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Molecular cloning and functional characterization of MdNHX1 reveals its involvement in salt tolerance in apple calli and Arabidopsis

https://doi.org/10.1016/j.scienta.2016.11.031

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What this work says

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

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Molecular and functional analyses of rice NHX-type Na+/H+ antiporter genes

inferredcites →https://doi.org/10.1007/s10529-010-0418-2openalex-snapshot

Enhanced V-ATPase activity contributes to the improved salt tolerance of transgenic tobacco plants overexpressing vacuolar Na+/H+ antiporter AtNHX1

inferredcites →https://doi.org/10.1007/s10725-013-9787-6openalex-snapshot

Apple gene function and gene family database: an integrated bioinformatics database for apple research

inferredcites →https://doi.org/10.1007/s11033-011-0823-1openalex-snapshot

Signal transduction during cold, salt, and drought stresses in plants

inferredcites →https://doi.org/10.1007/s11103-014-0278-6openalex-snapshot

The wheat NHX antiporter gene TaNHX2 confers salt tolerance in transgenic alfalfa by increasing the retention capacity of intracellular potassium

inferredcites →https://doi.org/10.1007/s11240-010-9738-0openalex-snapshot

Overexpression of a Malus vacuolar Na+/H+ antiporter gene (MdNHX1) in apple rootstock M.26 and its influence on salt tolerance

inferredcites →https://doi.org/10.1007/s11248-007-9085-zopenalex-snapshot

Salt tolerance conferred by overexpression of Arabidopsis vacuolar Na+/H+ antiporter gene AtNHX1 in common buckwheat (Fagopyrum esculentum)

inferredcites →https://doi.org/10.1007/s12033-011-9399-1openalex-snapshot

Enhanced Expression of AtNHX1, in Transgenic Groundnut (Arachis hypogaea L.) Improves Salt and Drought Tolerence

inferredcites →https://doi.org/10.1016/j.abb.2008.01.010openalex-snapshot

Calcium- and salt-stress signaling in plants: Shedding light on SOS pathway

inferredcites →https://doi.org/10.1016/j.bbamem.2016.05.008openalex-snapshot

Protein architecture and core residues in unwound α-helices provide insights to the transport function of plant AtCHX17

inferredcites →https://doi.org/10.1016/j.gene.2013.03.104openalex-snapshot

Comparative analysis of cation/proton antiporter superfamily in plants

inferredcites →https://doi.org/10.1016/j.jplph.2004.03.010openalex-snapshot

Molecular characterization of Na+/H+ antiporters (ZmNHX) of maize (Zea mays L.) and their expression under salt stress

inferredcites →https://doi.org/10.1016/j.jplph.2011.07.001openalex-snapshot

MdVHP1 encodes an apple vacuolar H+-PPase and enhances stress tolerance in transgenic apple callus and tomato

inferredcites →https://doi.org/10.1016/j.pbi.2014.08.002openalex-snapshot

The ins and outs of intracellular ion homeostasis: NHX-type cation/H + transporters

inferredcites →https://doi.org/10.1016/j.tplants.2007.09.007openalex-snapshot

Transgenic strategies for the nutritional enhancement of plants

inferredcites →https://doi.org/10.1038/90824openalex-snapshot

Transgenic salt-tolerant tomato plants accumulate salt in foliage but not in fruit

inferredcites →https://doi.org/10.1038/nbt766openalex-snapshot

Overexpression of a plasma membrane Na+/H+ antiporter gene improves salt tolerance in Arabidopsis thaliana

inferredcites →https://doi.org/10.1038/ng.654openalex-snapshot

The genome of the domesticated apple (Malus × domestica Borkh.)

inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01309.xopenalex-snapshot

Differential expression and function of Arabidopsis thaliana NHX Na+/H+ antiporters in the salt stress response

inferredcites →https://doi.org/10.1073/pnas.0504437102openalex-snapshot

Vacuolar Na + /H + antiporter cation selectivity is regulated by calmodulin from within the vacuole in a Ca 2+ - and pH-dependent manner

inferredcites →https://doi.org/10.1073/pnas.0604711103openalex-snapshot

The plasma membrane Na + /H + antiporter SOS1 interacts with RCD1 and functions in oxidative stress tolerance in Arabidopsis

inferredcites →https://doi.org/10.1073/pnas.122224699openalex-snapshot

Regulation of SOS1, a plasma membrane Na + /H + exchanger in Arabidopsis thaliana , by SOS2 and SOS3

inferredcites →https://doi.org/10.1074/jbc.m105043200openalex-snapshot

The Arabidopsis Na+/H+Exchanger AtNHX1 Catalyzes Low Affinity Na+ and K+ Transport in Reconstituted Liposomes

