Aug 2026· Journal of Sustainable Agriculture and Environment· Vol 5· 0 citations· 59 references
TL;DR
The novel synthesis offered here repositions epigenetic regulation, specifically H3K27ac and H3K27me3 dynamics at NRT2 , GS, and storage protein loci, as a principal determinant of cultivar‐specific nitrogen use efficiency operating independently of DNA sequence variation.
Abstract
Nitrogen is the most yield‐limiting macronutrient in wheat (
Triticum aestivum
L.), yet no prior review has integrated nitrogen deficiency symptomology, physiology, and multi‐omics approaches encompassing transcriptomics, proteomics, metabolomics, and epigenomics into a single mechanistic framework for wheat specifically. Wheat's hexaploid genome, distinctive nitrogen remobilisation architecture, and unique grain protein composition generate responses that cannot be extrapolated from diploid cereals. Two stress modes must be distinguished: acute nitrogen withdrawal induces rapid NLP7‐mediated
NRT2
transporter activation within minutes, whereas chronic low‐nitrogen supply drives sustained epigenetic and root architectural adaptations over weeks. Post‐translational modifications, including NRT2 phosphorylation and thioredoxin‐regulated starch biosynthetic enzyme activity, govern nitrogen remobilisation dynamics independently of transcript abundance. The novel synthesis offered here repositions epigenetic regulation, specifically H3K27ac and H3K27me3 dynamics at
NRT2
, GS, and storage protein loci, as a principal determinant of cultivar‐specific nitrogen use efficiency operating independently of DNA sequence variation. Sub‐genome homologue epigenetic asymmetry in hexaploid wheat provides phenotypic buffering capacity unavailable to diploid cereals. The rhizosphere microbiome is identified as an integral co‐regulator of nitrogen acquisition whose molecular interactions with plant signalling networks remain uncharacterised. Three wheat‐specific dimensions absent from rice and maize are identified: sub‐genome epigenetic asymmetry, an unusually high nitrogen harvest index amplifying remobilisation failure costs, and a gliadin‐glutenin quality trade‐off driven by differential chromatin accessibility. Five knowledge gaps define the immediate research agenda: single‐cell omics under nitrogen deficiency, developmental time‐series multi‐omics, CRISPR validation of NUE quantitative trait locus candidates, molecular characterisation of organic versus mineral nitrogen responses, and climate‐nitrogen epigenomics under elevated carbon dioxide. Wheat‐specific multi‐omics investment is required as a primary research objective rather than an agronomic supplement.
This study provides a systems-level view of posttranscriptional regulation during salt stress in wheat and identifies potential targets for enhancing salt tolerance.
J. Zang, Qian Zhang, Yuyu Zhang et al.· Plant Physiology· 0 citations
Sulfur availability is a major modulator of iron-responsive phenotypic, transcriptional, and metabolic traits in durum wheat and provides a systems-level framework for future functional studies of Fe/S crosstalk.
