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CATION EXCHANGER1 Cosegregates with Cadmium Tolerance in the Metal Hyperaccumulator Arabidopsis halleri and Plays a Role in Limiting Oxidative Stress in Arabidopsis Spp.

https://doi.org/10.1104/pp.15.01037

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What this work says

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

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Reactive oxygen species produced by NADPH oxidase are involved in pollen tube growth

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The role of Ca pathway in Cd uptake and translocation by the hyperaccumulator Sedum alfredii

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Expression of an Arabidopsis Ca2+/H+ antiporter CAX1 variant in petunia enhances cadmium tolerance and accumulation

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Evolution of metal hyperaccumulation required cis-regulatory changes and triplication of HMA4

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5′ end cDNA amplification using classic RACE

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3′ End cDNA amplification using classic RACE

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Heavy metal toxicity: cadmium permeates through calcium channels and disturbs the plant water status

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Zinc tolerance and accumulation in metallicolous and nonmetallicolous populations of Arabidopsis halleri (Brassicaceae)

inferredcites →https://doi.org/10.1046/j.1469-8137.2002.00432.xopenalex-snapshot

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Variation in HMA4 gene copy number and expression among Noccaea caerulescens populations presenting different levels of Cd tolerance and accumulation

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Zinc tolerance and hyperaccumulation are genetically independent characters

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Gene duplication as a mechanism of genomic adaptation to a changing environment

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Functional Association of Arabidopsis CAX1 and CAX3 Is Required for Normal Growth and Ion Homeostasis

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Zinc-Dependent Global Transcriptional Control, Transcriptional Deregulation, and Higher Gene Copy Number for Genes in Metal Homeostasis of the Hyperaccumulator Arabidopsis halleri

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A Major Quantitative Trait Locus for Cadmium Tolerance in Arabidopsis halleri Colocalizes with HMA4, a Gene Encoding a Heavy Metal ATPase

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Expression of Arabidopsis CAX2 in Tobacco. Altered Metal Accumulation and Increased Manganese Tolerance

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Reactive oxygen species produced by NADPH oxidase are involved in pollen tube growth

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inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02748.xopenalex-snapshot

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inferredcites →https://doi.org/10.1111/j.1469-8137.2009.02831.xopenalex-snapshot

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Gene duplication and evolutionary novelty in plants

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Quantitative trait loci analysis of mineral element concentrations in an Arabidopsis halleri × Arabidopsis lyrata petraea F2 progeny grown on cadmium‐contaminated soil

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Protein lysine methylation is involved in modulating the response of sensitive and tolerant Arabidopsis species to cadmium stress

inferred← citeshttps://doi.org/10.1101/859249openalex-snapshot

Constitutively enhanced genome integrity maintenance and direct stress mitigation characterize transcriptome of extreme stress-adapted Arabidopsis halleri

inferred← citeshttps://doi.org/10.1104/pp.16.01348openalex-snapshot

Calcium Deficiency Triggers Phloem Remobilization of Cadmium in a Hyperaccumulating Species

inferred← citeshttps://doi.org/10.1104/pp.17.00212openalex-snapshot

Photosynthetic Efficiency as Bioindicator of Environmental Pressure in A. halleri

inferred← citeshttps://doi.org/10.1111/mec.14800openalex-snapshot

Evolutionary dynamics of quantitative variation in an adaptive trait at the regional scale: The case of zinc hyperaccumulation in Arabidopsis halleri

inferred← citeshttps://doi.org/10.1111/nph.14093openalex-snapshot

Potential preadaptation to anthropogenic pollution: evidence from a common quantitative trait locus for zinc and cadmium tolerance in metallicolous and nonmetallicolous accessions of Arabidopsis halleri

inferred← citeshttps://doi.org/10.1111/nph.14948openalex-snapshot

Contrasting cadmium resistance strategies in two metallicolous populations of Arabidopsis halleri

inferred← citeshttps://doi.org/10.1111/nph.14949openalex-snapshot

Adaptation to high zinc depends on distinct mechanisms in metallicolous populations of Arabidopsis halleri