inferredcites →https://doi.org/10.1080/15592324.2016.1184810openalex-snapshot

AtNHX5 and AtNHX6: Roles in protein transport

inferredcites →https://doi.org/10.1093/aob/mcg058openalex-snapshot

Na+ Tolerance and Na+ Transport in Higher Plants

inferredcites →https://doi.org/10.1093/jxb/ers250openalex-snapshot

Cellular ion homeostasis: emerging roles of intracellular NHX Na+/H+ antiporters in plant growth and development

inferredcites →https://doi.org/10.1093/mp/ssn058openalex-snapshot

Overexpression of SOS (Salt Overly Sensitive) Genes Increases Salt Tolerance in Transgenic Arabidopsis

inferredcites →https://doi.org/10.1093/mp/sst017openalex-snapshot

The Salt Overly Sensitive (SOS) Pathway: Established and Emerging Roles

inferredcites →https://doi.org/10.1093/mp/sst091openalex-snapshot

Intracellular NHX-Type Cation/H+ Antiporters in Plants

inferredcites →https://doi.org/10.1093/pcp/pci028openalex-snapshot

Characterization of a Novel Na+/H+ Antiporter Gene InNHX2 and Comparison of InNHX2 with InNHX1, Which is Responsible for Blue Flower Coloration by Increasing the Vacuolar pH in the Japanese Morning Glory

inferredcites →https://doi.org/10.1093/pcp/pcv138openalex-snapshot

Arabidopsis Intracellular NHX-Type Sodium-Proton Antiporters are Required for Seed Storage Protein Processing

inferredcites →https://doi.org/10.1104/pp.15.01333openalex-snapshot

MdMYB1 Regulates Anthocyanin and Malate Accumulation by Directly Facilitating Their Transport into Vacuoles in Apples

inferredcites →https://doi.org/10.1104/pp.77.1.46openalex-snapshot

Proton-Translocating Inorganic Pyrophosphatase in Red Beet (Beta vulgaris L.) Tonoplast Vesicles

inferredcites →https://doi.org/10.1104/pp.78.1.163openalex-snapshot

Na+/H+ Antiport in Isolated Tonoplast Vesicles from Storage Tissue of Beta vulgaris

inferredcites →https://doi.org/10.1105/tpc.010021openalex-snapshot

Molecular Characterization of Functional Domains in the Protein Kinase SOS2 That Is Required for Plant Salt Tolerance

inferredcites →https://doi.org/10.1105/tpc.010371openalex-snapshot

The Putative Plasma Membrane Na + /H + Antiporter SOS1 Controls Long-Distance Na + Transport in Plants

inferredcites →https://doi.org/10.1105/tpc.111.095273openalex-snapshot

Ion Exchangers NHX1 and NHX2 Mediate Active Potassium Uptake into Vacuoles to Regulate Cell Turgor and Stomatal Function in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.13.6.1383openalex-snapshot

Molecular Characterization of Functional Domains in the Protein Kinase SOS2 That Is Required for Plant Salt Tolerance

inferredcites →https://doi.org/10.1111/j.1365-3040.2009.01971.xopenalex-snapshot

The plasma membrane Na+/H+ antiporter SOS1 is essential for salt tolerance in tomato and affects the partitioning of Na+ between plant organs

inferredcites →https://doi.org/10.1111/j.1365-3040.2009.02086.xopenalex-snapshot

Na + transport in glycophytic plants: what we know and would like to know

inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02177.xopenalex-snapshot

Characterization of AtCHX17, a member of the cation/H+ exchangers, CHX family, from Arabidopsis thaliana suggests a role in K+ homeostasis

inferredcites →https://doi.org/10.1111/j.1365-313x.2009.04073.xopenalex-snapshot

The AtNHX1 exchanger mediates potassium compartmentation in vacuoles of transgenic tomato

inferredcites →https://doi.org/10.1111/j.1399-3054.2008.01060.xopenalex-snapshot

The HAL1 function on Na+ homeostasis is maintained over time in salt‐treated transgenic tomato plants, but the high reduction of Na+ in leaf is not associated with salt tolerance

inferredcites →https://doi.org/10.1111/j.1399-3054.2009.01269.xopenalex-snapshot

Molecular characterization of putative vacuolar NHX‐type Na+/H+ exchanger genes from the salt‐resistant tree Populus euphratica

inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02461.xopenalex-snapshot

Overexpression of the tomato K+/H+ antiporter LeNHX2 confers salt tolerance by improving potassium compartmentalization

inferredcites →https://doi.org/10.1111/pce.12109openalex-snapshot

The K+ / H+ antiporter LeNHX2 increases salt tolerance by improving K+ homeostasis in transgenic tomato

inferredcites →https://doi.org/10.1128/mcb.01989-06openalex-snapshot

An Enhancer Mutant of Arabidopsis salt overly sensitive 3 Mediates both Ion Homeostasis and the Oxidative Stress Response