E. Coppa, Mutsumi Watanabe, Moez Maghrebi et al.· New Phytologist· 0 citations
Synthetic nitrogen fertilizers have greatly increased crop yields, yet much of the applied nitrogen is lost from agroecosystems and contributes to environmental pollution and higher economic costs. Improving nitrogen uptake efficiency (NUpE) benefits from understanding how root system architecture (RSA) governs soil nitrogen capture. Although root traits have seldom been explicit breeding targets, selection for variation in above-ground nitrogen accumulation has also likely shaped differences in RSA. The Illinois Protein Strain Recombinant Inbred population, derived from more than a century of divergent selection for seed protein concentration, offers a powerful resource for dissecting RSA variation. Using multi-year field phenotyping of excavated root crowns and genome-wide association analysis, we identified a quantitative trait locus on chromosome 10 containing E1OGDH1, which encodes the E1 subunit of the 2-oxoglutarate dehydrogenase (OGDH) complex. OGDH performs a key step in the tricarboxylic acid cycle that also modulates 2-oxoglutarate, an important entry point into nitrogen metabolism and a co-factor for enzymes involved in hormone and secondary product synthesis. Long-read sequencing of inbreds derived from the divergent IHP and ILP parental populations revealed promoter polymorphisms defining E1OGDH1 alleles and differed in E1OGDH1 expression in root tissue. Field experiments in IPSRI lines carrying IHP- or ILP-associated E1OGDH1 alleles showed differences in root architectural traits over two years. CRISPR-Cas9 knockout mutants confirmed a functional role for E1OGDH1 in whole-plant performance and nitrogen-responsive root development. Mutants were shorter, had reduced biomass, and exhibited altered architectural responses to soil nitrogen levels. Transcriptome analysis further showed that loss of E1OGDH1 altered basal and nitrogen-responsive expression of genes associated with root development and nitrogen uptake and metabolism. Together, these findings identify E1OGDH1 as a strong candidate quantitative regulator of maize RSA and nitrogen plasticity, suggesting that central carbon–nitrogen metabolic genes can contribute to root developmental responses relevant to NUpE.
Michelle S. Cho, Zhengbin Liu, Collin Luebbert et al.· bioRxiv· 0 citations
A four-tier closed-loop conceptual framework comprising signal perception, transport reprogramming, metabolic redistribution, and genetic redesign is developed that yields three testable predictions: the sequential activation of regulatory tiers; a quantitative relationship between Ca2+ signal amplitude and the extent of C–N metabolic redistribution; and salt-concentration thresholds that distinguish basal homeostatic buffering from full adaptive reprogramming.
Ran-Ran Liu, Long-Yu Wang, Shulei Wang et al.· Frontiers in Plant Science· 0 citations
Soil salinization severely limits forage crop productivity, yet the regulatory networks that govern salt stress adaptation in alfalfa, a moderately salt-tolerant leguminous forage, remain largely unexplored. Here, we examined the physiological and transcriptomic dynamics of alfalfa leaves under 200 mM NaCl stress across three time points. Salt stress induced a progressive elevation of the Na+/K+ ratio, biphasic activation of antioxidant enzymes and concurrent accumulation of malondialdehyde. Time-course RNA-seq analysis identified 3631 differentially expressed genes (DEGs) and 132 core salt-responsive transcription factors (TFs). Pathway and functional annotation analyses indicated that these DEGs were prominently involved in cell wall biogenesis, redox homeostasis, and the carotenoid biosynthesis pathway, with carotenoid accumulation strongly activated under salt stress. Using weighted gene co-expression network analysis (WGCNA), nine distinct co-expression clusters were constructed. Notably, the brown module, which showed a positive correlation with Na+ accumulation and the Na+/K+ ratio, was significantly enriched in the plant hormone signal transduction pathway, within which 72.7% of the enriched genes belonged to the TIFY family. Among them, a core hub gene, MsTIFY11B, was isolated for functional characterization. Subcellular localization demonstrated that MsTIFY11B is exclusively localized to the nucleus. Heterologous expression in yeast showed that MsTIFY11B overexpression enhanced tolerance to salinity and alkalinity, whereas it conferred negligible protection against mannitol-induced drought stress. Taken together, our findings provide a comprehensive temporal framework of the alfalfa transcriptomic response to salinity and suggest that MsTIFY11B may contribute to salt–alkali tolerance, making it a promising candidate for further functional characterization and potential application in the development of stress-adapted alfalfa varieties.
Lin Cheng, Yan-Feng Liu, Qing-Chun Liu et al.· Plants· 0 citations
A genomics‐enabled roadmap for developing heat‐resilient rice cultivars under intensifying global warming and supporting sustainable global rice production is outlined.
Prabhat Rana, Chanderkant Chaudhary, Rajat Pruthi et al.· The Plant Genome· 0 citations
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