inferred← citeshttps://doi.org/10.1111/nph.19168openalex-snapshot

Intronic microRNA‐directed regulation of mitochondrial reactive oxygen species enhances plant stress tolerance in Arabidopsis

inferred← citeshttps://doi.org/10.1111/pce.12711openalex-snapshot

NADPH oxidases differentially regulate ROS metabolism and nutrient uptake under cadmium toxicity

inferred← citeshttps://doi.org/10.1111/pce.13362openalex-snapshot

CAX1 suppresses Cd‐induced generation of reactive oxygen species in Arabidopsis halleri

inferred← citeshttps://doi.org/10.1111/pce.13592openalex-snapshot

The Arabidopsis defensin gene AtPDF2.5 mediates cadmium tolerance and accumulation

inferred← citeshttps://doi.org/10.1111/pce.13692openalex-snapshot

Protein lysine methylation contributes to modulating the response of sensitive and tolerant Arabidopsis species to cadmium stress

inferred← citeshttps://doi.org/10.1111/pce.13806openalex-snapshot

The two copies of the zinc and cadmium ZIP6 transporter ofArabidopsis hallerihave distinct effects on cadmium tolerance

inferred← citeshttps://doi.org/10.1111/pce.14756openalex-snapshot

Sequential removal of cation/H + exchangers reveals their additive role in elemental distribution, calcium depletion and anoxia tolerance

inferred← citeshttps://doi.org/10.1111/pce.14862openalex-snapshot

Reduced expression of bZIP19 and bZIP23 increases zinc and cadmium accumulation in Arabidopsis halleri

inferred← citeshttps://doi.org/10.1111/plb.12460openalex-snapshot

CAX ‐ing a wide net: Cation/H+ transporters in metal remediation and abiotic stress signalling

inferred← citeshttps://doi.org/10.1111/plb.13698openalex-snapshot

CAX control: multiple roles of vacuolar cation/H + exchangers in metal tolerance, mineral nutrition and environmental signalling

inferred← citeshttps://doi.org/10.1111/ppl.13488openalex-snapshot

Comparative analysis identifies micro‐RNA associated with nutrient homeostasis, development and stress response in Arabidopsis thaliana upon high Zn and metal hyperaccumulator Arabidopsis halleri

inferred← citeshttps://doi.org/10.1111/tpj.14610openalex-snapshot

Intertwined metal homeostasis, oxidative and biotic stress responses in the Arabidopsis frd3 mutant

inferred← citeshttps://doi.org/10.1111/tpj.15544openalex-snapshot

Constitutively enhanced genome integrity maintenance and direct stress mitigation characterize transcriptome of extreme stress‐adapted Arabidopsis halleri

inferred← citeshttps://doi.org/10.1111/tpj.15740openalex-snapshot

Altered metal distribution in the sr45‐1 Arabidopsis mutant causes developmental defects

inferred← citeshttps://doi.org/10.1111/tpj.16966openalex-snapshot

A dominant‐negative Arabidopsis cation exchanger 1 ( CAX1 ): N‐terminal autoinhibition and membrane topology

inferred← citeshttps://doi.org/10.1186/s12870-021-02866-1openalex-snapshot

Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters

inferred← citeshttps://doi.org/10.15252/embr.202153698openalex-snapshot

Long‐distance mobile mRNA CAX3 modulates iron uptake and zinc compartmentalization

inferred← citeshttps://doi.org/10.15407/frg2022.04.279openalex-snapshot

Cadmium stress in plants: toxicity and resistance mechanisms

inferred← citeshttps://doi.org/10.2139/ssrn.6878958openalex-snapshot

Removal of the Self-inhibitory Domain of AtCAX3 Enhances As(III) Tolerance by Modulating Ca2+ Homeostasis and Antioxidant Defense in Arabidopsis

inferred← citeshttps://doi.org/10.30848/pjb2020-5(15)openalex-snapshot

Cadmium decreased superoxide anion derived from NADPH oxidase through overload of calcium in wheat seedling

