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Adaptive divergence in transcriptome response to heat and acclimation in Arabidopsis thaliana plants from contrasting climates
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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/bf02712120openalex-snapshot
Heat stress response in plants: a complex game with chaperones and more than twenty heat stress transcription factors
inferredcites →https://doi.org/10.1007/s10725-005-1536-zopenalex-snapshot
Effects of Abscisic Acid, Salicylic Acid, Ethylene and Hydrogen Peroxide in Thermotolerance and Recovery for Creeping Bentgrass
inferredcites →https://doi.org/10.1007/s10811-013-0188-zopenalex-snapshot
RNA-Seq revealed complex response to heat stress on transcriptomic level in Saccharina japonica (Laminariales, Phaeophyta)
inferredcites →https://doi.org/10.1016/j.bbrc.2013.01.104openalex-snapshot
Molecular mechanisms of the plant heat stress response
inferredcites →https://doi.org/10.1016/j.pbi.2007.04.011openalex-snapshot
Complexity of the heat stress response in plants
inferredcites →https://doi.org/10.1016/j.plantsci.2012.06.004openalex-snapshot
Some like it hot, some like it warm: Phenotyping to explore thermotolerance diversity
inferredcites →https://doi.org/10.1016/j.plantsci.2014.05.020openalex-snapshot
Constitutive camalexin production and environmental stress response variation in Arabidopsis populations from the Iberian Peninsula
inferredcites →https://doi.org/10.1016/j.tplants.2004.03.006openalex-snapshot
Role of plant heat-shock proteins and molecular chaperones in the abiotic stress response
inferredcites →https://doi.org/10.1016/j.tplants.2005.11.002openalex-snapshot
Abiotic stress, the field environment and stress combination
inferredcites →https://doi.org/10.1016/j.tplants.2010.08.002openalex-snapshot
Plant molecular stress responses face climate change
inferredcites →https://doi.org/10.1016/s1369-5266(03)00092-xopenalex-snapshot
Regulatory network of gene expression in the drought and cold stress responses
inferredcites →https://doi.org/10.1038/nprot.2012.016openalex-snapshot
Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks
inferredcites →https://doi.org/10.1038/nrg2484openalex-snapshot
RNA-Seq: a revolutionary tool for transcriptomics
inferredcites →https://doi.org/10.1046/j.1365-294x.2003.01833.xopenalex-snapshot
Genetics of drought adaptation in Arabidopsis thaliana: I. Pleiotropy contributes to genetic correlations among ecological traits
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01066.xopenalex-snapshot
Hsp101 is necessary for heat tolerance but dispensable for development and germination in the absence of stress
inferredcites →https://doi.org/10.1074/jbc.m313350200openalex-snapshot
The Zinc Finger Protein Zat12 Is Required for Cytosolic Ascorbate Peroxidase 1 Expression during Oxidative Stress in Arabidopsis
inferredcites →https://doi.org/10.1074/jbc.m611093200openalex-snapshot
The EAR-motif of the Cys2/His2-type Zinc Finger Protein Zat7 Plays a Key Role in the Defense Response of Arabidopsis to Salinity Stress
inferredcites →https://doi.org/10.1074/jbc.m709187200openalex-snapshot
The Transcriptional Co-activator MBF1c Is a Key Regulator of Thermotolerance in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/aobpla/plv101openalex-snapshot
Natural populations ofArabidopsis thalianadiffer in seedling responses to high temperature stress
inferredcites →https://doi.org/10.1093/jxb/erl164openalex-snapshot
Gene networks involved in drought stress response and tolerance
inferredcites →https://doi.org/10.1093/jxb/erq098openalex-snapshot
Regulation and function of SOC1, a flowering pathway integrator
inferredcites →https://doi.org/10.1093/oso/9780198577324.001.0001openalex-snapshot
Evolutionary Genetics and Environmental Stress
inferredcites →https://doi.org/10.1098/rspb.2004.3045openalex-snapshot
Stress-induced variation in evolution: from behavioural plasticity to genetic assimilation
inferredcites →https://doi.org/10.1101/gad.12.24.3788openalex-snapshot
Regulation of the heat shock transcriptional response: cross talk between a family of heat shock factors, molecular chaperones, and negative regulators
inferredcites →https://doi.org/10.1104/pp.006858openalex-snapshot
The Combined Effect of Drought Stress and Heat Shock on Gene Expression in Tobacco
inferredcites →https://doi.org/10.1104/pp.103.033431openalex-snapshot
When Defense Pathways Collide. The Response of Arabidopsis to a Combination of Drought and Heat Stress
inferredcites →https://doi.org/10.1104/pp.105.062257openalex-snapshot
Heat Stress Phenotypes of Arabidopsis Mutants Implicate Multiple Signaling Pathways in the Acquisition of Thermotolerance
inferredcites →https://doi.org/10.1104/pp.107.112060openalex-snapshot
Core Genome Responses Involved in Acclimation to High Temperature
inferredcites →https://doi.org/10.1105/tpc.010011openalex-snapshot
Growth Stage–Based Phenotypic Analysis of Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.107.050641openalex-snapshot
Natural Variation amongArabidopsis thalianaAccessions for Transcriptome Response to Exogenous Salicylic Acid
inferredcites →https://doi.org/10.1105/tpc.11.5.949openalex-snapshot
