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Salt Tolerant Gene 1 contributes to salt tolerance by maintaining photosystem II activity in maize

https://doi.org/10.1111/pce.14578
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What this work says

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

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Lipid-protein Interactions in Crystals of Plant Light-harvesting Complex
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The Role of Phosphatidylglycerol in Photosynthesis
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Chapter 13 Biosynthesis and Function of Monogalactosyldiacylglycerol (MGDG), the Signature Lipid of Chloroplasts
inferredcites →https://doi.org/10.1007/s00122-018-3257-5openalex-snapshot
ZmAPRG, an uncharacterized gene, enhances acid phosphatase activity and Pi concentration in maize leaf during phosphate starvation
inferredcites →https://doi.org/10.1007/s11032-013-9895-zopenalex-snapshot
Fine mapping of quantitative trait loci for acid phosphatase activity in maize leaf under low phosphorus stress
inferredcites →https://doi.org/10.1007/s11033-014-3072-2openalex-snapshot
BcPMI2, isolated from non-heading Chinese cabbage encoding phosphomannose isomerase, improves stress tolerance in transgenic tobacco
inferredcites →https://doi.org/10.1007/s11099-010-0080-xopenalex-snapshot
Increase in unsaturated fatty acids in membrane lipids of Suaeda salsa L. enhances protection of photosystem II under high salinity
inferredcites →https://doi.org/10.1007/s12374-018-0162-zopenalex-snapshot
Molecular and Functional Characterization of ZmNF-YC14 in Transgenic Arabidopsis
inferredcites →https://doi.org/10.1016/0005-2728(90)90203-gopenalex-snapshot
Glycerolipids in various preparations of Photosystem II from spinach chloroplasts
inferredcites →https://doi.org/10.1016/j.cj.2021.05.010openalex-snapshot
ZmWRKY104 positively regulates salt tolerance by modulating ZmSOD4 expression in maize
inferredcites →https://doi.org/10.1016/j.envexpbot.2018.08.018openalex-snapshot
Silicon mediates sodium transport and partitioning in maize under moderate salt stress
inferredcites →https://doi.org/10.1016/j.jgg.2015.10.006openalex-snapshot
Efficiency and Inheritance of Targeted Mutagenesis in Maize Using CRISPR-Cas9
inferredcites →https://doi.org/10.1016/j.jplph.2010.09.019openalex-snapshot
A phytocyanin-related early nodulin-like gene, BcBCP1, cloned from Boea crassifolia enhances osmotic tolerance in transgenic tobacco
inferredcites →https://doi.org/10.1016/j.jplph.2019.01.012openalex-snapshot
Patellin protein family functions in plant development and stress response
inferredcites →https://doi.org/10.1016/j.pbi.2006.03.012openalex-snapshot
Non-vesicular and vesicular lipid trafficking involving plastids
inferredcites →https://doi.org/10.1016/j.phytochem.2004.06.021openalex-snapshot
Salt-induced lipid changes in Catharanthus roseus cultured cell suspensions
inferredcites →https://doi.org/10.1016/j.tplants.2015.10.011openalex-snapshot
Fatty Acid and Lipid Transport in Plant Cells
inferredcites →https://doi.org/10.1016/s0960-9822(00)00477-2openalex-snapshot
Membrane lipids: It’s only a phase
inferredcites →https://doi.org/10.1021/pr801083aopenalex-snapshot
Comparative Proteomic Analysis of Differentially Expressed Proteins in Shoots of Salicornia europaea under Different Salinity
inferredcites →https://doi.org/10.1038/s41467-022-29809-0openalex-snapshot
A dirigent family protein confers variation of Casparian strip thickness and salt tolerance in maize
inferredcites →https://doi.org/10.1038/s41477-019-0565-yopenalex-snapshot
A HAK family Na+ transporter confers natural variation of salt tolerance in maize
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.061500998openalex-snapshot
VIPP1 , a nuclear gene of Arabidopsis thaliana essential for thylakoid membrane formation
inferredcites →https://doi.org/10.1073/pnas.0704680104openalex-snapshot
Galactolipid synthesis in chloroplast inner envelope is essential for proper thylakoid biogenesis, photosynthesis, and embryogenesis