inferred← citeshttps://doi.org/10.3389/fpls.2016.00470openalex-snapshot

Hydrogen Peroxide, Signaling in Disguise during Metal Phytotoxicity

inferred← citeshttps://doi.org/10.3389/fpls.2016.01296openalex-snapshot

Calcium-Mediated Abiotic Stress Signaling in Roots

inferred← citeshttps://doi.org/10.3389/fpls.2016.01975openalex-snapshot

Paxillus involutus-Facilitated Cd2+ Influx through Plasma Membrane Ca2+-Permeable Channels Is Stimulated by H2O2 and H+-ATPase in Ectomycorrhizal Populus × canescens under Cadmium Stress

inferred← citeshttps://doi.org/10.3389/fpls.2017.01115openalex-snapshot

Transcriptomic Response of Purple Willow (Salix purpurea) to Arsenic Stress

inferred← citeshttps://doi.org/10.3389/fpls.2019.00201openalex-snapshot

Expression of the Tobacco Non-symbiotic Class 1 Hemoglobin Gene Hb1 Reduces Cadmium Levels by Modulating Cd Transporter Expression Through Decreasing Nitric Oxide and ROS Level in Arabidopsis

inferred← citeshttps://doi.org/10.3389/fpls.2019.00748openalex-snapshot

Toxic Effects of Cd and Zn on the Photosynthetic Apparatus of the Arabidopsis halleri and Arabidopsis arenosa Pseudo-Metallophytes

inferred← citeshttps://doi.org/10.3389/fpls.2020.00186openalex-snapshot

Chloroplast Calcium Signaling in the Spotlight

inferred← citeshttps://doi.org/10.3389/fpls.2021.752246openalex-snapshot

TypiCal but DeliCate Ca++re: Dissecting the Essence of Calcium Signaling Network as a Robust Response Coordinator of Versatile Abiotic and Biotic Stimuli in Plants

inferred← citeshttps://doi.org/10.3389/fpls.2022.843274openalex-snapshot

Editorial: Recent Insights Into the Double Role of Hydrogen Peroxide in Plants

inferred← citeshttps://doi.org/10.3389/fpls.2022.964059openalex-snapshot

Calcium channels and transporters: Roles in response to biotic and abiotic stresses

inferred← citeshttps://doi.org/10.3389/fpls.2025.1506461openalex-snapshot

Evolutionary dynamics of the calcium/cation antiporter superfamily in Brassicaceae: codon usage, selection pressure, and BnCaCAs role in abiotic stress response

inferred← citeshttps://doi.org/10.3390/agronomy13071793openalex-snapshot

A Systematic Review on the Improvement of Cd Stress Tolerance in Ramie Crop, Limitations and Future Prospective

inferred← citeshttps://doi.org/10.3390/biology9070177openalex-snapshot

Phytoremediation of Cadmium: Physiological, Biochemical, and Molecular Mechanisms

inferred← citeshttps://doi.org/10.3390/f14102028openalex-snapshot

Populus trichocarpa PtHSFA4a Enhances Heat Tolerance by Regulating Expression of APX1 and HSPs

inferred← citeshttps://doi.org/10.3390/ijms20071732openalex-snapshot

HvPAA1 Encodes a P-Type ATPase, a Novel Gene for Cadmium Accumulation and Tolerance in Barley (Hordeum vulgare L.)

inferred← citeshttps://doi.org/10.3390/ijms20133117openalex-snapshot

Dual Role of Metallic Trace Elements in Stress Biology—From Negative to Beneficial Impact on Plants

inferred← citeshttps://doi.org/10.3390/ijms22158186openalex-snapshot

The Rice Cation/H+ Exchanger Family Involved in Cd Tolerance and Transport

inferred← citeshttps://doi.org/10.3390/ijms241411587openalex-snapshot

Inhibition Roles of Calcium in Cadmium Uptake and Translocation in Rice: A Review

inferred← citeshttps://doi.org/10.3390/jof10020134openalex-snapshot

Combined Proteomic and Metabolomic Analyses Reveal the Comprehensive Regulation of Stropharia rugosoannulata Mycelia Exposed to Cadmium Stress

