →https://doi.org/10.1146/annurev.arplant.52.1.627openalex-snapshot
G UARD C ELL S IGNAL T RANSDUCTION
inferredcites →https://doi.org/10.1186/1471-2229-11-162openalex-snapshot
DOF-binding sites additively contribute to guard cell-specificity of AtMYB60 promoter
inferredcites →https://doi.org/10.1186/1746-4811-4-6openalex-snapshot
Isolation of a strong Arabidopsis guard cell promoter and its potential as a research tool
inferredcites →https://doi.org/10.1186/s13742-016-0149-yopenalex-snapshot
Circadian rhythms have significant effects on leaf-to-canopy scale gas exchange under field conditions
inferredcites →https://doi.org/10.1242/dev.125.3.485openalex-snapshot
The short-period mutant, toc1-1, alters circadian clock regulation of multiple outputs throughout development in Arabidopsis thaliana
inferredcites →https://doi.org/10.1271/bbb.66.2429openalex-snapshot
Compilation and Characterization of a Novel WNK Family of Protein Kinases inArabiodpsis thalianawith Reference to Circadian Rhythms
inferredcites →https://doi.org/10.1371/journal.pgen.1001350openalex-snapshot
REVEILLE8 and PSEUDO-REPONSE REGULATOR5 Form a Negative Feedback Loop within the Arabidopsis Circadian Clock
inferredcites →https://doi.org/10.1371/journal.pone.0096462openalex-snapshot
Strengths and Limitations of Period Estimation Methods for Circadian Data
inferredcites →https://doi.org/10.1534/genetics.107.072769openalex-snapshot
A Complex Genetic Interaction BetweenArabidopsis thalianaTOC1 and CCA1/LHY in Driving the Circadian Clock and in Output Regulation
inferredcites →https://doi.org/10.1626/jcs.65.652openalex-snapshot
Contributions of Capacity for Soil Water Extraction and Water Use Efficiency to Maintenance of Dry matter Production in Rice subjected to Drought.
inferredcites →https://doi.org/10.2307/2445286openalex-snapshot
Variance for Water-Use Efficiency Among Ecotypes and Recombinant Inbred Lines of Arabidopsis thaliana (Brassicaceae)
inferredcites →https://doi.org/10.3389/fpls.2019.00225openalex-snapshot
Impact of Stomatal Density and Morphology on Water-Use Efficiency in a Changing World
inferredcites →https://doi.org/10.3390/horticulturae3020031openalex-snapshot
Improving Plant Water Use Efficiency through Molecular Genetics
inferredcites →https://doi.org/10.3923/ajpp.2010.241.256openalex-snapshot
Drought Tolerance in Crop Plants
inferredcites →https://doi.org/10.3929/ethz-b-000105397openalex-snapshot
Fitting Linear Mixed-Effects Models Using lme4
inferredcites →https://doi.org/10.4161/psb.3.9.5820openalex-snapshot
Gene trap-based identification of a guard cell promoter in Arabidopsis
inferredcites →https://doi.org/10.4161/psb.5.4.10792openalex-snapshot
Up-regulation of biosynthetic processes associated with growth by trehalose 6-phosphate

What points at this work

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

inferred← citeshttps://doi.org/10.1093/jxb/erad274openalex-snapshot
Inhibition of RNA degradation integrates the metabolic signals induced by osmotic stress into the Arabidopsis circadian system
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