inferredcites →https://doi.org/10.1186/1471-2229-13-97openalex-snapshot

Different evolutionary histories of two cation/proton exchanger gene families in plants

inferredcites →https://doi.org/10.1371/journal.pgen.1006273openalex-snapshot

Glucose Sensor MdHXK1 Phosphorylates and Stabilizes MdbHLH3 to Promote Anthocyanin Biosynthesis in Apple

inferredcites →https://doi.org/10.1371/journal.pone.0078098openalex-snapshot

Functional Characterization of a Wheat NHX Antiporter Gene TaNHX2 That Encodes a K+/H+ Exchanger

inferredcites →https://doi.org/10.3389/fpls.2012.00025openalex-snapshot

Conserved and Diversified Gene Families of Monovalent Cation/H+ Antiporters from Algae to Flowering Plants

inferredcites →https://doi.org/10.3389/fpls.2013.00410openalex-snapshot

Sodium transport system in plant cells

inferredcites →https://doi.org/10.3390/plants3030409openalex-snapshot

Vacuolar Na+/H+ NHX-Type Antiporters Are Required for Cellular K+ Homeostasis, Microtubule Organization and Directional Root Growth

What points at this work

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

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inferred← citeshttps://doi.org/10.1002/clen.201600574openalex-snapshot

Metabolic Profiling to Elucidate Genetic Elements Due to Salt Stress

inferred← citeshttps://doi.org/10.1007/s00344-020-10264-4openalex-snapshot

Na+ Efflux from Apple Dwarfing Rootstocks is Associated with High-Salt Resistance of Their Scions

inferred← citeshttps://doi.org/10.1007/s00425-020-03366-6openalex-snapshot

Engineering salinity tolerance in plants: progress and prospects

inferred← citeshttps://doi.org/10.1007/s13562-021-00741-6openalex-snapshot

Adaptation of plants to salt stress: the role of the ion transporters

inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.04.021openalex-snapshot

Overexpression of PbrNHX2 gene, a Na+/H+ antiporter gene isolated from Pyrus betulaefolia, confers enhanced tolerance to salt stress via modulating ROS levels

inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.04.022openalex-snapshot

Comparative transcriptome analysis of NaCl and KCl stress response in Malus hupehensis Rehd. Provide insight into the regulation involved in Na+ and K+ homeostasis

inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108507openalex-snapshot

Stress salinity in plants: New strategies to cope with in the foreseeable scenario

inferred← citeshttps://doi.org/10.1016/j.scienta.2022.111704openalex-snapshot

A Na+/H+ antiporter localized on the Golgi-to-vacuole transport system from Camellia sinensis, CsNHX6, plays a positive role in salt tolerance

inferred← citeshttps://doi.org/10.1038/s41598-023-47024-9openalex-snapshot

MdNup62 involved in salt and osmotic stress tolerance in apple

inferred← citeshttps://doi.org/10.1093/plcell/koae102openalex-snapshot

Structure, biogenesis, and evolution of thylakoid membranes

inferred← citeshttps://doi.org/10.1104/pp.17.01472openalex-snapshot

The Glucose Sensor MdHXK1 Phosphorylates a Tonoplast Na + /H + Exchanger to Improve Salt Tolerance

inferred← citeshttps://doi.org/10.1111/ppl.14589openalex-snapshot

Fungal endophyte symbionts enhance plant adaptation in Antarctic habitats

inferred← citeshttps://doi.org/10.1111/tpj.16395openalex-snapshot

MdHB7 ‐like positively modulates apple salt tolerance by promoting autophagic activity and Na+ efflux

inferred← citeshttps://doi.org/10.1186/s12870-026-09156-8openalex-snapshot

Genome-wide identification of the NHX gene family in sweet cherry and functional dissection of PavNHX37, a key salt tolerance gene

inferred← citeshttps://doi.org/10.17660/ejhs.2021/86.5.12openalex-snapshot

Salt stress in apple seedlings was mitigated by n-propyl dihydrojasmonate, a synthetic analog of jasmonic acid

inferred← citeshttps://doi.org/10.3389/fbioe.2019.00022openalex-snapshot

Antarctic Extremophiles: Biotechnological Alternative to Crop Productivity in Saline Soils

inferred← citeshttps://doi.org/10.3390/horticulturae10050510openalex-snapshot

Physiological Studies and Transcriptomic Analysis Reveal the Mechanism of Saline-Alkali Stress Resistance of Malus sieversii f. niedzwetzkyan

inferred← citeshttps://doi.org/10.3390/ijms21207712openalex-snapshot

Genome-Wide Identification of the Gossypium hirsutum NHX Genes Reveals That the Endosomal-Type GhNHX4A Is Critical for the Salt Tolerance of Cotton

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Genome-Wide Identification and Functional Characterization of the Cation Proton Antiporter (CPA) Family Related to Salt Stress Response in Radish (Raphanus sativus L.)

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