inferred← citeshttps://doi.org/10.3390/plants10071342openalex-snapshot

The Different Faces of Arabidopsis arenosa—A Plant Species for a Special Purpose

inferred← citeshttps://doi.org/10.3390/plants11091146openalex-snapshot

Novel QTL for Low Seed Cadmium Accumulation in Soybean

inferred← citeshttps://doi.org/10.3390/plants14121736openalex-snapshot

Selenium Alleviates Cadmium Toxicity by Regulating Carbon Metabolism, AsA-GSH Cycle, and Cadmium Transport in Glycyrrhiza uralensis Fisch. Seedlings

inferred← citeshttps://doi.org/10.3390/plants15193042openalex-snapshot

Molecular Mechanism of AtCAX3-Induced BPA Tolerance in Plants

inferred← citeshttps://doi.org/10.3390/plants9020223openalex-snapshot

Reducing Cadmium Accumulation in Plants: Structure–Function Relations and Tissue-Specific Operation of Transporters in the Spotlight

inferred← citeshttps://doi.org/10.3390/su151612158openalex-snapshot

Cadmium Accumulation in Plants: Insights from Phylogenetic Variation into the Evolution and Functions of Membrane Transporters

inferred← citeshttps://doi.org/10.35550/vbio2018.03.010openalex-snapshot

Plants and heavy metals: perception and signaling

inferred← citeshttps://doi.org/10.5599/jese.2729openalex-snapshot

Ion-imprinted polyaniline-based polymer for selective electrochemical detection of cadmium

inferred← citeshttps://doi.org/10.6084/m9.figshare.13787524openalex-snapshot

Additional file 10 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters

inferred← citeshttps://doi.org/10.6084/m9.figshare.13787530openalex-snapshot

Additional file 11 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters

inferred← citeshttps://doi.org/10.6084/m9.figshare.13787533openalex-snapshot

Additional file 12 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters

inferred← citeshttps://doi.org/10.6084/m9.figshare.13787539openalex-snapshot

Additional file 13 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters

inferred← citeshttps://doi.org/10.6084/m9.figshare.13787542openalex-snapshot

Additional file 14 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters

inferred← citeshttps://doi.org/10.6084/m9.figshare.13787548openalex-snapshot

Additional file 15 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters

inferred← citeshttps://doi.org/10.6084/m9.figshare.13787551openalex-snapshot

Additional file 16 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters

inferred← citeshttps://doi.org/10.6084/m9.figshare.13787557openalex-snapshot

Additional file 17 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters

inferred← citeshttps://doi.org/10.6084/m9.figshare.13787560openalex-snapshot

Additional file 18 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters

inferred← citeshttps://doi.org/10.6084/m9.figshare.13787563openalex-snapshot

Additional file 1 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters

inferred← citeshttps://doi.org/10.6084/m9.figshare.13787566openalex-snapshot

Additional file 2 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters

inferred← citeshttps://doi.org/10.6084/m9.figshare.13787572openalex-snapshot

Additional file 3 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters

inferred← citeshttps://doi.org/10.6084/m9.figshare.13787575openalex-snapshot

Additional file 4 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters

inferred← citeshttps://doi.org/10.6084/m9.figshare.13787578openalex-snapshot

Additional file 5 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters

inferred← citeshttps://doi.org/10.6084/m9.figshare.13787581openalex-snapshot

Additional file 6 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters

inferred← citeshttps://doi.org/10.6084/m9.figshare.13787584openalex-snapshot

Additional file 7 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters

inferred← citeshttps://doi.org/10.6084/m9.figshare.13787590openalex-snapshot

Additional file 8 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters

inferred← citeshttps://doi.org/10.6084/m9.figshare.13787593openalex-snapshot

Additional file 9 of Genome-wide analysis of the apple CaCA superfamily reveals that MdCAX proteins are involved in the abiotic stress response as calcium transporters

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.