FLOWERING LOCUS C Encodes a Novel MADS Domain Protein That Acts as a Repressor of Flowering
inferredcites →https://doi.org/10.1105/tpc.13.7.1499openalex-snapshot
Growth Stage-Based Phenotypic Analysis of Arabidopsis: A Model for High Throughput Functional Genomics in Plants
inferredcites →https://doi.org/10.1111/1365-3040.ep11587620openalex-snapshot
An analysis of photosynthetic response and adaptation to temperature in higher plants: temperature acclimation in the desert evergreen Nerium oleander L*
inferredcites →https://doi.org/10.1111/j.0031-9317.2005.00582.xopenalex-snapshot
Reactive oxygen species and temperature stresses: A delicate balance between signaling and destruction
inferredcites →https://doi.org/10.1111/j.1365-294x.2008.03690.xopenalex-snapshot
Heat shock protein 101 effects in A. thaliana : genetic variation, fitness and pleiotropy in controlled temperature conditions
inferredcites →https://doi.org/10.1111/j.1365-294x.2011.05397.xopenalex-snapshot
Thermal adaptation and ecological speciation
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03479.xopenalex-snapshot
Arabidopsis thaliana populations show clinal variation in a climatic gradient associated with altitude
inferredcites →https://doi.org/10.1111/j.1541-4337.2004.tb00057.xopenalex-snapshot
Adaptation of Microorganisms to Cold Temperatures, Weak Acid Preservatives, Low pH, and Osmotic Stress: A Review
inferredcites →https://doi.org/10.1111/j.1558-5646.2012.01689.xopenalex-snapshot
CLINAL VARIATION IN SEED TRAITS INFLUENCING LIFE CYCLE TIMING INARABIDOPSIS THALIANA
inferredcites →https://doi.org/10.1111/mec.12240openalex-snapshot
Thermal adaptation and acclimation of ectotherms from differing aquatic climates
inferredcites →https://doi.org/10.1111/mec.13047openalex-snapshot
RNA ‐seq reveals regional differences in transcriptome response to heat stress in the marine snail C hlorostoma funebralis
inferredcites →https://doi.org/10.1111/nph.12485openalex-snapshot
Adaptation to spring heat and drought in northeastern S panish A rabidopsis thaliana
inferredcites →https://doi.org/10.1126/science.1143153openalex-snapshot
The Evolution of Selfing in Arabidopsis thaliana
inferredcites →https://doi.org/10.1146/annurev.arplant.53.091401.143329openalex-snapshot
S ALT AND D ROUGHT S TRESS S IGNAL T RANSDUCTION IN P LANTS
inferredcites →https://doi.org/10.1146/annurev.pp.31.060180.002423openalex-snapshot
Photosynthetic Response and Adaptation to Temperature in Higher Plants
inferredcites →https://doi.org/10.1152/ajpregu.00306.2010openalex-snapshot
Transcriptional responses to thermal acclimation in the eurythermal fish Gillichthys mirabilis (Cooper 1864)
inferredcites →https://doi.org/10.1152/physiolgenomics.00026.2013openalex-snapshot
RNA-Seq reveals expression signatures of genes involved in oxygen transport, protein synthesis, folding, and degradation in response to heat stress in catfish
inferredcites →https://doi.org/10.1186/1471-2148-12-170openalex-snapshot
Investigating the molecular basis of local adaptation to thermal stress: population differences in gene expression across the transcriptome of the copepod Tigriopus californicus
inferredcites →https://doi.org/10.1186/gb-2009-10-6-r66openalex-snapshot
Global expression analysis of the brown alga Ectocarpus siliculosus (Phaeophyceae) reveals large-scale reprogramming of the transcriptome in response to abiotic stress
inferredcites →https://doi.org/10.1186/s12864-015-1246-5openalex-snapshot
Transcriptomic response to heat stress among ecologically divergent populations of redband trout
inferredcites →https://doi.org/10.1242/jeb.02260openalex-snapshot
Intraspecific variation in thermal tolerance and heat shock protein gene expression in common killifish, Fundulus heteroclitus
inferredcites →https://doi.org/10.1242/jeb.058735openalex-snapshot
Comparative genomics in ecological physiology: toward a more nuanced understanding of acclimation and adaptation
inferredcites →https://doi.org/10.1371/journal.pone.0007213openalex-snapshot
Demographic and Genetic Patterns of Variation among Populations of Arabidopsis thaliana from Contrasting Native Environments
inferredcites →https://doi.org/10.1371/journal.pone.0046244openalex-snapshot
Transcriptomic Responses to Salinity Stress in the Pacific Oyster Crassostrea gigas
inferredcites →https://doi.org/10.1371/journal.pone.0082634openalex-snapshot
RNA-Seq Transcriptome Profiling of Upland Cotton (Gossypium hirsutum L.) Root Tissue under Water-Deficit Stress
inferredcites →https://doi.org/10.1641/0006-3568(2000)050[0217:esaaef]2.3.co;2openalex-snapshot
Environmental Stress as an Evolutionary Force
inferredcites →https://doi.org/10.4161/15592324.2014.992741openalex-snapshot
A geographic cline in leaf salicylic acid with increasing elevation inArabidopsis thaliana
inferredcites →https://doi.org/10.5962/bhl.title.122577openalex-snapshot
Plant-geography upon a physiological basis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Intensive herbicide use has selected for constitutively elevated levels of stress‐responsive mRNAs and proteins in multiple herbicide‐resistant Avena fatua L
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