inferredcites →https://doi.org/10.1074/jbc.275.9.6509openalex-snapshot
Phosphatidylglycerol Is Involved in the Dimerization of Photosystem II
inferredcites →https://doi.org/10.1093/jxb/erab157openalex-snapshot
Maize transcription factor ZmNF-YC13 regulates plant architecture
inferredcites →https://doi.org/10.1093/molbev/msw054openalex-snapshot
MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets
inferredcites →https://doi.org/10.1093/pcp/pcf185openalex-snapshot
Phosphatidylglycerol is Essential for the Development of Thylakoid Membranes in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/plphys/kiab498openalex-snapshot
miR169q and NUCLEAR FACTOR YA8 enhance salt tolerance by activating PEROXIDASE1 expression in response to ROS
inferredcites →https://doi.org/10.1097/00024382-200209000-00016openalex-snapshot
Annual Review of Cell and Developmental Biology 2001
inferredcites →https://doi.org/10.1104/pp.002725openalex-snapshot
The pgp1 Mutant Locus of Arabidopsis Encodes a Phosphatidylglycerolphosphate Synthase with Impaired Activity
inferredcites →https://doi.org/10.1104/pp.114.238899openalex-snapshot
Maintenance of Chloroplast Structure and Function by Overexpression of the RiceMONOGALACTOSYLDIACYLGLYCEROL SYNTHASEGene Leads to Enhanced Salt Tolerance in Tobacco
inferredcites →https://doi.org/10.1104/pp.123.3.1047openalex-snapshot
Ionic and Osmotic Effects of NaCl-Induced Inactivation of Photosystems I and II in Synechococcus sp.
inferredcites →https://doi.org/10.1104/pp.124.2.795openalex-snapshot
Direct Evidence for Requirement of Phosphatidylglycerol in Photosystem II of Photosynthesis
inferredcites →https://doi.org/10.1104/pp.125.4.1842openalex-snapshot
Unsaturated Fatty Acids in Membrane Lipids Protect the Photosynthetic Machinery against Salt-Induced Damage inSynechococcus
inferredcites →https://doi.org/10.1111/j.1399-3054.2012.01623.xopenalex-snapshot
Effects of salt stress on the structure and function of the photosynthetic apparatus in Cucumis sativus and its protection by exogenous putrescine
inferredcites →https://doi.org/10.1111/j.1432-1033.1994.tb18785.xopenalex-snapshot
Heterogenous lipid distribution among chlorophyll‐binding proteins of photosystem II in maize mesophyll chloroplasts
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01487.xopenalex-snapshot
Genes and salt tolerance: bringing them together
inferredcites →https://doi.org/10.1111/nph.14882openalex-snapshot
A retrotransposon in an HKT1 family sodium transporter causes variation of leaf Na + exclusion and salt tolerance in maize
inferredcites →https://doi.org/10.1111/nph.15605openalex-snapshot
A domestication‐associated reduction in K+‐preferring HKT transporter activity underlies maize shoot K+ accumulation and salt tolerance
inferredcites →https://doi.org/10.1111/tpj.14184openalex-snapshot
An updated gene atlas for maize reveals organ‐specific and stress‐induced genes
inferredcites →https://doi.org/10.1126/science.42.1074.161openalex-snapshot
The Proceedings of the National Academy of Sciences
inferredcites →https://doi.org/10.1146/annurev.cellbio.042308.113414openalex-snapshot
Mechanisms of Lipid Transport Involved in Organelle Biogenesis in Plant Cells
inferredcites →https://doi.org/10.1199/tab.0161openalex-snapshot
Acyl-Lipid Metabolism
inferredcites →https://doi.org/10.1214/009053606000000425openalex-snapshot
On the Benjamini–Hochberg method
inferredcites →https://doi.org/10.1371/journal.pone.0104423openalex-snapshot
Bioinformatic Indications That COPI- and Clathrin-Based Transport Systems Are Not Present in Chloroplasts: An Arabidopsis Model
inferredcites →https://doi.org/10.1371/journal.pone.0148572openalex-snapshot
Overexpression of the NDR1/HIN1-Like Gene NHL6 Modifies Seed Germination in Response to Abscisic Acid and Abiotic Stresses in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pone.0221949openalex-snapshot
Overexpression of the maize transcription factor ZmVQ52 accelerates leaf senescence in Arabidopsis

What points at this work

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

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Chlorophyll Fluorescence Explains More than 70% of Moso Bamboo Forests Productivity Variations During the Leaf-Expansion Stage
inferred← citeshttps://doi.org/10.2139/ssrn.4790089openalex-extracted
Chlorophyll Fluorescence of Moso Bamboo at the Leaf-Expansion Stage in Response to the Environment and its Effect on Gross Primary Productivity
inferred← citeshttps://doi.org/10.1002/9781394192595.ch18openalex-snapshot
Customizing Crops for Salinity Tolerance: Toward Resilient Crop Production Systems
inferred← citeshttps://doi.org/10.1007/s00299-023-03003-yopenalex-snapshot
Thermosensitivity of pollen: a molecular perspective
inferred← citeshttps://doi.org/10.1007/s11104-025-08067-1openalex-snapshot
The halophyte-derived salt-responsive gene HgS3 enhances salinity tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11427-025-3022-6openalex-snapshot
Decades’ progress and prospects on maize functional genomics and molecular breeding
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.121499openalex-snapshot
Synergistic responses of physiological, transcriptomic, and metabolomic levels in soybean (Glycine max (Linn.) Merr) under combined salt-alkali stress
inferred← citeshttps://doi.org/10.1016/j.jafr.2026.103138openalex-snapshot
Genome-scale analysis of maize ALA genes identifies ZmALA9 as a regulator of saline-alkali tolerance during germination
inferred← citeshttps://doi.org/10.1016/j.jenvman.2024.121185openalex-snapshot
Effects of chlorophyll fluorescence on environment and gross primary productivity of moso bamboo during the leaf-expansion stage
inferred← citeshttps://doi.org/10.1016/j.jplph.2025.154677openalex-snapshot
The JmjC domain-containing histone demethylase ZmJMJ703 orchestrates salt stress adaptation in maize
inferred← citeshttps://doi.org/10.1016/j.molp.2023.07.005openalex-snapshot
Genetic and molecular exploration of maize environmental stress resilience: Toward sustainable agriculture
inferred← citeshttps://doi.org/10.1016/j.synbio.2024.06.008openalex-snapshot
Advances in stress-tolerance elements for microbial cell factories
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Genomics‐assisted breeding for designing salinity‐smart future crops
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Autophagy Regulates Plant Tolerance to Submergence by Modulating Photosynthesis
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GhWRKY41 Confers Salt Tolerance by Enhancing Photosynthetic Capacity in Cotton ( Gossypium hirsutum )
inferred← citeshttps://doi.org/10.1186/s12870-024-05773-3openalex-snapshot
Physiological, transcriptomic, and metabolomic analyses of the chilling stress response in two melon (Cucumis melo L.) genotypes
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Integrative transcriptomic and metabolomic analysis elucidates the vital pathways underlying the differences in salt stress responses between two chickpea (Cicer arietinum L.) varieties
inferred← citeshttps://doi.org/10.21926/obm.genet.2402232openalex-snapshot
Salinity Stress in Maize: Consequences, Tolerance Mechanisms, and Management Strategies
inferred← citeshttps://doi.org/10.3390/agronomy13102484openalex-snapshot
Genome-Wide Identification of the Phytocyanin Gene Family and Its Potential Function in Salt Stress in Soybean (Glycine max (L.) Merr.)
inferred← citeshttps://doi.org/10.3390/horticulturae11010017openalex-snapshot
Transcriptome-Wide Identification of miRNAs and Their Targets During Riboflavin-Promoted Dormancy Release in Lilium ‘Siberia’
inferred← citeshttps://doi.org/10.3390/plants14132054openalex-snapshot
The Transcription Factor ZmMYBR24 Gene Is Involved in a Variety of Abiotic Stresses in Maize (Zea mays L.)
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